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Showing articles 0 to 6 of 6 Filter Applied: genetic screening (Click to remove) Melas Syndrome Stat PearlsPubl Jan 25, Pia,S. & Lui,F., 2025 Molecular and Neurological Features of MELAS Syndrome in Paediatric Patients: A Case Series and Review of the Literature Mal Genet Genomic Med 10:e1955, Seed,L.M.,et al, 2022 Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019 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 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