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Differential
(Click to cross reference)
abdominal muscle paralysis
acid maltase deficiency
acid maltase deficiency, adult
activities of daily living scale
alpha glucosidase
aneurysm
anterior horn cell disease
aspartate aminotransferase
asymptomatic
calf hypertrophy
cardiomegaly
cardiomyopathy
congestive heart failure
consanguinity
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
delay in diagnosis
developmental retardation
diaphragmatic paralysis
difficulty climbing stairs
distal muscle atrophy
distal muscle weakness
dyspnea
efficacy
electrocardiogram, abnormal
electromyogram
electron microscopy
enzyme treatment
enzyme, defect
enzyme, muscle disease
exercise
exercise intolerance
facial weakness
falling
familial
fatigue
fibrillations
floppy infant
gene
gene mutation
gene therapy
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
hepatomegaly
hip flexor weakness
histochemistry of muscle
hypoglycemia
hypotonia
hypotonia, infants
hypoxia
imbalance
inborn errors of metabolism, screening
ischemic exercise test
leg weakness, bilateral
low back pain
lysosomal storage disease
lysosomes, abnoral
McArdle's disease
misdiagnosis
mortality
MRI, muscle
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle phosphorylase deficiency
muscle stiffness
muscle strength, testing
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
myoglobinuria
myopathy
myopathy, distal, vacuolar
myopathy, genetic
myopathy, metabolic
myopathy, necrotizing
myopathy, vacuolar
myotonic discharges
neck weakness
neurologic disease
neurologic disease, diagnoses of
orthopnea
pain, back
paraspinal muscle
paraspinal muscle weakness
PAS positive
patient in waiting
phosphorylase b kinase deficiency
Pompe's disease of glycogen storage
preclinical
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
pseudomyotonia
pulmonary function tests
pulmonary hypertension
renal failure
respiratory failure
review article
screening
second wind phenomena
short stature
subarachnoid hemorrhage
tongue, enlarged
tongue, weakness
treatment of neurologic disorder
urine, dark
vital capacity
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
winging of scapula
Showing articles 1350 to 1400 of 1619 << Previous Next >>

Nearly Fatal Muscle Carnitine Deficiency with Full Recovery after Replacement Therapy
Neurol 33:1629-1631, Prockop,L.D.,et al, 1983

Limbic Encephalopathy as a Nonmetastatic Complication of Oat Cell Lung Cancer
Am J Med 75:518-520, Brennan,L.V.,et al, 1983

Downbeat Nystagmus
Arch Neurol 40:754-755, Coppeto,J.R.,et al, 1983

Ultrastructure & Electrodiagnosis of Peripheral Neuropathy in Cockayne's Syndrome
Neurol 33:1606-1609, Grunnet,M.L.,et al, 1983

Familial Spastic Paraplegia, Mental Retardation, & Precocious Puberty
Arch Neurol 40:809-810, Raphaelson,M.I.,et al, 1983

Effect of Carbamazepine on Coumadin Metabolism
Ann Neurol 13:691-692, Massey,E.W., 1983

Unrecognized Chronic Lithium Neurotoxic Reactions
JAMA 250:2029-2030, Lewis,D.A., 1983

Action Tremor as a Manifestation of Chylomicron Retention Disease
Ann Neurol 14:591, Gauther,S.,et al, 1983

CSF Enzymes in Lacunar & Cortical Stroke
Stroke 14:266-269, Donnan,G.A.,et al, 1983

Treatment of Dystonia with Tetrahydrobiopterin
NEJM 308:157-158, LeWitt,P.A.,et al, 1983

"Lhermitte's Sign"as a Presenting Symptom of Subacute Combined Degeneration of the Cord
Ann Neurol 13:215, Sandyk,R.,et al, 1983

Vitamin E & Neurological Function
Lancet 1:225-228, Muller,D.P.R.,et al, 1983

The Early Clinical Manifestations of Lyme Disease
Ann Int Med 99:76-82, Steere,A.C.,et al, 1983

Creatine Kinase BB Isoenzyme in CSF in Neurologic Diseases
Arch Neurol 40:169-172, Pfeiffer,F.E.,et al, 1983

Wernicke's Encephalopathy Induced by Tolazamide
NEJM 309:599-600, Kwee,I.L.,et al, 1983

Myeloneuropathy & Macrocytosis Associated with Nitrous Oxide Abuse
Arch Neurol 40:416-418, Bianco,G.,et al, 1983

Pyridoxine-Dependency Seizure:Report of a Rare Presentation
Ann Neurol 13:103-104, Krishnamoorthy,K.S., 1983

Serum Folate Concentra. During Pregnancy in Women with Epilepsy:Relation to Antiepileptic Drug Concentrations
BMJ 287:577-579, Hiilesmaa,V.K.,et al, 1983

Safe Readministration of Valproate after an Episode of Hepatotoxicity
Ann Neurol 13:688, Ramsay,R.E., 1983

Glutamate Dehydrogenase Deficiency in Patients with Olivopontocerebellar Atrophy
Neurol 33:1322-1326, Duvoisin,R.C.,et al, 1983

Primary Position Upbeating Nystagmus:A Variety of Central Positional Nystagmus
Brain 106:949-964, Fisher,A.,et al, 1983

Fibrodysplasia Ossificans Progressiva, The Clinical Features & Natural Hx of 34 Pts
J Bone Joint Surg 64B:76-83, Connor,J.M.&Evans,D.A.P., 1982

Deprenyl In Parkinson's Disease
Lancet 2:695-696, , 1982

Nevoid Basal Cell Carcinoma Syndrome & Epilepsy
Ann Neurol 11:372-376, Murphy,M.J.,et al, 1982

The Child Who is Slow to Talk
BMJ 285:671-672, Robinson,R.J., 1982

Cockayne Syndrome
J Comput Assist Tomogr 6:1172-1174, Levinson,E.D.,et al, 1982

Generalized Paroxysmal Fast Activity:Electoencephalographic & Clinical Features
Ann Neurol 11:386-390, Brenner,R.P.,et al, 1982

Maternal Seizure Disorder, Outcome of Pregnancy, & Neurologic Abnormalities in the Children
Neurol 32:1247-1254, Nelson,K.B.,et al, 1982

Lhermitte's Sign in Multiple Sclerosis:A Clinical Survey & Review of the Literature
JNNP 45:308-312, Kanchandani,R.,et al, 1982

Spinocerebellar Degeneration Secondary to Chronic Intestinal Malabsorption:A Vitamin E Deficiency Syndrome
Ann Neurol 12:419-424, Harding,A.E.,et al, 1982

Hypomelanosis of Ito (incontinentia pigmenti achromians) :Macrocephaly & Gray Matter Heterotopias
Neurol 32:1013-1016, Ross,D.L.,et al, 1982

Colpocephaly, An Error of Morphogenesis
Arch Neurol 39:243-246, Garg,B.P., 1982

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

Brain Damage After Open-heart Surgery
Editorial, Lancet 1:1161-11631982., , 1982

Two Cases of Van Buchem's Disease
JNNP 45:913-918, Dixon,J.M.,et al, 1982

Wernicke-Korsakoff Encephalopathy after Gastric Plication
JAMA 247:2566-2567, Haid,R.W.,et al, 1982

Benign Intracranial Hypertension Induced by Deficiency of Vitamin A During Infancy
Neurol 32:1292-1295, Kasarskis,E.J.,et al, 1982

Wernicke's Encephalopathy Following"Hunger Strike"
Postgrad Med J 58:427-428, Pentland,B.,et al, 1982

Wernicke's Encephalopathy In Prolonged Fasting
Lancet 2:1108-1109, Devathasan,G.,et al, 1982

Anorexia Nervosa & Wernicke's Encephalopathy:An Underdiagnosed Association
Lancet 2:771-772, Handler,O.E.,et al, 1982

Impaired Biotin Status in Anticonvulsant Therapy
Ann Neurol 12:485-486, Krause,K-H.,et al, 1982

Fragile X Chromosome & X-Linked Mental Retardation
CMA Journal 127:123-126, Larbrisseau,A.,et al, 1982

Cerebrospinal Fluid:A Selective Review
Ann Neurol 11; 1-101982., Cutler,R.W.P.,et al, 1982

Prenatal Diagnosis of Fragile X Chromosome
Lancet 1:99-100, Shapiro,L.R.,et al, 1982

Diagnostic Delay in Duchenne's Muscular Dystrophy
JAMA 247:478-480, Crisp,D.E.,et al, 1982

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

Neurologic Disease & Nutrition
Res & Staff Physician August 1981, pp. 77-81., Dreyfus,P.M., 1981

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981



Showing articles 1350 to 1400 of 1619 << Previous Next >>