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acromegaly
Addison's disease
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arthrogryposis multiplex
Asians
asymptomatic
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cerebrospinal fluid, elevated protein of
cerebrovascular accident
Charcot-Marie-Tooth
chemosis
chorea
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
coenzyme Q10
collagen vascular disease
coma
complications
concentration, impaired
confusion
congestive heart failure
conjunctival injection
craniopharyngioma
creatine phosphokinase(CPK)elevated
Cushing's syndrome
deafness
deep tendon reflexes
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diabetes mellitus, neurologic manifestations of
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digitalis intoxication
diplopia
disorientation
dropped head syndrome
dysarthria
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dysthyroid ocularmyopathy
edema, periorbital
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
emotional lability
encephalopathy
epidemiology of neurology
exercise
exophthalmus
extraocular muscle enlargement
eye movement, disorders of
eye, pain in
facial nerve palsy
fasciculation
fatigue
fever
Fisher C.M.
gag reflex, depressed
gait disorder
gait, spastic
genetic neurologic disorders
Graves ophthalmopathy
Guillain Barre syndrome
gynecomastia
hallucination
hallucination, auditory
Hand-Schuller-Christian disease
headache
hearing loss
heat intolerance
hemianopia, homonymous
hippus
HLA
hoarseness
hung reflex
hyperadrenalism
hypercalcemia
hyperinsulinism
hyperkalemia
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hypersomnia
hyperthermia
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hypokalemic paralysis
hypokalemic periodic paralysis
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hypoparathyroidism, idiopathic
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hyporeflexia
hypothalamus
hypothalamus, disturbance of
hypothyroidism
immunology and the nervous system
impotence
insomnia
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
islet cell tumor
Kearns-Sayre syndrome
klippel feil syndrome
leg numbness
leg weakness, bilateral
level of consciousness, decreased
lid abnormalities
lid retraction, lower
mania
marche a petits pas
memory, impairment of
meningitis, TB
mental retardation
mental status, abnormal
mononeuropathy
mortality
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muscle biopsy
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myasthenia gravis
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myopathy, mitochondrial
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myopathy, steroid induced
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myositis
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myotonia dystrophica
myxedema coma
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nasal speech
neck weakness
Nelson's syndrome
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obesity
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ocular myopathy
one and a half syndrome
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ophthalmoplegia, painful
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic disc edema
optic neuritis
optic neuropathy
orbit
orbit, lesions of
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papilledema
paralysis, acute areflexic
paranoia
paraparesis
paraplegia, acute
parathyroid adenoma
paresthesias
Parkinsonism syndrome
periodic paralysis
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personality change
pheochromocytoma
photophobia
photophobia, central
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porphyria
potassium
primary aldosteronism
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proptosis, bilateral
psychiatric problems in neurologic disorders
psychosis
ptosis
ptosis, bilateral
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, dilated and fixed, unilateral
quadriparesis
quadriplegia
quadriplegia, transient
ragged-red fibers
rash
review article
rhabdomyolysis
sarcoidosis
scintillations
seizure
sensorineural hearing loss
skin, biopsy
skin, lesions in neurologic disorders
sleep apnea
somnolence
spasticity
statin therapy
steroid therapy, CNS treatment and complications with
stiff man syndrome
systemic lupus erythematosus
tachycardia
telangiectases
telangiectases, periungual
tetany
thymectomy
thymoma
thyroid function tests
thyroid gland, enlarged
thyroiditis
thyrotoxicosis
tongue, enlarged
torticollis
treatment of neurologic disorder
tremor
Trousseau's sign
tuberculosis
visual loss
walking, difficulty with
weakness
weakness, acute
weakness, episodic
weakness, generalized
weakness, proximal
weight loss
Werdnig-Hoffman disease
xanthopsia
Showing articles 750 to 800 of 1222 << Previous Next >>

Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction
Ann Neurol 29:606-614, Mhiri,C.,et al, 1991

Depletion of Muscle Mitochondrial DNA in AIDS Patients with Zidovudine-Induced Myopathy
Lancet 337:508-510, Arnaudo,E.,et al, 1991

Hashimoto's Encephalopathy:A Steroid-Responsive Disorder Associated with High Anti-Thyroid Antibody Titers-Report of 5 Cases
Neurol 41:228-233, Shaw,P.J.,et al, 1991

Adult Reye's Syndrome:A Review with New Evidence for a Generalized Defect in Intramitochondrial Enzyme Processing
Neurol 41:1815-1821, VanCoster,R.N.,et al, 1991

Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation
NEJM 325:1673-1681, Rousseau,F.,et al, 1991

Complete Ophthalmoplegia as a Complication of Acute Corticosteroid-and Pancuronium-Associated Myopathy
Neurol 41:921-922, Sitwell,L.D.,et al, 1991

Thyroid Function after Treatment of Brain Tumors in Children
J Pediatr 119:733-737, Ogilvy-Stuart,A.L.,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

Clinicopath Conf
Case 40-1991, Inclusion-Body Myositis, NEJM 325:1026-1035991., , 1991

Chronic Cardiomyopathy and WEakness or Acute Coma in Children with a Defect in Carnitine Uptake
Ann Neurol 30:709-716, Stanley,C.A.,et al, 1991

The Bruns-Garland Syndrome (Diabetic Amyotrophy) , Revisited 100 Years Later
Arch Neurol 48:1130-1135, Barohn,R.J.,et al, 1991

Necrotizing Myopathy with Pipestem Capillaries, Microvasc Depos
Neurol 41:936-939, Emslie-Smith,A.M.&Engel,A.G., 1991

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

A Disorder of Azonal Development, Necrotizing Myopathy, Cardiomyopathy, and Cataracts:A New Familial Disease
Ann Neurol 27:193-199, Lyon,G.,et al, 1990

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

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

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

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 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

Progressive Myopathy in Hyperkalemic Periodic Paralysis
Arch Neurol 47:1013-1017, Bradkey,W.G.,et al, 1990

Graves'Ophthalmopathy
BMJ 300:1352-1353, Fleck,B.W.&Toft,A.D., 1990

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

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

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990

Clinicopath Conf
Eosinophilic Fasciitis, Case Study 4-1990, NEJM 322:252-261, 93190., , 1990

Development of Diffuse Fasciitis with Eosinophilia During L-Tryptophan Treatment:Elevated Type I Collagen Gene
Ann Int Med 112:344-351, Varga,J.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Night-Time Nasal Ventilation in Neuromuscular Disease
Lancet 335:579-582, Heckmatt,J.Z.,et al, 1990

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



Showing articles 750 to 800 of 1222 << Previous Next >>