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K P Figueroa

Showing results (1-10 of 10) with videos related to

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Drugs of the Future|September 25, 2009
SOLUBLE CD40 LIGAND IN DEMENTIAB Giunta, K P Figueroa, T Town, et al.
American Journal of Human Genetics|February 11, 1999
Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22L Zu, K P Figueroa, R Grewal, et al.
Genomics|April 16, 1998
Genomic structure of the human gene for spinocerebellar ataxia type 2 (SCA2) on chromosome 12q24.1S Sahba, A Nechiporuk, K P Figueroa, et al.
Muscle & Nerve|May 16, 2001
Rippling muscle disease: evidence for phenotypic and genetic heterogeneityY T So, L Zu, C Barraza, et al.
Neurology. Genetics|May 24, 2017
Genetic analysis of age at onset variation in spinocerebellar ataxia type 2K P Figueroa, Hilary Coon, Nieves Santos, et al.
Neurology|December 31, 1997
Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlationsD H Geschwind, S Perlman, K P Figueroa, et al.
Neurology|November 18, 1998
Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxiaR P Grewal, E Tayag, K P Figueroa, et al.
Archives of Neurology|October 27, 2001
Association of moderate polyglutamine tract expansions in the slow calcium-activated potassium channel type 3 with ataxiaK P Figueroa, P Chan, L Schöls, et al.
Neurology|September 2, 2005
An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?M F Waters, D Fee, K P Figueroa, et al.
Neurology|February 15, 2018
Comprehensive systematic review summary: Treatment of cerebellar motor dysfunction and ataxia [RETIRED]: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of NeurologyTheresa A Zesiewicz, George Wilmot, Sheng-Han Kuo, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Drugs of the Future|September 25, 2009
SOLUBLE CD40 LIGAND IN DEMENTIAB Giunta, K P Figueroa, T Town, et al.
American Journal of Human Genetics|February 11, 1999
Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22L Zu, K P Figueroa, R Grewal, et al.
Genomics|April 16, 1998
Genomic structure of the human gene for spinocerebellar ataxia type 2 (SCA2) on chromosome 12q24.1S Sahba, A Nechiporuk, K P Figueroa, et al.
Muscle & Nerve|May 16, 2001
Rippling muscle disease: evidence for phenotypic and genetic heterogeneityY T So, L Zu, C Barraza, et al.
Neurology. Genetics|May 24, 2017
Genetic analysis of age at onset variation in spinocerebellar ataxia type 2K P Figueroa, Hilary Coon, Nieves Santos, et al.
Neurology|December 31, 1997
Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlationsD H Geschwind, S Perlman, K P Figueroa, et al.
Neurology|November 18, 1998
Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxiaR P Grewal, E Tayag, K P Figueroa, et al.
Archives of Neurology|October 27, 2001
Association of moderate polyglutamine tract expansions in the slow calcium-activated potassium channel type 3 with ataxiaK P Figueroa, P Chan, L Schöls, et al.
Neurology|September 2, 2005
An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?M F Waters, D Fee, K P Figueroa, et al.
Neurology|February 15, 2018
Comprehensive systematic review summary: Treatment of cerebellar motor dysfunction and ataxia [RETIRED]: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of NeurologyTheresa A Zesiewicz, George Wilmot, Sheng-Han Kuo, et al.
Pageof 1