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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Gait Ataxia and FMR1[original query]
Screen for expanded FMR1 alleles in patients with essential tremor.
Movement disorders : official journal of the Movement Disorder Society 2004 Aug 19 (8): 930-3.
Garcia Arocena Dolores, Louis Elan D, Tassone Flora, Gilliam T Conrad, Ottman Ruth, Jacquemont Sébastien, Hagerman Paul
FMR1 CGG repeat length predicts motor dysfunction in premutation carriers.
Neurology 2008 Apr 70 (16 Pt 2): 1397-402.
Leehey M A, Berry-Kravis E, Goetz C G, Zhang L, Hall D A, Li L, Rice C D, Lara R, Cogswell J, Reynolds A, Gane L, Jacquemont S, Tassone F, Grigsby J, Hagerman R J, Hagerman P
Screening for FXTAS in 95 Spanish patients negative for Huntington disease.
Genetic testing 2008 Mar 12 (1): 135-8.
Rodriguez-Revenga Laia, Santos M Mònica, Sánchez Aurora, Pujol Montserrat, Gómez-Anson Beatriz, Badenas Celia, Jiménez Dolores, Madrigal Irene, Milà Montserr
Screening for the presence of FMR1 premutation alleles in women with parkinsonism.
Archives of neurology 2009 Feb 66 (2): 244-9.
Cilia Roberto, Kraff Jeremy, Canesi Margherita, Pezzoli Gianni, Goldwurm Stefano, Amiri Khalid, Tang Hiu-Tung, Pan Ruiqin, Hagerman Paul J, Tassone Flo
Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome.
Neuropsychology 2011 May 25 (3): 404-11.
Allen Emily Graves, Hunter Jessica E, Rusin Michele, Juncos Jorge, Novak Gloria, Hamilton Debra, Shubeck Lisa, Charen Krista, Sherman Stephanie
Characterization and Early Detection of Balance Deficits in Fragile X Premutation Carriers With and Without Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS).
Cerebellum (London, England) 2015 Mar .
O'Keefe Joan A, Robertson-Dick Erin, Dunn Emily J, Li Yan, Deng Youping, Fiutko Amber N, Berry-Kravis Elizabeth, Hall Deborah
'Essential Tremor' Phenotype in FMR1 Premutation/Gray Zone Sibling Series: Exploring Possible Genetic Modifiers.
Twin research and human genetics : the official journal of the International Society for Twin Studies 2021 3 24 (2): 95-102.
Loesch Danuta Z, Duffy David L, Martin Nicholas G, Tassone Flora, Atkinson Anna, Storey Elsd
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