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Differential
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acetylcholine receptor antibody
adverse drug reaction
amyotrophic lateral sclerosis, differential diagnosis
anterior tibial muscle weakness
antistriational muscle antibody
areflexia
arrhythmia, cardiac
Bell's phenomenon
botulism
brainstem, lesion of
bulbar palsy
calf atrophy
canned food
cardiac arrest
cardiac arrest and resuscitation
cataracts
central core disease
chewing, impaired
children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
Coats syndrome
Collier's sign
congenital myopathy
creatine phosphokinase(CPK)elevated
descending paralysis
diplopia
distal muscle weakness
dysarthria
dysphagia
dyspnea
electromyogram
electromyogram, decremental response
eye closure
face, elongated
facial appearance, abnormal
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
false negative
familial
fatigable chewing
fatigue
fibrillations
food poisoning
foot drop
gag reflex, depressed
gait disorder
gammaglobulin therapy, intravenous
gaze palsy
gaze palsy, horizontal
gaze palsy, vertical
gene mutation
genetic neurologic disorders
genetic testing
hand weakness
histochemistry of muscle
hypophonia
hypotonia
immunohistochemistry
immunosuppressive agents
inclusion body myositis
internuclear ophthalmoplegia
intrinsic hand muscles, wasting of
Kearns-Sayre syndrome
leg weakness, bilateral
lid abnormalities
lid closure, weakness of
lid twitch
lordosis
mediastinum, mass of
Melkersson's syndrome
mestinon
misdiagnosis
mitochondrial disease
motor neuron disease
multicore myopathy
muscle atrophy, progressive
muscle biopsy
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, diagnosis
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, drug induced
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, ocular
myasthenia gravis, presenting manifestations
myasthenia gravis, prognosis of
myasthenia gravis, remission of
myasthenia gravis, seronegative
myasthenia gravis, treatment of
myasthenic sneer
myopathy
myopathy, centronuclear
myopathy, inflammatory
myopathy, mitochondrial
myotonia
myotonia dystrophica
nasal regurgitation
nasal speech
nausea and vomiting
neck weakness
nemaline rod myopathy
nerve conduction studies
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuroophthalmology
neurotoxin
nystagmus
ocular motility, disorders of
ocular myopathy
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
orbicularis oculi muscle
oropharyngeal weakness
overlap syndrome
penicillamine
percussion induced muscle contraction
plasmapheresis
polymyositis
positive sharp waves
prognosis
progressive neurologic disorder
pseudointernuclear ophthalmoplegia
ptosis
ptosis, alternating
ptosis, bilateral
quadriparesis, acute
quinine
ragged-red fibers
rapidly progressing neurologic illness
repetitive nerve stimulation
respiratory failure
review article
saccadic eye movements
saccadic eye movements, abnormal
scoliosis
seronegative
shoulder-girdle wasting
single-fiber electromyography
sleep
sloped shoulders
spinal muscular atrophy
standing difficulty
steroid
steroid therapy, CNS treatment and complications with
temporalis muscle wasting
tensilon
tensilon test, false negative
tensilon test, false positive
tensilon test, paradoxical
thymectomy
thymoma
tongue, weakness
toxins, nervous system
transverse smile
treatment of neurologic disorder
trinucleotide repeats
upgaze, paralysis of
voice, abnormality of
walking, difficulty with
weakness
weakness, acute
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weaning from respirator, failure to
weight loss
wheelchair
whistle, inability to
winging of scapula
Showing articles 2050 to 2100 of 3180 << Previous Next >>

The Role of Plasmapheresis in Childhood Guillain-Barre Syndrome
Ann Neurol 28:65-69, Epstein,M.A.&Sladky,J.T., 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Mitochondrial Myopathy with a Defect of Mitochondrial-Protein Transport
NEJM 323:37-42, Schapira,A.H.V.,et al, 1990

Myopathy and Rhabdomyolysis Associated with Lovastatin-Gemfibrozil Combination Therapy
JAMA 264:71-75, Pierce,L.R.,et al, 1990

Peripheral Neuropathy in the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Neurol 40 1035-1040, Smith,B.E.&Dyck,P.J., 1990

The Clinical Spectrum of the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Ann Int Med 113:124-134, Martin,R.W.,et al, 1990

L-Tryptophan-Associated Eosinophilic Perimyositis, Neuritis, and Fasciitis
Medicine 69:187-199, Kaufman,L.D.,et al, 1990

Autosomal Dominant Cramping Disease
Arch Neurol 47:810-812, Ricker,K.&Moxley,R.T., 1990

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Paraneoplastic Motor Neuron Disease and Renal Cell Carcinoma:Improvement after Nephrectomy
Neurol 40:960-962, Evans,B.K.,et al, 1990

Poliomyelitis Outbreak in Isreal in 1988:A Report with two Commentaries
Lancet 335:1192-1198, Slater,P.E.,et al, 1990

Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
Neurol 40:1450-1453, Defesche,J.C.,et al, 1990

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990

Clinicopath Conf
Eosinophilic Fasciitis, Case Study 4-1990, NEJM 322:252-261, 93190., , 1990

Development of Diffuse Fasciitis with Eosinophilia During L-Tryptophan Treatment:Elevated Type I Collagen Gene
Ann Int Med 112:344-351, Varga,J.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

HIV-Related Neuromuscular Syndrome Simulating Motor Neuron Disease
Neurol 40:544-546, Verma,R.K.,et al, 1990

Acute Relapsing Guillain-Barre Syndrome after Long Asymptomatic Intervals
Arch Neurol 47:82-84, Wijdicks,E.F.&Ropper,A.H., 1990

Benefit of Intravenously Administered Immune Serum Globulin in Patients with Guillain-Barre Syndrome
J Pediatr 116:141-144, Shahar,E.,et al, 1990

Lyme Polyradiculoneuropathy Presenting as Increasing Abdominal Girth
Neurol 40:373-375, Daffner,K.R.,et al, 1990

Night-Time Nasal Ventilation in Neuromuscular Disease
Lancet 335:579-582, Heckmatt,J.Z.,et al, 1990

Muscle Cramps
Arch Int Med 150:511-518, McGee,S.R., 1990

How Frequently Does Classic Amyotrophic Lateral Sclerosis Develop in Survivors of Poliomyelitis
Neurol 40:172-174, Armon,C.,et al, 1990

Amyotrophic Lateral Sclerosis:A Case-Control Study Following Detection of a Cluster in a Small Wisconsin Community
Arch Neurol 47:38-41, Sienko,D.G.,et al, 1990

Bismuth Absorption and Myoclonic Encephalopathy During Bismuth Subsalicylate Therapy
Ann Int Med 112:140-141, Mendelowitz,P.C.,et al, 1990

Neuromuscular Blockade
Lancet 335:382-384, , 1990

Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,et al, 1990

Clinicopath Conf
Primary CNS Lymphoma with AIDS, Am J Med 88:169-1761990., , 1990

Benign Plexus Neuropathy in Children
J Pediatr 116:276-278, Zeharia,A.,et al, 1990

Distal Ulnar Neuropathy as a Cause of Finger Tremor:A Case Report
Neurol 40:153-154, Streib,E.W., 1990

Extrapyramidal Involvement in Rett's Syndrome
Neurol 40:293-295, FitzGerald,P.M.,et al, 1990

Scleroderma, fasciitis, and Eosinophilia Associated with the Ingestion of Tryptophan
NEJM 322:874-881, 9261990., Silver,R.M.,et al, 1990

Association of the Eosinophilia-Myalgia Syndrome with the Ingestion of Tryptophan
NEJM 322:869-873, 9261990., Hertzman,P.A.,et al, 1990

Left Ventricular Thrombosis and Stroke Following Myocardial Infarction
Editorial, Lancet 335:759-7601990., , 1990

The Effect of Warfarin on Mortality and Reinfarction after Myocardial Infarction
NEJM 323:148-152, Smith,P.,et al, 1990

Clinical Study of 227 Patients with Lacunar Infarcts
Stroke 21:842-847, Arboix,A.,et al, 1990

Acute Disseminated Encephalomyelitis, MRI Findings & the Distinction from Multiple Sclerosis
Brain 113:291-302, Kesselring,J.,et al, 1990

Botulinum Toxin Treatment of Cranial-Cervical Dystonia, Spasmodic Dystonia, Focal Dystonias & Hemifacial Spasm
JNNP 53:633-639, Jankovic,J.,et al, 1990

Assessment:The Clinical Usefulness of Botulinum Toxin-A in Treating Neurologic Disorders
Subcommittee Report, Neurol 40:1332-13361990., , 1990

Cortical-Basal Ganglionic Degeneration
Neurol 40:1203-1212, Riley,D.E.,et al, 1990

Neurological Findings in Alzheimer's Disease and Normal Aging
Arch Neurol 47:625-627, Glasko,D.,et al, 1990

Treatment of Spasticity with Botulinum Toxin:A Double-Blind Study
Ann Neurol 28:512-515, Snow,B.J.,et al, 1990

Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl
Clin genet 37:355-362, Clarke,J.T.,et al, 1990

Skeletal Muscle Pathology in AIDS:An Autopsy Study
Muscle & Nerve, 13:508-51590., Wrzolek,M.A.,et al, 1990

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

Hypoxic-Ischemic Damage of the Basal Ganglia
Mov Disord 5:219-224, Hawker, K. & Lang, A.E., 1990

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989



Showing articles 2050 to 2100 of 3180 << Previous Next >>