Enter your terms above and click the 'Search' button.

Showing articles 0 to 10 of 10 Filter Applied: genetic screening (Click to remove) Spinal Muscular Atrophy UpToDate, Oct, Bodamer,O.A., 2022 Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019 Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome) UpToDate, Feb, Shovlin, C., 2011 Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts & Leukoencephalopathy (CADASIL) UpToDate (www.uptodate.com) Aug 21, Dichgans,M.,et al., 2007 The Tuberous Sclerosis Complex NEJM 355:1345-1356, Crino,P.B.,et al, 2006 Adrenoleukodystrophy JAMA 294:3131-3134, Moser,H.W.,et al, 2005 Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population JAMA 291:460-469, Jacquemont,S.,et al, 2004 What Level of Care for the Neurofibromatoses? Lancet 353:1114-1116, Huson,S.M., 1999 Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992 Neurologic Crises in Hereditary Tyrosinemia NEJM 322:432-437, Mitchell,G.,et al, 1990 Showing articles 0 to 10 of 10