Neudle.com: "distal myasthenia gravis"

Neurology Specific Literature Search

Differential
(Click to cross reference)

acetylcholine receptor antibody

acetylcholinesterase

acetylcholinesterase deficiency

acute intermittant porphyria

Addison's disease

alveolar hypoventilation

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, neurologic complications with

arthrogryposis multiplex

ataxia, cerebellar

autoimmune disease

autonomic dysfunction

benign congenital hypotonia

bitemporal visual field defect

brachial neuritis

bulbar palsy, acute

calcification, intracranial

carpo-pedal spasm

central core disease

cerebellar degeneration

cerebrovascular accident

Charcot-Marie-Tooth

Chinese paralytic syndrome

chronic polyneuritis, children

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

collagen vascular disease

compression neuropathy

congenital myasthenic syndromes

congenital myopathy

congestive heart failure

controversies in neurology

conversion reaction

cortical hand knob

cost effectiveness

craniopharyngioma

creatine phosphokinase(CPK)elevated

Cushing's syndrome

degenerative diseases of CNS

dermatomyositis

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diaphragmatic paralysis

differential diagnosis

distal muscle weakness

dysferlinopathy

entrapment neuropathy

epidemiology of neurology

evidence-based research

facioscapulohumeral syndrome

Fazio-Londe's disease

finger weakness

gammaglobulin therapy, intravenous

genetic neurologic disorders

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

hallucination, auditory

Hand-Schuller-Christian disease

heavy metal intoxication

hyperadrenalism

hyperinsulinism

hyperparathyroidism

hyperthyroidism

hypokalemic periodic paralysis

hypoparathyroidism

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

limbic encephalitis

median neuropathy

mental retardation

mononeuritis multiplex

motor neuron disease

movement disorder

multiple sclerosis

muscle atrophy, progressive

muscle atrophy, static

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

muscular dystrophy, neurogenic hypothesis of

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

myasthenic crisis

myasthenic syndrome

myelopathy, necrotizing

myopathy, carcinomatous

myopathy, centronuclear

myopathy, distal

myopathy, inflammatory

myopathy, mitochondrial

myopathy, neurogenic hypothesis of

myopathy, thyroid disease causing

myotonia dystrophica

myxedema, neurologic manifestations of

nemaline rod myopathy

neoplasm, pituitary

neuritis, causes of

neuroendocrinology

neurofibrillary degeneration

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neuromuscular blockade

neuromuscular junction

neuromuscular junction, abnormality of

neuronopathy, sensory

neuropathy, acute

neuropathy, diabetic

neuropathy, diphtheritic

neuropathy, motor, multifocal

neuropathy, peripheral

neuropathy, peripheral, treatment

ophthalmoplegia

ophthalmoplegia, total

Oppenheim muscular dystrophy

overlap syndrome

palliative care

parathyroid adenoma

Parkinson disease

pheochromocytoma

poison, mercury

poison, neurologic problems with

polyneuropathy, chronic inflammatory demyelinating

posterior interosseous neuropathy

practice guidelines

primary aldosteronism

progressive muscular dystrophy

progressive neurologic disorder

remote effect of cancer on the nervous system

repetitive nerve stimulation

respiratory depression

respiratory failure

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

seizure, children

seizure, treatment of

shell fish poisoning

spinal cord, injury of

spinal muscular atrophy

stiff man syndrome

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

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tensilon test, false positive

thoracic outlet syndromes

treatment of neurologic disorder

tricresylphosphate

Trousseau's sign

ulnar neuropathy

viral infection

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

whistle, inability to

winging of scapula

Showing articles 0 to 50 of 1417 Next >>

A Woman with Subacute Progression of Distal Upper Extremity Weakness
Neurol 105:e214212, Zhao,A.J.,et al, 2025

Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020

Acetylcholine Receptor-Antibody-Positive Myasthenia Gravis Presenting with Early Atrophy and Nonfluctuating Weakness of Proximal Limb Muscles
J Clin Neurol 16:714-716, Pancheri, E.,et al, 2020

Mechanisms, Causes, and Effects of Hypercapnia
UptoDate Dec, Feller-Kopman, D.J. & Schwartzstein, R.M., 2016

Differential Diagnosis of Finger Drop
Neurologist 19:128-131, Varatharaj, A.,et al, 2015

Palliative Care and Neurology
Neurol 83:561-567, Boersma, I.,et al, 2014

Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., et al, 2010

Distal Myasthenic Gravis
Neurol 52:632-634, Nations,S.P.,et al, 1999

Myasthenic Hand
Neurol 51:913-914, Janssen,J.C.,et al, 1998

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

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

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

Neuromuscular Blockade
Lancet 335:382-384, , 1990

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

The Remote Effects of Cancer on the Nervous System
in Neurol Manif of Systemic Dis, W. B. Saunders, Co, Phila, Neurologic Clinics 7:579-603, Dropcho,E.J., 1989

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Clinical Syndromes of Myasthenia in Infancy & Childhood
Arch Neurol 35:97, Fenichel,G.M., 1978

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Neurological Problems in Endocrine Diseases
Med Clin North Am 56:1029, Dale,A., 1972

"Sick"Motoneurones A Unifying Concept of Muscle Disease
Lancet 321, 1971 Feb., McComas,A.J.,et al, 1971

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

Myasthenic Syndrome in Patients with ALS
et al Neurol 9:627, Mulder,D.W., 1959

Neuro CPC of MGH
Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958

Risk of False Acetylcholine Receptor Autoantibody Positivity by Radioimmunoprecipitation Assay in Clinical Practice
Neurol 104:e213498, Zara,P.,et al, 2025

A 72-Year-Old Man with Progressive Pan-Dysautonomia
Neurol 105:e213994, Zelikovich,A.S.,et al, 2025

A Phase 3 Trial of Inebilizumab in Generalized Myasthenia Gravis
NEJM 392:2309-2320, Nowak,R.J.,et al, 2025

Myasthenia Gravis - Redemption for B-Cell Depletion
NEJM 392:2382-2384, Wolfe,G.I. & Shelly,S., 2025

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

Clinicopathologic Conference, Brain Abscess Due to Infection with Listeria Monocytogeneses
NEJM 391:1529-1538, Case 33-2024, 2024

Cancer Frequency in MuSK Myasthenia Gravis and Histological Evidence of Paraneoplastic Etiology
Ann Neurol 96:1020-1025, Falso,S.,et al, 2024

Chronic Immunotherapy for Myasthenia Gravis
www.UptoDate.Com, Bird,S.J., 2024

Ocular Myasthenia Gravis, Central Ocular Motor Signs and Unilateral Visual Loss Caused by the Great Neuro-Ophthalmologic Impersonator
Neurol 102:e209260, Young,A. & Johnston,J.L., 2024

The "Chameleon Eyes Sign" in Myasthenia Gravis
Neurol 103:e209756, Zara,P.,et al, 2024

Curtain Sign
NEJM 387:e7, Sherman, S.V., 2022

Rituximab Therapy in the Treatment of Juvenile Myasthenia Gravis
Neurol 98:e2368-e2376, Molimard, A.,et al, 2022

A New Option is Approved for Patients with Myasthenia Gravis
JAMA 327:417, Voelker, R., 2022

Myasthenia Grais
www.mda.org, , 2021

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

Useful Bedside Testing for Myasthenia Gravis
Neurol 94:e1870-e1871, Gomes del Carvalho Neto, E.,et al, 2020

Thymectomy for Myasthenia Gravis
Neurol 94:705-709, Gronseth, G.S.,et al, 2020

Severe Neurological Toxicity of Immune Checkpoint Inhibitors: Growing Spectrum
Ann Neurol 87:659-669, Dubey, D.,et al, 2020

Severe Neurological Toxicity of Immune Checkpoint Inhibitors: Growing Spectrum
Ann Neurol 87:659-669, Dubey, D.,et al, 2020

The Face of Myasthenia Gravis
Neurol 95:89-90, Ruiter, A.M.,et al, 2020

Ptosis that Resolves with Application of an Ice Pack
BMJ 369:m1147, Chakraborty, A. & Jacob, J., 2020

Myasthenic Crisis Demanding Mechanical Ventilation
Neurol 94:e299-e313, Neumann, B.,et al, 2020

Long-Term Follow-Up, Quality of Life, and Survival of Patients with Lambert-Eaton Myasthenic Syndrome
Neurol 94:e511-e520, Lipka, A.F.,et al, 2020

Showing articles 0 to 50 of 1417 Next >>