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Differential
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acyl CoA dehydrogenase deficiency
adverse drug reaction
aminoacidopathies
anticonvulsants
anticonvulsants, untoward effects of
carbamazepine
cardiomyopathy
carnitine deficiency
carnitine deficiency myopathy
children
coma
complications
congestive heart failure
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
dilantin
drug interactions
enzyme, muscle disease
enzyme, serum
exercise
exercise intolerance
exercise-induced neurologic dysfunction
fatigue
fluctuate
gene mutation
genetic neurologic disorders
glycogen storage disease
hepatomegaly
hypoglycemia
hypoglycemic coma
hyporeflexia
hypotonia
lactic dehydrogenase(LDH)
leg weakness, bilateral
level of consciousness, decreased
lipid storage myopathy
metabolic acidosis
mortality
mucopolysaccharidoses
muscle biopsy
muscle cramp
muscle pain
muscle weakness
muscle weakness, proximal
myoglobinuria
myopathy
myopathy, metabolic
myopathy, proximal
neck weakness
neurologic complications of, surgery
pain, abdominal
pain, leg
phenobarbital
postpartum
precipitating factors
pregnancy, neurologic complications in
progressive neurologic disorder
propranolol
proteinuria
quadriplegia
recurrent
review article
rhabdomyolysis
seizure, children
seizure, intractable
sodium valproate
sodium valproate, toxicity
sphingolipodoses
spinocerebellar degeneration
treatment of neurologic disorder
type 1 muscle fiber
urine, dark
weakness
weakness, chronic
weakness, fluctuating
weakness, generalized
weakness, progressive
weakness, proximal
Showing articles 1100 to 1150 of 1265 << Previous Next >>

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

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

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

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

The Aicardi Syndrome:Report of 4 Cases & Review of the Literature
Ann Neurol 5:475-482, Bertoni,J.M.,et al, 1979

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

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Reversibility of Human Myopathy Caused by Vitamin E Deficiency
Neurol 29:1182-1186, Tomasi,L.G., 1979

Myasthenia Gravis, Pernicious Anemia, & Hashimoto's Thyroiditis
Arch Neurol 36:594-595, Krol,T.C., 1979

Spinocerebellar Degeneration:Hexosaminidase A & B Deficiency in Two Adult Sisters
Neurol 29:380-384, Oonk,J.G.W.,et al, 1979

Familial Psychosis & Diverse Neurologic Abnormalities in Adult-Onset Gaucher's Disease
Arch Neurol 36:95-99, Neil,J.F.,et al, 1979

Visual Evoked Responses in Pernicious Anemia
Arch Neurol 36:168-169, Troncoso,J.,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

Spinal Cord Compression by Extramedullary Hemopoietic Tissue in Pyruvate-Kinase-Deficiency-Caused Hemolytic Anemia
Neurol 29:510-513, Rutgers,M.J.,et al, 1979

Progressive Myelopathy Due to Extramedullary Hematopoiesis:Case Report & Review of the Literature
Ann Neurol 5:485-489, Stahl,S.M.,et al, 1979

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Clinical Syndromes of Myasthenia in Infancy & Childhood
Arch Neurol 35:97, Fenichel,G.M., 1978

Role of Magnesium Depletion in Wernicke-Korsakoff Syndrome
NEJM 298:743, Flink,E.B., 1978

Prevention of the Wernicke-Korsakoff Syndrome
NEJM 299:285, Centerwall,B.S.,et al, 1978

Marchiafava-Bignami Disease
Neurol 28:290, Koeppen,A.H.,et al, 1978

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Possible Biochemical Basis of Memory Disorder in Alzheimer Disease
Ann Neurol 3:471, Smith,C.M.,et al, 1978

Neurological Involvement in the Epidermal Naevus Syndrome
JNNP 41:466, McAuley,D.L.,et al, 1978

A Syndrome of Progressive Muscle Spasm, Alopecia, & Diarrhea
Neurol 28:458, Satoyoshi,E., 1978

Leigh's Disease in an Adult with Evidence of"Inhibitor Factor"in Family Members
Ann Neurol 3:519, Whetsell,W.O.,et al, 1978

Glycine Encephalopathy
NEJM 298:687, Ch'ien,L.T., 1978

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Kearns-Sayre Syndrome & Hypoparathyroidism
Ann Neurol 3:455, Pellock,J.M.,et al, 1978

Vitamin B-6-Dependent Seizures:Pathology & Chemical Findings in Brain
Neurol 28:47, Lott,I.T.,et al, 1978

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

Status Epilepticus in Pregnancy:Effect of Phenytoin Malabsorption on Seizure Control
Neurol 28:85, Ramsay,R.E.,et al, 1978

The Cherry-red Spot-Myoclonus Syndrome
Ann Neurol 3:234, Rapin,I.,et al, 1978

A Synd of Methylmal Acid, Homocystinuria, Megaloblas. Anemia & Neurol Abnor. in a Vit B-12-def Breast-fed Infant of veget
NEJM 299:317, Higginbottom,M.C., 1978

Celiac Sprue & Refractory Sprue
Gastroenter. 75:3071978., Trier,J.S.,et al, 1978

Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978

Cobalamin Analog Present In Human Plasma Mask Cobalamin Defic Current Radioistope Dil. Assays Not Spec for Cobalamin
NEJM 299:785, Kolhouse,J.F.,et al, 1978

Evidence That Some Patients With Pernicious Anemia Are Not Recogn By Radiodil Assay For Cobalamin In Serum
NEJM 299:816, Cooper,B.A.,et al, 1978



Showing articles 1100 to 1150 of 1265 << Previous Next >>