Abnormal nerve conduction features in fragile X premutation carriers.
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Advances in the Understanding of the Gabaergic Neurobiology of FMR1 Expanded Alleles Leading to Targeted Treatments for Fragile X Spectrum DisorderFragile X spectrum disordersFragile X-associated tremor/ataxia syndrome.Unstable mutations in the FMR1 gene and the phenotypesAltered Translational Control of FMRP on Myelin Proteins in Neuropsychiatric DisordersFragile X-associated tremor/ataxia syndrome: clinical phenotype, diagnosis, and treatmentIn the Gray Zone in the Fragile X Gene: What are the Key Unanswered Clinical and Biological Questions?Advances in understanding the molecular basis of FXTASEmerging topics in FXTAS.Fragile x-associated tremor ataxia syndrome: the expanding clinical picture, pathophysiology, epidemiology, and update on treatment.Premutation CGG-repeat expansion of the Fmr1 gene impairs mouse neocortical development.A voxel-based morphometry study of grey matter loss in fragile X-associated tremor/ataxia syndrome.A Quantitative Assessment of Tremor and Ataxia in Female FMR1 Premutation Carriers Using CATSYS.Widespread non-central nervous system organ pathology in fragile X premutation carriers with fragile X-associated tremor/ataxia syndrome and CGG knock-in mice.Axonal neuropathy in female carriers of the fragile X premutation with fragile x-associated tremor ataxia syndrome.FMR1 premutation and full mutation molecular mechanisms related to autism.Modest alterations in patterns of motor neuron dendrite morphology in the Fmr1 knockout mouse model for fragile X.Fragile X syndrome: an aging perspective.Prevalence and risk of migraine headaches in adult fragile X premutation carriersA multimodal imaging analysis of subcortical gray matter in fragile X premutation carriers.Molecular pathogenesis of fragile X-associated tremor/ataxia syndromeFragile X-associated tremor/ataxia syndrome (FXTAS): pathology and mechanisms.Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome.Neurocognitive endophenotypes in CGG KI and Fmr1 KO mouse models of Fragile X-Associated disorders: an analysis of the state of the fieldLinking oligodendrocyte and myelin dysfunction to neurocircuitry abnormalities in schizophrenia.Therapeutic approach to pain in neurodegenerative diseases: current evidence and perspectives.Implications of the FMR1 Premutation for Children, Adolescents, Adults, and Their Families.Late Onset Tremor and Ataxia Syndrome: FXTAS and its Ignored Peripheral Nervous System Findings in Diagnostic Criteria.Clinical Phenotype of Adult Fragile X Gray Zone Allele Carriers: a Case Series.Small fiber neuropathy in a woman with fragile X-associated tremor/ataxia syndrome (FXTAS).
P2860
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P2860
Abnormal nerve conduction features in fragile X premutation carriers.
description
2008 nî lūn-bûn
@nan
2008 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Abnormal nerve conduction features in fragile X premutation carriers.
@ast
Abnormal nerve conduction features in fragile X premutation carriers.
@en
type
label
Abnormal nerve conduction features in fragile X premutation carriers.
@ast
Abnormal nerve conduction features in fragile X premutation carriers.
@en
prefLabel
Abnormal nerve conduction features in fragile X premutation carriers.
@ast
Abnormal nerve conduction features in fragile X premutation carriers.
@en
P2093
P2860
P1433
P1476
Abnormal nerve conduction features in fragile X premutation carriers.
@en
P2093
Davis Hessl
Flora Tassone
Grace Fenton-Farrell
Kultida Soontarapornchai
Paul J Hagerman
Randi J Hagerman
Ricardo Maselli
P2860
P304
P356
10.1001/ARCHNEUR.65.4.495
P577
2008-04-01T00:00:00Z