Neudle.com: metabolic myopathy

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Differential
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abdominal distention

abdominal muscle paralysis

abducens nerve paralysis

abscess, intracerebral

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

activities of daily living scale

acyl CoA dehydrogenase deficiency

adrenoleukodystrophy

advances in neurology

adverse drug reaction

alcohol intolerance

alcohol, heart involvement with

alcohol, neurologic complications with

alkylating agents

alpha glucosidase

altered states of consciousness

aminoacidopathies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

aneurysm, intracranial

ankle, swelling of

anterior horn cell disease

anterior tibial muscle weakness

antiarrhythmic drugs

anticholinesterase

arrhythmia, cardiac

arthrogryposis multiplex

ascending paralysis

aspartate aminotransferase

ataxia, cerebellar

ataxia, progressive

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

azidodeoxythymidine

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

bent spine syndrome

biological warfare

blindness, sudden

blood dyscrasias, neurologic findings with

bone marrow suppression

bone marrow transplantation

brainstem, dysfunction

brainstem, lesion of

burning paresthesia

calcification, intracranial

calf hypertrophy

caloric testing

cancer, cerebrovascular accident complicating patients with

carbon monoxide poisoning

carbon monoxide poisoning, chronic

carboxyhemoglobin

carcinoid tumor

carnitine deficiency

carnitine deficiency myopathy

CAT scan, abnormal

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, muscle

cataracts, congenital

central core disease

central nervous system, infection of

cerebellar atrophy, secondary

cerebellar degeneration

cerebral cortical atrophy

cerebral glucose metabolism

cerebro hepato renal syndrome

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure low

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chemical weapons

chemotherapy, CNS treatment and complications with

cherry red spot-myoclonus syndrome

chronic fatigue syndrome

chronic graft versus host disease

chronic progressive external ophthalmoplegia

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

coenzyme Q10 deficiency

compartment syndrome

congenital myopathy

congestive heart failure

contractures, joint

conversion reaction

cortical blindness

corticotropin level

corticotropin-releasing factor

cortisol, elevated

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cricopharyngeal bar

critical care unit

cultured skin fibroblasts

Cushing's syndrome

cyclic vomiting

cytochrome c oxidase

cytochrome c oxidase, deficiency

degenerative diseases of CNS

delay in diagnosis

dementia, rapidly progressive

dermatomyositis

descending paralysis

developmental milestones, loss of

developmental retardation

diabetes mellitus

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

distal muscle atrophy

distal muscle weakness

down-beat nystagmus

dropped head syndrome

drug induced neurologic disorders

echocardiogram, LVH

electrocardiogram, abnormal

electron microscopy

electronystagmography

electroretinograph

emergencies, medical

emergencies, neurologic

encephalitis, autoimmune

encephalomyopathy

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

enzyme treatment

enzyme, muscle disease

epidemiology of neurology

epilepsia partialis continua

episodic disorders

episodic neurologic deficits

evoked potentials

exercise intolerance

exercise-induced neurologic dysfunction

exercise-related muscle strength increase

extraocular muscle atrophy

eye movement, disorders of

facial appearance, abnormal

facial hair, excessive

facial nerve palsy

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failure to thrive

Fazio-Londe's disease

feeding disorder

fingernails, abnormal

fundus, abnormality of

gag reflex, depressed

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastroenteritis

gastrointestinal motility

Gaucher's disease

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

glucocerebrosidase

glycogen debranching enzyme deficiency

glycogen storage disease

gonadal dysgenesis

Gowers maneuver

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Gulf War syndrome

Hallervorden Spatz disease

headache, sudden onset of

heavy metal intoxication

hemianopia, transient

hexosaminidase-A

hip flexor weakness

histochemistry of muscle

human immunodeficiency virus type 1

hydroxychloroquine

hyperamylasemia

hyperbaric oxygen

hypoglycemic coma

hypomyelination

hypoparathyroidism

hypoparathyroidism, idiopathic

hypotension, systemic

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

ileus, paralytic

immune checkpoint inhibitors

immune-related adverse events

immunologic disease

immunosuppression

immunosuppressive agents

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion body myositis

insect repellent

intellectual deficit

intellectual deterioration

intelligence quotient

intestinal pseudoobstruction

intracerebral hemorrhage

ischemic exercise test

Kearns-Sayre syndrome

klippel feil syndrome

Korsakoff's psychosis

Kugelberg-Welander syndrome

lactic acidemia

lactic dehydrogenase(LDH)

Lafora's disease

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

lens, dislocation of

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy

level of consciousness, decreased

lid closure, weakness of

life expectancy

limb-girdle weakness

lipid storage disorder of CNS

lipid storage myopathy

liver function enzymes

lysosomal storage disease

lysosomes, abnoral

macular degeneration

McArdle's disease

McArdle's disease, adult onset

melanoma, malignant

memory, impairment of

meningitis, leukemic

meningoencephalopathy

mental retardation

mental status, abnormal

metabolic acidosis

metabolic alkalosis

metabolic disorder, primary

methylhydrazine derivatives

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

molybdenum cofactor deficiency

monoamine oxidase inhibitors

motor neuron disease

movement disorder

MRI, disappearing lesion on

MRI, hypointense signal foci on

mucopolysaccharidoses

multiple organ failure

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle hypertrophy

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle stiffness

muscle strength, testing

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, ocular

myasthenic crisis

myasthenic syndrome

myoclonus, epilepsy

myopathy, acute

myopathy, alcoholic

myopathy, carcinomatous

myopathy, centronuclear

myopathy, critically ill

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, genetic

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, necrotizing, immune-mediated

myopathy, proximal

myopathy, steroid induced

myopathy, thyroid disease causing

myopathy, toxic

myopathy, vacuolar

myotonia congenita

myotonia dystrophica

myotonia, treatment of

myotonic discharges

nausea and vomiting

nemaline rod myopathy

neonatal screening, genetic neurologic disorders

neoplasm, hormone producing, ectopic

neoplasm, metastatic

neoplasm, metastatic to CNS

nephrotic syndrome

nerve conduction studies

nerve conduction studies, sensory

neuritis, causes of

neuritis, heavy metals causing

neuroendocrinology

neurofibrillary degeneration

neurogenic vs.myopathic atrophy

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, peripheral nerves

neuropathy, acute

neuropathy, ataxia, retinitis pigmentosa

neuropathy, diabetic

neuropathy, diphtheritic

neuropathy, hereditary peripheral

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, peripheral

neuropathy, sensory

neuropathy, toxic

newborn, evaluation of

night blindness

nitrogen mustard

numbness, extremity

occupational neurologic disorders

ocular motility, disorders of

ocular myopathy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, total

optic neuropathy

orbit, lesions of

organ transplantation

orthostatic hypotension

paramyotonia congenita

paraspinal muscle

paraspinal muscle weakness

paresthesias, feet

paresthesias, hands

Parkinson disease

patient information and support

pediatric neurology

pericardial effusion

periodic paralysis

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

peroxisomal disease

personality change

phosphorylase b kinase deficiency

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleural effusion

poison, mercury

poison, neurologic problems with

poison, organophosphate

polymerase chain reaction

polymyalgia rheumatica

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, critically ill

Pompe's disease of glycogen storage

position sensation, abnormal

postural abnormality

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

progressive neurologic disorder

proprioception, abnormal

proximal muscle atrophy

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

ptosis, bilateral

pulmonary embolism

pulmonary function tests

pulmonary hypertension

pulmonary infiltrates

quadriparesis, acute

quadriparesis, progressive

quadriplegia, transient

radionuclide imaging, heart

ragged-red fibers

rapidly progressing neurologic illness

recurrent laryngeal nerve paralysis

refractive errors

Refsum's disease

respiratory failure

retinal degeneration

retinitis pigmentosa

reversible neurologic disorder

second wind phenomena

seizure, intractable

seizure, neonatal

sensorineural hearing loss

sensory symptoms

sensory testing

sensory testing, quantitative

skin, lesions in neurologic disorders

sleep pathology and physiology

sodium channel dysfunction

sodium valproate

sodium valproate, toxicity

somatosensory evoked potentials

Southern immunoblot test

spinal cord, compression of

spinal cord, metastasis to

spinal muscular atrophy

spinocerebellar degeneration

spongy degeneration of brain

standing difficulty

startle reaction

status asthmaticus

steroid therapy, CNS treatment and complications with

stiff man syndrome

stooped posture

strokelike episodes

subarachnoid hemorrhage

sweating, abnormality of

systemic illness

tapetoretinal degeneration

Tay-Sachs disease

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

tone, muscle, increased

tongue, enlarged

tongue, weakness

toxic oil syndrome

toxins, nervous system

transverse smile

treatment of neurologic disorder

tricresylphosphate

Unverricht-Lundborg disease

upgaze, paralysis of

urinary frequency

urinary incontinence

urine test in toxic screen

Usher's syndrome

vaccination, neurologic complications with

vincristine neurotoxicity

visual field defect

vocal cord paralysis

walking, difficulty with

weakness, acute

weakness, chronic

weakness, episodic

weakness, fluctuating

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

Werdnig-Hoffman disease

whistle, inability to

white matter disease

winging of scapula

Showing articles 50 to 100 of 1903 << Previous Next >>

Atrophy of Bilateral Extraocular Muscles
J Neuro-Ophthalmol 16:286-288, Okamoto,K.,et al, 1996

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

Late-Onset Mitochondrial Myopathy
Ann Neurol 37:16-23, 31995., Johnston,W.,et al, 1995

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

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

Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994

Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994

Acute Neuromuscular Respiratory Paralysis
JNNP 56:334-343, Hughes,R.A.C.&Bihari,D., 1993

Ophthalmologic Manifestations in MELAS Syndrome
Arch Neurol 50:977-980, Fang,W.,et al, 1993

Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
NEJM 329:241-245, Tsujino,S.,et al, 1993

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

Acute Myopathy and Neuropathy in Status Asthmaticus:Case Report and Literature Review
Muscle & Nerve 16:84-90993., Lacomis,D.,et al, 1993

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,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

Genetic Diagnosis of Gaucher's Disease
Lancet 339:889-892, Mistry,P.K.,et al, 1992

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

Travel and Ciguatera Fish Poisoning
Arch Int Med 152:2049-2053, Lange,W.R.,et al, 1992

Polymyalgia Rheumatica and Mitochondrial Myopathy:Clinicopathologic and Biochemical Studies in Five Cases
Am J Med 92:167-172, Harle,J.,et al, 1992

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

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation
Neurol 42:545-550, Goto,Y.,et al, 1992

The Neuropsychological Features of Mitochondrial Myopathies and Encephalomyopathies
Arch Neurol 49:158-160, Kartsounis,L.D.,et al, 1992

Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction
Ann Neurol 29:606-614, Mhiri,C.,et al, 1991

Muscle Carnitine Deficiency in Patients Using Valproic Acid
J Pediatr 118:646-649, Shapira,Y.&Gutman,A., 1991

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

Depletion of Muscle Mitochondrial DNA in AIDS Patients with Zidovudine-Induced Myopathy
Lancet 337:508-510, Arnaudo,E.,et al, 1991

Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
NEJM 324:364-369, 4111991., Haller,R.G.&Lewis,S.F., 1991

Mitochondrial Myopathy Caused by Long-Term Ziduvudine Therapy
NEJM 322:1098-1105, Dalakas,M.C.,et al, 1990

Mitochondrial Myopathy with a Defect of Mitochondrial-Protein Transport
NEJM 323:37-42, Schapira,A.H.V.,et al, 1990

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

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

Mitochondrial DNA and Genetic Disease
Editorial, Lancet 1:250-2511989., , 1989

Mitochondrial Myopathies, Mechanisms Now Better Understood
BMJ 298:1127-1128, Schapira,A.H.V., 1989

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
NEJM 320:1293-1299, Moraes,C.T.,et al, 1989

Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship
J Pediatr 115:81-88, Sooth,F.A.,et al, 1989

McArdle's Disease:Biochemical and Molecular Genetic Studies
Ann Neurol 24:774-781, Servidei,S.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
Neurol 38:751-754, Montagne,P.,et al, 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

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

Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
P. D. , et al, Muscle & Nerve 10:114-120, , 1987

Unusual Neurotoxicity Associated with Amiodarone Therapy
Arch Int Med 147:881-884, Palakurthy,P.R.,et al, 1987

Clinicopath Conf
Kearns-Sayre Syndrome (Oculocraniosomatic Neuromuscular Disease with Mitochondrial Myopathy) , Case, 4-1,NEJM 317:493-501,1987., 1987

Neurotoxic Effects of Organophosphorus Insecticides:An Intermediate Syndrome
NEJM 316:761-763, 807-8081987., Senanayake,N.&Karalliedde,L., 1987

Chloroquine Neuromyotoxicity, Clinical & Pathological Perspective
Am J Med 82:447-455, Estes,M.L.,et al, 1987

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

Clinicopath Conf
Myopathy Due to Adult Acid Maltase Deficiency, 36-1986, NEJM 315:694-701986., , 1986

Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986

Neurologic Complications of Carcinoid
Neurol 36:745-749, Parchell,R.A.&Posner,J.B., 1986

Showing articles 50 to 100 of 1903 << Previous Next >>