Differential (Click to cross reference) abdominal distention abducens nerve paralysis acanthocytosis acetazolamide achondroplasia acromicria adverse drug reaction alcohol alcohol, neurologic complications with algorithm alopecia amenorrhea amniocentesis anatomy of anemia Angelman syndrome anorexia nervosa aphasia aqueduct of Sylvius, stenosis aqueductal stenosis areflexia arthralgia arthritis arylsulfatase B asymptomatic ataxia ataxia, cerebellar ataxia, progressive ataxic gait atlanto-axial subluxation autoimmune disease basal ganglia, calcification of basal ganglia, lesion, bilateral basilar impression Bassen-Kornzweig syndrome battered child syndrome behavior, combative behavioral disorder bitemporal visual field defect blepharophimosis blepharospasm blind spot, enlarged blindness blindness, sudden bone age bone biopsy bone marrow transplantation brachial plexus neuropathy brachial plexus neuropathy, familial brain atrophy brain biopsy brainstem, atrophy breech delivery cachexia calcification, gyral calcification, intracranial carbonic anhydrase II deficiency cardiomyopathy caries CAT scan CAT scan, abnormal CAT scan, false negative cataracts celiac disease, adult celiac disease, childhood cerebellar ataxia, primary cerebellar degeneration cerebral cortical atrophy cerebral palsy cerebrospinal fluid, cytology cerebrospinal fluid, elevated protein of cerebrospinal fluid, lactic acid concentration cerebrospinal fluid, pressure increased cerebrovascular accident cerebrovascular accident, familial occurrence cerebrovascular accident, infancy and childhood cerebrovascular accident, mimics cerebrovascular accident, multiple cerebrovascular accident, recurrent cerebrovascular accident, young adult chemotherapy, CNS treatment and complications with child abuse children choreoathetosis chorionic gonadotropin chromosomal abnormality chromosome 14 chromosome 15 chromosome 8 chronic graft versus host disease chronic progressive external ophthalmoplegia cisternogram, radionuclide cleft palate Clinical Pathologic Conference(C.P.C.) Cockayne's syndrome codfish vertebrae cold hands sign collagen vascular disease coma complications compression fracture congenital heart disease congenital heart disease, CNS complications with congenital malformation conjunctivitis consanguinity contractures, joint cornea, abnormal cornea, opacity of corpus callosotomy corpus callosum, atrophy of corpus callosum, thinning cortical blindness cranial nerve palsies craniopharyngioma cry, abnormal cry, weak cryopyrin-associated periodic syndrome cryptorchidism cultured skin fibroblasts cystinuria cytochrome c oxidase cytochrome c oxidase, deficiency deafmute deafness degenerative diseases of CNS dementia dementia, rapidly progressive dentate nuclei, lesion of dermatitis herpetiformis developmental milestones, loss of developmental retardation diabetes insipidus diabetes mellitus diagnostic criteria diarrhea differential diagnosis difficulty climbing stairs diplopia dislocated hip, congenital dissociated sensory loss distal muscle atrophy distal muscle weakness dopa responsive dystonia drooling dural sinus thrombosis dwarfism dysmorphic dysphagia dyspraxia dystonia ear, abnormal eating disorder echocardiogram ectopic pinealoma electroencephalogram electroencephalogram, abnormalities of electromyogram electron microscopy empty sella encephalopathy encephalopathy, progressive endovascular therapy enophthalmous enzyme treatment enzyme, defect enzyme, muscle disease epicanthal folds episodic disorders evoked potentials exercise intolerance exostosis eye movement, disorders of eyes, sunken facial anomalies facial appearance, abnormal facial hypoplasia facial nerve palsy failure to thrive false negative familial feeding disorder fetal alcohol syndrome fetus fever fever, recurrent fibrillations finger tapping floppy infant foam cells follicle stimulating hormone foot drop foot drop, bilateral fracture, pathologic Friedreich's ataxia frontal bossing gadolinium gait disorder gangliosidosis GM1 gangliosidosis GM2 gargoylism gastrointestinal disease, neurologic complications gastrointestinal motility gender gene gene mutation genetic counselling genetic diagnosis genetic diagnosis, prenatal genetic neurologic disorders genetic testing genital hypoplasia genu valgum glaucoma gluten ataxia gluten sensitivity gluten-free diet glycogen debranching enzyme deficiency glycogen storage disease Gowers maneuver gray hair growth hormone growth hormone deficiency growth retardation hair, darkening of hair, loss Hallgren's syndrome hamartoma hand flapping hand weakness head circumference head injury head injury, hypothalamic and pituitary damage head injury, pediatric headache hearing loss heart block heart murmur hemiparesis hemorrhage, intracranial, newborn hemorrhagic diathesis hepatitis hepatomegaly hepatosplenomegaly heralding manifestation hereditary multiple exostoses high arched palate hip dysplasia hirsutism HLA homocystinuria Hunter's syndrome Hurler's syndrome hydrocephalus hydrocephalus, normal pressure hydrocephalus, normal pressure in children hyperhomocysteinemia hyperphagia hyperreflexia hypertelorism hypertrophic cardiomyopathy hypertrophic intracranial pachymeningitis hypodontia hypoglycemia hypogonadism hypomagnesemia hypomyelination hypoparathyroidism hypopigmentation of skin hypopituitarism hyporeflexia hypotelorism hypothalamus hypothalamus, disturbance of hypothalamus, lesion of hypothalamus, neoplasm of hypothermia hypothermia, causes of hypothyroidism hypotonia hypotonia, infants iatrogenic neurologic disorders imbalance imperforate anus impulsivity inability to stand on tiptoes inclusion bodies, intranuclear insulin resistance intellectual deficit intellectual deterioration intestinal biopsy intestinal pseudoobstruction intracranial hemorrhage intracranial hypertension, benign intracranial hypertension, benign, differential diagnosis intracranial hypertension, benign, pathogenesis of intracranial pressure, increased joint hypermobility Kearns-Sayre syndrome keratoconus Krabbe's disease kyphoscoliosis, neurologic causes of lactate lactic acidemia laminar necrosis, cortical Laurence-Moon-Bardet-Biedl syndrome L-dopa Leber's hereditary optic neuropathy leg weakness, bilateral Leigh's disease lens, dislocation of lens, ectopic leuko-araiosis leukodystrophy leukodystrophy, 4H leukoencephalopathy lip, abnormal lipid storage disorder of CNS livedo reticularis lumbar puncture luteinizing hormone macrocephaly malabsorption malformation, CNS, congenital megalencephaly melanomatosis, primary malignant MELAS syndrome meningitis, aseptic menses mental retardation MERRF syndrome metabolic acidosis metabolic disorder, primary metachromatic leukodystrophy microcephaly micrognathia microspherophakia migraine misdiagnosis mitochondrial disease mitochondrial encephalomyopathy MNGIE syndrome molecular genetics Morquio syndrome mortality movement disorder movement disorder, extrapyramidal MRI MRI, abnormal MRI, CAT scan compared to MRI, contrast enhanced MRI, disappearing lesion on MRS mucopolysaccharidoses muscle biopsy muscle stiffness muscle weakness muscle weakness, proximal myasthenia gravis, differential diagnosis myasthenia gravis, misdiagnosis of myelopathy myoclonus myoclonus, epilepsy myopathy myopathy, distal myopathy, distal, vacuolar myopathy, inclusion body myopathy, inclusion body, hereditary myopathy, mitochondrial myopathy, vacuolar myopia myotonia nasal bridge, wide nausea and vomiting neck, webbed negative neoplasm, primary of CNS neoplasm, primary of CNS-children neoplasm, primary of CNS-incidence of neoplasm, primary of CNS-treatment of neuritis neurocutaneous disease neuroendocrinology neurologic complications of, systemic cancer neurologic complications of, systemic disease neurologic disease neurologic disease, diagnoses of neurologic examination, focal neuroophthalmology neuropathology, brain neuropathy neuropathy, peripheral Niemann-Pick disease Noonan Syndrome normal nose, abnormal nystagmus nystagmus, see-saw obesity ocular myopathy ophthalmoplegia ophthalmoplegia, progressive external optic atrophy optic atrophy, bilateral optic foramina optic foramina, abnormal optic nerve sheath fenestration optic nerve, decompression of optic neuropathy oral ulcerations osteogenesis imperfecta osteopetrosis osteoporosis otosclerosis P300 Pallister-Hall syndrome palpebral fissure, short pancytopenia papilledema paraparesis paraparesis, spastic Parkinson disease, differential diagnosis of Parkinsonism syndrome pectus carinatum pectus excavatum personality change philtrum, hypoplastic photosensitivity, skin pigmentary retinopathy pinched face pituitary pituitary stalk pituitary, hyppoplasia PLEDs PLEDs, bilateral independent PLEDs, etiology of pleocytosis of cerebrospinal fluid polydactyly polyhydramnios posterior pituitary ectopia postural abnormality Prader-Labhart-Willi syndrome precocious puberty pregnancy, neurologic complications in prenatal diagnosis by amniocentesis progeria prognathism progressive neurologic disorder proteinuria pseudoretinitis pigmentosa psychiatric disorder psychiatric problems in neurologic disorders psychomotor retardation psychosis ptosis puberty puberty, delayed pulmonary stenosis pupil, abnormality in neurologic disorders putamen, lesion of putamen, lesion of, bilateral quadriparesis radiation therapy, CNS treatment and complications with ragged-red fibers rapidly progressing neurologic illness rash recurrent red eye renal failure renal tubular acidosis respiratory failure retinal degeneration retinitis pigmentosa retinopathy Rett's syndrome review article risk factors root lesion, nerve Sanfilippo syndrome schizophrenia Schwartz-Jampel syndrome sclerae, blue scoliosis scoliosis, neurologic association with seizure seizure, children seizure, focal seizure, injury following sella turcica, enlargement of sella turcica, hypoplasia of sensorineural hearing loss serologic testing short neck short stature shunt procedure, lumboperitoneal skin, biopsy skin, darkening of skin, lesions in neurologic disorders skull bone, thickening skull x-ray, abnormal skull x-ray, bony defect on small vessel disease somatosensory evoked potentials spasticity Spielmeyer Vogt syndrome spinal cord, compression of spongy degeneration of brain standing difficulty stem cell transplantation stent, venous sinus steppage gait stereotyped behavior stooped posture strabismus strokelike episodes subarachnoid hemorrhage subdural hematoma subdural hematoma, neonates and infants suck, poor systemic illness teeth, abnormal temper tantrums temporal lobe, lesion teratoma third ventricle, mass of toe walking tongue, enlarged tongue, protrusion of treatment of neurologic disorder tremor tremor, postural tremulousness upgaze, paralysis of Usher's syndrome valvulopathy visual acuity, decreased visual field defect visual field testing visual fields, constricted visual impairment visual loss vomiting, recurrent walking, difficulty with weakness weakness, generalized weight gain weight loss Werner's syndrome wheelchair white matter disease wide based gait xeroderma pigmentosa x-ray, cervical spine

Showing articles 50 to 59 of 59 << Previous Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome Arch Neurol 35:337, Brumback,R.A.,et al, 1978 Chronic Hydrocephalus Associated with Short Stature & Growth Hormone Deficiency Ann Neurol 2:246, Hier,D.B.,et al, 1977 Prader-Willi-Syndrome, In Endocrine & Genetic Diseases of Childhood & Adolescence (Ed) , 1975. W. B. Saunders Co, p, Gardner,L.I., 1975 Germinoma of third Ventricle (Case Record of MGH) NEJM 293:653, Locke,S.,et al, 1975 Genetic Counseling in Retinitis Pigmentosa MCV Quart 8:283, Noah,V., 1972 Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue (Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972 Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue (Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972 The Mucopolysaccharidoses (Ed) , 4th Edition, the C. V. Mosby Co, 1971, Chp. 11, p. p. 521-686., McKusick,V.A., 1971 Hunter's Syndrome, In Recognizable Patterns Of Human Malformation, Genetic, Embryologic, & Clinical Aspects, by Smith W. B. , Saunders Co. , 1970, 248-249., David,W., 1970 Morquio's Disease, A Radiologic & Morphologic Study Pediatrics 34:839-850, Schenk,E.A.&Haggerty,J., 1964 Showing articles 50 to 59 of 59 << Previous