Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal.
about
Machado-Joseph Disease: from first descriptions to new perspectives.Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics.Autosomal dominant cerebellar ataxias: a systematic review of clinical features.Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestryHereditary Cerebellar Ataxias: A Korean Perspective.Epidemiological, clinical, and molecular characterization of Cuban families with spinocerebellar ataxia type 3/Machado-Joseph disease.First report of a Japanese family with spinocerebellar ataxia type 10: The second report from Asia after a report from ChinaNystagmus as an early ocular alteration in Machado-Joseph disease (MJD/SCA3).A comprehensive review of spinocerebellar ataxia type 2 in Cuba.Fragile X-associated tremor/ataxia syndrome: phenotypic comparisons with other movement disorders.Spinocerebellar ataxia type 3 in Israel: phenotype and genotype of a Jew Yemenite subpopulation.Spinocerebellar ataxias in Venezuela: genetic epidemiology and their most likely ethnic descent.Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation.Spinocerebellar ataxias in Brazil--frequencies and modulating effects of related genes.Clinical and genetic analysis of spinocerebellar ataxia type 7 (SCA7) in Zambian families.A shared haplotype for dentatorubropallidoluysian atrophy (DRPLA) in Italian families testifies of the recent introduction of the mutation.Clinical course of patients with familial early-onset Alzheimer's disease potentially lacking senile plaques bearing the E693Δ mutation in amyloid precursor protein.Current molecular insight to reveal the dynamics of CAG repeating units in spinocerebellar ataxia.
P2860
Q21202868-A1479B9E-D5EA-424E-848D-7B9EF472DC61Q34323333-D95E574C-6576-4BEA-A4AA-EA1F59814E64Q34417063-0D576DA9-E2CE-40CE-9DF1-10144421889AQ35054026-3CCA441F-A52A-47C7-8CC8-231CF97E4649Q35699775-5BEF0EDE-3395-44C8-A8FE-EA061CA38719Q36003053-01F65A71-8555-4363-B84E-BCD6AE6F971BQ36380255-8166959A-76E2-4FAF-BD66-B97EEE0DFB96Q37514583-DE89A393-42DB-4322-82DC-7FC18C87B647Q37852582-C2CAA07A-BB63-4888-87DF-24F03EA32846Q38896237-4E8A3304-96E9-488F-8C7A-8B0AEA4389B5Q39200544-43B9149E-EE1F-4CE4-A387-164D433725CCQ41148958-0638DF44-E238-4DF1-B04B-D7084254404BQ42690468-36A9E023-8446-40E1-96EB-8DB6A7A54808Q45893158-3071C4EA-A65E-40D2-9625-EC9EDE43D879Q47112261-AD78B4CA-5AAC-4DBB-9EA1-5BEB4FA4FFB2Q47222677-A088263B-1BB2-46AB-B51C-75E7860EB6DAQ48946574-A88F9A82-4104-44E6-8E19-0CE182942E13Q54935894-257CB860-D132-42BA-8E0D-40120C05D184
P2860
Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
Autosomal dominant cerebellar ...... of 45 families from Portugal.
@en
Autosomal dominant cerebellar ...... of 45 families from Portugal.
@nl
type
label
Autosomal dominant cerebellar ...... of 45 families from Portugal.
@en
Autosomal dominant cerebellar ...... of 45 families from Portugal.
@nl
prefLabel
Autosomal dominant cerebellar ...... of 45 families from Portugal.
@en
Autosomal dominant cerebellar ...... of 45 families from Portugal.
@nl
P2860
P50
P1476
Autosomal dominant cerebellar ...... of 45 families from Portugal.
@en
P2093
P2860
P304
P356
10.1111/J.1468-1331.2009.02757.X
P577
2009-07-29T00:00:00Z