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Differential
(Click to cross reference)
agenesis of corpus callosum
basal ganglia, degeneration
blindness
calcification, intracranial
CAT scan
CAT scan, abnormal
cerebral cortical atrophy
corpus callosum, lesion of
familial
hydrocephalus
hypotonia
inborn errors of metabolism
intellectual deterioration
lens, dislocation of
mental retardation
microcephaly
quadriparesis
seizure
seizure, neonatal
spasticity
sulfite oxidase deficiency
uric acid, low
urinalysis, abnormal
Showing articles 1100 to 1150 of 1308 << Previous Next >>

Septo-optic Dysplasia in an Infant of a Diabetic Mother
Arch Neurol 38:590-591, Donat,J.F.G., 1981

Penicillamine-Induced Neuropathy in Rheumatoid Arthritis
Ann Int Med 95:457-458, Pool,K.D.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Evoked Responses in Vitamin B12 Deficiency
Ann Neurol 9:407-409, Krumholz,A.,et al, 1981

Lhermitte's Sign in Cobalamin (Vitamin B12) Deficiency
JAMA 245:1059, Butler,W.M.,et al, 1981

Dystrophic Axons & Spinal Cord Demyelination in Cystic Fibrosis
Neurol 31:714-718, Cavalier,S.J.,et al, 1981

Lipid Storage Myopathy:Successful Treatment with Propranolol
BMJ 282:1997-1999, Martyn,C.,et al, 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Effects of Prophyl. Treat. of CNS on Intellect. Funct. of Children with Acute lymph. Leuk
Am J Med 71:47-52, Moss,H.A., 1981

Deprenyl in Parkinson Disease
Neurol 31:19-23, Eisler,T.,et al, 1981

Depression, Intellectual Impairment & Parkinson Disease
Neurol 31:645-650, Mayeux,R.,et al, 1981

Prognostic Indicators in Hemiparetic Cerebral Palsy
Ann Neurol 9:353-357, Cohen,M.E.,et al, 1981

Ataxia with Aniridia of Gillespie:A Case Report
Neurol 31:95-97, Lechtenberg,R.,et al, 1981

Minor Brain Damage & Alcoholism
Editorial, BMJ 283:455-4561981., , 1981

Von Recklinghausen Neurofibromatosis
NEJM 305:1617-1627, Riccardi,V.M., 1981

Biochemical Evidence Of Dysfunction Of Brain Neurotransmitters In The Lesch-Nyhan Syndrome
NEJM 305:1106-1111, Lloyd,K.G.,et al, 1981

Hemoglobin H Disease & Mental Retardation
NEJM 305:607-612, Weatherall,D.J.,et al, 1981

Association Of Spinocerebellar Disorders With Cystic Fibrosis Or Chronic Childhood Cholestasis & Very Low Serum Vit. E
Lancet 2:1319-1321, Elias,E.,et al, 1981

Biochemical Genetics Of Neurologic Disease
NEJM 305:1181-1193, Rosenberg,R.N., 1981

Neurological Manifestation of Accidental Hypothermia
Ann Neurol 10:384-387, Fischbeck,K.H.,et al, 1981

The Intelligence of Hydrocephalic Children
Arch Neurol 38:607-615, Dennis,M.,et al, 1981

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,et al, 1981

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Extramedullary Hematopoiesis & Spinal Cord Compression Complicating Polycythemia Rubra Vera
Ann Neurol 7:81-84, Rice,G.P.A.,et al, 1980

Fetal Methylmercury Poisoning:Clinical & Toxicological Data on 29 Cases
Ann Neurol 7:348-353, Marsh,D.O.,et al, 1980

Neonatal Polycythemia Causing Multiple Cerebral Infarcts
Arch Neurol 37:109-110, Amit,M.,et al, 1980

Maternal & Fetal Sequelae of Anticoagulation During Pregnancy
Am J Med 68:122-140, Hall,J.G.,et al, 1980

Hazards of Oral Anticoagulants During Pregnancy
JAMA 243:1549-1551, Stevenson,R.E.,et al, 1980

Cognitive Function in Patients With Multiple Sclerosis
Arch Neurol 37:577-579, Peyser,J.M.,et al, 1980

The Neuropsychiatry of Megaloblastic Anaemia
BMJ 281:1036-1038, Shorvon,S.D.,et al, 1980

Unreliability of Radiodilution Assays as Screening Tests for Cobalamin (Vitamin B12) Deficiency
JAMA 244:1942-1945, Cohen,K.L.,et al, 1980

Studies Of A Patient With Megaloblastic Anemia & An Abnormal Transcobalamin II
NEJM 303:1209-1212, Seligman,P.A.,et al, 1980

Abetalipoproteinemia, Report of Two Cases & Review of Therapy
Arch Neurol 37:659-662, Illingworth,D.R.,et al, 1980

Proximal Myopathy after Prolonged Total Therapeutic Starvation
BMJ 280:1212-1213, Scobie,I.N.,et al, 1980

Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
Am J Med 69:64-74, Whythe,M.P.,et al, 1980

Wernicke's Encephalopathy in Patients With Tumors of the Lymphoid-Hemopoietic Systems
Arch Neurol 37:338-341, DeReuck,J.L.,et al, 1980

Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
NEJM 303:377-380, Hirschhorn,R.,et al, 1980

Heterozygous Expression Of X-Linked Mental Retardation & X-chromosome Marker fra (X) (q27)
NEJM 303:662-664, Turner,G.,et al, 1980

Acquired Hemophilia, Meningioma, & Diphenyl-hydantoin Therapy
J Neurosurg 53:600-605, O'Reilly,R.A.,et al, 1980

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

The Fragile X-Chromosome Mental Retardation & Large Testes
Arizona Med 37:764-766, Hecht,F.,et al, 1980

X-Linked Mental Retardation
Am J Med Genet 7:407-415, Turner,G.,et al, 1980

Alternating Hemiplegia in Infants:Report of Five Cases
Dev Med Child Neurol 22:784-791, Krageloh,I.&Aicardi,J., 1980

Cerebral Infarcts with Arterial Occlusion in Neonates
Ann Neurol 6:495-502, Barmada,M.A.,et al, 1979

Iatrogenic Night Blindness & Keratoconjunctival Xerosis
NEJM 301:943-944, Partamian,L.G.,et al, 1979

Familial Tapetorentinal Degeneration & Epilepsy
Arch Neurol 36:544-546, Cohan,S.L.,et al, 1979

Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Periodic Lateralized Epileptiform Discharges in Infants & Children
Ann Neurol 6:47-50, PeBenito,R.,et al, 1979

Multiple Molecular Forms of Arylsulfatase in Different Forms of Metachromatic Leukodystrophy (MLD)
Neurol 29:16-20, Farrell,D.F.,et al, 1979



Showing articles 1100 to 1150 of 1308 << Previous Next >>