Differential (Click to cross reference) acromicria amniocentesis Angelman syndrome anorexia antitoxin apraxia of eye movements aspartate aminotransferase ataxia athetosis autonomic dysfunction basal ganglia, lesion of basal ganglia, lesion, bilateral behavior, combative behavioral disorder bilirubin encephalopathy botulinum toxin botulism botulism antitoxin botulism immune globulin botulism, infant breast feeding bulbar palsy bulbar palsy, childhood CAT scan, abnormal cerebral cortical atrophy cerebrospinal fluid cerebrospinal fluid, cell count, normal children chromosome 15 Clinical Pathologic Conference(C.P.C.) contractures, joint cry, abnormal cry, high-pitched cry, weak crying developmental disability developmental milestones developmental milestones, loss of developmental retardation drooling dysarthria dysmorphic dysphagia eating disorder efficacy electroencephalogram, abnormalities of encephalitis, viral encephalopathy enzyme, defect facial appearance, abnormal failure to thrive feeding disorder fetal movements, reduced fetus fever floppy infant food poisoning food-borne infection gait disorder gammaglobulin therapy, intravenous gastroenteritis Gaucher's disease gaze palsy gaze palsy, supranuclear gaze palsy, vertical gene genetic counselling genetic diagnosis, prenatal genetic neurologic disorders globus pallidus, lesion of globus pallidus, lesion of, bilateral glucocerebrosidase growth hormone deficiency hand flapping head bobbing head lag hearing loss hepatic failure hepatic failure, acute hepatitis histochemistry histochemistry of muscle honey hot, red, angry babies human parechovirus hyperbilirubinemia hyperbilirubinemia, CNS abnormality after hyperphagia hyperreflexia hypertension hypogonadism hypopigmentation of skin hyporeflexia hypotonia hypotonia, infants imbalance infant, evaluation of infection intellectual deficit irritability irritable baby jaundice kernicterus lactic dehydrogenase(LDH) Leigh's disease lethargy liver function enzymes meningoencephalitis mental retardation merosin microcephaly misdiagnosis mitochondrial disease molecular genetics molybdenum cofactor deficiency moro reflex mortality MRI MRI, abnormal MRI, high signal foci on MRI, high signal intensity of basal ganglia muscle biopsy muscular dystrophy muscular dystrophy, central nervous system abnormality muscular dystrophy, congenital muscular dystrophy, congenital, Fukuyama type myoclonic jerks neck weakness neurologic disease, diagnoses of neuromuscular junction, abnormality of neurotoxin nystagmus obesity oculogyric crisis ophthalmoplegia ophthalmoplegia, neonatal opisthotonus parechovirus encephalitis pediatric neurology polymerase chain reaction Prader-Labhart-Willi syndrome premature infant prenatal diagnosis by amniocentesis prognosis psychomotor retardation ptosis ptosis, bilateral rash rash, hand respiratory failure respiratory tract infection review article season seizure seizure, neonatal sensorineural hearing loss septicemia setting sun phenomena short stature spongy degeneration of brain strabismus suck, poor tachycardia temper tantrums term infant tongue, protrusion of tonic spasms treatment of neurologic disorder tremulousness upgaze, paralysis of uric acid, low vertical gaze viral infection viral infection, CNS walking, difficulty with weakness weakness, congenital weakness, generalized weakness, infant white matter disease wide based gait

Showing articles 150 to 153 of 153 << Previous Corticodentatonigral Degeneration with Neuronal Achromasia Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968 Central Nervous System Manifestations of Periarteritis Nodosa Neurol 15:114, Ford,R.G.,et al, 1965 Carbon Monoxide Asphyxia, A Common Clinical Entity Canad M A J 78:182-185, Katz,M., 1958 Clinical Study of Nine Patients with ReNU Syndrome , Okamoto,N.,et al, Showing articles 150 to 153 of 153 << Previous