Differential (Click to cross reference) adverse drug reaction agenesis of corpus callosum aminoacidurias anticonvulsants anticonvulsants, blood level determination of anticonvulsants, selection of anticonvulsants, teratogenicity of anticonvulsants, untoward effects of aphasia, children apraxia, speech attention deficit disorder with hyperactivity autism Benedict's solution test benzodiazepine bifid uvula bone age brachial plexus neuropathy brachial plexus neuropathy, familial bulbar palsy bulbar palsy, acute caffeine calcification, intracranial carbamazepine carbamazepine, toxicity cerebral palsy cerebral palsy, associated problems with cerebral palsy, pure ataxic cervical spine abnormality chromosomal abnormality cleft lip cleft palate clinodactyly clonazepam complications congenital birth defects congenital deformities congenital heart disease congenital heart disease, CNS complications with congenital malformation congenital malformation, dilantin therapy causing congenital malformation, non CNS Cornelia de Lange syndrome Craniosynostosis cry, abnormal deafness deafness, unilateral developmental abnormality of brain digits, abnormal dilantin dilantin, toxicity dinitrophenylhydrazine(D.N.P.H.)reaction diphtheria diplegia, atonic diplegia, spastic cerebral Duane syndrome dysarthria dysmorphic dysplasia of C.N.S. ear, abnormal electroencephalogram ethantoin eyebrows, abnormal facial anomalies facial nerve palsy failure to thrive ferric chloride test fetal alcohol syndrome gender genetic neurologic disorders growth retardation hearing problems in children hemorrhagic diathesis heterotopia Hirschprung's disease hirsutism holoprosencephaly Holt-Oram syndrome hypertelorism hypospadias hypotelorism intellectual deficit intellectual deficit, treatable causes of intelligence quotient karyotyping klippel feil syndrome lamotrigine language disorders in children low birth weight malformation, CNS, congenital malformation, vascular maple syrup urine disease mental retardation microcephaly micrognathia micromelia midline defect in children myelodysplasia nasal speech neural tube defect neuropathy, diphtheritic neurotoxin oligodactyly ophthalmoplegia palate, paralysis palatopharyngeal incompetence phenobarbital phenylketonuria phocomelia polydactyly polypharmacy pregnancy, anticonvulsants during pregnancy, neurologic complications in psychological testing, neurologic problems psychosis psychosis, childhood psychosocial aspects ptosis ptosis, unilateral pupil, abnormality in neurologic disorders pupil, ectopic-congenital pyramidal tract dysfunction respiratory failure risk factors saddle nose safety seizure seizure, advice to parents and teachers regarding seizure, maternal seizure, pregnancy seizure, psychosocial aspects of seizure, treatment of septicemia short stature simian crease skin, lesions in neurologic disorders sodium valproate speech disorder, childhood spina bifida stuttering syndactyly synophrys syringomyelia teratogenesis teratogenic drugs topiramate trimethadione urine test for metabolic disorders Wildervanck's syndrome

Showing articles 50 to 62 of 62 << Previous Treatment of Ocular Myoclonus with Valproic Acid Ann Neurol 17:103-104, Lefkowitz,D.,et al, 1985 Syndrome of Palatal Myoclonus & Progressive Ataxia:Two Cases with Magnetic Resonance Imaging Neurol 35:1212-1214, Sperling,M.R.&Herrman,C., 1985 Palatal Myoclonus in Behcet's Disease Arch Int Med 145:949-950, Shuttleworth,E.C.,et al, 1985 Unilateral Palatal Paralysis Caused by Lesion in the Corticobulbar Tract Arch Neurol 41:782-784, Iwata,M., 1984 Brainstem Auditory Evoked Potentials in 20 Patients with Palatal Myoclonus Arch Neurol 40:155-158, Westmoreland,B.F.,et al, 1983 Adult Celiac Disease Presenting as Cerebellar Syndrome Neurol 30:245-249 1980., Finelli,P.F.,et al, 1980 Locked-In Syndrome with Recovery Ann Neurol 8:439-441, Khurana,R.K.,et al, 1980 Dominant Spinopontine Atrophy Arch Neurol 35:156, Pogacar,S.,et al, 1978 Nemaline (Rod) Myopathy:The Need for Histochemical Evaluation of Affected Families Ann Neurol 4:37, Bender,A.N.,et al, 1978 Granulomatous Inflammation of Mouth & Larynx, Consistent with Crohn's Disease, Case 35-1978 NEJM 299:538-544, Scully,R.E.,et al, 1978 Prader-Willi-Syndrome, In Endocrine & Genetic Diseases of Childhood & Adolescence (Ed) , 1975. W. B. Saunders Co, p, Gardner,L.I., 1975 Palatal Myoclonus & Diphenylhydantoin Therapy Letter, NEJM 290:10881974., Rhee,R.S.,et al, 1974 Acquired Pendular Nystagmus with Oscillopsia in Multiple Sclerosis:A Sign of Cerebellar Nuclei Disease JNNP 37:570, Aschoff,J.C.,et al, 1974 Showing articles 50 to 62 of 62 << Previous