Neudle.com: myotonia

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abortion, spontaneous

acetazolamide

acid maltase deficiency

advances in neurology

adverse drug reaction

adynamia episodica hereditaria

airway obstruction

alopecia

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, familial

amniocentesis

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

anasarca

anemia

anesthesia, general

anterior interosseous neuropathy

antiarrhythmic drugs

antibodies to voltage-gated calcium channels

anticoagulant, treatment

anticoagulant, treatment in CVD

anticonvulsants

anticonvulsants, untoward effects of

antihistamines

arrhythmia, cardiac

arthrogryposis multiplex

atrioventricular block

audiogram

auditory and vestibular pathways

auditory evoked brainstem potentials

autoantibodies

autoimmune disease

autoimmune encephalopathy

automatic implantable cardioverter-defibrillator

autonomic dysfunction

axonal degeneration

axonopathy, distal

baldness

basal ganglia, calcification of

behavioral disorder

beta adrenergic agonist

calcification, intracranial

calcium antagonist

calcium channel dysfunction

calf hypertrophy

cancer of colon

carbamazepine

carbamazepine, toxicity

carcinoma

carcinoma of ovary

carcinoma of pancreas

carcinoma of uterus

cardiac arrest

cardiac arrest and resuscitation

cardiac surgery, neurologic complications with

cardiac transplantation

central nervous system, infection of

cerebral blood flow

cerebral embolism

cerebral embolism, cardiac origin

cerebral ischemia

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, prevention of

cerebrovascular accident, young adult

chloride channel dysfunction

cholestasis

chromosomal abnormality

chromosome 19

chromosome 3

chronic progressive external ophthalmoplegia

Chvostek sign

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

compression neuropathy

conduction block

confidentiality

confusion

congenital birth defects

congenital heart disease

congenital myopathy

congestive heart failure

consanguinity

constipation

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

corneal dystrophy

corpus callosum

corpus callosum, thinning

coumarin

cranial nerve palsies

cranial neuropathy

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

cylindrical spiral

dantrolene sodium

defibrillator, implanted

degenerative diseases of CNS

delay in diagnosis

delayed muscle relaxation

dementia, thalamic

dentatorubral-pallidoluysian atrophy

dermatomyositis

diabetes mellitus

diaphragmatic paralysis

diet

differential diagnosis

difficulty climbing stairs

dilantin

dilantin, toxicity

diplopia

disability, neurological

distal muscle weakness

DNA probes

down-beat nystagmus

droperidol

dropped head syndrome

drug induced neurologic disorders

electrocardiogram, abnormal

electromyogram

electron microscopy

electronystagmography

electronystagmography, abnormal

electrophoretic pattern, serum

electroretinograph

embolism

emergencies, neurologic

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

entrapment neuropathy

enzyme treatment

eosinophilia

eosinophilic fasciitis

epidemiology of neurology

episodic disorders

episodic neurologic deficits

erythrocyte

evoked potentials

exercise

exercise electrocardiography

exercise intolerance

eye closure

eye movement, disorders of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial weakness

facial weakness, bilateral

falling

false negative

familial

familial hemiplegic migraine

fasciculation

Fazio-Londe's disease

fibrillations

fine motor function, impaired

floppy infant

fluorescein angiography

gammaglobulin therapy, intravenous

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glioma

glucose tolerance test, abnormal

Guillain Barre syndrome

heart block, complete

heavy metal intoxication

heralding manifestation

histochemistry of muscle

hoarseness

H-reflex testing

human diploid cell rabies vaccine

hyperkalemic periodic paralysis

hypokalemic periodic paralysis

hyponatremia

hypoparathyroidism

hypoparathyroidism, idiopathic

hypoxic encephalopathy

iatrogenic neurologic disorders

immunosuppressive agents

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion body myositis

intelligence quotient

iris, abnormal

Isaacs syndrome

kaliuresis

Kearns-Sayre syndrome

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

laryngeal spasm

leg swelling

leg weakness, bilateral

leucine rich glioma inactivated 1 antibodies

lid abnormalities

lid closure, weakness of

lid lag

lid retraction, lower

lymphoma, primary of CNS

malignancy screen

malignant hyperpyrexia

manic-depressive

meclizine

median neuropathy

Melkersson's syndrome

mental retardation

mental status, abnormal

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

Morvan's fibrillary chorea

multiple sclerosis, diet in

multiple sclerosis, treatment of

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, non motor symptoms

myasthenic crisis

myasthenic syndrome

myasthenic syndrome, treatment of

myopathy, carcinomatous

myopathy, distal

myopathy, drug-induced

myopathy, genetic

myopathy, hereditary

myopathy, metabolic

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, proximal

myopathy, thyroid disease causing

myotonia dystrophica, classification

myotonia dystrophica, type 2

myotonia, causes of

myotonia, treatment of

myotonic crisis

myotonic discharges

neck weakness

neoplasm, metastatic to CNS

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve injury

neuritis, causes of

neurocutaneous disease

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurogenic vs.myopathic atrophy

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neuromuscular disease, electrodiagnosis of

neuromyotonia

neuromyotonia and axonal neuropathy

neuromyotonia, ocular

neuronal migration disorder

neuropathy, hereditary peripheral

neuropathy, medication induced

neuropathy, motor, multifocal

neuropathy, peripheral

neurosyphilis

newborn, evaluation of

next-generation sequencing

oculovestibular reflex

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegic migraine

optic atrophy

orbicularis oculi muscle

orbit, lesions of

ovarian tumor

pacemaker, cardiac-transvenous

paramyotonia congenita

paroxysmal neurologic deficits

percussion induced muscle contraction

pericardial effusion

periodic paralysis

peripheral nerve, lesion of

platelet inhibiting drugs

pleural effusion

pneumonia

poison, mercury

poison, neurologic problems with

poliomyelitis

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polymyositis

polyneuropathy

Pompe's disease of glycogen storage

posterior interosseous neuropathy

postoperative neurologic complications

potassium channel antibodies

potassium channel dysfunction

prayer sign

precipitating factors

pregnancy, neurologic complications in

premature infant

prevention of neurologic disorders

primary episodic ataxia

procainamide

prognosis

progressive neurologic disorder

proptosis

proximal muscle atrophy

proximal myotonic myopathy

pruritus

pseudomyotonia

psoriasis

psychiatric problems in neurologic disorders

psychological testing

ptosis

ptosis, bilateral

pulmonary function tests

pulmonary hypertension

radiation neuropathy

radiation therapy, CNS treatment and complications with

radiculopathy

radionuclide angiocardiography

ragged-red fibers

recombinant DNA

red cell aplasia

remote effect of cancer on the nervous system

renal failure

respiratory failure

respiratory tract infection

rippling muscle disease

risk factors

risk-benefit assessment

saccadic eye movements

saccadic eye movements, abnormal

safety

salivation, excessive

sarcoidosis

Schwartz-Jampel syndrome

screening

second wind phenomena

sedimentation rate, elevated

seizure

sensorineural hearing loss

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

skin, thickened

sleep apnea

sleep pathology and physiology

slit lamp examination

sodium channel dysfunction

somnolence

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 6

spinocerebellar degeneration

standing difficulty

statin therapy

steroid therapy, CNS treatment and complications with

sweating, abnormality of

syphilis, neurologic complications with

taste

taurine

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

thoracic outlet syndromes

thymoma

thyrotoxicosis

tocainide

tone, muscle, increased

torticollis

transient ischemic attack

treatment of neurologic disorder

tricresylphosphate

trigeminal nerve

trigeminal nerve, lesion of

trigeminal neuropathy

trinucleotide repeats

tubular aggregates, muscle

ventricular tachycardia

vertigo

vertigo, cervical

vertigo, treatment of

viral infection, CNS

visual evoked response

vitamin deficiency

vocal cord paralysis

walking, difficulty with

weakness

weakness, acute

weakness, episodic

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

weight loss

Werdnig-Hoffman disease

Wernicke's encephalopathy

wheelchair

white matter disease

white matter disease, periventricular

winging of scapula

workup

X-linked bulbospinal neuronopathy

X-linked myopathy

x-linked myopathy with excessive autophagy

Showing articles 100 to 138 of 138 << Previous

Cardiac Involvement in Myotonic Muscular Dystrophy
Medicine 64:371-387, Moorman,J.R.,et al, 1985

Tubular Aggregates, Their Association with Neuromuscular Diseases, Including the Syndrome of Myalgias/Cramps
Arch Neurol 42:973-976, Rosenberg,N.L.,et al, 1985

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

Isaacs'Syndrome with Muscle Hypertrophy Reversed by Phenytoin Therapy
Arch Neurol 40:241-242, Zisfein,J.,et al, 1983

Radionuclide Angiocardiographic Analysis of Myocardial Function in Myotonic Muscular Dystrophy
Neurol 33:657-660, Hartwign,G.B.,et al, 1983

The Treatment of Myotonia:Evaluation of Chronic Oral Taurine Therapy
Neurol 33:599-603, Durelli,L.,et al, 1983

Abnormal Visual Evoked Potentials in Myotonic Dystrophy
Neurol 33:1622-1625, Cott,P.S.,et al, 1983

Families with Myotonic Dystrophy with & without Cardiac Involvement
Arch Int Med 143:2134-2136, Hawley,R.J.,et al, 1983

Myotonic Dystrophy, Mitral Valve Prolapse, and Cerebral Embolism
Stroke 13:93-94, Morris,L.K.,et al, 1982

Respiratory Muscle Function and Ventilatory Control in Patients with Myotonic Dystrophy
Q J Med 202:205-226, Serisier,D.E.,et al, 1982

Myotonia Associated With Cancer
NEJM 304:358, Laso,F.J.,et al, 1981

Hypersomnia Associated with Alveolar Hypoventilation in Myotonic Dystrophy
Neurol 31:1336-1337, Hansotia,P.,et al, 1981

Echocardiographic Evaluation of Cardiac Abnormalities in Duchenne's Dystrophy & Myotonic Muscular Dystrophy
Arch Neurol 37:273-277, Reeves,W.C.,et al, 1980

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

Cylindrical Spirals in a Familial Neuromuscular Disorder
Ann Neurol 7:550-556, Bove,K.E.,et al, 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Retraction of the Lower Eyelid
Neurol 29:386-389, Cohen,M.M.,et al, 1979

Cholestasis & Myotonic Dystrophy
(letter) NEJM 301:329-330979., Theodore,Ch.,et al, 1979

Isaac Syndrome with Laryngeal Involvement:An Unusual Presentation of Myokymia
Neurol 29:1612-1615, Jackson,D.L.,et al, 1979

Abnormal Iris Vasculature in Myotonic Dystrophy
Arch Neurol 35:224, Stern,L.Z.,et al, 1978

Effects of Acetazolamide on Myotonia
Ann Neurol 3:531, Griggs,R.C.,et al, 1978

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978

Peripheral Neuropathy in Myotonic Dystrophy
Arch Neurol 35:741-745, Olson,N.D.,et al, 1978

Erythrocyte Metabolism in Muscular Dystrophy
Arch Neurol 35:592-595, Danon,M.J.,et al, 1978

Hypothyroidism with True Myotonia
JNNP 41:1013-1015, Venables,G.S.,et al, 1978

Myasthenia Gravis & Myotonic Dystrophy in a 13-year-old Girl
Neurol 27:546, Schoen,R.T., 1977

Cardiac Features of Unusual X-linked Humeroperoneal Neuromuscular Disease
et al NEJM 293:1017, Waters,D.D., 1975

Important Advances in Clinical Medicine
West J Med 123:128, Mosier,J.M.,et al, 1975

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

Pathology of Malignant Hyperpyrexia
BMJ Editorial 249, 1973, Feb., , 1973

Thalmic Neuronal Inclusion Disease
Neurol 22, 3961972., Segarra,J., 1972

Diphenylhydantoin for Myotonia Congenita-Correspondence
NEJM 286:893, , 1972

Congenital Dystrophia Myotonica
Neurol 22:443, Dyken,P.D., 1972

Preclinical Detection of Dystrophia Myotonica
BMJ 124, 1972 April., , 1972

Electrodiagnosis of Neuromuscular Disease
Bull Univ Maryland School Med 56:33, Kemble,F., 1971

Ophthalmoplegia In Myotonic Dystrophy
Am J Ophthalmol 71:1231-1235, Lessell,S.,et al, 1971

Early Recognition of Heterozygotes for the Gene for Dystrophia Myotonica
JNNP 33:279, Bundey,S.,et al, 1970

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

The Cerebral Defect & Myopathy in Myotonic Dystrophy
Neurol 17:1106, Rosman,N.,et al, 1967

Showing articles 100 to 138 of 138 << Previous