Neudle.com: "Harvey-Masland test"

Differential
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abdominal distention

abducens nerve paralysis, bilateral

acetylcholine receptor antibody

adverse drug reaction

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, prognosis

anal wink response

antibodies to voltage-gated calcium channels

antistriational muscle antibody

autonomic dysfunction

autonomic dysfunction, acute

autonomic neuropathy

Bell's phenomenon

botulinum toxin

botulinum toxin, complications of

cerebrovascular accident, mimics

chewing, impaired

children

choking

Clinical Pathologic Conference(C.P.C.)

Collier's sign

complications

congenital myasthenic syndromes

constipation

contractures, joint

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

critical care unit

denervation of muscle

denervation potentials

diaminopyridine, 3, 4

diarrhea

difficulty climbing stairs

diplopia

diplopia, transient

dropped head syndrome

electromyogram, decremental response

electromyogram, electrical silence

electromyogram, incremental response

encephalitis, autoimmune

encephalitis, brainstem

facial weakness, bilateral

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

genetic neurologic disorders

guanidine

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

gynecomastia

heat intolerance

heralding manifestation

iatrogenic neurologic disorders

immunosuppressive agents

impotence

intrinsic hand muscles, wasting of

leg weakness, bilateral

leg weakness, unilateral

lid abnormalities

lid closure, weakness of

lid twitch

limbic encephalitis

lordosis

lymphadenopathy, hilar

malignancy, occult

mediastinum, mass of

mediastinum, widening

muscle strength, testing

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

myasthenia gravis

myasthenia gravis, cold test for

myasthenia gravis, congenital

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, etiology of

myasthenia gravis, familial incidence of

myasthenia gravis, late-onset

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, neuromuscular junction in

myasthenia gravis, ocular

myasthenia gravis, paraneoplastic

myasthenia gravis, presenting manifestations

myasthenia gravis, prognosis of

myasthenia gravis, receptor site in

myasthenia gravis, remission of

myasthenia gravis, seronegative

myasthenia gravis, treatment of

myasthenic syndrome

myasthenic syndrome, treatment of

nerve conduction studies

neuroblastoma

neurologic disease, diagnoses of

neurologic examination

neurologic history

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

ocular motility, disorders of

old age, neurology of

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, total

progressive neurologic disorder

proximal muscle atrophy

pseudointernuclear ophthalmoplegia

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

remote effect of cancer on the nervous system

repetitive nerve stimulation

respiratory arrest

respiratory failure

respiratory paralysis, pharmacologic

review article

saccadic eye movements

saccadic eye movements, abnormal

seronegative

single-fiber electromyography

sleep

standing difficulty

steroid

steroid therapy, CNS treatment and complications with

temporalis muscle wasting

tensilon

tensilon test

tensilon test, false negative

tensilon test, false positive

tensilon test, paradoxical

thymectomy

thymoma

tongue, fasciculations of

tongue, pain

tongue, weakness

transient neurologic deficit

treatment of neurologic disorder

voice, abnormality of

walking, difficulty with

weakness

weakness, end of day

weakness, fatiguable

weakness, generalized

weakness, progressive

Showing articles 0 to 25 of 25

Clinicopathologic Conference, Myasthenia Gravis
NEJM 391:1441-1450, Case 32-2024, 2024

A 71-Year-Old Man Presenting with Acute Onset Dysarthria and Dysphagia
Neurol 96:180-184, Spagni, G.,et al, 2021

A 68-Year-Old Man with Proximal Weakness and Seizures
Neurol 97:e423-e428, Chen, T., 2021

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

Diagnosis of Lambert-Eaton Myasthenic Syndrome in Children
Neurol 80:e220-e222, Morgan-Followell,B.& de los Reyes,E., 2013

Clinicopathologic Conference, Thymoma with Paraneoplastic Myasthenia Gravis, Polymyositis and Myocarditis, and Brain Stem Encephalitis
NEJM 365:2413-2422, Case 39-2011, 2011

Severe Botulism After Focal Injection of Botulinum Toxin
Neurol 67:1855-1856, Souayah,N.,et al, 2006

Does This Patient Have Myasthenia Gravis?
JAMA 293:1906-1914, Scherer,K.,et al, 2005

Dysphagia as the Sole Manisfestation of Myasthenia Gravis
JNNP 76:1297-1300, Llabrs,M.,et al, 2005

Adult Botulism
Muscle & Nerve, 20:100-10297., Shapiro,B.E.,et al, 1997

Clinicopath Conf
Botulism, Case 22-1997, NEJM 337:184-190997., , 1997

Lambert-Eaton Myasthenic Syndrome Presenting with Severe Respiratory Failure
Muscle & Nerve 19:1328-1333996., Nicolle,M.W.,et al, 1996

Congenital Myasthenic Syndromes
In:Neurologic Clinics, 12:401-4371994., Engel,A.G., 1994

Clinicopath Conf
Small Cell CA (of lung) with Lambert-Eaton Myasthenic Syndr, Case 32-1994, NEJM 331:528-5354., , 1994

Ocular Myasthenia:A Protean Disorder
Survey of Ophthalmology 39:169-210, Weinberg,D.A.,et al, 1994

Prolonged Paralysis Due to Nondepolarizing Neuromuscular Blocking Agents and Corticosteroids
Muscle & Nerve 17:647-654994., Barohn,R.J.,et al, 1994

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

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

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

The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
Brain 111, 577-5961988., O'Neill,J.H.,et al, 1988

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

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Clin. Path. Conference
Type B Botulism, Unclassified Form, Case Record 48-1980, NEJM 303:1347-135580., , 1980

Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978

The Eaton-Lambert Syndrome in Ocular Myasthenia Gravis
Arch Neurol 31:183-186, Oh,S.J., 1974

Showing articles 0 to 25 of 25