Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
aminoacidurias
anticonvulsants
anticonvulsants, teratogenicity of
anticonvulsants, untoward effects of
aphasia, children
apraxia, speech
attention deficit disorder with hyperactivity
autism
Benedict's solution test
bifid uvula
calcification, intracranial
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cleft lip
cleft palate
congenital malformation, dilantin therapy causing
developmental abnormality of brain
dilantin
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
dysarthria
dysplasia of C.N.S.
electroencephalogram
facial anomalies
ferric chloride test
hearing problems in children
holoprosencephaly
hypotelorism
intellectual deficit
intellectual deficit, treatable causes of
intelligence quotient
karyotyping
klippel feil syndrome
language disorders in children
maple syrup urine disease
mental retardation
microcephaly
midline defect in children
myelodysplasia
nasal speech
palatopharyngeal incompetence
phenylketonuria
pregnancy, anticonvulsants during
psychological testing, neurologic problems
psychosis
psychosis, childhood
psychosocial aspects
seizure
seizure, advice to parents and teachers regarding
seizure, pregnancy
seizure, psychosocial aspects of
seizure, treatment of
speech disorder, childhood
spina bifida
stuttering
urine test for metabolic disorders
Showing articles 300 to 350 of 5336 << Previous Next >>

Tourette Syndrome and Other Tic Disorders, Diagnosis, Pathophysiology, and Treatment
Medicine 70:15-32, Singer,H.S.&Walkup,J.T., 1991

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Maternal Cocaine Abuse:The Spectrum of Radiologic Abnormalities in the Neonatal CNS
AJR 157:1105-1110, Heier,L.A.,et al, 1991

Craniopharyngyoma in Children
In Brain Tumors in Children, W B Saunders Co, Phila, Neurologic Clinics 9:453-46591., Sanford,R.A.&Muhbauer,S., 1991

Creutzfeldt-Jakob Disease and Other Transmissible Spongiform Encephalopathies
Ed, F. O. Bastian, Mosby Year Book, St. Louis 9:153, Maertens,P.&Quindlen,E.A., 1991

Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
Stroke 21:633-636, Cros,D.,et al, 1990

Genetic Testing for Huntington's Disease
BMJ 300:1089-1090, Harper,P.,et al, 1990

Perinatal Loss and Neurological Abnormalities Among Children of the Atomic Bomb
JAMA 264:605-609, 6221990., Yamazaki,J.N.&Schull,W.J., 1990

Neurologic Sequelae of Open-Heart Surgery in Children
Am J Dis Child 144:369-373, Ferry,P.C., 1990

Vision and Hearing During Deferoxamine Therapy
J Pediatr 117:326-330, Cohen,A.,et al, 1990

Hematologic Disorders and Ischemic Stroke
Stroke 21:1111-1121, Hart,R.G.&Kanter,M.C., 1990

Epilepsy Octet, Epidemiology, Classification, Natural History, and Genetics of Epilepsy
Lancet 336:93-96, Shorvon,S.D., 1990

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

Premature Stroke in a Family with Lupus Anticoagulant and Antiphospholipid Antibodies
Stroke 21:66-71, Ford,P.M.,et al, 1990

The Infant with Anencephaly
Med Task Force on Anencephaly, NEJM 322:669-6741990., , 1990

Chiasmal Apoplexy:Haemorrhage from a Cavernous Malformation in the Optic Chiasm
JNNP 52:1095-1099, Regli,L.,et al, 1989

Dyslexia
Editorial, Lancet 2:719-7201989., , 1989

Cardioembolic Stroke in Primary Oxalosis with Cardiac Involvement
DiPasquale. G. , et al, Stroke 20:1403-14069., , 1989

Anterior Choroidal Artery Territory Infarction:A Small Vessel Disease
Stroke 20:616-619, Bruno,A.,et al, 1989

Problems in Genetic Prediction for Huntington's Disease
Lancet 2:601-603, Morris,M.J.,et al, 1989

Uptake of Presymptomatic Predictive Testing for Huntington's Disease
Lancet 2:603-605, Craufurd,D.,et al, 1989

The Acquired Immunodeficiency Syndrome (AIDS) Dementia Complex
Ann Int Med 111:400-410, Ho,D.D.,et al, 1989

A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
NEJM 320:1300-1305, Singh,G.,et al, 1989

Magnetic Resonance Imaging in a Family with Hereditary Cerebral Arteriovenous Malformations
Arch Neurol 46:184-187, Allard,J.C.,et al, 1989

Predictive Testing for Huntington's Disease, Progress and Problems
BMJ 298:404-405, 1989, Harper,P.S.&Morris,M.J., 1989

The Use of Anencephalic Infants as Organ Sources, A Critique
JAMA 261:1773-1781, Shewmon,D.A.,et al, 1989

Anencephalic Organ Donors, Guidelines Available from Britain and North America
BMJ 298:622-623, Salaman,J.R., 1989

Cerebral Infarction and Ventricular Septal Defect
Stroke 20:957-958, Shuiab,A., 1989

Neurofibromatosis Type 1 (Recklinghausen's Disease) , Neurologic and Cognitive Assessment
Am J Dis Child 143:833-837, Eldridge,R.,et al, 1989

Neurofibromatosis and Other Disorders Among Children with CNS Tumors and Their Families
Neurol 39:487-492, Baptiste,M.,et al, 1989

Follow-up and Diagnostic Reappraisal of 75 Patients with Leber's Congenital Amaurosis
Am J Ophthalmol 107:624-631, Lambert,S.R.,et al, 1989

MR of Neuronal Migration Anomalies
AJR 150:179-187, Barkovich,A.J.,et al, 1988

Cerebrovascular Disorders of Infancy
In Handbk of Clin Neurol, Elsevier Sci Publ, NY, 2:3188., Salam-Adams,M.&Adams,R.D., 1988

Hysterical Conversion Reactions Mimicking Neurological Disease
Am J Dis Child 142:1203-1206, Bangash,I.H.,et al, 1988

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

The Molecular Genetic Revolution, Its Impact on Clinical Neurology
Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988

Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage
Lancet 2:603-604, Palsdottir,A.,et al, 1988

Livedo Reticularis, Porcelain-White Scars, and Cerebral Thromboses
Lancet 1:1263-1265, Burton,J.L., 1988

MR Imaging of Intrachiasmatic Hemorrhage
J Comput Assist Tomogr 12:535-536, Moffit,B.,et al, 1988

Primary Intraventricular Hemorrhage:Clinical & Neuropsychological Fundings in a Prospective Stroke Series
Neurol 38:68-75, Darby,D.G.,et al, 1988

Predictive Testing for Huntington's Disease with Use of a Linked DNA Marker
NEJM 318:535-542, Meissen,G.J.,et al, 1988

Cerebral Cavernous Malformations:Incidence and Familial Occurrence
NEJM 319:343-347, Rigamonti,D.,et al, 1988

The Combined Use of Positron Emission Tomography & DNA Polymorphisms for Preclinical Detection of Huntington's Disease
Neurol 37:1441-1447, Hayden,M.R.,et al, 1987

CT in Ceroid Lipofuscinosis
Neurol 37:1025-1026, Dunn,D.W., 1987

Familial Cavernous Malformations of the Central Nervous System & Retina
Ann Neurol 21:578-583, Dobyns,W.B.,et al, 1987

Childhood Stroke Associated with Protein C or S Deficiency
J Pediatr 111:562-564, Israels,S.J.&Seshia,S.S., 1987

Mendelian Etiologies of Stroke
Ann Neurol 22:175-192, Natowicz,M.&Kelley,R.I., 1987

Pimozide Treatment of Tic & Tourette Disorders
Pediatrics 79:1032-1039, Shapiro,A.K.,et al, 1987

Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987

Neurologic Manifestations of Infection with Human Immunodeficiency Virus, Clinical Features & Pathogenesis
Ann Int Med 107:383-391, Gabuzda,D.H.,et al, 1987



Showing articles 300 to 350 of 5336 << Previous Next >>