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You searched for subject:(genetic epilepsy). Showing records 1 – 30 of 40 total matches.

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University of Melbourne

1. Parsons, Nicholas James. Using single subject manual independent component analysis on resting-state fMRI data.

Degree: 2019, University of Melbourne

 It is important to understand the influence of common artefacts when processing fMRI data, and how best to remove these in order to produce reliable… (more)

Subjects/Keywords: FMRI; epilepsy; genetic generalised epilepsy; ICA

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APA (6th Edition):

Parsons, N. J. (2019). Using single subject manual independent component analysis on resting-state fMRI data. (Masters Thesis). University of Melbourne. Retrieved from http://hdl.handle.net/11343/227442

Chicago Manual of Style (16th Edition):

Parsons, Nicholas James. “Using single subject manual independent component analysis on resting-state fMRI data.” 2019. Masters Thesis, University of Melbourne. Accessed January 15, 2021. http://hdl.handle.net/11343/227442.

MLA Handbook (7th Edition):

Parsons, Nicholas James. “Using single subject manual independent component analysis on resting-state fMRI data.” 2019. Web. 15 Jan 2021.

Vancouver:

Parsons NJ. Using single subject manual independent component analysis on resting-state fMRI data. [Internet] [Masters thesis]. University of Melbourne; 2019. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/11343/227442.

Council of Science Editors:

Parsons NJ. Using single subject manual independent component analysis on resting-state fMRI data. [Masters Thesis]. University of Melbourne; 2019. Available from: http://hdl.handle.net/11343/227442


University of Melbourne

2. Perucca, Piero Cesare. The role of genetic factors in the aetiology of focal epilepsy and in the outcomes of epilepsy treatment.

Degree: 2017, University of Melbourne

Epilepsy is one of the most common neurological disorders, affecting people of all ages, races, social classes, and nationalities. It is characterised by an enduring… (more)

Subjects/Keywords: Epilepsy; Focal; Genetics; Genetic testing; Whole exome sequencing; Temporal lobe epilepsy

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APA (6th Edition):

Perucca, P. C. (2017). The role of genetic factors in the aetiology of focal epilepsy and in the outcomes of epilepsy treatment. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/194133

Chicago Manual of Style (16th Edition):

Perucca, Piero Cesare. “The role of genetic factors in the aetiology of focal epilepsy and in the outcomes of epilepsy treatment.” 2017. Doctoral Dissertation, University of Melbourne. Accessed January 15, 2021. http://hdl.handle.net/11343/194133.

MLA Handbook (7th Edition):

Perucca, Piero Cesare. “The role of genetic factors in the aetiology of focal epilepsy and in the outcomes of epilepsy treatment.” 2017. Web. 15 Jan 2021.

Vancouver:

Perucca PC. The role of genetic factors in the aetiology of focal epilepsy and in the outcomes of epilepsy treatment. [Internet] [Doctoral dissertation]. University of Melbourne; 2017. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/11343/194133.

Council of Science Editors:

Perucca PC. The role of genetic factors in the aetiology of focal epilepsy and in the outcomes of epilepsy treatment. [Doctoral Dissertation]. University of Melbourne; 2017. Available from: http://hdl.handle.net/11343/194133


University of Melbourne

3. KIM, TAE HWAN. Genetic, metabolic and pharmacological modulation of seizure susceptibility in mouse models of genetic epilepsy.

Degree: 2013, University of Melbourne

Epilepsy is a common neurological disorder that is poorly understood. A large proportion of epilepsies have a strong familial component. The GABAA γ2 (R43Q) mutation… (more)

Subjects/Keywords: epilepsy; diet; genetic; mouse model; absence epilepsy; febrile seizures

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APA (6th Edition):

KIM, T. H. (2013). Genetic, metabolic and pharmacological modulation of seizure susceptibility in mouse models of genetic epilepsy. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/38492

Chicago Manual of Style (16th Edition):

KIM, TAE HWAN. “Genetic, metabolic and pharmacological modulation of seizure susceptibility in mouse models of genetic epilepsy.” 2013. Doctoral Dissertation, University of Melbourne. Accessed January 15, 2021. http://hdl.handle.net/11343/38492.

MLA Handbook (7th Edition):

KIM, TAE HWAN. “Genetic, metabolic and pharmacological modulation of seizure susceptibility in mouse models of genetic epilepsy.” 2013. Web. 15 Jan 2021.

Vancouver:

KIM TH. Genetic, metabolic and pharmacological modulation of seizure susceptibility in mouse models of genetic epilepsy. [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/11343/38492.

Council of Science Editors:

KIM TH. Genetic, metabolic and pharmacological modulation of seizure susceptibility in mouse models of genetic epilepsy. [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/38492


University of Adelaide

4. Wallace, Robyn, 1967-. Molecular genetics of epilepsy / by Robyn Wallace.

Degree: 1997, University of Adelaide

Subjects/Keywords: Epilepsy Genetic aspects.

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APA (6th Edition):

Wallace, Robyn, 1. (1997). Molecular genetics of epilepsy / by Robyn Wallace. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/19283

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wallace, Robyn, 1967-. “Molecular genetics of epilepsy / by Robyn Wallace.” 1997. Thesis, University of Adelaide. Accessed January 15, 2021. http://hdl.handle.net/2440/19283.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wallace, Robyn, 1967-. “Molecular genetics of epilepsy / by Robyn Wallace.” 1997. Web. 15 Jan 2021.

Vancouver:

Wallace, Robyn 1. Molecular genetics of epilepsy / by Robyn Wallace. [Internet] [Thesis]. University of Adelaide; 1997. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/2440/19283.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wallace, Robyn 1. Molecular genetics of epilepsy / by Robyn Wallace. [Thesis]. University of Adelaide; 1997. Available from: http://hdl.handle.net/2440/19283

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Melbourne

5. Casillas Espinosa, Pablo Miguel. Genetic and molecular determinants of acquired and genetic epilepsy.

Degree: 2016, University of Melbourne

 Introduction: Despite the differences in the pathophysiological mechanisms and clinical features of both genetic and acquired epilepsies, dysfunction of both voltage- and ligand-gated ion channels… (more)

Subjects/Keywords: epileptogenesis; epilepsy; acquired epilepsy; genetic epilepsy; T-type calcium channels; TARPs; AMPA receptors; whole genome sequencing; GAERS; Z944

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Casillas Espinosa, P. M. (2016). Genetic and molecular determinants of acquired and genetic epilepsy. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/108875

Chicago Manual of Style (16th Edition):

Casillas Espinosa, Pablo Miguel. “Genetic and molecular determinants of acquired and genetic epilepsy.” 2016. Doctoral Dissertation, University of Melbourne. Accessed January 15, 2021. http://hdl.handle.net/11343/108875.

MLA Handbook (7th Edition):

Casillas Espinosa, Pablo Miguel. “Genetic and molecular determinants of acquired and genetic epilepsy.” 2016. Web. 15 Jan 2021.

Vancouver:

Casillas Espinosa PM. Genetic and molecular determinants of acquired and genetic epilepsy. [Internet] [Doctoral dissertation]. University of Melbourne; 2016. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/11343/108875.

Council of Science Editors:

Casillas Espinosa PM. Genetic and molecular determinants of acquired and genetic epilepsy. [Doctoral Dissertation]. University of Melbourne; 2016. Available from: http://hdl.handle.net/11343/108875


Brandeis University

6. Feinbaum, Rhonda. Parent Experience with Genetic Testing for Pediatric Epileptic Encephalopathy: What Can We Do Better?.

Degree: 2018, Brandeis University

 Epileptic encephalopathies are a group of severe childhood disorders characterized by seizures and cognitive and developmental deficits. Genetic testing is frequently used in the diagnosis… (more)

Subjects/Keywords: epileptic encephalopathy; pediatric epilepsy; genetic testing; parent experience; genetic counselor; understanding; family

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APA (6th Edition):

Feinbaum, R. (2018). Parent Experience with Genetic Testing for Pediatric Epileptic Encephalopathy: What Can We Do Better?. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/35681

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Feinbaum, Rhonda. “Parent Experience with Genetic Testing for Pediatric Epileptic Encephalopathy: What Can We Do Better?.” 2018. Thesis, Brandeis University. Accessed January 15, 2021. http://hdl.handle.net/10192/35681.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Feinbaum, Rhonda. “Parent Experience with Genetic Testing for Pediatric Epileptic Encephalopathy: What Can We Do Better?.” 2018. Web. 15 Jan 2021.

Vancouver:

Feinbaum R. Parent Experience with Genetic Testing for Pediatric Epileptic Encephalopathy: What Can We Do Better?. [Internet] [Thesis]. Brandeis University; 2018. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10192/35681.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Feinbaum R. Parent Experience with Genetic Testing for Pediatric Epileptic Encephalopathy: What Can We Do Better?. [Thesis]. Brandeis University; 2018. Available from: http://hdl.handle.net/10192/35681

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Hong Kong

7. Guo, Youling. Genetic and genomic mapping of common diseases.

Degree: 2012, University of Hong Kong

  Genome-wide mapping of susceptibility genes was conducted in two complex disorders of hypertension and epilepsy, allowing the dissection of the genetic architecture of these… (more)

Subjects/Keywords: Epilepsy - Genetic aspects.; Hypertension - Genetic aspects.

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APA (6th Edition):

Guo, Y. (2012). Genetic and genomic mapping of common diseases. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/188267

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Guo, Youling. “Genetic and genomic mapping of common diseases.” 2012. Thesis, University of Hong Kong. Accessed January 15, 2021. http://hdl.handle.net/10722/188267.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Guo, Youling. “Genetic and genomic mapping of common diseases.” 2012. Web. 15 Jan 2021.

Vancouver:

Guo Y. Genetic and genomic mapping of common diseases. [Internet] [Thesis]. University of Hong Kong; 2012. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10722/188267.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Guo Y. Genetic and genomic mapping of common diseases. [Thesis]. University of Hong Kong; 2012. Available from: http://hdl.handle.net/10722/188267

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Melbourne

8. Scheffer, Ingrid Eileen. Inherited epilepsy syndromes in multiplex families.

Degree: 1988, University of Melbourne

 The epilepsies are a common group of disorders where genetic factors are known to be important. The challenging search for genes for the idiopathic epilepsies… (more)

Subjects/Keywords: genetic aspects of epilepsy

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APA (6th Edition):

Scheffer, I. E. (1988). Inherited epilepsy syndromes in multiplex families. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/35866

Chicago Manual of Style (16th Edition):

Scheffer, Ingrid Eileen. “Inherited epilepsy syndromes in multiplex families.” 1988. Doctoral Dissertation, University of Melbourne. Accessed January 15, 2021. http://hdl.handle.net/11343/35866.

MLA Handbook (7th Edition):

Scheffer, Ingrid Eileen. “Inherited epilepsy syndromes in multiplex families.” 1988. Web. 15 Jan 2021.

Vancouver:

Scheffer IE. Inherited epilepsy syndromes in multiplex families. [Internet] [Doctoral dissertation]. University of Melbourne; 1988. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/11343/35866.

Council of Science Editors:

Scheffer IE. Inherited epilepsy syndromes in multiplex families. [Doctoral Dissertation]. University of Melbourne; 1988. Available from: http://hdl.handle.net/11343/35866


University of Hong Kong

9. Fong, Chung-yan, Gardian. Electro-clinical study and gene mapping of epilepsies.

Degree: 2002, University of Hong Kong

Subjects/Keywords: Epilepsy in children - Genetic aspects.

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Fong, Chung-yan, G. (2002). Electro-clinical study and gene mapping of epilepsies. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/29438

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Fong, Chung-yan, Gardian. “Electro-clinical study and gene mapping of epilepsies.” 2002. Thesis, University of Hong Kong. Accessed January 15, 2021. http://hdl.handle.net/10722/29438.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Fong, Chung-yan, Gardian. “Electro-clinical study and gene mapping of epilepsies.” 2002. Web. 15 Jan 2021.

Vancouver:

Fong, Chung-yan G. Electro-clinical study and gene mapping of epilepsies. [Internet] [Thesis]. University of Hong Kong; 2002. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10722/29438.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Fong, Chung-yan G. Electro-clinical study and gene mapping of epilepsies. [Thesis]. University of Hong Kong; 2002. Available from: http://hdl.handle.net/10722/29438

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Vanderbilt University

10. Huang, Xuan. Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities.

Degree: PhD, Neuroscience, 2014, Vanderbilt University

Epilepsy is a neurological disorder affecting almost one percent of the population, and genetic epilepsy are those caused by a presumed or unknown genetic factor(s).… (more)

Subjects/Keywords: GABA(A) receptors; GABRG2; genetic epilepsy; mutation; therapy

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APA (6th Edition):

Huang, X. (2014). Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14755

Chicago Manual of Style (16th Edition):

Huang, Xuan. “Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed January 15, 2021. http://hdl.handle.net/1803/14755.

MLA Handbook (7th Edition):

Huang, Xuan. “Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities.” 2014. Web. 15 Jan 2021.

Vancouver:

Huang X. Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1803/14755.

Council of Science Editors:

Huang X. Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/14755


Michigan State University

11. Feng, Huijie. Mechanisms of GNAO1-associated neurological disorders.

Degree: 2019, Michigan State University

Thesis Ph. D. Michigan State University. Pharmacology and Toxicology 2019.

Tremendous advances in the genetics of neurodevelopmental disorders have markedly improved the understanding of disease… (more)

Subjects/Keywords: Nervous system – Diseases – Genetic aspects – Animal models; Infantile spasms – Genetic aspects – Animal models; Epilepsy – Genetic aspects – Animal models; Pharmacology

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APA (6th Edition):

Feng, H. (2019). Mechanisms of GNAO1-associated neurological disorders. (Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:48132

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Feng, Huijie. “Mechanisms of GNAO1-associated neurological disorders.” 2019. Thesis, Michigan State University. Accessed January 15, 2021. http://etd.lib.msu.edu/islandora/object/etd:48132.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Feng, Huijie. “Mechanisms of GNAO1-associated neurological disorders.” 2019. Web. 15 Jan 2021.

Vancouver:

Feng H. Mechanisms of GNAO1-associated neurological disorders. [Internet] [Thesis]. Michigan State University; 2019. [cited 2021 Jan 15]. Available from: http://etd.lib.msu.edu/islandora/object/etd:48132.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Feng H. Mechanisms of GNAO1-associated neurological disorders. [Thesis]. Michigan State University; 2019. Available from: http://etd.lib.msu.edu/islandora/object/etd:48132

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Michigan State University

12. Larrivee, Casandra Lynn. Analysis of mice carrying human GNAO1 mutations as a model to study associated movement disorders.

Degree: 2019, Michigan State University

Thesis M.S. Michigan State University. Comparative Medicine and Integrative Biology 2019

"Due to the increased availability of genetic screening, patients with idiopathic epilepsy and movement… (more)

Subjects/Keywords: Movement disorders – Genetic aspects – Animal models; Epilepsy – Genetic aspects – Animal models; Convulsions – Genetic aspects – Animal models; Neurosciences; Pharmacology

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Larrivee, C. L. (2019). Analysis of mice carrying human GNAO1 mutations as a model to study associated movement disorders. (Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:47791

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Larrivee, Casandra Lynn. “Analysis of mice carrying human GNAO1 mutations as a model to study associated movement disorders.” 2019. Thesis, Michigan State University. Accessed January 15, 2021. http://etd.lib.msu.edu/islandora/object/etd:47791.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Larrivee, Casandra Lynn. “Analysis of mice carrying human GNAO1 mutations as a model to study associated movement disorders.” 2019. Web. 15 Jan 2021.

Vancouver:

Larrivee CL. Analysis of mice carrying human GNAO1 mutations as a model to study associated movement disorders. [Internet] [Thesis]. Michigan State University; 2019. [cited 2021 Jan 15]. Available from: http://etd.lib.msu.edu/islandora/object/etd:47791.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Larrivee CL. Analysis of mice carrying human GNAO1 mutations as a model to study associated movement disorders. [Thesis]. Michigan State University; 2019. Available from: http://etd.lib.msu.edu/islandora/object/etd:47791

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Vanderbilt University

13. Misra, Sunita N. Characterization of Mutant Human Brain Sodium Channels Associated with Familial Epilepsy.

Degree: PhD, Pharmacology, 2008, Vanderbilt University

 Investigating genetic forms of epilepsy allows for improved understanding of epilepsy pathophysiology in general. Mutations in voltage-gated sodium channels are a frequent cause of genetic(more)

Subjects/Keywords: Sodium channels  – Pathophysiology; electrophysiology; epilepsy; Epilepsy  – Genetic aspects; Epilepsy  – Molecular aspects

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APA (6th Edition):

Misra, S. N. (2008). Characterization of Mutant Human Brain Sodium Channels Associated with Familial Epilepsy. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12753

Chicago Manual of Style (16th Edition):

Misra, Sunita N. “Characterization of Mutant Human Brain Sodium Channels Associated with Familial Epilepsy.” 2008. Doctoral Dissertation, Vanderbilt University. Accessed January 15, 2021. http://hdl.handle.net/1803/12753.

MLA Handbook (7th Edition):

Misra, Sunita N. “Characterization of Mutant Human Brain Sodium Channels Associated with Familial Epilepsy.” 2008. Web. 15 Jan 2021.

Vancouver:

Misra SN. Characterization of Mutant Human Brain Sodium Channels Associated with Familial Epilepsy. [Internet] [Doctoral dissertation]. Vanderbilt University; 2008. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1803/12753.

Council of Science Editors:

Misra SN. Characterization of Mutant Human Brain Sodium Channels Associated with Familial Epilepsy. [Doctoral Dissertation]. Vanderbilt University; 2008. Available from: http://hdl.handle.net/1803/12753

14. Chatzistefanidis, Dimitrios. Ο μεταβολισμός του βαλπροϊκού οξέος: o ρόλος των πολυμορφισμών των γονιδίων UGT1A6 και UGT2B7 στην ηπατική γλυκουρονίδωση του βαλπροϊκού οξέος σε ανήλικους και ενήλικους ασθενείς.

Degree: 2016, University of Ioannina; Πανεπιστήμιο Ιωαννίνων

Aim: To clarify the impact of UGT1A6 and UGT2B7 gene polymorphisms on the metabolism of valproic acid.Method/Patients: Adult patients (age ≥ 16 years) hospitalized in… (more)

Subjects/Keywords: Βαλπροϊκό οξύ; Γενετικοί πολυμορφισμοί; Επιληψία; Valproic acid; Genetic polymorphisms; Epilepsy; UGT1A6; UGT2B7

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APA (6th Edition):

Chatzistefanidis, D. (2016). Ο μεταβολισμός του βαλπροϊκού οξέος: o ρόλος των πολυμορφισμών των γονιδίων UGT1A6 και UGT2B7 στην ηπατική γλυκουρονίδωση του βαλπροϊκού οξέος σε ανήλικους και ενήλικους ασθενείς. (Thesis). University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Retrieved from http://hdl.handle.net/10442/hedi/43395

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chatzistefanidis, Dimitrios. “Ο μεταβολισμός του βαλπροϊκού οξέος: o ρόλος των πολυμορφισμών των γονιδίων UGT1A6 και UGT2B7 στην ηπατική γλυκουρονίδωση του βαλπροϊκού οξέος σε ανήλικους και ενήλικους ασθενείς.” 2016. Thesis, University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Accessed January 15, 2021. http://hdl.handle.net/10442/hedi/43395.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chatzistefanidis, Dimitrios. “Ο μεταβολισμός του βαλπροϊκού οξέος: o ρόλος των πολυμορφισμών των γονιδίων UGT1A6 και UGT2B7 στην ηπατική γλυκουρονίδωση του βαλπροϊκού οξέος σε ανήλικους και ενήλικους ασθενείς.” 2016. Web. 15 Jan 2021.

Vancouver:

Chatzistefanidis D. Ο μεταβολισμός του βαλπροϊκού οξέος: o ρόλος των πολυμορφισμών των γονιδίων UGT1A6 και UGT2B7 στην ηπατική γλυκουρονίδωση του βαλπροϊκού οξέος σε ανήλικους και ενήλικους ασθενείς. [Internet] [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2016. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10442/hedi/43395.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chatzistefanidis D. Ο μεταβολισμός του βαλπροϊκού οξέος: o ρόλος των πολυμορφισμών των γονιδίων UGT1A6 και UGT2B7 στην ηπατική γλυκουρονίδωση του βαλπροϊκού οξέος σε ανήλικους και ενήλικους ασθενείς. [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2016. Available from: http://hdl.handle.net/10442/hedi/43395

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Vanderbilt University

15. Hawkins, Nicole Alise. Identification of epilepsy modifier genes in a mouse model.

Degree: PhD, Neuroscience, 2013, Vanderbilt University

Epilepsy is a neurological disorder affecting approximately 3 million Americans. Two-thirds of patients diagnosed with epilepsy have no known cause for their disease, however recent… (more)

Subjects/Keywords: voltage-gated ion channels; voltage-gated sodium channels; mouse models; Epilepsy; genetic modifier; seizure

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APA (6th Edition):

Hawkins, N. A. (2013). Identification of epilepsy modifier genes in a mouse model. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14623

Chicago Manual of Style (16th Edition):

Hawkins, Nicole Alise. “Identification of epilepsy modifier genes in a mouse model.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed January 15, 2021. http://hdl.handle.net/1803/14623.

MLA Handbook (7th Edition):

Hawkins, Nicole Alise. “Identification of epilepsy modifier genes in a mouse model.” 2013. Web. 15 Jan 2021.

Vancouver:

Hawkins NA. Identification of epilepsy modifier genes in a mouse model. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1803/14623.

Council of Science Editors:

Hawkins NA. Identification of epilepsy modifier genes in a mouse model. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/14623


Stellenbosch University

16. Carr, Jonathan. Familial adult myoclonus epilepsy : a clinical, neurophysiological and genetic study of a familial form of myoclonic epilepsy.

Degree: Medicine, 2009, Stellenbosch University

Thesis (DMed (Medicine. Internal Medicine)) – University of Stellenbosch, 2009.

ENGLISH ABSTRACT: Progressive Myoclonic Epilepsies (PME) are characterized by progressive neurological impairment with myoclonus, seizures and… (more)

Subjects/Keywords: Internal medicine; Myoclonus; Epilepsy; Genetic disorders

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APA (6th Edition):

Carr, J. (2009). Familial adult myoclonus epilepsy : a clinical, neurophysiological and genetic study of a familial form of myoclonic epilepsy. (Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/1201

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Carr, Jonathan. “Familial adult myoclonus epilepsy : a clinical, neurophysiological and genetic study of a familial form of myoclonic epilepsy.” 2009. Thesis, Stellenbosch University. Accessed January 15, 2021. http://hdl.handle.net/10019.1/1201.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Carr, Jonathan. “Familial adult myoclonus epilepsy : a clinical, neurophysiological and genetic study of a familial form of myoclonic epilepsy.” 2009. Web. 15 Jan 2021.

Vancouver:

Carr J. Familial adult myoclonus epilepsy : a clinical, neurophysiological and genetic study of a familial form of myoclonic epilepsy. [Internet] [Thesis]. Stellenbosch University; 2009. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10019.1/1201.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Carr J. Familial adult myoclonus epilepsy : a clinical, neurophysiological and genetic study of a familial form of myoclonic epilepsy. [Thesis]. Stellenbosch University; 2009. Available from: http://hdl.handle.net/10019.1/1201

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Arizona

17. Al-Humayyd, Mohammad Saad Abdulrahman. Birth defects in epilepsy: role of phenytoin and convulsion .

Degree: 1979, University of Arizona

Subjects/Keywords: Abnormalities, Human  – Genetic aspects.; Epilepsy  – Genetic aspects.; Teratogenic agents.

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APA (6th Edition):

Al-Humayyd, M. S. A. (1979). Birth defects in epilepsy: role of phenytoin and convulsion . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/557257

Chicago Manual of Style (16th Edition):

Al-Humayyd, Mohammad Saad Abdulrahman. “Birth defects in epilepsy: role of phenytoin and convulsion .” 1979. Masters Thesis, University of Arizona. Accessed January 15, 2021. http://hdl.handle.net/10150/557257.

MLA Handbook (7th Edition):

Al-Humayyd, Mohammad Saad Abdulrahman. “Birth defects in epilepsy: role of phenytoin and convulsion .” 1979. Web. 15 Jan 2021.

Vancouver:

Al-Humayyd MSA. Birth defects in epilepsy: role of phenytoin and convulsion . [Internet] [Masters thesis]. University of Arizona; 1979. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10150/557257.

Council of Science Editors:

Al-Humayyd MSA. Birth defects in epilepsy: role of phenytoin and convulsion . [Masters Thesis]. University of Arizona; 1979. Available from: http://hdl.handle.net/10150/557257


University of Michigan

18. MacDonald, Bryan Thomas. Phenotype to genotype: Genetic variants of SCN1A and Dkk1.

Degree: PhD, Molecular biology, 2004, University of Michigan

 In the era of sequenced genomes, forward genetic approaches to identify mutations in humans and mice must include the utilization of genomic sequence comparisons and… (more)

Subjects/Keywords: Dkk1; Epilepsy; Genetic; Genotype; Limb Development; Phenotype; Scn1a; Variants

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APA (6th Edition):

MacDonald, B. T. (2004). Phenotype to genotype: Genetic variants of SCN1A and Dkk1. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/124127

Chicago Manual of Style (16th Edition):

MacDonald, Bryan Thomas. “Phenotype to genotype: Genetic variants of SCN1A and Dkk1.” 2004. Doctoral Dissertation, University of Michigan. Accessed January 15, 2021. http://hdl.handle.net/2027.42/124127.

MLA Handbook (7th Edition):

MacDonald, Bryan Thomas. “Phenotype to genotype: Genetic variants of SCN1A and Dkk1.” 2004. Web. 15 Jan 2021.

Vancouver:

MacDonald BT. Phenotype to genotype: Genetic variants of SCN1A and Dkk1. [Internet] [Doctoral dissertation]. University of Michigan; 2004. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/2027.42/124127.

Council of Science Editors:

MacDonald BT. Phenotype to genotype: Genetic variants of SCN1A and Dkk1. [Doctoral Dissertation]. University of Michigan; 2004. Available from: http://hdl.handle.net/2027.42/124127


Columbia University

19. Dhindsa, Ryan Singh. Deciphering gene dysregulation in disease through population and functional genomics.

Degree: 2020, Columbia University

Genetic discoveries have highlighted the role of gene expression dysregulation in both rare and common diseases. In particular, a large number of chromatin modifiers, transcription… (more)

Subjects/Keywords: Gene expression; Chromatin; Chromatographic analysis; Transcription factors; RNA-protein interactions; Nervous system – Diseases; Epilepsy; Genetic regulation

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APA (6th Edition):

Dhindsa, R. S. (2020). Deciphering gene dysregulation in disease through population and functional genomics. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/d8-fkv2-1q39

Chicago Manual of Style (16th Edition):

Dhindsa, Ryan Singh. “Deciphering gene dysregulation in disease through population and functional genomics.” 2020. Doctoral Dissertation, Columbia University. Accessed January 15, 2021. https://doi.org/10.7916/d8-fkv2-1q39.

MLA Handbook (7th Edition):

Dhindsa, Ryan Singh. “Deciphering gene dysregulation in disease through population and functional genomics.” 2020. Web. 15 Jan 2021.

Vancouver:

Dhindsa RS. Deciphering gene dysregulation in disease through population and functional genomics. [Internet] [Doctoral dissertation]. Columbia University; 2020. [cited 2021 Jan 15]. Available from: https://doi.org/10.7916/d8-fkv2-1q39.

Council of Science Editors:

Dhindsa RS. Deciphering gene dysregulation in disease through population and functional genomics. [Doctoral Dissertation]. Columbia University; 2020. Available from: https://doi.org/10.7916/d8-fkv2-1q39


University of Ottawa

20. Ghinda, Cristina Diana. Neuronal and Electrophysiological Markers of Glioma .

Degree: 2020, University of Ottawa

 The research performed in this thesis aims to improve our understanding about one of the most malignant tumors of the human brain – glioma. From… (more)

Subjects/Keywords: glioma; awake craniotomy; functional MRI; electrocorticography; power-law exponent; glioblastoma; glioma-related epilepsy; peritumoral tissue; neuroplasticity; genetic markers

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APA (6th Edition):

Ghinda, C. D. (2020). Neuronal and Electrophysiological Markers of Glioma . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/40218

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ghinda, Cristina Diana. “Neuronal and Electrophysiological Markers of Glioma .” 2020. Thesis, University of Ottawa. Accessed January 15, 2021. http://hdl.handle.net/10393/40218.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ghinda, Cristina Diana. “Neuronal and Electrophysiological Markers of Glioma .” 2020. Web. 15 Jan 2021.

Vancouver:

Ghinda CD. Neuronal and Electrophysiological Markers of Glioma . [Internet] [Thesis]. University of Ottawa; 2020. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10393/40218.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ghinda CD. Neuronal and Electrophysiological Markers of Glioma . [Thesis]. University of Ottawa; 2020. Available from: http://hdl.handle.net/10393/40218

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

21. Correard, Solenne. Analyses génétiques et génomiques de maladies neurologiques chez le chien comme modèle de maladies rares humaines : Genetic and genomic analyses of neurological diseases in dogs as a model of rare human diseases.

Degree: Docteur es, Génétique, Génomique, Bioinformatique, 2018, Rennes 1

L’identification des mutations génétiques impliquées dans les maladies rares est un prérequis pour mieux les comprendre, les traiter et accompagner les patients. Pour se faire,… (more)

Subjects/Keywords: Modèle chien; Maladies rares; Epilepsie; Neuropathie; Génétique; Séquençage; Dog model; Rare diseases; Epilepsy; Neuropathy; Genetic, Sequencing

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APA (6th Edition):

Correard, S. (2018). Analyses génétiques et génomiques de maladies neurologiques chez le chien comme modèle de maladies rares humaines : Genetic and genomic analyses of neurological diseases in dogs as a model of rare human diseases. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2018REN1B028

Chicago Manual of Style (16th Edition):

Correard, Solenne. “Analyses génétiques et génomiques de maladies neurologiques chez le chien comme modèle de maladies rares humaines : Genetic and genomic analyses of neurological diseases in dogs as a model of rare human diseases.” 2018. Doctoral Dissertation, Rennes 1. Accessed January 15, 2021. http://www.theses.fr/2018REN1B028.

MLA Handbook (7th Edition):

Correard, Solenne. “Analyses génétiques et génomiques de maladies neurologiques chez le chien comme modèle de maladies rares humaines : Genetic and genomic analyses of neurological diseases in dogs as a model of rare human diseases.” 2018. Web. 15 Jan 2021.

Vancouver:

Correard S. Analyses génétiques et génomiques de maladies neurologiques chez le chien comme modèle de maladies rares humaines : Genetic and genomic analyses of neurological diseases in dogs as a model of rare human diseases. [Internet] [Doctoral dissertation]. Rennes 1; 2018. [cited 2021 Jan 15]. Available from: http://www.theses.fr/2018REN1B028.

Council of Science Editors:

Correard S. Analyses génétiques et génomiques de maladies neurologiques chez le chien comme modèle de maladies rares humaines : Genetic and genomic analyses of neurological diseases in dogs as a model of rare human diseases. [Doctoral Dissertation]. Rennes 1; 2018. Available from: http://www.theses.fr/2018REN1B028


Michigan State University

22. Fakhrai, Habibollah, 1942-. A population study in human biochemical genetics : the relationships of several metabolites in epilepsy and mental retardation.

Degree: PhD, Department of Zoology, 1974, Michigan State University

Subjects/Keywords: Human genetics; Medical genetics; Epilepsy – Genetic aspects; Intellectual disability – Genetic aspects

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APA (6th Edition):

Fakhrai, Habibollah, 1. (1974). A population study in human biochemical genetics : the relationships of several metabolites in epilepsy and mental retardation. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:39936

Chicago Manual of Style (16th Edition):

Fakhrai, Habibollah, 1942-. “A population study in human biochemical genetics : the relationships of several metabolites in epilepsy and mental retardation.” 1974. Doctoral Dissertation, Michigan State University. Accessed January 15, 2021. http://etd.lib.msu.edu/islandora/object/etd:39936.

MLA Handbook (7th Edition):

Fakhrai, Habibollah, 1942-. “A population study in human biochemical genetics : the relationships of several metabolites in epilepsy and mental retardation.” 1974. Web. 15 Jan 2021.

Vancouver:

Fakhrai, Habibollah 1. A population study in human biochemical genetics : the relationships of several metabolites in epilepsy and mental retardation. [Internet] [Doctoral dissertation]. Michigan State University; 1974. [cited 2021 Jan 15]. Available from: http://etd.lib.msu.edu/islandora/object/etd:39936.

Council of Science Editors:

Fakhrai, Habibollah 1. A population study in human biochemical genetics : the relationships of several metabolites in epilepsy and mental retardation. [Doctoral Dissertation]. Michigan State University; 1974. Available from: http://etd.lib.msu.edu/islandora/object/etd:39936


Stellenbosch University

23. Thomas, Saralene Iona. Genetic markers in the differential diagnosis in a family setting of episodic loss of consciousness.

Degree: MSc, Biomedical Sciences, 2000, Stellenbosch University

ENGLISH ABSTRACT: Please see fulltext for abstract

AFRIKAANSE OPSOMMING: Sien asb volteks vir opsomming

Advisors/Committee Members: Corfield, Valerie, Stellenbosch University. Faculty of Medicine & Health Sciences. Dept. of Biomedical Sciences. Medical Physiology..

Subjects/Keywords: Consciousness; Cardiovascular system  – Diseases  – Genetic aspects; Epilepsy  – Genetic aspects; Arrhythmia; Dissertations  – Medicine; Myoclonic epilepsy

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APA (6th Edition):

Thomas, S. I. (2000). Genetic markers in the differential diagnosis in a family setting of episodic loss of consciousness. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/51777

Chicago Manual of Style (16th Edition):

Thomas, Saralene Iona. “Genetic markers in the differential diagnosis in a family setting of episodic loss of consciousness.” 2000. Masters Thesis, Stellenbosch University. Accessed January 15, 2021. http://hdl.handle.net/10019.1/51777.

MLA Handbook (7th Edition):

Thomas, Saralene Iona. “Genetic markers in the differential diagnosis in a family setting of episodic loss of consciousness.” 2000. Web. 15 Jan 2021.

Vancouver:

Thomas SI. Genetic markers in the differential diagnosis in a family setting of episodic loss of consciousness. [Internet] [Masters thesis]. Stellenbosch University; 2000. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10019.1/51777.

Council of Science Editors:

Thomas SI. Genetic markers in the differential diagnosis in a family setting of episodic loss of consciousness. [Masters Thesis]. Stellenbosch University; 2000. Available from: http://hdl.handle.net/10019.1/51777


Michigan State University

24. Firpi, Hiram A. On prediction and detection of epileptic seizures by means of genetic programming artificial features.

Degree: PhD, Department of Electrical and Computer Engineering, 2005, Michigan State University

Subjects/Keywords: Epilepsy – Genetic aspects; Neural networks (Computer science); Genetic programming (Computer science); Electroencephalography; Signal generators – Data processing; Genetic algorithms; Bioengineering; Vector analysis

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APA (6th Edition):

Firpi, H. A. (2005). On prediction and detection of epileptic seizures by means of genetic programming artificial features. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:33476

Chicago Manual of Style (16th Edition):

Firpi, Hiram A. “On prediction and detection of epileptic seizures by means of genetic programming artificial features.” 2005. Doctoral Dissertation, Michigan State University. Accessed January 15, 2021. http://etd.lib.msu.edu/islandora/object/etd:33476.

MLA Handbook (7th Edition):

Firpi, Hiram A. “On prediction and detection of epileptic seizures by means of genetic programming artificial features.” 2005. Web. 15 Jan 2021.

Vancouver:

Firpi HA. On prediction and detection of epileptic seizures by means of genetic programming artificial features. [Internet] [Doctoral dissertation]. Michigan State University; 2005. [cited 2021 Jan 15]. Available from: http://etd.lib.msu.edu/islandora/object/etd:33476.

Council of Science Editors:

Firpi HA. On prediction and detection of epileptic seizures by means of genetic programming artificial features. [Doctoral Dissertation]. Michigan State University; 2005. Available from: http://etd.lib.msu.edu/islandora/object/etd:33476


University of Adelaide

25. Kolc, Kristy Louise. Variable Clinical and Molecular Expressivity of PCDH19 Variants and Girls Clustering Epilepsy A disorder of cellular "mosaics".

Degree: 2020, University of Adelaide

 Girls Clustering Epilepsy is the second most common developmental and epileptic encephalopathy. GCE is due to variants in the X chromosome gene PCDH19 and is… (more)

Subjects/Keywords: X-linked clustering epilepsy; PCDH19; cellular mosaicism; X-chromosome inactivation; genetic; developmental and epileptic encephalopathy; autism spectrum disorder; attention-deficit hyperactivity disorder; executive dysfunction; obsessive-compulsive disorder

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APA (6th Edition):

Kolc, K. L. (2020). Variable Clinical and Molecular Expressivity of PCDH19 Variants and Girls Clustering Epilepsy A disorder of cellular "mosaics". (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/126965

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kolc, Kristy Louise. “Variable Clinical and Molecular Expressivity of PCDH19 Variants and Girls Clustering Epilepsy A disorder of cellular "mosaics".” 2020. Thesis, University of Adelaide. Accessed January 15, 2021. http://hdl.handle.net/2440/126965.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kolc, Kristy Louise. “Variable Clinical and Molecular Expressivity of PCDH19 Variants and Girls Clustering Epilepsy A disorder of cellular "mosaics".” 2020. Web. 15 Jan 2021.

Vancouver:

Kolc KL. Variable Clinical and Molecular Expressivity of PCDH19 Variants and Girls Clustering Epilepsy A disorder of cellular "mosaics". [Internet] [Thesis]. University of Adelaide; 2020. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/2440/126965.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kolc KL. Variable Clinical and Molecular Expressivity of PCDH19 Variants and Girls Clustering Epilepsy A disorder of cellular "mosaics". [Thesis]. University of Adelaide; 2020. Available from: http://hdl.handle.net/2440/126965

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Melbourne

26. LEAW, BRYAN. Sodium channels and epilepsy: neuronal dysfunction in genetic mouse models.

Degree: 2014, University of Melbourne

 Mutations in sodium channels have long been linked to inherited epilepsies. Recent clinical findings identified patients with Dravet syndrome that were homozygous for a mutation… (more)

Subjects/Keywords: neuroscience; epilepsy; sodium channel; genetic; mouse model; animal model; patching; cellular biology; neurophysiology; network; excitability; development; splice variant; behavior; immunohistochemistry; staining; confocal; microscopy; tracing; morphology

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APA (6th Edition):

LEAW, B. (2014). Sodium channels and epilepsy: neuronal dysfunction in genetic mouse models. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/40951

Chicago Manual of Style (16th Edition):

LEAW, BRYAN. “Sodium channels and epilepsy: neuronal dysfunction in genetic mouse models.” 2014. Doctoral Dissertation, University of Melbourne. Accessed January 15, 2021. http://hdl.handle.net/11343/40951.

MLA Handbook (7th Edition):

LEAW, BRYAN. “Sodium channels and epilepsy: neuronal dysfunction in genetic mouse models.” 2014. Web. 15 Jan 2021.

Vancouver:

LEAW B. Sodium channels and epilepsy: neuronal dysfunction in genetic mouse models. [Internet] [Doctoral dissertation]. University of Melbourne; 2014. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/11343/40951.

Council of Science Editors:

LEAW B. Sodium channels and epilepsy: neuronal dysfunction in genetic mouse models. [Doctoral Dissertation]. University of Melbourne; 2014. Available from: http://hdl.handle.net/11343/40951

27. Kuo, Chia-Hung. THE ANALYSIS OF HIGH FREQUENCY OSCILLATIONS AND SUPPRESSION IN EPILEPTIC SEIZURE DATA.

Degree: PhD, EECS - System and Control Engineering, 2014, Case Western Reserve University School of Graduate Studies

 In this study, several techniques for the variability analysis of electroencephalography (EEG) have been developed with application to the detection of high-frequency oscillations (HFOs) and… (more)

Subjects/Keywords: Biomedical Engineering; Biomedical Research; Electrical Engineering; EEG; HFOs; High Frequency Oscillations; Line-Length; Adaptive Neuro-Fuzzy Inference System; ANFIS; Epilepsy; Genetic Algorithm

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APA (6th Edition):

Kuo, C. (2014). THE ANALYSIS OF HIGH FREQUENCY OSCILLATIONS AND SUPPRESSION IN EPILEPTIC SEIZURE DATA. (Doctoral Dissertation). Case Western Reserve University School of Graduate Studies. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1396411237

Chicago Manual of Style (16th Edition):

Kuo, Chia-Hung. “THE ANALYSIS OF HIGH FREQUENCY OSCILLATIONS AND SUPPRESSION IN EPILEPTIC SEIZURE DATA.” 2014. Doctoral Dissertation, Case Western Reserve University School of Graduate Studies. Accessed January 15, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=case1396411237.

MLA Handbook (7th Edition):

Kuo, Chia-Hung. “THE ANALYSIS OF HIGH FREQUENCY OSCILLATIONS AND SUPPRESSION IN EPILEPTIC SEIZURE DATA.” 2014. Web. 15 Jan 2021.

Vancouver:

Kuo C. THE ANALYSIS OF HIGH FREQUENCY OSCILLATIONS AND SUPPRESSION IN EPILEPTIC SEIZURE DATA. [Internet] [Doctoral dissertation]. Case Western Reserve University School of Graduate Studies; 2014. [cited 2021 Jan 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1396411237.

Council of Science Editors:

Kuo C. THE ANALYSIS OF HIGH FREQUENCY OSCILLATIONS AND SUPPRESSION IN EPILEPTIC SEIZURE DATA. [Doctoral Dissertation]. Case Western Reserve University School of Graduate Studies; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1396411237


Georgia Tech

28. Smart, Otis Lkuwamy. Evolutionary algorithms and frequent itemset mining for analyzing epileptic oscillations.

Degree: PhD, Electrical and Computer Engineering, 2007, Georgia Tech

 This research presents engineering tools that address an important area impacting many persons worldwide: epilepsy. Over 60 million people are affected by epilepsy, a neurological… (more)

Subjects/Keywords: Epileptic oscillations; Epilepsy; Evolutionary algorithms; Frequent itemset mining; Intracranial EEG; Feature extraction; Artificial feature; Epilepsy; Brain mapping; Electroencephalography; Evolutionary computation; Genetic programming (Computer science); Algorithms

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APA (6th Edition):

Smart, O. L. (2007). Evolutionary algorithms and frequent itemset mining for analyzing epileptic oscillations. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/22709

Chicago Manual of Style (16th Edition):

Smart, Otis Lkuwamy. “Evolutionary algorithms and frequent itemset mining for analyzing epileptic oscillations.” 2007. Doctoral Dissertation, Georgia Tech. Accessed January 15, 2021. http://hdl.handle.net/1853/22709.

MLA Handbook (7th Edition):

Smart, Otis Lkuwamy. “Evolutionary algorithms and frequent itemset mining for analyzing epileptic oscillations.” 2007. Web. 15 Jan 2021.

Vancouver:

Smart OL. Evolutionary algorithms and frequent itemset mining for analyzing epileptic oscillations. [Internet] [Doctoral dissertation]. Georgia Tech; 2007. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1853/22709.

Council of Science Editors:

Smart OL. Evolutionary algorithms and frequent itemset mining for analyzing epileptic oscillations. [Doctoral Dissertation]. Georgia Tech; 2007. Available from: http://hdl.handle.net/1853/22709

29. Klainer, Nira. Epilepsy in Pregnancy: Current Practices of Prenatal Genetic Counselors.

Degree: 2013, Brandeis University

Epilepsy is a neurological disorder affecting approximately 1% of the general population. There are over 1 million women with epilepsy in the US alone, making… (more)

Subjects/Keywords: AEDs; Current practices; Epilepsy; Molecular genetics; Pregnancy; Seizure control; Risk assessment; Prenatal genetic counselors; Women with epilepsy

Genetic factors, while not always the primary cause of epilepsy, play an important role in… …questions/concerns about pregnancy and epilepsy. Genetic counselors can also provide patients with… …guidelines for genetic counseling of women with epilepsy published by the American Congress of… …that genetic counseling of women with epilepsy can contribute to a reduction of adverse… …indicated that when they see women with epilepsy who present for genetic counseling during an… 

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APA (6th Edition):

Klainer, N. (2013). Epilepsy in Pregnancy: Current Practices of Prenatal Genetic Counselors. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/25054

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Klainer, Nira. “Epilepsy in Pregnancy: Current Practices of Prenatal Genetic Counselors.” 2013. Thesis, Brandeis University. Accessed January 15, 2021. http://hdl.handle.net/10192/25054.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Klainer, Nira. “Epilepsy in Pregnancy: Current Practices of Prenatal Genetic Counselors.” 2013. Web. 15 Jan 2021.

Vancouver:

Klainer N. Epilepsy in Pregnancy: Current Practices of Prenatal Genetic Counselors. [Internet] [Thesis]. Brandeis University; 2013. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10192/25054.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Klainer N. Epilepsy in Pregnancy: Current Practices of Prenatal Genetic Counselors. [Thesis]. Brandeis University; 2013. Available from: http://hdl.handle.net/10192/25054

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

30. O'Brien, Janelle Elizabeth. Regulation and Mutation of Voltage-Gated Sodium Channel SCN8A (Nav1.6).

Degree: PhD, Human Genetics, 2013, University of Michigan

 The gene SCN8A encodes voltage-gated sodium channel Nav1.6, which is widely expressed in the nervous system and contributes to firing patterns in many types of… (more)

Subjects/Keywords: Voltage-gated Sodium Channels; Human Genetic Disease; Epilepsy; Alternative Splicing; Protein Trafficking; Genetics; Science

epilepsy (Papale et al., 2009), disrupted sleep architecture (Papale et al., 2010… …Mutations of human SCN8A. Filled circles, mutations identified in patients with epilepsy. Grey… …recently identified by exome sequencing of patients with epilepsy (M. Hammer, personal… …hyperexcitability 11 ! and leads to epilepsy (Veeramah et al., 2012). The magnitude of… 

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

O'Brien, J. E. (2013). Regulation and Mutation of Voltage-Gated Sodium Channel SCN8A (Nav1.6). (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/100063

Chicago Manual of Style (16th Edition):

O'Brien, Janelle Elizabeth. “Regulation and Mutation of Voltage-Gated Sodium Channel SCN8A (Nav1.6).” 2013. Doctoral Dissertation, University of Michigan. Accessed January 15, 2021. http://hdl.handle.net/2027.42/100063.

MLA Handbook (7th Edition):

O'Brien, Janelle Elizabeth. “Regulation and Mutation of Voltage-Gated Sodium Channel SCN8A (Nav1.6).” 2013. Web. 15 Jan 2021.

Vancouver:

O'Brien JE. Regulation and Mutation of Voltage-Gated Sodium Channel SCN8A (Nav1.6). [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/2027.42/100063.

Council of Science Editors:

O'Brien JE. Regulation and Mutation of Voltage-Gated Sodium Channel SCN8A (Nav1.6). [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/100063

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