Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
antibodies to voltage-gated calcium channels
areflexia
autonomic dysfunction
carcinoma
carcinoma of lung
CAT scan, chest
Clinical Pathologic Conference(C.P.C.)
creatine phosphokinase(CPK)elevated
difficulty climbing stairs
electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
electromyogram, incremental response
encephalitis, autoimmune
enzyme, defect
exercise
exercise intolerance
exercise-related muscle strength increase
familial
fatigue
gamma amino butyric acid receptor antibody
genetic neurologic disorders
glycogen storage disease
H-reflex testing
hyporeflexia
hypothyroidism
ischemic exercise test
limbic encephalitis
lymphadenopathy, hilar
McArdle's disease
McArdle's disease, adult onset
misdiagnosis
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle stiffness
muscle strength, testing
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset of
myasthenic syndrome
myoglobinuria
myotonia
neck weakness
nerve conduction studies
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
PAS positive
percussion induced muscle contraction
pericardial effusion
phosphorylase b kinase deficiency
remote effect of cancer on the nervous system
renal failure
repetitive nerve stimulation
review article
second wind phenomena
urine, dark
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
xerostomia
Showing articles 1250 to 1300 of 2786 << Previous Next >>

Neurogenic Muscle Hypertrophy
Muscle & Nerve 19:811-818996., Gutmann,L., 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

Kobberling-Dunnigan Syndrome:A Rare Cause of Generalized Muscular Hypertrophy
Muscle & Nerve 19:843-847996., Wildermuth,S.,et al, 1996

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

Brain and Spinal Cord MRI in Motor Neuron Disease
JNNP 61:314-317, Thorpe,J.W.,et al, 1996

Amyotrophic Lateral Sclerosis and Occupational History
Arch Neurol 53:730-733, Strickland,D.,et al, 1996

Avoiding False Positive Diagnoses of Motor Neuron Disease:Lessons from the Scottish Motor Neuron Disease Register
JNNP 60:147-151, Davenport,R.J.,et al, 1996

Diagnosing Motor Neurone Disease
BMJ 312:650-651, Chancellor,A.M., 1996

Motor Neuron Disease
BMJ 313:244, Shneerson,J.M., 1996

Motor Neuron Disease Presenting as Acute Respiratory Failure:A Clinical and Pathological Study
JNNP 60:455-458, Chen,R.,et al, 1996

Dose-Ranging Study of Riluzole in Amyotrophic Lateral Sclerosis
Lancet 347:1425-1431, Lacomblez,L.,et al, 1996

Skin Involvement in Amyotrophic Lateral Sclerosis
lancet 347:1226-1227, Kolde,G.,et al, 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

AAEM Case Report#13:Diabetic Amyotrophy
Muscle & Nerve 19:939-945996., Chokroverty,S.&Sander,H.W., 1996

Ethylene Oxide Neurotoxicity:A Cluster of 12 Nurses with Peripheral and Central Nervous System Toxicity
Neurol 46:992-998, Brashear,A.,et al, 1996

Clinicopath Conf
Hypertension, MI, and Cerebral Infarctions with Pheochromocytoma, Am J Med 100:357-36496., , 1996

Opsoclonus
Semin Neurol 16:21-26, Averbuch-Heller,L.&Remler,B., 1996

Diffuse Lewy Body Disease:Clinical Features in Nine Cases without Coexistent Alzheimer's Disease
JNNP 60:531-538, Hely,M.A.,et al, 1996

Development of General Weakness in a Patient with Amyotrophic Lateral Sclerosis after Focal Botulinum Toxin Injection
Neurol 46:845-846, Mezaki,T.,et al, 1996

Yelling Attacks and Wasted Hands
Lancet 348:238, Bosboom,W.M.J.,et al, 1996

Acute Focal Neuropathy in Male Weight Lifters
Muscle & Nerve 19:897-899996., Bird,S.J.&Brown,M.J., 1996

Axillary Neuropathy in Volleyball Players:Report of Two Cases and Literature Review
JNNP 60:345-347, Paladini,D.,et al, 1996

Critical Illness Myopathy and Neuropathy
Lancet 347:1579-1582, Latronico,N.,et al, 1996

Clinicopath Conf
Tangier Disease, Case 16-1996, NEJM 334:1389-1394996., , 1996

Motor Neuropathy Due to Docetaxel and Paclitaxel
Neurol 47:115-118, Freilich,R.J.,et al, 1996

Ten Steps in Characterizing and Diagnosing Patients with Peripheral Neuropathy
Neurol 47:10-17, Dyck,P.J.,et al, 1996

Multifocal Motor Neuropathy
JNNP 60:599-603, Nobile-Orazio,E., 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

Syringomyelia as a Cause of Body Hypertrophy
Lancet 347:1593-1595, Sudo,K.,et al, 1996

Progressive Encephalomyelitis with Rigidity Responsive to Plasmapheresis and Immunosuppression
Ann Neurol 40:451-453, Fogan,L., 1996

Neuralgic Amyothrophy Misdiagnosed as Diaphragmatic Rupture
Muscle & Nerve 19:1181-1182996., Beydoun,S.R.&Rodriquez,R., 1996

Erroneous Diagnosis Corrected After 28 Years
Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996

Atrophy of Bilateral Extraocular Muscles
J Neuro-Ophthalmol 16:286-288, Okamoto,K.,et al, 1996

Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
Lancet 348:1068-1069, Wevrick,R.&Francke,U., 1996

Management of Patients Receiving Interferon Beta-1b for MS:Report of a Consensus Conf
Neurol 46:12-18, Lublin,F.D.,et al, 1996

Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
Neurol 46:68-74, Scott,B.L.,et al, 1996

Progressive Ataxia, Focal Seizures, and Malabsorption Syndrome in a 41 Year Old Woman
JNNP 60:225-230, Mumford,C.J.,et al, 1996

Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
NEJM 334:362-366, Fadic,R.,et al, 1996

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

Exacerbation of Myasthenia Gravis Associated with Cocaine Use
Neurol 46:271-272, Daras,M.,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

Peripheral Neurotoxicity Induced by Docetaxel
Neurol 46:104-108, 21996., Hilkens,P.H.E.,et al, 1996

Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
Neurol 46:461-465, North,K.N.,et al, 1996

Clinical Heterogeneity of Adhalin Deficiency
Ann Neurol 39:196-202, Morandi,L.,et al, 1996

Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
Lancet 347:582-584, Sewry,C.A.,et al, 1996



Showing articles 1250 to 1300 of 2786 << Previous Next >>