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

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

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 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

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 50 to 100 of 119 << Previous Next >>

An Unusual Cause of Cerebral Venous Thrombosis in a Four-Year-Old Child
Stroke 24:603-605, Rich,C.,et al, 1993

Cerebral Abnormalities in Myotonic Dystrophy
Arch Neurol 50:917-923, Chang,L.,et al, 1993

Protein S Deficiency in Middle-Aged Women with Stroke
Neurol 42:1029-1033, Green,D.,et al, 1992

Oculomotor, Auditory, and Vestib ular Responses in Myotonic Dystrophy
Arch Neurol 49:954-960, Verhagen,W.I.M.,et al, 1992

Unstable DNA Sequence in Myotonic Dystrophy
Lancet 339:1125-1128, Harley,H.G.,et al, 1992

Phenotypic Expression of the Myotonic Dystrophy Gene in Monozygotic Twins
Neurol 42:1815-1817, Dubel,J.R.,et al, 1992

Superior Sagittal Sinus Thrombosis in a Child with Protein S Deficiency
Neurol 42:2303-2305, Prats,J.M.,et al, 1992

The Heart in Myotonic Dystrophy
Editorial, Lancet 339:528-5291992., , 1992

Ventricular Late Potentials in Myotonic Dystrophy
Ann Int Med 115:607-613, Milner,M.R.,et al, 1991

Myotonic Heart Disease:A Clinical Follow-Up
Neurol 41:259-262, Hawley,R.J.,et al, 1991

Response to Treatment with Antihistamines in a Family with Myotonia Congenita
Lancet 337:28-30, Hughes,E.F.&Wilson,J., 1991

Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
Stroke 21:633-636, Cros,D.,et al, 1990

Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
Neurol 40:671-676, Speer,M.C.,et al, 1990

Hematologic Disorders and Ischemic Stroke
Stroke 21:1111-1121, Hart,R.G.&Kanter,M.C., 1990

Criteria for Establishing the Validity of Genetic Recombination in Myotonic Dystrophy
Neurol 39:420-421, Griggs,R.C.,et al, 1989

Magnetic Resonance Imaging and Clinical Correlates of Intellectual Impairment in Myotonic Dystrophy
Arch Neurol 46:536-540, Huber,S.J.,et al, 1989

The Molecular Genetic Revolution, Its Impact on Clinical Neurology
Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988

Hearing Loss in Myotonic Dystrophy
Ann Neurol 23:202-203, Wright,R.B.,et al, 1988

Central Nervous System Magnetic Resonance Imaging Findings in Myotonic Dystrophy
Arch Neurol 45:36-37, Glantz,R.H.,et al, 1988

Peripheral Neuropathy in Myotonic Dystrophy:A Nerve Biopsy Study
Ann Neurol 23:470-476, Cros,D.,et al, 1988

Hydrops and Pleural Effusions in Congenital Myotonic Dystrophy
J Pediatr 113:555-557, Curry,C.J.R.,et al, 1988

Cerebral Ischemia with Mitral Valve Prolapse
Am Heart J 113:1308-1315, Wolf,P.A.,et al, 1987

Genetic Linkage in Neurologic Diseases
Editorial, NEJM 316:1018-10201987., Martin,J.B., 1987

Association of Primary Hyperparathyroidism with Myotonic Dystrophy in Two Patients
Arch Int Med 147:777-778, Harada,S.,et al, 1987

Acetazolamide-Responsive Myotonia Congenita
Neurol 37:488-491, Trudell,R.G.,et al, 1987

Childhood Stroke Associated with Protein C or S Deficiency
J Pediatr 111:562-564, Israels,S.J.&Seshia,S.S., 1987

Computed Tomographic Findings of Brain & Skull in Myotonic Dystrophy
JNNP 50:435-438, Avrahami,E.,et al, 1987

Cerebral Ventricular Dilation in Congenital Myotonic Dystrophy
J Pediatr 111:372-376, Regev,R.,et al, 1987

Treatment of Myotonia
Editorial, Lancet 1:1242-12441987., , 1987

Frequency of Cerebral Infarction in Patients with Inherited Neuromuscular Disease
Stroke 18:805-807, Biller,J.,et al, 1987

Successful Treatment with Tocainide of Recessive Generalized Congenital Myotonia
Ann Neurol 19:501-504, Streib,E.W., 1986

Cardiac Side Effects of Phenytoin & Carbamazepine, A Dose-Related Phenomenon
Arch Neurol 42:1067-1068, Durelli,L.,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

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

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

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

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

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

Drug-Induced Myopathies In Man
Lancet 2:562-566, Lane,R.J.M.,et al, 1978

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

Showing articles 50 to 100 of 119 << Previous Next >>