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Showing articles 0 to 14 of 14 Filter Applied: trinucleotide repeats (Click to remove) Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022 A Neonate with Micrognathia and Hypotonia Neurol 86:e80-e84, Vawter-Lee, M.M.,et al, 2016 Newborn Screening for Fragile X Syndrome JAMA Neurol 71:355-359, Tassone, F., 2014 Brugada Syndrome in Spinal and Bulbar Muscular Atrophy Neurol 82:1813-1821, Araki, A.,et al, 2014 Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy) Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014 Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene Arch Neurol 65:19-25, Amiri,K.,et al, 2008 Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population JAMA 291:460-469, Jacquemont,S.,et al, 2004 Kennedy Disease Arch Neurol 60:893-894, Paparounas,K.,et al, 2003 Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction. AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002 Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS Neurol 49:568-572, Parboosingh,J.S.,et al, 1997 Advances in Molecular Analysis of Fragile X Syndrome 552, Warren,W.T.&Nelson,D.L.JAMA 271:536-553, 1994 Trinucleotide Repeat Expansion in Neurological Disease Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994 Molecular Genetics in Neurology Ann Neurol 34:757-773, Martin,J.B., 1993 Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test JAMA 270:1569-1575, Brown,W.,et al, 1993 Showing articles 0 to 14 of 14