Neudle.com: myasthenia gravis distal weakness

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acetylcholine receptor antibody

acetylcholinesterase

acetylcholinesterase deficiency

Addison's disease

alveolar hypoventilation

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, myasthenic syndrome with

amyotrophic lateral sclerosis, treatment of

anterior interosseous neuropathy

anterior tibial muscle weakness

antibiotics

antibiotics, neurologic complications with

apnea

arm weakness

arthrogryposis multiplex

ataxia, cerebellar

autoimmune disease

benign congenital hypotonia

bitemporal visual field defect

botulism

brachial neuritis

bulbar palsy, acute

calcification, intracranial

calf atrophy

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children

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Chvostek sign

Clinical Pathologic Conference(C.P.C.)

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controversies in neurology

creatine phosphokinase(CPK)elevated

Cushing's syndrome

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dermatomyositis

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diabetes mellitus, neurologic manifestations of

diaphragmatic paralysis

differential diagnosis

diplopia

distal muscle weakness

entrapment neuropathy

epidemiology of neurology

evidence-based research

exophthalmus

facioscapulohumeral syndrome

familial

fasciculation

Fazio-Londe's disease

finger drop

finger weakness

foot drop

gammaglobulin therapy, intravenous

gene

genetic neurologic disorders

Guillain Barre syndrome

Guyon's canal

hallucination, auditory

hand weakness

Hand-Schuller-Christian disease

head injury

headache

heavy metal intoxication

hypokalemic periodic paralysis

hypoparathyroidism

hypothalamus

hypothalamus, disturbance of

immune complexes

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion body myositis

intrinsic hand muscles, wasting of

islet cell tumor

klippel feil syndrome

Kugelberg-Welander syndrome

leg weakness, unilateral

level of consciousness, decreased

lid closure, weakness of

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle diseases, characteristics of

muscle relaxant

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, familial incidence of

myasthenia gravis, infantile and juvenile

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, neonatal

myasthenia gravis, treatment of

myopathy, carcinomatous

myopathy, centronuclear

myopathy, distal

myopathy, mitochondrial

myopathy, thyroid disease causing

myositis

myotonia dystrophica

myxedema coma

myxedema, neurologic manifestations of

neck weakness

nemaline rod myopathy

neoplasm, pituitary

neuritis, causes of

neuroendocrinology

neurofibrillary degeneration

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neuromuscular blockade

neuromuscular junction

neuromuscular junction, abnormality of

neuropathy

neuropathy, diabetic

neuropathy, motor, multifocal

neuropathy, peripheral, treatment

ophthalmoplegia

ophthalmoplegia, total

Oppenheim muscular dystrophy

poison, neurologic problems with

poliomyelitis

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

porphyria

posterior interosseous neuropathy

practice guidelines

primary aldosteronism

prognosis

progressive muscular dystrophy

psychosis

ptosis

repetitive nerve stimulation

respiratory depression

respiratory failure

review article

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

sarcoidosis

seizure

seizure, children

seizure, treatment of

sleep apnea

spinal cord, injury of

spinal muscular atrophy

stiff man syndrome

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

syringomyelia

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tensilon test, false positive

tetany

thoracic outlet syndromes

thyrotoxicosis

torticollis

treatment of neurologic disorder

Werdnig-Hoffman disease

wheelchair

whistle, inability to

winging of scapula

Showing articles 300 to 350 of 1329 << Previous Next >>

Abnormalities of Eyelid Closure
In Walsh & Hoyt's Clinical Neuro-ophthalmology, Williams & Wilkins, Baltimore, 2:967, Miller,M.R., 1985

Sharing of Antigenic Determinants Between the Nicotinic Ach Receptor & Proteins in Ecoli, Prot Vulgaris & Pneumoniae
NEJM 312:221-225, Stefansson,K.,et al, 1985

Familial Infantile Myasthenia Gravis
Arch Neurol 42:143-144, Gieron,M.A.,et al, 1985

Worsening of Myasthenia Gravis with Timolol Maleate Eyedrops
Ann Neurol 17:211-212, Verkijk,A., 1985

Clinical Decisions in Neuro-Ophthalmology
CV Mosby:154-156, Burde,R.M.,et al, 1985

Heart Disease in Myasthenia Gravis
Acta Neurol Scand 70:176-184, Hofstad,H.,et al, 1984

Chronic Long-Interval Plasma Exchange in Myasthenia Gravis
Arch Neurol 41:715-717, Rodnitzky,R.L.,et al, 1984

Bell's Phenomenon in Diagnosis of Myasthenia Gravis
Lancet 2:1090-1091, Furukawa,T.,et al, 1984

Treatment of Lambert-Eaton Syndrome:3, 4-Diaminopyridine & Pyridostigmine
Neurol 34:1324-1330, Lundh,H.,et al, 1984

High-Dose Intravenous Gammaglobulin for Myasthenia Gravis
Lancet 1:406-407, Gajdos,Ph.,et al, 1984

Respiratory Failure in Myasthenia Gravis Due to Vocal Cord Paresis
Arch Neurol 41:567-568, Schmidt-Nowara,W.W.,et al, 1984

Long-Term Corticosteroid Treatment of Myasthenia Gravis:Report of 116 Patients
Ann Neurol 15:291-298, Pascuzzi,R.M.,et al, 1984

Myasthenia Gravis:Prolonged Treatment with Steroids
Neurol 34:170-174, Sghirlanzoni,A.,et al, 1984

Plasma Exchange & Immunosuppressive Drug Treatment in the Lambert-Eaton Myasthenic Syndrome
Neurol 34:480-485, Newsom-Davis,J.,et al, 1984

Azathioprine in the Treatment of Myasthenia Gravis
Ann Neurol 15:602-605, Witte,A.S.,et al, 1984

The Neurotoxicity of Antibacterial Agents
Ann Int Med 101:92-104, Snavely,S.R.,et al, 1984

Myasthenia Gravis & Myasthenic Syndromes
Ann Neurol 16:519-534, Engel,A.G., 1984

Prognosis of Ocular Myasthenia
Ann Neurol 14:516-519, Bever,C.T.,et al, 1983

Mechanical Ventilation for Respiratory Failure in Myasthenia Gravis
Mayo Clin Proc 58:597-602, Gracey,D.R.,et al, 1983

Myasthenia Gravis after Bone-Marrow Transplantation
NEJM 309:1565-1568, Smith,C.I.E.,et al, 1983

Myasthenia Gravis:Mechanisms & Management
Hospital Practice, (March) , 101-1093., Lisak,R.P., 1983

Myasthenia Gravis
JAMA 250:2516-2521, Seybold,M.D., 1983

Multiple Sclerosis & Autoimmune Diseases
Neurol 33:97-98, Lo,R.,et al, 1983

Juvenile Progressive Bulbar Palsy
Arch Neurol 40:351-353, Albers,J.W.,et al, 1983

Radiologic Evaluation of the Mediastinum in Myasthenia Gravis
Neurol 33:534-539, Janssen,R.S.,et al, 1983

Pure RBC Aplasia & Myasthenia Gravis
Arch Int Med 143:543-546, Socinski,M.A.,et al, 1983

Myasthenia Gravis In Children:Long-Term Follow-up
Ann Neurol 13:504-510, Rodriguez,M.,et al, 1983

Left-handedness:Association with Immune Disease, Migraine, & Developmental Learning Disorder
Proc Natl Acad Sci 79:5097-5100, Geschwind,N.,et al, 1982

Beta-Adrenoreceptor Antagonists & Diplopia
Lancet 2:826-827, Weber,J.C.P., 1982

Management of Myasthenia Gravis
Editorial, Lancet 2:135-1361982., , 1982

The Laboratory Diagnosis of Mild Myasthenia Gravis
Ann Neurol 12:238-242, Kelly,J.J.,et al, 1982

Electrophysiological & Clinical Correlation in Myasthenia Gravis
Ann Neurol 12:348-354, Oh,S.J.,et al, 1982

Functional Activities Of Autoantibodies To Acetylcholine Receptors & The Clinical Severity of Myasthenia Gravis
NEJM 307:769-775, Drachman,D.B.,et al, 1982

Ventilatory Failure in Myasthenia Gravis
JNNP 45:217-222, Ferguson,I.T.,et al, 1982

Plasmapheresis & Immunosuppressive Drug Therapy in the Eaton-Lambert Syndrome
Ann Neurol 11:570-575, Da,P.C.,et al, 1982

Progressive Multifocal Leukoencephalopathy in Myasthenia Gravis
Ann Neurol 11:218-219, Dawson,D.M., 1982

Thymectomy in Late-Onset Myasthenia Gravis
Arch Neurol 39:82-83, Olanow,C.W.,et al, 1982

Ocular Myasthenia, Multiple Recurrences & Spontaneous Remissions
JAMA 247:62, Hochman,M.S., 1982

Enhanced Ptosis in Myasthenia Gravis
Arch Neurol 38:531, Gorelick,P.B.,et al, 1981

Eaton-Lambert Myasthenic Syndrome:Long-term Treatment of Three Patients with Prednisone
Ann Neurol 10:448-453, Streib,E.W.,et al, 1981

Myasthenia Gravis & Premature Ovarian Failure
Arch Int Med 141:1230-1232, Kuki,S.,et al, 1981

Pathogenesis & Treatment of Myasthenia Gravis
BMJ 283:1008-1012, Scadding,G.K.,et al, 1981

No Direct Correl. of Serum Ach Receptor Antib. Levels & Clin. State of Individual Patients with Myasthenia Gravis
Neurol 31:220-224, Roses,A.D.,et al, 1981

Plasma Pyridostigmine Levels in Myasthenia Gravis
Neurol 31:145-150, White,M.C.,et al, 1981

Relapsing Ocular Myasthenia
Neurol 31:325-326, Rollinson,R.D.,et al, 1981

Treatment with Oral 4-aminopyridine in Disorders of Neuromuscular Transmission
Neurol 31:265-271, Murray,N.M.F.,et al, 1981

Stable Remissions in Myasthenia Gravis
Neurol 31:32-37, Perez,M.C.,et al, 1981

Procainamide-Induced Myasthenia-like Weakness in a Patient with Peripheral Neuropathy
Arch Neurol 38:378-379, Niakan,E.,et al, 1981

Juvenile Myasthenia Gravis
Neurol 30:732-739, Snead,O.C.,et al, 1980

Heat-Induced Myasthenic Crisis
Arch Neurol 37:671-672, Gutmann,L., 1980

Showing articles 300 to 350 of 1329 << Previous Next >>