Neudle.com: Steinert s disease

Differential
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acetazolamide

acid maltase deficiency

acquired immunodeficiency syndrome

activated protein C resistance

addiction, heroin

advances in neurology

adverse drug reaction

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, familial

amniocentesis

amphotericin B

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

anasarca

anesthesia, general

anterior interosseous neuropathy

antiarrhythmic drugs

antibodies to voltage-gated calcium channels

anticardiolipin antibodies

anticoagulant, treatment

anticoagulant, treatment in CVD

anticonvulsants

anticonvulsants, untoward effects of

antihistamines

antiphospholipid antibodies

antithrombin III deficiency

arrhythmia, cardiac

arthrogryposis multiplex

atrioventricular block

audiogram

auditory evoked brainstem potentials

autoimmune disease

automatic implantable cardioverter-defibrillator

axonopathy, distal

baldness

basal ganglia, calcification of

Behcet's syndrome

blood dyscrasias, neurologic findings with

calcification, intracranial

calcium antagonist

calcium channel dysfunction

cancer of colon

carbamazepine

carbamazepine, toxicity

carbenoxolone

carcinoma

carcinoma of ovary

carcinoma of pancreas

carcinoma of uterus

cardiac arrest

cardiac arrest and resuscitation

cardiac surgery, neurologic complications with

cardiac transplantation

CAT scan, delta sign, empty

central nervous system, infection of

cerebral blood flow

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral ischemia

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebral venous thrombosis, etiology

cerebral venous thrombosis, recurrent

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, cost of

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, thrombolytic agents in treatment

cerebrovascular accident, women

cerebrovascular accident, work up for

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

cerebrovascular disease, treatment of

Charcot-Marie-Tooth

chewing, impaired

children

chloride channel dysfunction

chloroquine

cholestasis

cholesterol

chromosomal abnormality

chromosome 19

chromosome 3

chronic progressive external ophthalmoplegia

clofibrate

clubfoot as related to neurologic disease

coagulopathy

complications

compression neuropathy

conduction block

confidentiality

congenital birth defects

congenital heart disease

congenital myopathy

congestive heart failure

contractures, joint

controversies in neurology

corneal dystrophy

corpus callosum

corpus callosum, thinning

cost effectiveness

coumarin

craniectomy, decompressive

creatine phosphokinase(CPK)elevated

D-dimer

defibrillator, implanted

degenerative diseases of CNS

dementia, thalamic

dentatorubral-pallidoluysian atrophy

dermatomyositis

diabetes mellitus

diaphragmatic paralysis

differential diagnosis

disseminated intravascular coagulation(DIC)

distal muscle weakness

diuretic

DNA probes

dropped head syndrome

drug induced neurologic disorders

dural sinus thrombosis

dysphagia

echocardiogram

efficacy

electrocardiogram, abnormal

electromyogram

electron microscopy

electronystagmography

electronystagmography, abnormal

electrophoretic pattern, serum

encephalopathy, anoxic

encephalopathy, neonatal

endovascular therapy

enolase

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

epsilon-aminocaproic acid(E.A.C.A.)

erythrocyte

evidence-based research

evoked potentials

exercise

exercise electrocardiography

eye closure

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial weakness

facial weakness, bilateral

familial hemiplegic migraine

Fazio-Londe's disease

fibrinolytic agents

fibrinolytic agents, intra-venous local infusion

floppy infant

fluorescein angiography

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glioma

glucose tolerance test, abnormal

gray matter

Guillain Barre syndrome

Guyon's canal

hand weakness

head injury

head injury, pediatric

heart block, complete

heavy metal intoxication

hemiparesis

hemoglobin abnormality, neurologic complications of

high arched feet

high arched palate

histochemistry

histochemistry of muscle

H-reflex testing

human immunodeficiency virus type 1

hyperkalemic periodic paralysis

hypokalemic periodic paralysis

hypotonia

hypotonia, causes of

hypotonia, infants

hypoxic encephalopathy

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion body myositis

infantile hemiplegia

intellectual deficit

intelligence quotient

interobserver agreement

intracranial hypertension, benign

intracranial pressure, increased

ipecac

iris, abnormal

kaliuresis

Kearns-Sayre syndrome

klippel feil syndrome

Kugelberg-Welander syndrome

leukemia

leukemia, neurologic findings assoc.with

level of consciousness, decreased

lid abnormalities

lid closure, weakness of

lid retraction, lower

malignant hyperpyrexia

manic-depressive

median neuropathy

Melkersson's syndrome

middle cerebral artery territory infarction

middle cerebral artery, occlusion of

migraine

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

MRI, CAT scan compared to

MRI, contrast enhanced

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

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

myasthenic crisis

myasthenic syndrome

myeloproliferative disorder

myopathy, carcinomatous

myopathy, distal

myopathy, drug-induced

myopathy, hypokalemic

myopathy, mitochondrial

myopathy, proximal

myopathy, steroid induced

myopathy, thyroid disease causing

myotonia dystrophica, classification

myotonia dystrophica, type 2

myotonia, causes of

myotonia, treatment of

nausea and vomiting

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

neuritis, causes of

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurogenic vs.myopathic atrophy

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination, focal

neuromuscular disease, electrodiagnosis of

neuron specific enolase

neuronal migration disorder

neuropathy

neuropathy, amyloid

neuropathy, diabetic

neuropathy, motor, multifocal

neuropathy, peripheral

newborn, evaluation of

nifedipine

nonsteroidal anti-inflammatory drug

ocular myopathy

oculovestibular reflex

ophthalmoplegia

optic atrophy

oral contraceptives

oral contraceptives, cerbrovascular disease and

oral contraceptives, neurologic complications with

orbicularis oculi muscle

orbit, lesions of

ovarian tumor

pacemaker, cardiac-transvenous

paramyotonia congenita

paresthesias

paroxysmal neurologic deficits

paroxysmal nocturnal hemoglobinuria

percussion induced muscle contraction

plasminogen deficiency

platelet inhibiting drugs

pleural effusion

pneumonia

poison, mercury

poison, neurologic problems with

poliomyelitis

polycythemia, primary

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polymyositis

polyneuropathy

porphyria

posterior interosseous neuropathy

postoperative neurologic complications

potassium channel antibodies

potassium channel dysfunction

practice guidelines

pregnancy, neurologic complications in

prethrombotic state

prevention of neurologic disorders

primary thrombocythemia

proximal myotonic myopathy

psychological testing

ptosis

ptosis, bilateral

pulmonary embolism

pulmonary function tests

radionuclide angiocardiography

saccadic eye movements

saccadic eye movements, abnormal

sensorineural hearing loss

sickle cell disease

single photon emission computed tomography

sleep apnea

slit lamp examination

sodium channel dysfunction

somnolence

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 6

spinocerebellar degeneration

superior sagittal sinus thrombosis

taurine

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

term infant

testicular atrophy

thoracic outlet syndromes

thrombocytopenia

thrombophlebitis

thyrotoxicosis

tissue plasminogen activator, intravenous

tocainide

torticollis

transient ischemic attack

transient ischemic attack, treatment of

treatment of neurologic disorder

tricresylphosphate

triglycerides

trinucleotide repeats

tubular aggregates, muscle

twins

ulnar neuropathy

ultrasonography

ventricular tachycardia

vincristine neurotoxicity

viral infection, CNS

visual evoked response

weakness

weaning from respirator, failure to

Werdnig-Hoffman disease

wheelchair

white matter disease

white matter disease, periventricular

workup

X-linked bulbospinal neuronopathy

Showing articles 100 to 120 of 120 << Previous

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

Clofibrate-Induced Muscle Damage with Myoglobinuria & Cardiomyopathy
NEJM 296:942, Smals,A.G.H., 1977

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

Platelet-Inhibiting Drugs in the Prevention of Clinical Thrombotic Disease
NEJM 293:174, Genton,E.,et al, 1975

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

The Treatment of Cerebrovascular Disease with Clofibrate
VA Cooperative Study Group, Stroke 4:6841973., , 1973

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

Clofibrate for the Treatment of Occlusive CVD-Correspondence
NEJM 287:671, Hirsch,S.,et al, 1972

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

Muscular Syndrome after Clofibrate
NEJM 286:1110, Katsilambros,N., 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

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

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

Showing articles 100 to 120 of 120 << Previous