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Showing articles 2800 to 2850 of 3162 << Previous Next >>

Arrhythmic Complications in the Guillain-Barre Syndrome
Arch Int Med 140:1053-1055, Greenland,P.,et al, 1980

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

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

Cylindrical Spirals in a Familial Neuromuscular Disorder
Ann Neurol 7:550-556, Bove,K.E.,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

Pseudotumor Cerebri, Clinical Profile & Visual Outcome in 63 Patients
Mayo Clin Proc 55:541-546, Rush,J.A., 1980

Progressive Supranuclear Palsy & Hyperkalemic Periodic Paralysis
Arch Neurol 37:461-462, Foster,N.L.,et al, 1980

Demyelinative Chiasmal Lesions
Arch Neurol 37:757-762, Spector,R.H.,et al, 1980

Traumatic Chiasmal Syndrome
Neurol 30:963-970, Savino,P.J.,et al, 1980

Leber's Optic Neuropathy
Editorial, BMJ 280:1097-10981980., , 1980

Palinopsia:Cerebral Localization with Computed Tomography
Neurol 30:887-889, Michel,E.M.,et al, 1980

Ocular Defects in Children with Cerebral Palsy
BMJ 281:487-488, Black,P.D., 1980

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

Perinatal Neuropathy as an Early Manifestation of Krabbe's Disease
Arch Neurol 37:446-447, Lieberman,J.S.,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

Computed tomography in Hallervorden-Spatz disease
Neurol 30:1128-1130, Dooling,E.C.,et al, 1980

Enlarged Cerebral Ventricular System in Infant Achondroplastic Dwarf
Neurol 30:767-769, Mueller,S.M., 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

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

Transient Global Amnesia
Ann Neurol 7:281-285, Shuping,J.R.,et al, 1980

Idiopathic Hyperammonemia Associated with Cerebral arteriovenous Malformation
Arch Neurol 37:111-112, Michaelson,P.S., 1980

Controlled Study of 24-hr Ambulatory EKG Monitoring in Patients with Transient Neurological Symptoms
JNNP 43:37-41, Luxon,Lm.,et al, 1980

Familial Stroke Syndrome Associated with Mitral Valve Prolapse
Ann Neurol 7:130-134, Rice,G.P.A.,et al, 1980

Lyme Carditis:Cardiac Abnormalities of Lyme Disease
Ann Int Med 93:8-16, Steere,A.C.,et al, 1980

Nervous System Toxicity of Chemo Agents
Young, DF, in Vinken PJ, Bruyn GW, Handbook of Clin Neurol, North-Holland Publ Co, Amster, Vol 39, 1, 80, p 104, 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Quadruple Sectoranopia and Sectorial Optic Atrophy:A Syndrome of the Distan Anterior Choroidal Artery
JNNP 42:590-594, Frisen,L., 1979

Seizures & Intraventricular Conduction Defect in Propranolol Poisoning
Ann Int Med 91:860-862, Buiumsohn,A.,et al, 1979

Familial Inverted Choreoathetosis
Neurol 29:1627-1631, Fisher,M.,et al, 1979

Congenital Ocular Motor Apraxia
Arch Neurol 36:29-31, Orrison,W.W.,et al, 1979

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

Clinical & Biochemical Aspects of Trichopoliodystrophy
Ann Neurol 5:65-71, Grover,W.D.,et al, 1979

CT Scans in Menkes Disease
Neurol 29:304-312, Seay,A.R.,et al, 1979

Reduction of Angiotensin-Converting Enzyme in Substantia Nigra in Early-Onset Schizophrenia
NEJM 300:502-503, Arregui,A.,et al, 1979

Fetal Alcohol Syndrome & Related CNS Problems
Neurol 29:1429-1430, Wisniewski,K.,et al, 1979

Familial Arteriovenous Malformation
Ann Neurol 5:585-587, Snead,O.C.III.,et al, 1979

The Pregnant Epileptic, A Review & Recommendations
Arch Neurol 36:601-603, Montouris,G.D.,et al, 1979

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

Hereditary Myoclonus & Progressive Distal Muscular Atrophy
Ann Neurol 6:227-231, Jankovic,J.,et al, 1979

Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations
Ann Neurol 6:349-354, Parrish,M.L.,et al, 1979

Dorsal Thalamic Lesion in a Noted Case of Human Memory Dysfunction
Ann Neurol 6:503-506, Squire,L.R.,et al, 1979

Abnormalties In Cultured Muscle & Periphral Nerve Of A Patient With Adrenomyeloneuropathy
NEJM 301:588-590, Askanas,V.,et al, 1979

Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Neurol 29:880-881, Kuritzky,A.,et al, 1979

Studies in Aging of the Brain:IV. Familial Alzheimer Dis. :Relat. to Transmiss. Demetia, Aneuploidy, & Microtubular Defects
Neurol 29:1402, Book,R.H.,et al, 1979

Huntington's Disease:Abnormality of Lymphocyte Capping
Ann Neurol 6:447-450, Noronha,A.B.C.,et al, 1979

Reversal of an Afferent Pupillary Defect with Cold Water Drinking
Ann Neurol 6:456, Czarnecki,J.S., 1979

Familial Periodic Ataxia
Arch Neurol 36:568-569, Donat,J.R.,et al, 1979

Marfan's Syndrome
NEJM 301:273, Barr,M., 1979



Showing articles 2800 to 2850 of 3162 << Previous Next >>