Neudle.com: cardiomyopathy

Differential
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acanthocytosis

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, infants and children

acyl CoA dehydrogenase deficiency

adriamycin

advances in neurology

adverse drug reaction

alcohol

alcohol intoxication

alcohol, heart involvement with

alcohol, neurologic complications with

alcoholic blackout

alcoholic coma

alcoholic dementia

alcoholic polyneuropathy

alcoholic withdrawal states, DT's, convulsions, etc.

amyotrophic chorea-acanthocytosis

aneurysm, intracranial

aneurysm, intracranial, familial

angiography, cerebral, beaded vessels

angiography, cerebral

angiotensin-converting enzyme

ankle edema

anosmia

anterior horn cell disease

anti signal recognition particle antibody

anticholinergic drugs

anticoagulant, restarting

anticoagulant, treatment

anticoagulant, treatment in CVD

antineutrophil cytoplasmic autoantibodies

antiphospholipid antibody syndrome

anxiety

aortic valve, stenosis

arterial dissection, carotid

arterial dissection, vertebral

arthralgia

arthritis

ascending paralysis

aspartate aminotransferase

atrioventricular block

autoantibodies

autoimmune disease

automatic implantable cardioverter-defibrillator

autonomic cardiovascular reflexes

autonomic dysfunction

basal ganglia, calcification of

basophilic stippling of red blood cells

blacks

blood pressure

bone marrow suppression

bradycardia

brain natriuretic peptide

brainstem, lesion of

burning paresthesia

calcification, intracranial

calf hypertrophy

carcinoma

cardiac enzymes

cardiac surgery, neurologic complications with

cardiac transplantation

cardiomegaly

cardiomyopathy

cardiovascular disease

carnitine deficiency

carnitine deficiency myopathy

carotid artery disease

carotid artery occlusion, intracranial

carotid sinus syndrome

carpal tunnel syndrome

CAT scan

CAT scan, abdomen

CAT scan, abnormal

CAT scan, angiography

CAT scan, dense artery sign

central pontine myelinolysis

cerebellar degeneration

cerebellar infarction

cerebral atherosclerosis

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, carotid origin

cerebral infarction

cerebral infarction, hemorrhagic

cerebral ischemia

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, clinical diagnosis

cerebrovascular accident, familial occurrence

cerebrovascular accident, incidence of

cerebrovascular accident, infancy and childhood

cerebrovascular accident, location of

cerebrovascular accident, nonvascular territory

cerebrovascular accident, postpartum

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, secondary prevention

cerebrovascular accident, silent

cerebrovascular accident, women

cerebrovascular accident, young adult

cerebrovascular disease, cardiovascular disease with

cerebrovascular disease, risk factors in

chest x-ray, abnormal

chromosomal abnormality

chromosome 9

chronic progressive external ophthalmoplegia

Churg-Strauss syndrome

cirrhosis

Clinical Pathologic Conference(C.P.C.)

collateral circulation

coma

complications

conduction block

congenital heart disease

congenital heart disease, CNS complications with

congestive heart failure

conjunctivitis

consanguinity

contractures, joint

controversies in neurology

conversion reaction

copper

copper metabolism, abnormal

corpus callosum, atrophy of

corpus callosum, infarction of

cortical infarction

coumarin

coumarin, restarting treatment

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

cryptorchidism

cultured skin fibroblasts

cyclophosphamide

cyst, bone

cytochrome c oxidase

cytochrome c oxidase, deficiency

Danon disease

deep tendon reflexes

degenerative diseases of CNS

developmental retardation

dexterity, impaired

diabetes mellitus

diamond on quadriceps

diarrhea

differential diagnosis

difficulty climbing stairs

diplopia

disability, neurological

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

disulfiram

dropped head syndrome

drug induced neurologic disorders

dystrophic calcification

dystrophin

dystrophin associated proteins

echocardiogram

echocardiogram, contrast

echocardiogram, LVH

echocardiogram, transesophageal

echocardiogram, transesophageal, false negative

edema, leg

edema, pedal

edema, periorbital

Ehlers-Danlos syndrome

ejection fraction

ejection fraction, abnormal

ejection fraction, abnormal, transient

electrocardiogram, abnormal

electrocardiogram, LVH

electromyogram

electron microscopy

embolic stroke of unknown source

embolism

embolism, air

embolism, amniotic fluid

embolism, fat

embolism, paradoxical

embolism, systemic

Emery-Dreifuss muscular dystrophy

Emery-Dreifuss muscular dystrophy, carrier

encephalopathy

endarterectomy, carotid

endocardial fibrosis

endocarditis

endocarditis, marantic

endocarditis, subacute bacterial

enzyme treatment

enzyme, defect

enzyme, muscle disease

eosinophilia

eosinophilic granulomatosis with polyangiitis

epidemiology of neurology

episcleritis

erythrocyte

evidence-based research

exercise

exercise intolerance

exercise-induced neurologic dysfunction

extraocular muscle enlargement

Fabry's disease

facial anomalies

facial appearance, abnormal

fetal alcohol syndrome

fever

fibrillations

fibromuscular dysplasia

fingernails, abnormal

fluorescein angiography

frataxin

Friedreich's ataxia

frontal balding

fundus, abnormality of

gait disorder

gait, waddling

gastrocnemius muscle weakness

gastroenteritis

gastrointestinal bleeding

genetic neurologic disorders

genetic testing

glycogen debranching enzyme deficiency

glycogen storage disease

Gowers maneuver

granuloma, eosinophilic

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

headache, progressive

headache, recurrent

headache, severe

headache, throbbing

headache, thunderclap

headache, worst of life

heart valve, prosthetic

heart wall motion dysfunction

heavy metal intoxication

hemianopia

hemisensory loss

hemoglobin abnormality, neurologic complications of

hemoglobinuria

hemorrhagic diathesis

heparin

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

hereditary hemorrhagic telangiectasia(HHT)

histochemistry of muscle

Holter monitoring

homocystinuria

hormone replacement

human immunodeficiency virus type 1

hypertensive emergency

hypertrophic cardiomyopathy

hypertrophy, ventricular

hypokinetic left ventricle

hypomagnesemia

hypoparathyroidism

hypoparathyroidism, idiopathic

hypoplastic left heart syndrome

hyporeflexia

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

idiopathic hypertrophic subaortic stenosis

imbalance

immunosuppressive agents

inability to stand on tiptoes

inclusion body myositis

intellectual deterioration

intestinal pseudoobstruction

intracardiac electrophysiologic testing

intracerebral hemorrhage

intracerebral hemorrhage, young adult

intracranial pressure, increased

ipecac

isolated left ventricular noncompaction

jaundice

joint hypermobility

Kayser-Fleischer ring

Kearns-Sayre syndrome

ketamine

kyphoscoliosis, neurologic causes of

kyphosis

lactic acidemia

laminopathies

Leber's hereditary optic neuropathy

left ventricular dilatation

left ventricular dysfunction

leg swelling

leg weakness, bilateral

lipid storage myopathy

liver disease

liver function enzymes

liver transplantation

LMNA gene

lordosis

lung biopsy

lysosomal storage disease

lysosomes, abnoral

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

malignant hyperpyrexia

Marchiafava-Bignami disease

Mees lines

MELAS syndrome

meningeal enhancement

mental retardation, familial

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitoxantrone

mitral valve prolapse

mitral valve vegetation

molecular genetics

mononeuritis multiplex

MRI, CAT scan compared to

MRI, contrast enhanced

multiple sclerosis, treatment of

muscle atrophy, progressive

muscle atrophy, static

muscle strength, testing

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

myasthenia gravis

myasthenia gravis, familial incidence of

myasthenia gravis, misdiagnosis of

myasthenia gravis, ocular

myasthenic syndrome

myelopathy

myocardial biopsy

myocardial infarction

myocardial infarction, acute

myopathy, drug-induced

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, painful

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myotonia dystrophica, classification

myotonia dystrophica, type 2

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, metastatic to CNS

nephritis

nephrotic syndrome

nerve biopsy

nerve conduction studies

neuritis, heavy metals causing

neurocardiology

neurocutaneous disease

neurofibromatosis 1

neurogenic stunned myocardium

neurologic complications

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, peripheral, treatment

non-dominant hemisphere

Noonan Syndrome

nutritional deficiency

nystagmus

occipital lobe, infarction, bilateral

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy

optic nerve, lesion of

optic neuropathy

optic neuropathy, nutritional

oral contraceptives

oral contraceptives, cerbrovascular disease and

oral contraceptives, neurologic complications with

orthopnea

orthostatic hypotension

overlap syndrome

pacemaker, cardiac-transvenous

Parkinsonism syndrome

patent foramen ovale

patent foramen ovale, surgical treatment of

peripheral blood smear

peripheral blood smear, abnormal

pes cavus

pheochromocytoma

physical therapy

pigmentary retinopathy

platelet inhibiting drugs

pleural effusion

poison, neurologic problems with

POLG1 gene

polycythemia, primary

polyhydramnios

polymyositis

polyneuropathy

Pompe's disease of glycogen storage

position sensation, abnormal

posterior leukoencephalopathy syndrome

postoperative neurologic complications

postpartum

postpartum cardiomyopathy

postpartum cortical blindness

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progeria

prognosis

progressive neurologic disorder

proprioception, abnormal

protein C deficiency

proteinuria

protozoan infection

proximal muscle atrophy

pseudohypertrophy

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

pulmonary infiltrates

radionuclide imaging, heart

ragged-red fibers

RAPID CT perfusion maps

repetitive nerve stimulation

reversible cerebral vasoconstrictive syndromes

review article

rhabdomyolysis

rheumatic heart disease

rhinitis

rigid spine syndrome

rippling muscle disease

scoliosis, neurologic association with

screening

sedimentation rate, elevated

seizure

seizure, children

seizure, injury following

seizure, withdrawal

sensorineural hearing loss

skin, lesions in neurologic disorders

South America

spinocerebellar ataxia

status epilepticus

steroid

steroid therapy, CNS treatment and complications with

Stokes-Adams syndrome

stress, emotional

strokelike episodes

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subarachnoid hemorrhage, prognosis

sudden death

sweating, abnormality of

symptomatic

syncope

syncope, differential diagnosis of

systemic illness

tachycardia

Takotsubo cardiomyopathy

tetany

the metabolic syndrome

thrombin inhibitor

thrombocytopenia

thrombophlebitis

thrombotic microangiopathy

thrombotic thrombocytopenia purpura

thrombus, atrial

thrombus, intracardiac

top of the basilar syndrome

toxins, nervous system

transdermal medication

transderm-V

transient ischemic attack

trauma

treatment of neurologic disorder

tremor

trinucleotide repeats

urinary catecholamines

urinary tract infection

urine test in toxic screen

urine, dark

uveitis

valvulopathy

vanilmandelic acid, urine

vertebral-basilar insufficiency

viral myopathy

visual acuity, decreased

visual evoked response

walking, difficulty with

weakness

weakness, acute

weakness, chronic

weakness, fluctuating

weakness, progressive

weakness, proximal

weaning from respirator, failure to

web sites

weight loss

Wernicke's encephalopathy

wheelchair

winging of scapula

word-finding difficulty

workup

ximelagatran

Showing articles 50 to 100 of 123 << Previous Next >>

Churg-Strauss Syndrome, Clinical Study and Long-Term Follow-Up of 96 Patients
Medicine 78:26-37, Guillevin,L.,et al, 1999

Signs and Symptoms of Duchenne Muscular Dystrophny and Becker Muscular Dystrophy Among Carriers in the Netherlands: A Cohort Study
Lancet 353:2116-2119, Hoogerwaard,E.M.,et al, 1999

Autosomal Dominant Myofibrillar Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy Linked to Chromosome 10q
Ann Neurol 46:684-692,681, Melberg,A.,et al, 1999

Difficult Asthma or Churg-Strauss Syndrome? Steroids May be Masking Undiagnosed Cases of Churg-Strauss Syndrome
BMJ 318:475-476, D'Cruz,D.P.,et al, 1999

Incidence of Dilated Cardiomyopathy and Detection of HIV in Myocardial Cells of HIV-Positive Patients
NEJM 339:1093-1099,1153, Barbaro,G.,et al, 1998

The Wide Spectrum of Myofibrillar Myopathy Suggests a Multifactorial Etiology and Pathogenesis
Neurol 51:1646-1655, Amato,A.A.,et al, 1998

A Boy with Heart Failure, A Thick Tongue, and Double Vision
Lancet 349:1516, Karstein,J.,et al, 1997

Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
NEJM 334:362-366, Fadic,R.,et al, 1996

Development of Cardiomyopathy in Female Carriers of Duchenne and Becker Muscular Dystrophies
JAMA 275:1335-1338, Politano,L.,et al, 1996

Cerebral Infarction Associated with Kearns-Sayre Syndrome-Related Cardiomyopathy
Neurol 46:826-828, Provenzale,J.M.,et al, 1996

Treatment of End Stage Dilated Cardiomyopathy
Br Heart J 72:S52-S56, O'Connell,J.B.,et al, 1996

Age on Onset, Sex, & Cardiomyopathy as Predictors of Disability and Survival in Friedreich's Disease
Neurol 47:1260-1264, DeMichele,G.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340, LeForestier,N.,et al, 1995

Evaluation of the Cardiomyopathy in Becker Muscular Dystrophy
Muscle & Nerve 18:283-291995., Nigro,G.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Relation of Alcoholic Myopathy to Cardiomyopathy
Ann Int Med 120:529-536, Fernandez-Sola,J.,et al, 1994

Neurologic Complications of Pediatric Heart Transplantation
Arch Pediatr Adolesc Med 148:973-979, Lynch,B.J.,et al, 1994

Liver Transplantation as a Treatment for Familial Amyloidotic Polyneuropathy
Ann Int Med 120:133-134, Skinner,M.,et al, 1994

Cardiomyopathy May Be the Only Clinical Manifestation in Female Carriers of Duchenne Muscular Dystrophy
Neurol 43:2342-2345, Mirabella,M.,et al, 1993

Sudden Death of a Carrier of X-Linked Emery-Dreifuss Muscular Dystrophy
Ann Int Med 119:900-905, Fishbein,M.C.,et al, 1993

Brief Report:Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated Cardiomyopathy
NEJM 329:921-925, 9601993., Muntoni,F.,et al, 1993

Sudden Onset of Profound Weakness in a Toddler
J Pediatr 122:663-667, Carraccio,C.,et al, 1993

Ipecac Myopathy and Cardiomyopathy
JNNP 56:560-562, Dresser,L.P.,et al, 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

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

Cardioskeletal Mitochondrial Myopathy Associated with Chronic Magnesium Deficiency
Neurol 42:128-130, Riggs,J.E.,et al, 1992

Clinicopath Conf
Systemic Amyloidosis with Involvement of Heart, Autonomic Nerves, Kidneys, and Lungs, Case 38-1992,, EJM 33-950,1992., 1992

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

Chronic Cardiomyopathy and WEakness or Acute Coma in Children with a Defect in Carnitine Uptake
Ann Neurol 30:709-716, Stanley,C.A.,et al, 1991

Brain Magnetic Resonance Imaging & Neuropsychologic Evaluation of Patients with Idiopathic Dilated Cardiomyopathy
Stroke 22:195-199, Schmidt,R.,et al, 1991

Ischemic Cerebrovascular Complications and Risk Factors in Idiopathic Hypertrophic Subaortic Stenosis
Stroke 22:1143-1147, Russell,J.W.,et al, 1991

Recurrent Embolic Stroke and Cocaine-Related Cardiomyopathy
Stroke 22:1203-1205, Sauer,C.M., 1991

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991

Embolic Stroke After Smoking"Crack"Cocaine
Stroke 21:1632-1635, Petty,G.W.,et al, 1990

Neurosarcoidosis:Signs, Course and Treatment in 35 Confirmed Cases
Medicine 69:261-276, Chapelon,C.,et al, 1990

Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990

Kearns-Sayre Syndrome and Dilated Cardiomyopathy
Neurol 40:553-554, Tveskov,C.&Angelo-Nielsen,K., 1990

Stroke in Pediatric Acquired Immunodeficiency Syndrome
Ann Neurol 28:303-311, Park,Y.D.,et al, 1990

Echocardiography
NEJM 323:165-172, Popp,R.L., 1990

Syncope:Current Diagnostic Evaluation and Management
Ann Int Med 112:850-863, Manolis,A.S.,et al, 1990

A Disorder of Azonal Development, Necrotizing Myopathy, Cardiomyopathy, and Cataracts:A New Familial Disease
Ann Neurol 27:193-199, Lyon,G.,et al, 1990

Heart Disease is Myasthenia Gravis
Tidsskr Nor Laegeforen 110:1209-1211, Mygland,A.,et al, 1990

Friedreich Ataxia
In Rowland, L. P. Merritt's Textbook of Neurology, 8th Ed, Lea & Febiger, Phila, Ch 13, p627, Rosenberg,R.N., 1989

The Effects of Alcoholism on Skeletal and Cardiac Muscle
NEJM 320:409-415, 458-4601989., Urbano-Marquez,A.,et al, 1989

Cardiogenic Brain Embolism
The Second Report of the Cerebral Embolism Task Force, Cerebral Embolism Task Force, Arch Neurol 46:, 2743,1989., 1989

Current Concepts in the Idiopathic Inflammatory Myopathies:Polymyositis, Dermatomyositis, and Related Disorders
Ann Int Med 111:143-157, Plotz,P.H.,et al, 1989

Duchenne Muscular Dystrophy:Patterns of Clinical Progression and Effects of Supportive Therapy
Neurol 39:475-481, Brooke,M.H.,et al, 1989

Cardiac Transplantation in a Patient with Muscular Dystrophy and Cardiomyopathy
Arch Neurol 46:705-707, Donofrio,P.D.,et al, 1989

Left Ventricular Thrombus and Systemic Emboli Complicating the Cardiomyopathy of Duchenne's Muscular Dystrophy
Arch Neurol 46:1249-1252, Gaffney,J.F.,et al, 1989

Showing articles 50 to 100 of 123 << Previous Next >>