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Showing articles 0 to 11 of 11 Filter Applied: microcephaly (Click to remove) Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder Brain 133:655-670, Leen,W.G., et al, 2010 The Expanding Phenotype of GLUT1-Deficiency Syndrome Brain & Dev 31:545-552, Brockmann,K., 2009 Congenital Cytomegalovirus Infection BMJ 373:m1212, Pesch, M.H.,et al, 2021 Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss Neurol 90:e625-e631, Set, K.K.,et al, 2018 FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018 Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 Practice Parameter: Evaluation of the Child with Microcephaly (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society Neurol 73:887-897, Ashwal,S.,et al, 2009 Aicardi-Gouti�res Syndrome Br Med Bull 89:183-201, Orcesi, S.,et al, 2009 Mutations in the Molybdenum Cofactor Biosynthetic Genes MOCS1, MOCS2, and GEPH Hum Mutat 21:569-576, Reiss,J. &Johnson,J.L., 2003 Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings Ann Neurol 31:64-68, Perlman,J.M.&Argyle,C., 1992 EEG Recognition of Aicardi's Syndrome Arch Neurol 34:563, Fariello,R.G.,et al, 1977 Showing articles 0 to 11 of 11