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Differential
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acid maltase deficiency
activities of daily living scale
adverse drug reaction
antibodies to voltage-gated calcium channels
areflexia
arrhythmia, cardiac
atrioventricular block
autonomic dysfunction
azidodeoxythymidine
carcinoma
carcinoma of lung
cardiomyopathy
cardiovascular disease
CAT scan, chest
cerebral palsy
Clinical Pathologic Conference(C.P.C.)
complications
congestive heart failure
contractures, joint
creatine kinase
creatine phosphokinase(CPK)elevated
dermatomyositis
difficulty climbing stairs
distal muscle weakness
drug induced neurologic disorders
dysphagia
dystrophic calcification
efficacy
electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
electromyogram, incremental response
encephalitis, autoimmune
enzyme treatment
enzyme, defect
enzyme, muscle disease
exercise
exercise intolerance
exercise-related muscle strength increase
falling
familial
fatigue
gait disorder
gamma amino butyric acid receptor antibody
genetic neurologic disorders
glycogen storage disease
heart block
hip flexor weakness
H-reflex testing
human immunodeficiency virus type 1
human immunodeficiency virus type 1, asymptomatic
hyporeflexia
hypothyroidism
imbalance
immunosuppressive agents
inclusion body myositis
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 tenderness
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset of
myasthenic syndrome
myocarditis
myoglobinuria
myopathy
myopathy, drug-induced
myositis
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
polymyositis
Pompe's disease of glycogen storage
prognosis
pulmonary function tests
remote effect of cancer on the nervous system
renal failure
repetitive nerve stimulation
review article
second wind phenomena
standing difficulty
statin therapy
steroid
treatment of neurologic disorder
urine, dark
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
Wingate Anaerobic Test
xerostomia
Showing articles 1500 to 1550 of 2856 << Previous Next >>

Cerebral Involvement in McLeod Syndrome
Neurol 44:117-120, Danek,A.,et al, 1994

Botulinum Toxin-A Improves the Rigidity of Progressive Supranuclear Palsy
Ann Neurol 35:237-239, Polo,K.B.&Jabbari,B., 1994

Myoclonus Associated with Propafenone
BMJ 308:113, Chua,T.P.,et al, 1994

The Clinical Correlates of High-Titer IgG Anti-GM1 Antibodies
Ann Neurol 35:234-237, Kornberg,A.J.,et al, 1994

Headache
JNNP 57:134-143, Pearce,J.M.S., 1994

Hypokalemic Myopathy Induced by Giardia Lamblia
NEJM 330:66-67, Addiss,D.G.&Lengerich,e.J., 1994

Concurrent Cerebral Venous Sinus Thrombosis and Myeloradiculopathy in Sjorgen's Syndrome
Neurol 44:554-556, Urban,E.,et al, 1994

Clinical Genetics in Neurological Disease
JNNP 57:7-15, MacMillan,J.C.&Harper,P.S., 1994

Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994

Rapidly Evolving Myopathy with Myosin-Deficient Muscle Fibers
Ann Neurol 35:273-279, 2571994., Al-Lozi,M.T.,et al, 1994

Amyotrophic Lateral Sclerosis:T2 Shortening in Motor Cortex at MR Imaging
Radiology 189:843-846, Oba,H.,et al, 1993

Evidence for a Dopaminergic Deficit in Sporadic Amyoptrophic Lateral Sclerosis on Positron Emission Scanning
Lancet 324:1016-1018, Takahashi,H.,et al, 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Tibial Muscular Dystrophy
Arch Neurol 50:604-608, Udd,B.,et al, 1993

Acute Myopathy and Neuropathy in Status Asthmaticus:Case Report and Literature Review
Muscle & Nerve 16:84-90993., Lacomis,D.,et al, 1993

Myositis-Specific Autoantibodies, Touchstones for Understanding the Inflammatory Myopathies
JAMA 270:1846-1849, Miller,F.W., 1993

Cardiomyopathy May Be the Only Clinical Manifestation in Female Carriers of Duchenne Muscular Dystrophy
Neurol 43:2342-2345, Mirabella,M.,et al, 1993

Differential Diagnosis of Guillain-Barre Synd, In Guillain-Barre Synd
Thieme Med Publ, Ch 3, p 42993., Parry,G.J., 1993

Ifosfamide-Induced Nonconvulsive Status Epilepticus
Arch Neurol 50:1104-1105, Wengs,W.J.,et al, 1993

Signs and Symptoms of Reflex Sympathetic Dystrophy:Prospective Study of 829 Patients
Lancet 342:1012-1016, Veldman,P.H.J.M.,et al, 1993

Frequency and Prognosis of Stroke/TIA Among 4808 Survivors of Acute Myocardial Infarction
Stroke 24:1490-1495, Tanne,D.,et al, 1993

Individual Risk Assessment for Intracranial Haemorrhage During Thrombolytic Therapy
Lancet 342:1523-1528, Simoons,M.L.,et al, 1993

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

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

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

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

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



Showing articles 1500 to 1550 of 2856 << Previous Next >>