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Differential
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ACTH, ectopic syndrome of
addiction, heroin
Addison's disease
advances in neurology
alcohol
alcohol, neurologic complications with
amphotericin B
ankle edema
antibodies to voltage-gated calcium channels
areflexia
arrhythmia, cardiac
Asians
asymptomatic
ataxia
ataxia, cerebellar
ataxia, paroxysmal
atrial fibrillation
autoimmune disease
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bitemporal visual field defect
brachial neuritis
brainstem, lesion of
cachexia
calcification, intracranial
calcium channel dysfunction
carbenoxolone
carcinoma of lung
carpo-pedal spasm
CAT scan
CAT scan, muscle
CD4 counts
central core disease
cerebellar degeneration
chloride channel dysfunction
chloroquine
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
clofibrate
coinfection
coma
congenital myopathy
conjunctival injection
craniopharyngioma
creatine phosphokinase(CPK)elevated
Cushing's syndrome
cystoisospora belli
deep tendon reflexes
Dengue fever
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diarrhea
diuretic
drug induced neurologic disorders
electrocardiogram, abnormal
electron microscopy
encephalitis
encephalopathy
enteritis
enzyme, muscle disease
epidemiology of neurology
epsilon-aminocaproic acid(E.A.C.A.)
exercise
exophthalmus
familial hemiplegic migraine
fasciculation
flavivirus
gait disorder
genetic neurologic disorders
giardiasis
Guillain Barre syndrome
gynecomastia
hallucination, auditory
Hand-Schuller-Christian disease
homosexual
human immunodeficiency virus type 1
hyperadrenalism
hypercalcemia
hyperinsulinism
hyperkalemia
hyperkalemic periodic paralysis
hyperparathyroidism
hyperthyroidism
hypocalcemia
hypokalemia
hypokalemic alkalosis
hypokalemic paralysis
hypokalemic periodic paralysis
hyponatremia
hypoparathyroidism
hyporeflexia
hypothalamus
hypothalamus, disturbance of
inclusion body myositis
India
infection
insomnia
insulin
intrinsic hand muscles, wasting of
ipecac
islet cell tumor
leg numbness
leg weakness, bilateral
leukocytosis
liquorice
liver function enzymes
malignant hyperpyrexia
migraine
migraine, hemiplegic
molecular genetics
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, muscle
muscle biopsy
muscle cramp
muscle pain
muscle swelling
muscle tenderness
muscle weakness
muscle weakness, causes of
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Duchenne
myasthenia gravis
myasthenic syndrome
myelopathy
myelopathy, carcinomatous
myoedema
myoglobinuria
myopathy
myopathy, alcoholic
myopathy, drug-induced
myopathy, hypokalemic
myopathy, mitochondrial
myopathy, proximal
myopathy, steroid induced
myositis
myotonia congenita
myotonia dystrophica
myxedema coma
myxedema, neurologic manifestations of
nausea and vomiting
neoplasm, hormone producing
neoplasm, hormone producing, ectopic
neoplasm, pituitary
Nepal
neuroendocrinology
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neuropathy, peripheral
ophthalmoplegia
ophthalmoplegia, total
pain, abdominal
pain, leg
papilledema
paralysis, acute areflexic
paramyotonia congenita
paranoia
paraparesis
parasitic infection, CNS
parathyroid adenoma
paroxysmal neurologic deficits
perhexiline maleate
periodic paralysis
periodic paralysis, thyrotoxic
pheochromocytoma
pleocytosis of cerebrospinal fluid
polymyositis
potassium
potassium channel antibodies
potassium channel dysfunction
primary aldosteronism
prognosis
protozoan infection
psychosis
quadriparesis
quadriplegia, transient
rash
remote effect of cancer on the nervous system
review article
rhabdomyolysis
risk factors
seizure
snuff dipping
sodium channel dysfunction
spinocerebellar ataxia
spinocerebellar ataxia type 6
steroid
tetany
thyroid function tests
thyroid gland, enlarged
thyrotoxicosis
travel, foreign
treatment of neurologic disorder
tremor
Trousseau's sign
tubular aggregates, muscle
vincristine neurotoxicity
viral infection
viral infection, CNS
walking, difficulty with
weakness
weakness, acute
weakness, episodic
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
yersinia enterocolitica
Showing articles 650 to 700 of 1024 << Previous Next >>

Eosinophilia-Myalgia Syndrome (L-Tryptophan-Associated Neuromyopathy)
Neurol 40:1793-1796, Turi,G.K.,et al, 1990

L-Tryptophan-Induced Eosinophila-Myalgia Syndrome and Myopathy
Neurol 40:1629-1630, Sagman,D.L.&Melamed,J.C., 1990

New Muscle Power Test in Neuromuscular Disease
Am J Dis Child 144:1083-1087, Tirosh,E.,et al, 1990

Myopathy with Human Immunodeficiency Virus Type I (HIV-1) Infection:HIV-1 or Zidovudine?
Ann Int Med 113:492-493, Till,M.&MacDonell,K., 1990

Human Immunodeficiency Virus Assoc Myopathy:Immunocytochemical Ident of an HIV Antigen (gp41) in Muscle Macrophages
Ann Neurol 28:579-582, Chad,D.A.,et al, 1990

Neurosarcoidosis:Signs, Course and Treatment in 35 Confirmed Cases
Medicine 69:261-276, Chapelon,C.,et al, 1990

Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990

Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
Ann Neurol 27:448-449, Katafuchi,Y.,et al, 1990

Scleroderma, fasciitis, and Eosinophilia Associated with the Ingestion of Tryptophan
NEJM 322:874-881, 9261990., Silver,R.M.,et al, 1990

Association of the Eosinophilia-Myalgia Syndrome with the Ingestion of Tryptophan
NEJM 322:869-873, 9261990., Hertzman,P.A.,et al, 1990

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

Mitochondrial Myopathy Caused by Long-Term Ziduvudine Therapy
NEJM 322:1098-1105, Dalakas,M.C.,et al, 1990

Clinicopath Conf
Acute Febrile Neutrophilic Dermatosis (Sweet's Syndrome) , Case 30-1990, NEJM 323:254-2630., , 1990

Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, and Intestinal Pseudo-Obstruction:POLIP Syndrome
Ann Neurol 28:349-360, Simon,L.T.,et al, 1990

Attitudes of Mothers to Neonatal Screening for Duchenne Muscular Dystrophy
BMJ 300:1112, Smith,R.A.,et al, 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
Neurol 40:671-676, Speer,M.C.,et al, 1990

Fluctuating MR Images with Mitochondrial Encephalopathy, Lactic Acidosis, Stroke-Like Syndrome (MELAS)
Neuroradiology 32:77, Abe,K.,et al, 1990

Mitochondrial Myopathy with a Defect of Mitochondrial-Protein Transport
NEJM 323:37-42, Schapira,A.H.V.,et al, 1990

Mitochondrial Encephalomyopathy (MELAS) with Mental Disorder, CT, MRI and SPECT Findings
Neuroradiology 32:74-76, Suzuki,T.,et al, 1990

Myopathy and Rhabdomyolysis Associated with Lovastatin-Gemfibrozil Combination Therapy
JAMA 264:71-75, Pierce,L.R.,et al, 1990

Peripheral Neuropathy in the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Neurol 40 1035-1040, Smith,B.E.&Dyck,P.J., 1990

The Clinical Spectrum of the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Ann Int Med 113:124-134, Martin,R.W.,et al, 1990

L-Tryptophan-Associated Eosinophilic Perimyositis, Neuritis, and Fasciitis
Medicine 69:187-199, Kaufman,L.D.,et al, 1990

Autosomal Dominant Cramping Disease
Arch Neurol 47:810-812, Ricker,K.&Moxley,R.T., 1990

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Graves Orbitopathy:Correlation of CT and Clinical Findings
Radiology 177:675-682, Nugent,R.A.,et al, 1990

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

Skeletal Muscle Pathology in AIDS:An Autopsy Study
Muscle & Nerve, 13:508-51590., Wrzolek,M.A.,et al, 1990

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Mitochondrial DNA and Genetic Disease
Editorial, Lancet 1:250-2511989., , 1989

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene
Neurol 39:1277-1280, Gospe,S.M.,et al, 1989

Eosinophilia-Myalgia Syndrome-New Mexico
JAMA 262:3116, Belvins,W.L.,et al, 1989

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

Diagnosis of Gerstmann-Straussler Syndrome in Familial Dementia with Prion Protein Gene Analysis
Lancet 2:15-17, Collinge,J.,et al, 1989

AIDS and the Nervous System
JAMA 261:2396-2399, Dalakas,M.,et al, 1989

Zidovudine-Associated Myopathy
Am J Med 86:814-818, Gertner,E.,et al, 1989

HTLV-I Polymyositis in a Patient Also Infected with the Human Immunodeficiency Virus
NEJM 320:992-995, Wiley,C.A.,et al, 1989

Computeritis, Who's Responsible When PCs Make Employees Sick?
Infoworld 11:51-54, Flynn,L., 1989

The Chronic Fatigue Syndrome-One Entity or Many?
NEJM 319:1726-1728, Swartz,M.N., 1989

Aseptic Meningitis Complicating Adult Kawasaki Disease:Case Report and Review of the Literature
Am J Med 87:106-110, McIlroy,M.A.,et al, 1989

Current Concepts in the Idiopathic Inflammatory Myopathies:Polymyositis, Dermatomyositis, and Related Disorders
Ann Int Med 111:143-157, Plotz,P.H.,et al, 1989

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Mitochondrial Myopathies, Mechanisms Now Better Understood
BMJ 298:1127-1128, Schapira,A.H.V., 1989

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
NEJM 320:1293-1299, Moraes,C.T.,et al, 1989

Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship
J Pediatr 115:81-88, Sooth,F.A.,et al, 1989

Inclusion Body Myositis, Observations in 40 Patients
Brain 112:727-747, Lotz,B.P.,et al, 1989



Showing articles 650 to 700 of 1024 << Previous Next >>