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Differential
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Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, early onset
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amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, misdiagnosis
ankle edema
apolipoprotein E
APP gene
arrhythmia, cardiac
arthrogryposis multiplex
Bence Jones protein
cardiomyopathy
carpal tunnel syndrome
Charcot-Marie-Tooth
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
congestive heart failure
Congo red stain
creatine phosphokinase(CPK)elevated
dermatomyositis
diarrhea
distal muscle atrophy
distal muscle weakness
dysphagia
dyspnea
edema, leg
electromyogram
electron microscopy
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fatigue
Friedreich's ataxia
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gene mutation
genetic counselling
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genetic neurologic disorders
genetic screening
genetic testing
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heralding manifestation
hoarseness
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immunoelectrophoresis, serum
immunohistochemistry
immunomodulation
immunosuppressive agents
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion body myositis
jaw pain
klippel feil syndrome
leg weakness, bilateral
misdiagnosis
molecular genetics
monoclonal gammopathy
monoclonal gammopathy of uncertain significance
mononeuropathy
motor neuron disease
MRI, abnormal
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multiple myeloma
muscle biopsy
muscle diseases, characteristics of
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muscle weakness, causes of
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muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
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myopathy, amyloid
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myopathy, thyroid disease causing
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myotonia dystrophica
nemaline rod myopathy
nemaline rod myopathy, adult onset
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neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuropathy
neuropathy, amyloid
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neuropathy, hereditary peripheral
old age, neurology of
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pain, calf
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plasma cell dyscrasia
plasma cell myeloma, CNS involvement associated with
poliomyelitis
polymyositis
polyneuropathy
polyneuropathy, familial
porphyria
practice guidelines
presenilin-1 gene
presenilin-2 gene
prognosis
proximal muscle atrophy
pseudohypertrophy
quadriceps atrophy
quadriceps weakness
review article
risk factors
sarcoidosis
sedimentation rate
sedimentation rate, elevated
stem cell transplantation
stiff man syndrome
systemic illness
tongue, enlarged
torticollis
treatment of neurologic disorder
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
weight loss
Werdnig-Hoffman disease
Showing articles 600 to 650 of 1362 << Previous Next >>

Polymyalgia Rheumatica and Temporal Arteritis:Diagnosis and Management
BMJ 314:1329-1332, Swannell,A.J., 1997

Diagnosis of Cerebral Amyloid Angiopathy
G. , Stroke 28:1418-1422997., Greenberg,S.M.&Vonsattel,J-P, 1997

High Frequency of Apolipoprotein E e2 Allele in Hemorrhage Due to Cerebral Amyloid Angiopathy
Ann Neurol 41:716-721, 7011997., Nicoli,J.A.R.,et al, 1997

Turning a Blind Eye
Lancet 349:1740, Bapat,V.N.&Tendolkar,A.G., 1997

Intravenous Immune Globulin Therapy for Neurologic Diseases
Ann Int Med 126:721-730, Dalakas,M.C., 1997

Quadriceps Weakness and Osteoarthritis of the Knee
Ann Int Med 127:97-104, 1541997., Slemenda,C.,et al, 1997

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 1997

Various Types of Hereditary Inclusion Body Myopathies Map to Chromosome 9p1-q1
Ann Neurol 41:548-551, Argov,Z.,et al, 1997

Obstetric Aspects in Women with FSH Muscular Dystrophy, Limb-Girdle Musc Dyst, & Cogen Myopathies
Arch Neurol 54:888-894, Rudnik-Schoneborn,S.,et al, 1997

A 9-Year-Old With Fever and Severe Muscle Pains
Lancet 349:1666, Punda-Polic,V.,et al, 1997

Treatment of Inflammatory Myopathies
Muscle & Nerve 20:651-664997., Mastaglia,F.L.,et al, 1997

Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy
Neurol 48:1227-1234, Eymard,B.,et al, 1997

Magnetic Resonance Imaging of the Forearm as a Diagnostic Aid in Pts with Sporadic Inclusion Body Myositis
Neurol 48:863-866, Sekul,E.A.,et al, 1997

Steroid Myopathy in Cancer Patients
Neurol 48:1234-1238, Batchelor,T.T.,et al, 1997

Clinicopath Conf
Acute Critical-Illness Myopathy, with Loss of Myosin Filaments, ? Induced by Steroid, Case 11-1997,, EJM 379-1088,1997., 1997

Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9
Ann Neurol 41:432-437, Ikeuchi,T.,et al, 1997

Painful Proximal Diabetic Neuropathy:Inflammatory Nerve Lesions and Spontaneous Favorable Outcome
Ann Neurol 41:762-770, Said,G.,et al, 1997

Clinicopath Conf
Skeletal-Muscle Infarction Associated with Diabetes Mellitus, Case 29-1997, NEJM 337:839-845997., , 1997

Granulomatous Angiitis of the Nervous System
In Vasculitis & The Nervous System, Neurol Clin 15:821-83497., Younger,D.S.,et al, 1997

Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
Arch Neurol 54:1226-1229, Roses,A.D., 1997

CIDP:Clinical Features & Responses to Trtm in 67 Consecutive Pts with/without a Monoclonal Gammopathy
Neurol 48:321-328, Gorson,K.G.,et al, 1997

Exploring the Etiology of Alzheimer Disease Using Molecular Genetics
JAMA 277:825-831, Lendon,C.L.,et al, 1997

The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
JAMA 277:832-836, Post,S.G.,et al, 1997

Thrombotic Thrombocytopenic Purpura:A Treatable Cause of Childhood Encephalopathy
J Pediatr 130:313-316, Lawlor,E.R.,et al, 1997

Few Psychological Consequences of Presymptomatic Testing for Huntington Disease
Lancet 349:4, Bundey,S., 1997

Collection and Normal Levels of the Amyloid Precursor Protein in Plasma
Ann Neurol 41:121-124, Whyte,S.,et al, 1997

Botulinum Toxin Treatment of Muscle Cramps, A Clinical & Neurophysiological Study
Ann Neurol 41:181-186, Bertolasi,L.,et al, 1997

Evaluation of Neuromuscular Symptoms in Veterans of the Persian Gulf War
Neurol 48:4-12, Amato,A.A.,et al, 1997

Is There a Gulf War Syndrome? Searching for Syndromes by Factor Analysis of Symptoms
JAMA 227:215-222, 2591997., Haley,R.W.,et al, 1997

Self-Reported Exposure to Neurotoxic Chemical Combinations in the Gulf War:A Cross-Sectional Epidemiologic Study
JAMA 227:231-237, 2591997., Haley,R.W.&Kurt,T.L., 1997

Evaluation of Neurologic Function in Gulf War Veterans:A Blinded Case-Control Study
JAMA 227:223-230, 2591997., Haley,R.W.,et al, 1997

Distal WEakness in Dystrophin-Deficient Muscular Dystrophy
Muscle & Nerve 19:1608-1610996., Felice,K.J., 1996

Practice Parameter:Genetic Testing Alert
Pract Comm Genet Testing Task Force AAN, Neurol 47:1343-13441996., , 1996

Clozapine-Induced Myotoxicity in Patients with Chronic Psychotic Disorders
Neurol 47:1518-1523, Scelsa,S.N.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Linomide Reduces the Rate of Active Lesions in Relapsing-Remitting Multiple Sclerosis
Neurol 47:895-900, Anderson,O.,et al, 1996

Angiotropic Large-Cell Lymphoma with Peripheral Nerve & Skeletal Muscle Involvement:Early Diagnosis & Treatment
Neurol 47:1009-1011, Levin,K.H.&Lutz,G., 1996

Electromagnetic Field Exposure May Cause Increased Production of Amyloid Beta & Eventually lead to Alzheimer's Disease
Neurol 47:1594-1600, Sobel,E.&Davanipour,Z., 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Acute Rectus Muscle Palsy in Children as a Result of Orbital Myositis
J Pediatr 128:230-233, Pollard,F.,et al, 1996

Peripheral Neuropathy Secondary to Docetaxel (Taxotere)
Neurol 46:108-111, 21996., New,P.Z.,et al, 1996

Influence of Apolipoprotein E Genotype on Cerebral Amyloid Angiopathy in the Elderly
Stroke 27:216-218, Itoh,Y.,et al, 1996

Primary Angiitis of Central Nervous System Assoc with Cerebral Amyloid Angiopathy:Two Cases & Review of Lit
Neurol 46:190-197, Fountain,N.B.&Eberhard,D.A., 1996

Acute Type II Myofiber Atrophy in Critical Illness
Neurol 46:819-821, 6001996., Gutman,L.,et al, 1996

Muscle is Electrically Inexcitable in Acute Quadriplegic Myopathy
Neurol 46:731-736, 6001996., Rich,M.M.,et al, 1996

Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
Neurol 47:579-580, El-Schahawi,M.,et al, 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Mushroom Myopathy
Muscle & Nerve 19:790-792996., Gonzalez,J.,et al, 1996

Isolated Neck Extensor Myopathy:A Common Cause of Dropped Head Syndrome
Neurol 46:917-921, Katz,J.S.,et al, 1996



Showing articles 600 to 650 of 1362 << Previous Next >>