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Showing articles 0 to 11 of 11 Filter Applied: microcephaly (Click to remove) A Middle-aged Woman with Severe Scoliosis and Encephalopathy JAMA Neurol 78:251-252, Mohan, G.,et al, 2021 Congenital Cytomegalovirus Infection BMJ 373:m1212, Pesch, M.H.,et al, 2021 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 Neonatal Abstinence Syndrome NEJM 375:2468-2479, McQueen, K. & Murphy-Oikonen, J., 2016 Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 Clinicopathologic Conference, Severe Methylenetetrahydrofolate Reductase Deficiency NEJM 371:847-858, Case 27-2014, 2014 Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up AJNR 30:1971-1976, Uggetti,C.,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 Causal Heterogeneity in Isolated Lissencephaly Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992 Angelman Syndrome: Clinical Profile J Child Neurol 7:270-280, Zori,R.T.,et al, 1992 Showing articles 0 to 11 of 11