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F Squitieri

Showing results (31-40 of 53) with videos related to

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The New England Journal of Medicine|May 19, 1994
A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeatsB Kremer, P Goldberg, S E Andrew, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1993
A double-blind cross-over trial of amantadine hydrochloride in Friedreich's ataxiaA Filla, G De Michele, G Orefice, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 5, 2003
Italian Huntington disease patients--data and tissue bankF Squitieri, M Cannella, L Gaudio, et al.
American Journal of Human Genetics|May 1, 1994
Huntington disease without CAG expansion: phenocopies or errors in assignment?S E Andrew, Y P Goldberg, B Kremer, et al.
Human Molecular Genetics|December 1, 1994
DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalenceF Squitieri, S E Andrew, Y P Goldberg, et al.
Clinical Genetics|August 17, 2000
Atypical movement disorders in the early stages of Huntington's disease: clinical and genetic analysisF Squitieri, A Berardelli, E Nargi, et al.
Human Molecular Genetics|October 1, 1993
Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parentH Telenius, H P Kremer, J Theilmann, et al.
Nature Genetics|August 1, 1993
The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's diseaseS E Andrew, Y P Goldberg, B Kremer, et al.
Neuroscience|July 18, 2008
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformationsF Gianfrancesco, T Esposito, S Penco, et al.
Nature Genetics|October 1, 1993
Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effectsY P Goldberg, B Kremer, S E Andrew, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
The New England Journal of Medicine|May 19, 1994
A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeatsB Kremer, P Goldberg, S E Andrew, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1993
A double-blind cross-over trial of amantadine hydrochloride in Friedreich's ataxiaA Filla, G De Michele, G Orefice, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 5, 2003
Italian Huntington disease patients--data and tissue bankF Squitieri, M Cannella, L Gaudio, et al.
American Journal of Human Genetics|May 1, 1994
Huntington disease without CAG expansion: phenocopies or errors in assignment?S E Andrew, Y P Goldberg, B Kremer, et al.
Human Molecular Genetics|December 1, 1994
DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalenceF Squitieri, S E Andrew, Y P Goldberg, et al.
Clinical Genetics|August 17, 2000
Atypical movement disorders in the early stages of Huntington's disease: clinical and genetic analysisF Squitieri, A Berardelli, E Nargi, et al.
Human Molecular Genetics|October 1, 1993
Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parentH Telenius, H P Kremer, J Theilmann, et al.
Nature Genetics|August 1, 1993
The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's diseaseS E Andrew, Y P Goldberg, B Kremer, et al.
Neuroscience|July 18, 2008
ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformationsF Gianfrancesco, T Esposito, S Penco, et al.
Nature Genetics|October 1, 1993
Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effectsY P Goldberg, B Kremer, S E Andrew, et al.
Pageof 6