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Differential
(Click to cross reference)
abdominal muscle paralysis
abdominal protrusion
acid maltase deficiency
acid maltase deficiency, adult
arthrogryposis multiplex
bent spine syndrome
bulbar palsy
bulbar palsy, progressive
camptocormia
CAT scan
CAT scan, abnormal
CAT scan, muscle
congenital myopathy
conversion reaction
creatine phosphokinase(CPK)elevated
difficulty climbing stairs
distal muscle weakness
dropped head syndrome
dysphagia
dyspnea
electrocardiogram, abnormal
electromyogram
enzyme, defect
facial weakness
familial
fibrillations
gait disorder
gene mutation
genetic neurologic disorders
histochemistry of muscle
hypotonia
inclusion body myositis
joint hypermobility
kyphosis
leg weakness, bilateral
low back pain
malignant hyperpyrexia
monoclonal gammopathy
movement disorder
MRI
MRI, abnormal
MRI, muscle
multicore myopathy
multiminicore disease
muscle atrophy, progressive
muscle biopsy
muscle weakness
muscle weakness, proximal
muscular dystrophy
myasthenia gravis
myopathy
myopathy, focal
myopathy, metabolic
myopathy, vacuolar
myositis
myositis, focal
neck extension
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
old age, neurology of
ophthalmoplegia
paraspinal muscle
paraspinal muscle weakness
Parkinson disease
postural abnormality
prognosis
progressive neurologic disorder
pseudomyotonia
respiratory failure
review article
scoliosis
standing difficulty
stem cell transplantation
steroid
steroid therapy, CNS treatment and complications with
stooped posture
tongue, enlarged
tongue, weakness
torticollis
treatment of neurologic disorder
weakness
weakness, progressive
weakness, proximal
wheelchair
winging of scapula
Showing articles 1650 to 1700 of 3161 << Previous Next >>

Evaluation Times for Patients with In-Hospital Strokes
Stroke 24:1817-1822, Alberts,M.J.,et al, 1993

Ischemic & Hemorrhagic Stroke in Pts on Oral Anticoagulants After Reconstruct for Chronic Lower Limb Ischemia
Stroke 24:1655-1663, Dawson,I.,et al, 1993

Guillain-Barre Syndrome (GBS) with Bilateral Optic Neuritis and Central White Matter Disease
Neurol 43:842-843, Nadkarni,M.&Lisak,R.P., 1993

MRI of Guillain-Barre Syndrome
J Comput Assist Tomogr 17:651-652, Patel,H.,et al, 1993

Elevated Serum Levels of Tumor Necrosis Factor-a in Guillain-Barre Syndrome
Ann Neurol 33:591-596, 5631993., Sharief,M.K.,et al, 1993

Relapse in Guillain-Barre Syndrome after Treatment with Human Immune Globulin
Neurol 43:872-875, 8571993., Inrani,D.N.,et al, 1993

Human Immune Globulin Infusion in Guillain-Barre Syndrome:Worsening During & After Treatment
Neurol 43:1034-1036, 8571993., Castro,L.H.M.&Ropper,A.H., 1993

Serologic Evidence of Previous Campylobacter Jejuni Infection in Patients with the Guillain-Barre Syndrome
Ann Int Med 118:947-953, Mishu,B.,et al, 1993

Fulminant Rhabdomyolysis in a Patient with Dermatomyositis
Neurol 43:844-845, Caccamo,D.V.,et al, 1993

Drug Therapy of Idiopathic Inflammatory Myopathies:Response to Prednisone Azathioprine, & Methotrexate
Am J Med 94:379-387, Joffe,M.M.,et al, 1993

The Treatment of Inclusion Body Myositis:A Retrospective Review & Random, Prospective Trial of Immunosupp Therapy
Medicine 72:225-235, Leff,R.L.,et al, 1993

Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
Ann Neurol 34:25-31, Koo,B.,et al, 1993

Ophthalmologic Manifestations in MELAS Syndrome
Arch Neurol 50:977-980, Fang,W.,et al, 1993

Treatment of Inclusion-Body Myositis with High-Dose Intravenous Immunoglobulin
Neurol 43:876-879, Soueidan,S.A.&Dalakas,M.C., 1993

Inclusion Body Myositis Presenting Solely as Dysphagia
Neurol 43:1241-1243, Riminton,D.S.,et al, 1993

Acute Myopathy Associated with Large Parenteral Dose of Corticosteroid in Myasthenia Gravis
JNNP 56:702-704, Panegyres,P.K.,et al, 1993

Sudden Onset of Profound Weakness in a Toddler
J Pediatr 122:663-667, Carraccio,C.,et al, 1993

Psychogenic Myoclonus
Neurol 43:349-352, Monday,K.&Jankovic,J., 1993

Klippel-Feil Syndrome:CT and MR of Acquired & Congen Abnormal of Cervical Spine & Cord
J Comput Assist Tomogr 17:215-244, Ulmer,J.L.,et al, 1993

Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
NEJM 329:241-245, Tsujino,S.,et al, 1993

Myopathy in the Elderly:Evaluation of the Histopathologic Spectrum and the Accuracy of Clinical Diagnosis
Neurol 43:825-828, Lacomis,D.,et al, 1993

Single-Photon Emission Computed Tomographic Investigation of Patients with Motor Neuron Disease
Neurol 43:1569-1573, Abe,K.,et al, 1993

Spinal Fluid Cells and Protein in Amyotrophic Lateral Sclerosis
Arch Neurol 50:489-491, Norris,F.H.,et al, 1993

The Natural History of Amyotrophic Lateral Sclerosis
Neurol 43:1316-1322, Ringel,S.P.,et al, 1993

Poliomyelitis:Hyperintensity of the Anterior Horn Cells on MRI Images of the Spinal Cord
AJR 161:863-865, Malzberg,M.S.,et al, 1993

Hereditary Motor-Sensory Neuropathy (Charcot-Marie-Tooth Disease) with Nerve Deafness:A New Variant
J Pediatr 123:431-434, Hamiel,O.P.,et al, 1993

Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene
NEJM 329:96-101, Roa,B.B.,et al, 1993

Magnetic Resonance Imaging of Brain and the Neuromotor Disorder in Endemic Cretinism
Ann Neurol 34:91-94, Ma,T.,et al, 1993

Encephalopathy from Abuse of Bismuth Subsalicylate (Popto-Bismol)
Neurol 43:1265, Jungreis,A.C.&Schaumburg,H.H., 1993

Life-Threatening Organophosphate-Induced Delayed Polyneurop in Child After Accidental Chlorpyrifos Ingest
J Pediatr 122:658-660, Aiuto,L.A.,et al, 1993

Early Severe Infantile Botulism
J Pediatr 122:909-911, Hurst,D.L.&Marsh,W.W., 1993

Arginase Deficiency Presenting as Cerebral Palsy
Pediatrics 91:995-996, Scheuerle,A.E.,et al, 1993

Sumatriptan and Chest Pain
Lancet 341:1564-1565, Hillis,W.S.&MacIntyre,P.D., 1993

Transmural Myocardial Infarction with Sumatriptan
Lancet 341:861-862, Ottervanger,J.P.,et al, 1993

Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
Arch Neurol 50:481-488, Hardiman,O.,et al, 1993

Gastric Carcinoma Metastases to Extraocular Muscles
J Comput Assist Tomogr 17:499-500, vanGelderen,W.F.C., 1993

Accelerated Neuropathy of Renal Failure
Arch Neurol 50:536-539, Ropper,A.H., 1993

Juvenile Myoclonic Epilepsy
Arch Neurol 50:594-598, Grunewald,R.A.&Panayiotopoulos,C.P., 1993

Clinicopath Conf
B-Cell Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma with Infilt of Orbital Muscle, Case 4, 193,NEJM 328:266-275,1993., 1993

Clinical and Magnetic Resonance Features of the Classic & Akinetic-Rigid Variants of Huntington's Dis
Arch Neurol 50:17-19, Oliva,D.,et al, 1993

Rapidly Progressive Aphasic Dementia and Motor Neuron Disease
Ann Neurol 33:200-207, Caselli,R.J.,et al, 1993

Competent Pts with Adv States of Perm Paralysis Have the Right to Forgo Life-Sustaining Therapy
Neurol 43:224-225, Bernat,J.L.,et al, 1993

Neuromuscular Manifestations of Wegener's Granulomatosis:A Case Report
Neurol 43:617-618, Finkelman,R.,et al, 1993

Intramedullary Spinal Sarcoidosis:Clinical and Magnetic Resonance Imaging Characteristics
Neurol 43:333-337, Junger,s.S.,et al, 1993

Double-Blind Trial of Intravenous Methylprednisolone in Guillain-Barre Syndrome
Guillain-Barre Steroid Trial Group, Lancet 341:586-5901993., , 1993

Nerve Root Enhancement with MRI in Inflammatory Demyelinating Polyradiculoneuropathy
Neurol 32:618-619, Morgan,G.W.,et al, 1993

Fatal Rabies Associated with Extensive Demyelination
Arch Neurol 50:317-323, Nelson,D.A.&Berry,R.G., 1993

The Neurological Complciations of Sepsis
Ann Neurol 33:94-100, Bolton,C.F.,et al, 1993

Clinicopath Conf
Tuberculosis of Mediastinal Lymph Nodes, Case 3-1993, NEJM 328:195-202993., , 1993

Diag of Occult Muscular Dystrophy:"Chance"Finding of Elevated Serum Aminotransferase Act
J Pediatr 122:254-256, Morse,R.P.&Rosman,N.P., 1993



Showing articles 1650 to 1700 of 3161 << Previous Next >>