Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred
about
Treatment for dysphagia (swallowing difficulties) in hereditary ataxiaGene, Stem Cell, and Alternative Therapies for SCA 1Spinocerebellar ataxia type 1--modeling the pathogenesis of a polyglutamine neurodegenerative disorder in transgenic mice.Milestones in ataxiaBrain pathology of spinocerebellar ataxias.Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1.Dominant spinocerebellar ataxias: a molecular approach to classification, diagnosis, pathogenesis and the future.Clinical, genetic, molecular, and pathophysiological insights into spinocerebellar ataxia type 1.Individual changes in preclinical spinocerebellar ataxia identified via increased motor complexity.Clinicopathology of spinocerebellar degeneration: its correlation to the unstable CAG repeat of the affected gene.Clinical aspects of CAG repeat diseases.The neuropathology of CAG repeat diseases: review and update of genetic and molecular features.Progressive cognitive decline with truncal/limb ataxia and ballistic movements.Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions.Loss of intrinsic organization of cerebellar networks in spinocerebellar ataxia type 1: correlates with disease severity and duration.Proton magnetic resonance spectroscopy in an Italian family with spinocerebellar ataxia type 1.Analysis of polyglutamine-coding repeats in the TATA-binding protein in different human populations and in patients with schizophrenia and bipolar affective disorder.Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis.Comparative studies of the CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene.Analysis of SCA1, DRPLA, MJD, SCA2, and SCA6 CAG repeats in 48 Portuguese ataxia families.Swallowing in degenerative ataxias.Spinocerebellar ataxia type 1 (SCA1): new pathoanatomical and clinico-pathological insights.Synchrotron X-ray fluorescence reveals abnormal metal distributions in brain and spinal cord in spinocerebellar ataxia: a case report.Spinocerebellar ataxia types 1, 2, 3 and 6: the clinical spectrum of ataxia and morphometric brainstem and cerebellar findings.Cognitive deficits in Machado-Joseph disease.Spinocerebellar ataxias: microsatellite and allele frequency in unaffected and affected individuals.
P2860
Q24187766-B461B64D-A8DA-422E-9190-33B40BD697A5Q26738497-CF8C1459-F485-4A84-BB01-D1F17B80DEF0Q33887985-FA15F229-23CF-4014-8EBE-6807C98BC873Q34188468-8F77AEDD-6F8A-4401-94F9-38853CCAA07DQ34298978-FC1C46F9-CCF7-4F81-9351-38E1CF750A30Q34377735-643EDBC9-86EE-492E-A0DD-6D2DF06EFB7DQ35589292-0655E5CC-A51D-4074-9A88-8F3888E2EDDAQ37140745-1A0821E3-4EBE-4390-B6D6-AA7878F9AE77Q38805432-F52CDDA2-E398-4F77-A84D-6FC9055169B9Q41364983-DA85373A-E16D-4F1C-B591-F13ED72522BFQ41527046-BC70297A-AAF2-41B1-9659-1B04A9BFE635Q41527060-1FF157B8-7602-4853-B5F5-83F9E1F0A229Q42448164-0C2318B1-F03A-46C8-B025-092EC933C330Q42528149-6E2C9184-438F-4B53-A377-29701537F9E6Q42731417-BEEC0C8A-C2E5-4E27-8258-CB3D682106AEQ44495068-F3AEBF4E-1E36-48B3-A65A-7D85F890DEE8Q45293240-E8372A4F-288E-4252-ADB5-82FB353238D6Q46474252-946E8C80-9908-4A7A-9603-33DC0C77D0D7Q46925753-83799253-B6D0-4FB1-A7B1-57DD9129F1C5Q48011436-391FDC36-56B8-468E-AF5A-7079D6C39BDBQ48581801-FB3125BA-CF99-4032-B769-8B5B821322C8Q48671892-60945A71-F5CF-49E1-BB1E-E45258FF68DAQ48691950-09CE6B55-EEED-4E80-8A7B-756887453439Q49131319-2E452A8B-00A0-474F-8BA0-C47416850C75Q52046710-30A54538-DD4F-46CE-BB7A-B1239D697544Q54446608-430FDB54-2E5F-4FBB-B37D-CC92D9235E29
P2860
Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred
description
im Januar 1995 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 01 January 1995
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в січні 1995
@uk
name
Clinical, neuropathologic, and ...... r ataxia type 1 (SCA1) kindred
@en
Clinical, neuropathologic, and ...... r ataxia type 1 (SCA1) kindred
@nl
type
label
Clinical, neuropathologic, and ...... r ataxia type 1 (SCA1) kindred
@en
Clinical, neuropathologic, and ...... r ataxia type 1 (SCA1) kindred
@nl
prefLabel
Clinical, neuropathologic, and ...... r ataxia type 1 (SCA1) kindred
@en
Clinical, neuropathologic, and ...... r ataxia type 1 (SCA1) kindred
@nl
P2093
P356
P1433
P1476
Clinical, neuropathologic, and ...... premonitory signs and symptoms
@en
P2093
P356
10.1212/WNL.45.1.24
P407
P577
1995-01-01T00:00:00Z