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You searched for subject:(Huntingtons disease). Showing records 1 – 14 of 14 total matches.

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Vanderbilt University

1. Kwakye, Gunnar Francis. Development of a novel high throughput assay: impaired manganese transport kinetics and homeostasis in Huntington’s disease.

Degree: PhD, Neuroscience, 2011, Vanderbilt University

 Expansion in the glutamine encoding CAG triplet-repeat in the Huntingtin (HTT) gene causes Huntington’s disease (HD). The susceptibility, age of onset, and severity of HD… (more)

Subjects/Keywords: manganese; striatal cells; high throughput assay; metal transport; Huntingtons disease

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APA (6th Edition):

Kwakye, G. F. (2011). Development of a novel high throughput assay: impaired manganese transport kinetics and homeostasis in Huntington’s disease. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14123

Chicago Manual of Style (16th Edition):

Kwakye, Gunnar Francis. “Development of a novel high throughput assay: impaired manganese transport kinetics and homeostasis in Huntington’s disease.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed January 15, 2021. http://hdl.handle.net/1803/14123.

MLA Handbook (7th Edition):

Kwakye, Gunnar Francis. “Development of a novel high throughput assay: impaired manganese transport kinetics and homeostasis in Huntington’s disease.” 2011. Web. 15 Jan 2021.

Vancouver:

Kwakye GF. Development of a novel high throughput assay: impaired manganese transport kinetics and homeostasis in Huntington’s disease. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1803/14123.

Council of Science Editors:

Kwakye GF. Development of a novel high throughput assay: impaired manganese transport kinetics and homeostasis in Huntington’s disease. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://hdl.handle.net/1803/14123

2. Färlin, Lena. Hur anhörigvårdare till personer med Huntingtons sjukdom upplever sin livssituation : En litteraturstudie.

Degree: Health and Caring Sciences, 2016, University of Gävle

Bakgrund: Huntingtons sjukdom (HS) är en neurologisk sjukdom som är genetiskt ärftlig och drabbar både kvinnor och män i lika stor utsträckning. Sjukdomen angriper… (more)

Subjects/Keywords: Huntington’s disease; family caregiver; experience; Huntingtons sjukdom; anhörigvårdare; upplevelser

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APA (6th Edition):

Färlin, L. (2016). Hur anhörigvårdare till personer med Huntingtons sjukdom upplever sin livssituation : En litteraturstudie. (Thesis). University of Gävle. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-21465

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):

Färlin, Lena. “Hur anhörigvårdare till personer med Huntingtons sjukdom upplever sin livssituation : En litteraturstudie.” 2016. Thesis, University of Gävle. Accessed January 15, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-21465.

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

MLA Handbook (7th Edition):

Färlin, Lena. “Hur anhörigvårdare till personer med Huntingtons sjukdom upplever sin livssituation : En litteraturstudie.” 2016. Web. 15 Jan 2021.

Vancouver:

Färlin L. Hur anhörigvårdare till personer med Huntingtons sjukdom upplever sin livssituation : En litteraturstudie. [Internet] [Thesis]. University of Gävle; 2016. [cited 2021 Jan 15]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-21465.

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

Council of Science Editors:

Färlin L. Hur anhörigvårdare till personer med Huntingtons sjukdom upplever sin livssituation : En litteraturstudie. [Thesis]. University of Gävle; 2016. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-21465

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


Vanderbilt University

3. Tidball, Andrew Martin. A Manganese-Handling Deficit in Huntington’s Disease Selectively Impairs ATM-p53 Signaling.

Degree: PhD, Neuroscience, 2014, Vanderbilt University

 The essential micronutrient manganese is enriched in brain, especially the basal ganglia. We sought to identify neuronal signaling pathways responsive to neurologically relevant manganese levels,… (more)

Subjects/Keywords: manganese; induced-pluripotent stem cells; ATM; p53; cell signaling; cytotoxicity; genomic instability; Huntingtons disease

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APA (6th Edition):

Tidball, A. M. (2014). A Manganese-Handling Deficit in Huntington’s Disease Selectively Impairs ATM-p53 Signaling. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14230

Chicago Manual of Style (16th Edition):

Tidball, Andrew Martin. “A Manganese-Handling Deficit in Huntington’s Disease Selectively Impairs ATM-p53 Signaling.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed January 15, 2021. http://hdl.handle.net/1803/14230.

MLA Handbook (7th Edition):

Tidball, Andrew Martin. “A Manganese-Handling Deficit in Huntington’s Disease Selectively Impairs ATM-p53 Signaling.” 2014. Web. 15 Jan 2021.

Vancouver:

Tidball AM. A Manganese-Handling Deficit in Huntington’s Disease Selectively Impairs ATM-p53 Signaling. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1803/14230.

Council of Science Editors:

Tidball AM. A Manganese-Handling Deficit in Huntington’s Disease Selectively Impairs ATM-p53 Signaling. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/14230


Vanderbilt University

4. Bichell, Terry Jo Vetters. Reduced Striatal Mn-accumulation in Huntington’s Disease Mouse Model Causes Reversible Alterations in Mn-dependent Enzyme Pathways.

Degree: PhD, Neuroscience, 2016, Vanderbilt University

 Huntington’s disease (HD) is caused by an increase in CAG repeats in exon 1 of the huntingtin gene (HTT), which results in a polyglutamine expansion… (more)

Subjects/Keywords: manganese; Huntingtons disease; arginase; gene environment interactions; neurodegeneration; mouse models; striatum; urea cycle

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APA (6th Edition):

Bichell, T. J. V. (2016). Reduced Striatal Mn-accumulation in Huntington’s Disease Mouse Model Causes Reversible Alterations in Mn-dependent Enzyme Pathways. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15162

Chicago Manual of Style (16th Edition):

Bichell, Terry Jo Vetters. “Reduced Striatal Mn-accumulation in Huntington’s Disease Mouse Model Causes Reversible Alterations in Mn-dependent Enzyme Pathways.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed January 15, 2021. http://hdl.handle.net/1803/15162.

MLA Handbook (7th Edition):

Bichell, Terry Jo Vetters. “Reduced Striatal Mn-accumulation in Huntington’s Disease Mouse Model Causes Reversible Alterations in Mn-dependent Enzyme Pathways.” 2016. Web. 15 Jan 2021.

Vancouver:

Bichell TJV. Reduced Striatal Mn-accumulation in Huntington’s Disease Mouse Model Causes Reversible Alterations in Mn-dependent Enzyme Pathways. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1803/15162.

Council of Science Editors:

Bichell TJV. Reduced Striatal Mn-accumulation in Huntington’s Disease Mouse Model Causes Reversible Alterations in Mn-dependent Enzyme Pathways. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/15162


Universidade Federal de Santa Maria

5. Nádia Aléssio Velloso. EFEITOS DA ESPERMINA SOBRE PARÂMETROS MOTORES, COGNITIVOS E NEUROMORFOLÓGICOS EM UM MODELO EXPERIMENTAL DA DOENÇA DE HUNTINGTON.

Degree: 2008, Universidade Federal de Santa Maria

A espermina (SPM) é uma amina alifática, contendo quatro centros nucleofílicos e é encontrada em todas as células eucarióticas, incluindo células nervosas. Ela pertence ao… (more)

Subjects/Keywords: neuroproteção; receptor NMDA; ácido quinolínico; poliaminas; espermina; BIOQUIMICA; spermine; polyamines; quinolinic acid; NMDA receptor; doença de Huntington; neuroprotection, Huntingtons disease

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APA (6th Edition):

Velloso, N. A. (2008). EFEITOS DA ESPERMINA SOBRE PARÂMETROS MOTORES, COGNITIVOS E NEUROMORFOLÓGICOS EM UM MODELO EXPERIMENTAL DA DOENÇA DE HUNTINGTON. (Thesis). Universidade Federal de Santa Maria. Retrieved from http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=2177

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):

Velloso, Nádia Aléssio. “EFEITOS DA ESPERMINA SOBRE PARÂMETROS MOTORES, COGNITIVOS E NEUROMORFOLÓGICOS EM UM MODELO EXPERIMENTAL DA DOENÇA DE HUNTINGTON.” 2008. Thesis, Universidade Federal de Santa Maria. Accessed January 15, 2021. http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=2177.

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

MLA Handbook (7th Edition):

Velloso, Nádia Aléssio. “EFEITOS DA ESPERMINA SOBRE PARÂMETROS MOTORES, COGNITIVOS E NEUROMORFOLÓGICOS EM UM MODELO EXPERIMENTAL DA DOENÇA DE HUNTINGTON.” 2008. Web. 15 Jan 2021.

Vancouver:

Velloso NA. EFEITOS DA ESPERMINA SOBRE PARÂMETROS MOTORES, COGNITIVOS E NEUROMORFOLÓGICOS EM UM MODELO EXPERIMENTAL DA DOENÇA DE HUNTINGTON. [Internet] [Thesis]. Universidade Federal de Santa Maria; 2008. [cited 2021 Jan 15]. Available from: http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=2177.

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

Council of Science Editors:

Velloso NA. EFEITOS DA ESPERMINA SOBRE PARÂMETROS MOTORES, COGNITIVOS E NEUROMORFOLÓGICOS EM UM MODELO EXPERIMENTAL DA DOENÇA DE HUNTINGTON. [Thesis]. Universidade Federal de Santa Maria; 2008. Available from: http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=2177

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


KTH

6. Håkansson, Mimmi. Huntingtin gene profiling, towards allele-specific treatment.

Degree: Biotechnology and Health (CBH), 2020, KTH

Huntington diseases(HD) is a fatal autosomal neurodegenerative genetic disorder, caused by a CAG trinucleotide repeat expansion in the huntingtin (HTT) gene, resulting in a… (more)

Subjects/Keywords: Huntington’s disease; huntingtin lowering; allele-selective; HD animal models; Huntingtons sjukdom; huntingtin sänkning; allel-specifik; Huntington djurmodeller; Medical Biotechnology; Medicinsk bioteknologi

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APA (6th Edition):

Håkansson, M. (2020). Huntingtin gene profiling, towards allele-specific treatment. (Thesis). KTH. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-278591

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):

Håkansson, Mimmi. “Huntingtin gene profiling, towards allele-specific treatment.” 2020. Thesis, KTH. Accessed January 15, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-278591.

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

MLA Handbook (7th Edition):

Håkansson, Mimmi. “Huntingtin gene profiling, towards allele-specific treatment.” 2020. Web. 15 Jan 2021.

Vancouver:

Håkansson M. Huntingtin gene profiling, towards allele-specific treatment. [Internet] [Thesis]. KTH; 2020. [cited 2021 Jan 15]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-278591.

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

Council of Science Editors:

Håkansson M. Huntingtin gene profiling, towards allele-specific treatment. [Thesis]. KTH; 2020. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-278591

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

7. Hamrebjörk, Frida. Erfarenheter av att vara närstående till personer med Huntingtons sjukdom : en beskrivande litteraturstudie.

Degree: Caring science, 2016, University of Gävle

Introduktion: Huntingtons sjukdom (HS) är en neurologisk sjukdom som är ärftlig. Sjukdomen påverkar hjärnans nervceller och ger symtom som ofrivilliga ryckningar i extremiteterna. Sväljsvårigheter… (more)

Subjects/Keywords: Experience; Huntington disease; Family; Erfarenheter; Huntingtons sjukdom; Närstående; Nursing; Omvårdnad

Huntingtons sjukdom? Vilka undersökningsgrupper och inklusionskriterier ingår i de valda artiklarna… …och sökstrategier Sökord som användes med hjälp av MeSH-termer var Huntington disease och… …AND. Huntington disease AND Family. 9 Tabell 1. Utfall av preliminära databassökningar… …engelska, adult:19+ years Headlines via Cinahl Free Full Text Peer reviewd Huntington disease… …disease (MeSH) AND Family (MeSH) 160901 Manuell sökning 160901 Totalt… 

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APA (6th Edition):

Hamrebjörk, F. (2016). Erfarenheter av att vara närstående till personer med Huntingtons sjukdom : en beskrivande litteraturstudie. (Thesis). University of Gävle. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-22883

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):

Hamrebjörk, Frida. “Erfarenheter av att vara närstående till personer med Huntingtons sjukdom : en beskrivande litteraturstudie.” 2016. Thesis, University of Gävle. Accessed January 15, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-22883.

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

MLA Handbook (7th Edition):

Hamrebjörk, Frida. “Erfarenheter av att vara närstående till personer med Huntingtons sjukdom : en beskrivande litteraturstudie.” 2016. Web. 15 Jan 2021.

Vancouver:

Hamrebjörk F. Erfarenheter av att vara närstående till personer med Huntingtons sjukdom : en beskrivande litteraturstudie. [Internet] [Thesis]. University of Gävle; 2016. [cited 2021 Jan 15]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-22883.

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

Council of Science Editors:

Hamrebjörk F. Erfarenheter av att vara närstående till personer med Huntingtons sjukdom : en beskrivande litteraturstudie. [Thesis]. University of Gävle; 2016. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-22883

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

8. Roe, Anne Jessica T. The role MAPK1 plays in Drp1 activation leading to mitochondrial dysfunction in Huntington's disease.

Degree: MSs, Physiology and Biophysics, 2016, Case Western Reserve University School of Graduate Studies

 Huntington’s disease (HD) is an incurable neurodegenerative disease withautosomal dominant inheritance caused by expanded CAG repeats in the huntingtingene that confers a toxic gain-of-function on… (more)

Subjects/Keywords: Physiology; Neurology; MAPK1; Drp1; Huntingtons disease; mitochondrial dysfunction

…and allowing me to conduct unique research with a neurodegenerative disease. I would also… …Huntington’s disease HeLa Henrietta Lacks IP immunoprecipitation iPS induced pluripotent stem… …MAPK1 Plays in Drp1 Activation Leading to Mitochondrial Dysfunction in Huntington’s Disease… …Abstract by ANNE J.T. ROE Huntington’s disease (HD) is an incurable neurodegenerative… …disease with autosomal dominant inheritance caused by expanded CAG repeats in the huntingtin… 

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APA (6th Edition):

Roe, A. J. T. (2016). The role MAPK1 plays in Drp1 activation leading to mitochondrial dysfunction in Huntington's disease. (Masters Thesis). Case Western Reserve University School of Graduate Studies. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1459431850

Chicago Manual of Style (16th Edition):

Roe, Anne Jessica T. “The role MAPK1 plays in Drp1 activation leading to mitochondrial dysfunction in Huntington's disease.” 2016. Masters Thesis, Case Western Reserve University School of Graduate Studies. Accessed January 15, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=case1459431850.

MLA Handbook (7th Edition):

Roe, Anne Jessica T. “The role MAPK1 plays in Drp1 activation leading to mitochondrial dysfunction in Huntington's disease.” 2016. Web. 15 Jan 2021.

Vancouver:

Roe AJT. The role MAPK1 plays in Drp1 activation leading to mitochondrial dysfunction in Huntington's disease. [Internet] [Masters thesis]. Case Western Reserve University School of Graduate Studies; 2016. [cited 2021 Jan 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1459431850.

Council of Science Editors:

Roe AJT. The role MAPK1 plays in Drp1 activation leading to mitochondrial dysfunction in Huntington's disease. [Masters Thesis]. Case Western Reserve University School of Graduate Studies; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1459431850


Queensland University of Technology

9. Brockhurst, Veronica. Development of novel DNA-based methods for the measurement of length polymorphisms (microsatellites).

Degree: 2001, Queensland University of Technology

Subjects/Keywords: Microsatellites (Genetics); microsatellites; STRs; ligase; LASA; A-SEal; Huntingtons disease; dinucleotide; tetranucleotide; trinucleotide; (CAG)n; mutation detection; thesis; doctoral

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APA (6th Edition):

Brockhurst, V. (2001). Development of novel DNA-based methods for the measurement of length polymorphisms (microsatellites). (Thesis). Queensland University of Technology. Retrieved from http://eprints.qut.edu.au/37113/

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):

Brockhurst, Veronica. “Development of novel DNA-based methods for the measurement of length polymorphisms (microsatellites).” 2001. Thesis, Queensland University of Technology. Accessed January 15, 2021. http://eprints.qut.edu.au/37113/.

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

MLA Handbook (7th Edition):

Brockhurst, Veronica. “Development of novel DNA-based methods for the measurement of length polymorphisms (microsatellites).” 2001. Web. 15 Jan 2021.

Vancouver:

Brockhurst V. Development of novel DNA-based methods for the measurement of length polymorphisms (microsatellites). [Internet] [Thesis]. Queensland University of Technology; 2001. [cited 2021 Jan 15]. Available from: http://eprints.qut.edu.au/37113/.

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

Council of Science Editors:

Brockhurst V. Development of novel DNA-based methods for the measurement of length polymorphisms (microsatellites). [Thesis]. Queensland University of Technology; 2001. Available from: http://eprints.qut.edu.au/37113/

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

10. Larsson, Matilda. Att leva med Huntingtons sjukdom : Ur ett personperspektiv.

Degree: Social and Health Sciences (HOS), 2014, Halmstad University

Huntingtons sjukdom är en ärftlig degenerativ sjukdom som förekommer hos 800-1000 personer i Sverige. Tidigare forskning visar på bristfällig kunskap om sjukdomen hos vårdpersonal… (more)

Subjects/Keywords: Experience; Huntington's disease; individuals perspective; suffering; Huntingtons sjukdom; lidande; personperspektiv; upplevelse

…genetic discrimination by people at risk for Huntingtons disease in the International RESPOND… …del av Huntington’s Disease Society of America (Huntington’s Disease Society of America… …behandlingen som redan finns (Riksförbundet Huntingtons sjukdom, 2014), med mål att öka… …moderkakan i vecka 10-11 eller genom ett fostervattenprov i vecka 14-18 (Huntington’s Disease… …Syfte Syftet var att belysa personers upplevelser av att leva med Huntingtons sjukdom. Metod… 

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

APA (6th Edition):

Larsson, M. (2014). Att leva med Huntingtons sjukdom : Ur ett personperspektiv. (Thesis). Halmstad University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:hh:diva-25329

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):

Larsson, Matilda. “Att leva med Huntingtons sjukdom : Ur ett personperspektiv.” 2014. Thesis, Halmstad University. Accessed January 15, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:hh:diva-25329.

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

MLA Handbook (7th Edition):

Larsson, Matilda. “Att leva med Huntingtons sjukdom : Ur ett personperspektiv.” 2014. Web. 15 Jan 2021.

Vancouver:

Larsson M. Att leva med Huntingtons sjukdom : Ur ett personperspektiv. [Internet] [Thesis]. Halmstad University; 2014. [cited 2021 Jan 15]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hh:diva-25329.

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

Council of Science Editors:

Larsson M. Att leva med Huntingtons sjukdom : Ur ett personperspektiv. [Thesis]. Halmstad University; 2014. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hh:diva-25329

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

11. Edlund, Hanna. Upplevelser av chorea och dess påverkan på fysisk aktivitet hos fem personer med Huntingtons sjukdom : En kvalitativ intervjustudie.

Degree: Physiotherapy, 2017, Uppsala University

Bakgrund: Huntingtons sjukdom innebär ofta såväl motoriska, kognitiva som psykiatriska symtom. Chorea är ett tidigt motoriskt symtom och innebär överrörelser som kan förekomma i… (more)

Subjects/Keywords: Huntington's disease; chorea; physical activity; experiences; interview; Huntingtons sjukdom; chorea; fysisk aktivitet; upplevelser; intervju; Physiotherapy; Sjukgymnastik

…personer med Huntingtons sjukdom av sin chorea? 2) Vilka upplevelser har fem personer med… …Huntingtons sjukdom av hur chorea påverkar deras förmåga till fysisk aktivitet? METOD Design I denna… …av 4 poäng Upplevelser av chorea hos fem personer med Huntingtons sjukdom Utifrån insamlad… …hur jag ska göra. (A) På grund av Huntingtons och chorea ska man helst gå framför… …personer med Huntingtons sjukdom Att finna sin plats i tillvaron Som tidigare nämnts så influeras… 

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APA (6th Edition):

Edlund, H. (2017). Upplevelser av chorea och dess påverkan på fysisk aktivitet hos fem personer med Huntingtons sjukdom : En kvalitativ intervjustudie. (Thesis). Uppsala University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-322573

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):

Edlund, Hanna. “Upplevelser av chorea och dess påverkan på fysisk aktivitet hos fem personer med Huntingtons sjukdom : En kvalitativ intervjustudie.” 2017. Thesis, Uppsala University. Accessed January 15, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-322573.

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

MLA Handbook (7th Edition):

Edlund, Hanna. “Upplevelser av chorea och dess påverkan på fysisk aktivitet hos fem personer med Huntingtons sjukdom : En kvalitativ intervjustudie.” 2017. Web. 15 Jan 2021.

Vancouver:

Edlund H. Upplevelser av chorea och dess påverkan på fysisk aktivitet hos fem personer med Huntingtons sjukdom : En kvalitativ intervjustudie. [Internet] [Thesis]. Uppsala University; 2017. [cited 2021 Jan 15]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-322573.

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

Council of Science Editors:

Edlund H. Upplevelser av chorea och dess påverkan på fysisk aktivitet hos fem personer med Huntingtons sjukdom : En kvalitativ intervjustudie. [Thesis]. Uppsala University; 2017. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-322573

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

12. Banduch, Kaitlin. Using the Theory of Motivated Information Management (TMIM) and Family Communication Patterns (FCP) to Understand Individual Decisions to Undergo Genetic Testing for Huntington's Disease (HD).

Degree: MA, College of Communication and Information / School of Communication Studies, 2014, Kent State University

 This study explored the relationship between family communication and individuals' decision-making process related to genetic testing for Huntington's disease (HD). HD is a rare genetic… (more)

Subjects/Keywords: Health; Communication; family communication; individual decision-making process; genetic testing; Huntingtons disease

disease. Finally, in the third scenario, genetic tests are used to diagnose autosomal dominant… …is 50 percent if only one parent is a carrier of the disease (Sheth, Dugdale, & Zieve… …and Huntington’s disease. The study focuses on Huntington’s disease. Huntington’s disease… …Neurological Disorders and Stroke, 2013). HD is a disease in which the brain and nerves… …and even the onset of dementia in later stages of the disease (Kent, 2004). The… 

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

APA (6th Edition):

Banduch, K. (2014). Using the Theory of Motivated Information Management (TMIM) and Family Communication Patterns (FCP) to Understand Individual Decisions to Undergo Genetic Testing for Huntington's Disease (HD). (Masters Thesis). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1397834101

Chicago Manual of Style (16th Edition):

Banduch, Kaitlin. “Using the Theory of Motivated Information Management (TMIM) and Family Communication Patterns (FCP) to Understand Individual Decisions to Undergo Genetic Testing for Huntington's Disease (HD).” 2014. Masters Thesis, Kent State University. Accessed January 15, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=kent1397834101.

MLA Handbook (7th Edition):

Banduch, Kaitlin. “Using the Theory of Motivated Information Management (TMIM) and Family Communication Patterns (FCP) to Understand Individual Decisions to Undergo Genetic Testing for Huntington's Disease (HD).” 2014. Web. 15 Jan 2021.

Vancouver:

Banduch K. Using the Theory of Motivated Information Management (TMIM) and Family Communication Patterns (FCP) to Understand Individual Decisions to Undergo Genetic Testing for Huntington's Disease (HD). [Internet] [Masters thesis]. Kent State University; 2014. [cited 2021 Jan 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1397834101.

Council of Science Editors:

Banduch K. Using the Theory of Motivated Information Management (TMIM) and Family Communication Patterns (FCP) to Understand Individual Decisions to Undergo Genetic Testing for Huntington's Disease (HD). [Masters Thesis]. Kent State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1397834101

13. Ranganathan, Megha. The Relationship Between Age-of-Onset and the Behavioral Phenotypic Manifestations in Huntington's Disease.

Degree: MS, Genetic Counseling, 2018, The Ohio State University

 Objective: The purpose of this study is to characterize behavioral manifestations of the Huntington's disease (HD) phenotype as associated with age-of-onset (AOO) of clinical presentation.… (more)

Subjects/Keywords: Genetics; Health Care; Neurology; Health Sciences; Huntingtons disease; HD; behavioral symptoms; behavioral manifestations; age of onset

…20 AIM 1: Compare difference in symptoms at disease presentation in individuals with early… …24 Table 3. Marginal comparison of AOO to symptom type at disease presentation with empiric… …AOO ......... 52 x Chapter 1. Background and Aims Background Huntington’s disease (… …HD) is a progressive neurodegenerative disease with an estimated prevalence of about… …article titled “On Chorea” (Huntington, 1872). He named the disease “hereditary chorea… 

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

APA (6th Edition):

Ranganathan, M. (2018). The Relationship Between Age-of-Onset and the Behavioral Phenotypic Manifestations in Huntington's Disease. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu152409456533713

Chicago Manual of Style (16th Edition):

Ranganathan, Megha. “The Relationship Between Age-of-Onset and the Behavioral Phenotypic Manifestations in Huntington's Disease.” 2018. Masters Thesis, The Ohio State University. Accessed January 15, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu152409456533713.

MLA Handbook (7th Edition):

Ranganathan, Megha. “The Relationship Between Age-of-Onset and the Behavioral Phenotypic Manifestations in Huntington's Disease.” 2018. Web. 15 Jan 2021.

Vancouver:

Ranganathan M. The Relationship Between Age-of-Onset and the Behavioral Phenotypic Manifestations in Huntington's Disease. [Internet] [Masters thesis]. The Ohio State University; 2018. [cited 2021 Jan 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu152409456533713.

Council of Science Editors:

Ranganathan M. The Relationship Between Age-of-Onset and the Behavioral Phenotypic Manifestations in Huntington's Disease. [Masters Thesis]. The Ohio State University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu152409456533713

14. Blanco, Maria Arone. Effects of herpes simplex virus 1 (HSV-1) infection on nuclear amyloid aggregation.

Degree: Biotechnology and Health (CBH), 2018, KTH

Huntington’s disease (HD) and Spinocerebellar ataxia (SCA) are incurable neurodegenerative diseases that affect the central nervous system. Amyloids, highly organized protein aggregates, are a… (more)

Subjects/Keywords: Huntington’s disease; Spinocerebellar ataxia; Amyloids; Protein aggregation; Herpes Simplex Virus 1; HSV-1; Virus infection; oligonucleotides; Filter retardation Assay; Dot Blot.; Huntingtons sjukdom; Spinocerebellära ataxier; Amyloider; Protein aggregering; Herpes Simplex Virus 1; HSV-1; Virus infektion; Oligonukleotider; Filter retardation Assay; Dot Blot.; Other Engineering and Technologies not elsewhere specified; Övrig annan teknik

…x22;Protein aggregates in Huntington’s disease," Experimental Neurology , vol. 238, no… …E. Marcocci, "HSV-1 and Alzheimer’s disease: more than a hypothesis," Frontiers… …Neurodegenerative Disorders: Alzheimer's Disease, Academic Press , 2017, pp. 1-16. [5] D… …Eidelberg and D. Surmeier, "Brain networks in Huntington disease," Journal Of Clinical… …x27;s Disease," Journal of Clinical and Experimental Neuropsychology, vol. 24, no. 2… 

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

APA (6th Edition):

Blanco, M. A. (2018). Effects of herpes simplex virus 1 (HSV-1) infection on nuclear amyloid aggregation. (Thesis). KTH. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-231319

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):

Blanco, Maria Arone. “Effects of herpes simplex virus 1 (HSV-1) infection on nuclear amyloid aggregation.” 2018. Thesis, KTH. Accessed January 15, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-231319.

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

MLA Handbook (7th Edition):

Blanco, Maria Arone. “Effects of herpes simplex virus 1 (HSV-1) infection on nuclear amyloid aggregation.” 2018. Web. 15 Jan 2021.

Vancouver:

Blanco MA. Effects of herpes simplex virus 1 (HSV-1) infection on nuclear amyloid aggregation. [Internet] [Thesis]. KTH; 2018. [cited 2021 Jan 15]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-231319.

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

Council of Science Editors:

Blanco MA. Effects of herpes simplex virus 1 (HSV-1) infection on nuclear amyloid aggregation. [Thesis]. KTH; 2018. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-231319

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

.