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Showing articles 0 to 8 of 8 Filter Applied: genetic counselling (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 10-year-old boy with Bilateral Vision Loss Neurol 88:e221-e224, Bulwa, Z.,et al, 2017 Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017 Neurological Management of Von Hippel-Lindau Disease Neurologist 21:73-78, Hodgson, T.S.,et al, 2016 Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders Arch Neurol 61:875-880, Smith,C.O.,et al, 2004 Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia Pediatrics 102:98-100, Cabana,M.D.,et al, 1998 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred Medicine 68:1-29, Lamiell,J.M.,et al, 1989 Showing articles 0 to 8 of 8