Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
adverse drug reaction
alveolar hypoventilation
anesthesia, general
anticonvulsants
arrhythmia, cardiac
aspiration
baldness
cachexia
calf hypertrophy
carbamazepine
cardiac arrest
cardiac arrest and resuscitation
cataracts
channelopathy
chewing, impaired
children
chromosome 19
cold temperature
coldness
creatine phosphokinase(CPK)elevated
delayed muscle relaxation
dilantin
disability, neurological
distal muscle weakness
electrocardiogram, abnormal
electromyogram
episodic disorders
exercise
facial appearance, abnormal
facial weakness
facial weakness, bilateral
falling
false negative
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
heart block
high arched palate
hypercapnia
hypothyroidism
lid closure, weakness of
lordosis
malignant hyperpyrexia
mexiletine
molecular genetics
muscle atrophy, progressive
muscle biopsy
muscle hypertrophy
muscle pain
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscular dystrophy
muscular dystrophy, cardiovascular changes with
myoedema
myotonia
myotonia congenita
myotonia dystrophica
neurologic disease, diagnoses of
neurologic evaluation
paramyotonia congenita
percussion induced muscle contraction
pericardial effusion
precipitating factors
pregnancy, neurologic complications in
prognosis
ptosis
ptosis, bilateral
respiratory failure
review article
rippling muscle disease
second wind phenomena
slit lamp examination
sodium channel dysfunction
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
treatment of neurologic disorder
trinucleotide repeats
weaning from respirator, failure to
wheelchair
Showing articles 1750 to 1800 of 3188 << Previous Next >>

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

Discrete Cortical Infarction with Prominent Impairment of Thumb Flexion
Stroke 24:2118-2120, Terao,Y.,et al, 1993

Ocular Myasthenia Gravis
J Natl Med Assoc 85:681-684, March,G.A.&Johnson,J.N., 1993

Serum anti-GQ1b IgG antibody is Associated with Ophthalmoplegia in Miller Fisher Syndrome and Guillain-Barre Syndrome: Clinical and Immunohistochemical Studies
Neurol 43:1911-1917, Chiba, A.,et al, 1993

Neuroleptic-Induced Catatonia as a Stage in the Progression Toward NMS
J Am Acad Child Adolesc Psychiatry 31:1161-1164, Woodbury,M.M.&Woodbury,M.A., 1992

Suprascapular Nerve Entrapment:Evaluation with MR Imaging
Radiology 182:437-444, Fritz,R.C.,et al, 1992

Myopathy in Severe Asthma
Am Rev Respir Dis 146:517-519, Douglass,J.A.,et al, 1992

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

Treatment of Hemifacial Spasm with Botulinum Toxin
Muscle & Nerve 15:1045-1049992., Yoshimura,D.M.,et al, 1992

Serum Antibodies to L-Type Calcium Channels in Patients with Amyotrophic Lateral Sclerosis
NEJM 327:1721-1728, 17521992., Smith,R.G.,et al, 1992

Botulinum Toxin, Useful in Adult Onset Focal Dystonias
BMJ 305:1169-1170, Lees,A.J., 1992

Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
Ann Neurol 32:577-580, vanEngelen,B.G.M.,et al, 1992

MRI and SPECT in Amyotrophic Lateral Sclerosis, Demonstr of Upper Motor Neurone Invol by Neuroimaging
Neuroradiology 34:389-393, Udaka,F.,et al, 1992

Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992

Needle Muscle Biopsy with the Automatic Biopsy Instrument
Neurol 42:2212-2213, Cote,A.M.,et al, 1992

Acute Quadriplegic Myopathy:A Complic of Treat with Steroids, Nondepolarizing Blocking Agents, or Both
Neurol 42:2082-2087, Hirano,M.,et al, 1992

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

Skeletal Muscle Toxoplasmosis in Patients with Acquired Immunodeficiency Syndrome:A Clinicopath Study
Ann Neurol 32:535-542, Gherardi,R.,et al, 1992

Hemifacial Spasm:Evaluation of Magnetic Resonance Imaging & Magnetic Resonance Tomographic Angiography
Ann Neurol 32:502-506, Adler,C.H.,et al, 1992

Neurologic Manifestations of Progressive Systemic Sclerosis
Arch Neurol 49:1292-1295, Averbuch-Heller,L.,et al, 1992

Long-Term Neurologic Consequences of Nutritional Vitamin B12 Deficiency in Infants
J Pediatr 121:710-714, Graham,S.M.,et al, 1992

Immunologic Aspects of Neurological and Neuromuscular Diseases
JAMA 268:2918-2922, Zweiman,B.&Levinson,A.I., 1992

Drug Induced Creutzfeldt-Jakob Like Syndrome
J Psychiatr Neurosci 17:103-105, Finelli,P.F., 1992

Bovine Gangliosides and Acute Motor Polyneuropathy
BMJ 305:1330-1331, Figueras,A.,et al, 1992

Prolonged Weakness after Long-Term Infusion of Vecuronium Bromide
Ann Int Med 117:484-486, Kupfer,Y.,et al, 1992

A Comparison of Two-Dimen Echocard vs Carotid Duplex Scanning in Older Pts with Cerebral Ischemia
Arch Int Med 152:2089-2093, Voyce,S.J.,et al, 1992

Stroke Complic Acute MI, A Meta-Analysis of Risk Modific by Antigoac & Thrombolytic Therapy
Arch Int Med 152:2020-2024, Viatkus,P.T.,et al, 1992

Treatment of Nocturnal Leg Cramps, A Crossover Trial of Quinine vs Vitamin E
Arch Int Med 152:1877-1880, Connolly,P.S.,et al, 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

Pravastatin-Associated Inflammatory Myopathy
NEJM 327:649-650, Schalke,B.B.,et al, 1992

'De Novo'Absence Status of Late Onset:Report of 11 Cases
Neurol 42:104-110, Thomas,P.,et al, 1992

The Dropped Head Syndrome
Neurol 42:1625-1627, Suarez,G.A.&Kelly,J.J., 1992

Decreased Glutamate Transport by the Brain and Spinal Cord in Amyotrophic Lateral Sclerosis
NEJM 326:1464-1468, 14931992., Rothstein,J.D.,et al, 1992

Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
Neurol 42:1488-1492, Applebaum,J.S.,et al, 1992

Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992

De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
Lancet 339:1081-1082, Hoogendijk,J.E.,et al, 1992

Amyotrophic Lateral Sclerosis and Lymphoma:Bone Marroe Examination and Other Diagnostic Tests
Neurol 42:1101-1102, Rowland,L.P.,et al, 1992

Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
Ann Neurol 32:404-407, Boylan,K.B.&Cornblath,D.R., 1992

Chronic Limb-Girdle Myasthenia Gravis
Neurol 42:1153-1156, Oh,S.J.&Kuruoglu,R., 1992

Clinical and Electrophysiologic Improvement in Lambert-Eaton Syndrome with Intravenous Immunoglobulin Therapy
Neurol 42:1422-1423, Bird,S.J., 1992

Electrodiagnosis Reliability in the Diagnosis of Infant Botulism
J Pediatr 120:747-749, Graf,W.D.,et al, 1992

Nerve Agents:A Review
Neurol 42:946-950, Gunderson,C.H.,et al, 1992

Anti-Hu-Associated Pareneoplastic Encephalomyelitis/Sensory Neuronopathy
Medicine 71:59-72, Dalmau,J.,et al, 1992

CNS Mycosis Fungoides:CT and MR Findings
J Comput Assist Tomogr 16:529-533, Tein,R.D.,et al, 1992

Unilateral Diaphragmatic Paralysis:An Electrophysiological Study
JNNP 55:316-318, Lagueny,A.,et al, 1992

Neurolymphomatosis:A Clinicopathologic Syndrome Re-emerges
Neurol 42:1136-1141, Diaz-Arrastia,R.,et al, 1992

Upper Arm Radial Nerve Palsy after Muscular Effort:Report of Three Cases
Neurol 42:1632-1634, Streib,E.,et al, 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992



Showing articles 1750 to 1800 of 3188 << Previous Next >>