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Showing articles 0 to 6 of 6 Filter Applied: genetic screening (Click to remove) Adrenoleukodystrophy JAMA 294:3131-3134, Moser,H.W.,et al, 2005 Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997 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 The Tuberous Sclerosis Complex NEJM 355:1345-1356, Crino,P.B.,et al, 2006 Clinical Spectrum of CADASIL:A Study of 7 Families Lancet 346:934-939, Chabriat,H.,et al, 1995 Showing articles 0 to 6 of 6