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Showing articles 0 to 11 of 11 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 Malignant Hyperthermia, Update on Susceptibility Testing JAMA 293:2918-2924,2958, Litman,R.S.&Rosenberg,H., 2005 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 The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective JAMA 277:832-836, Post,S.G.,et al, 1997 Statement of Use of Apolipoprotein E Testing for Alzheimer Disease JAMA 274:1627-1629, Farrer,L.A.,et al, 1995 Molecular Genetics in Neurology Ann Neurol 34:757-773, Martin,J.B., 1993 Detecting Susceptibility to Malignant Hyperthermia BMJ 304:791-792, Ellis,F.R., 1992 Neurologic Crises in Hereditary Tyrosinemia NEJM 322:432-437, Mitchell,G.,et al, 1990 Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening Lancet 2:425-427, Greenberg,C.R.,et al, 1988 Showing articles 0 to 11 of 11