Differential (Click to cross reference) ACTH advances in neurology Alzheimer's disease Alzheimer's disease, early onset Alzheimer's disease, familial Alzheimer's disease, familial, late onset Alzheimer's disease, pathogenesis Alzheimer's disease, treatment of amnesia amniocentesis amyloid beta protein amyloid imaging aneuploidy Angelman syndrome anticholinesterase antioxidant apolipoprotein E APP apraxia apraxia, constructional ataxia atrial septal defect atrioventricular septal defect autism CAT scan, emission CAT scan, emission, abnormal cataracts cataracts, congenital central nervous system, infection of cerebral glucose metabolism children choroid plexus choroid plexus, abnormality of choroid plexus, cyst chromosomal abnormality chromosome 1 chromosome 14 chromosome 21 complications congenital heart disease congenital infection, CNS congenital infection, viral dementia dementia, familial developmental milestones, loss of developmental retardation differential diagnosis DNA probes donepezil dysarthria dysnomia echolalia electroencephalogram, abnormalities of executive dysfunction familial fetal alcohol syndrome fetus fragile-X syndrome gene gene mutation genetic neurologic disorders genetic testing head bobbing hypsarrhythmia inborn errors of metabolism infantile spasm intelligence quotient intrauterine infection Jakob-Creutzfeldt disease learning disability learning disability, in children lymphoma involving CNS malformation, CNS, congenital memory, impairment of mild cognitive impairment molecular genetics mongolism mortality myoclonus myoclonus, epilepsy N-acetylcysteine neurofibrillary degeneration neurologic disease, diagnoses of neuropathology paranoia personality change Pittsburgh Compound B Prader-Labhart-Willi syndrome prenatal diagnosis by amniocentesis presenilin-1 gene presenilin-2 gene prognosis psychiatric disorder psychological testing psychological testing, children review article risk factors rubella syndrome seizure seizure, crying as manifestation of senile plaques single photon emission computed tomography skin, lesions in neurologic disorders trauma treatment of neurologic disorder trisomes trisomy 18 tuberous sclerosis ultrasonography ultrasonography, head ultrasonography, head, fetus-neonate Unverricht-Lundborg disease ventricular septal defect viral infection viral infection, CNS visuospatial disturbance workup

Showing articles 1350 to 1359 of 1359 << Previous Screening for Inborn Errors of Metabolism Associated with Mental Deficiency or Neurologic Disorders or Both NEJM 274:384, Renuart,A., 1966 Inherited Aminoacidopathies Demonstrating Vitamin Dependency NEJM 281:145, Rosenberg,L., 1965 Morquio's Disease, A Radiologic & Morphologic Study Pediatrics 34:839-850, Schenk,E.A.&Haggerty,J., 1964 Familial and Conjugal Multiple Sclerosis Brain 86:315-332, Schapira,K.,et al, 1963 The Cornelia de Lange Syndrome J Pediatr 63:1000-1020, Ptacek,L.J., 1963 Neuro CPC of MGH Multiple Cerebral Abscesses & Infarcts, NEJM 266:610-61762., , 1962 Angiokeratoma Corporis Diffusum Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962 Microcephaly Arch Dis Child 37:623-627, Davies,H.,et al, 1962 Cerebrovascular Accidents in Patients with Congenital Heart Disease Arch Neurol & Psychiat 77:483957., Tyler,H.R.,et al, 1957 Clinical Study of Nine Patients with ReNU Syndrome , Okamoto,N.,et al, Showing articles 1350 to 1359 of 1359 << Previous