Differential (Click to cross reference) agenesis of corpus callosum aminoacidurias anemia anemia, hemolytic aphonia basal ganglia, degeneration biologic markers CAT scan, abnormal cerebral cortical atrophy children choreoathetosis cirrhosis cirrhosis, causes of childhood corpus callosum, lesion of developmental retardation dysmorphic dysphagia dystonia dystonia, treatment of facial appearance, abnormal failure to thrive familial feeding disorder genetic counselling genetic diagnosis, prenatal genetic neurologic disorders handwriting hepatitis hepatolenticular degeneration(Wilson's disease) hyperuricemia hypotonia inborn errors of metabolism Kayser-Fleischer ring lens, dislocation of metabolic disorder, primary microcephaly misdiagnosis molybdenum cofactor deficiency MRI, abnormal nose, abnormal pancytopenia Parkinson disease Parkinson disease, prognosis of penicillamine prognosis psychiatric problems in neurologic disorders psychomotor retardation psychosis salivation, excessive schizophrenia screaming seizure seizure, intractable seizure, neonatal slit lamp examination splenomegaly suck, poor sulfite oxidase deficiency treatment of neurologic disorder tremor uric acid, low urinalysis, abnormal

Showing articles 0 to 5 of 5 Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 Serum Uric Acid and Clinical Progression in Parkinson Disease: Potential Biomarker for Nigrostriatal Failure Arch Neurol 65:698-699, Schiess,M. &Oh,I., 2008 Mutations in the Molybdenum Cofactor Biosynthetic Genes MOCS1, MOCS2, and GEPH Hum Mutat 21:569-576, Reiss,J. &Johnson,J.L., 2003 Dipsticks and Convulsions Lancet 352:1824, Koch,H., 1998 Diagnosis of Treatable Wilson's Disease NEJM 298:1347, Cartwright,G.E., 1978 Showing articles 0 to 5 of 5