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Differential
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abdominal distention

abdominal muscle paralysis

abdominal x-ray

abducens nerve paralysis

abducens nerve paralysis, bilateral

abscess, intracerebral

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

activities of daily living scale

acute disseminated encephalomyelitis

acute intermittant porphyria

acyl CoA dehydrogenase deficiency

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adenosine deaminase deficiency

advances in neurology

adverse drug reaction

agenesis of corpus callosum

alcohol intolerance

alkylating agents

alpha glucosidase

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

aminoacidopathies

aminoacylase 1 deficiency

amyloid angiopathy, cerebral

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

anemia, hemolytic

anesthesia, general

aneurysm, intracranial

angiitis, granulomatous of CNS

angiitis, isolated of CNS

ankle, swelling of

anorexia nervosa

anterior horn cell disease

anterior tibial muscle weakness

antiarrhythmic drugs

antibiotics, neurologic complications with

anticholinesterase

anticonvulsants

antiphospholipid antibodies

antiviral agents

aphasia, global

aromatic amino acid decarboxylase deficiency

arrhythmia, cardiac

arthrogryposis multiplex

ascending paralysis

aspartate aminotransferase

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

autoimmune disease

autonomic dysfunction

autonomic dysfunction, acute

autonomic nervous system

autonomic neuropathy

azidodeoxythymidine

B 12 deficiency

B cell lymphocytes

bacterial infection

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery stenosis

basophilic stippling of red blood cells

bath salts, psychoactive

behavior, combative

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

bent spine syndrome

biological warfare

biotin deficiency

biotin deficiency, juvenile form

biotinidase deficiency

black toenail sign

blindness, sudden

blood brain barrier

blood dyscrasias, neurologic findings with

bone marrow suppression

bone marrow transplantation

botulinum toxin

botulism antitoxin

botulism immune globulin

botulism, infant

brain biopsy, false negative

brainstem, dysfunction

brainstem, lesion of

bulbar palsy, acute

burning feet, differential diagnosis of

burning paresthesia

burst suppression pattern, electroencephalogram

calcification, heart

calcification, intracranial

calcification, muscle

calcium oxalate crystals

calf hypertrophy

Canavan's disease

cancer, cerebrovascular accident complicating patients with

candida albicans

carbon monoxide poisoning

carbon monoxide poisoning, chronic

carboxyhemoglobin

carcinoid tumor

carnitine deficiency

carnitine deficiency myopathy

carpo-pedal spasm

CAT scan, abnormal

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, hyperattenuation

CAT scan, muscle

CAT scan, pelvis

cataracts, congenital

central core disease

central nervous system, infection of

central pontine myelinolysis

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral death, EEG in

cerebral embolism

cerebral embolism, cardiac origin

cerebral glucose metabolism

cerebral infarction

cerebral ischemia

cerebral vasculature, calcification

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, proteincytologic dissociation

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

cerebrovascular disease

ceruloplasmin, serum

Charcot-Marie-Tooth

chasing the dragon

chemical weapons

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

Chinese paralytic syndrome

cholinergic crisis

chorioretinitis

chromosomal abnormality

chronic fatigue syndrome

chronic graft versus host disease

chronic progressive external ophthalmoplegia

ciguatera poisoning

cirrhosis, infancy

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

cluster, geographic

coenzyme Q10 deficiency

cognitive delay

cogwheel rigidty

coma, classification of

coma, electroencephalography in

coma, sudden onset

compartment syndrome

congenital myopathy

congestive heart failure

contractures, joint

conversion reaction

cornea, abnormal

corpus callosum

corpus callosum, lesion of

cortical blindness

cortical blindness, transient

cortical deafness

cortical hemorrhage

corticotropin level

corticotropin-releasing factor

cortisol, elevated

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

creatinine, elevated

cricopharyngeal bar

critical care unit

crying, pathologic

cryptococcal meningitis

cultured skin fibroblasts

Cushing's syndrome

cyclic vomiting

cytochrome c oxidase

cytochrome c oxidase, deficiency

cytomegalic inclusion disease

cytomegalovirus infection

cytosine arabinoside

decontamination

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, rapidly progressive

dementia, reversible

dementia, treatment of

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei, lesion of

dermatomyositis

descending paralysis

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diagnostic criteria

dialysis dementia

dialysis disequilibrium syndrome

diaphragmatic paralysis

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

disability, neurological

disseminated intravascular coagulation(DIC)

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

down-beat nystagmus

downward deviation of eyes

dropped head syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

drug abuse, toxic screen In

drug induced neurologic disorders

dural sinus thrombosis

dysequilibrium syndrome

dysostosis multiplex

dystonia, children

echocardiogram, LVH

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electron microscopy

emergencies, medical

emergencies, neurologic

encephalitis, autoimmune

encephalitis, human immunodeficiency virus type 1

encephalitis, viral

encephalomalacia

encephalomyelitis, postinfectious

encephalomyopathy

encephalopathy, acute

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, parainfectious

encephalopathy, progressive

enzyme treatment

enzyme, muscle disease

epidemiology of neurology

epilepsia partialis continua

episodic disorders

episodic neurologic deficits

escherichia coli

evoked potentials

exercise intolerance

exercise-induced neurologic dysfunction

exome sequencing

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

flaccid paralysis

follow commands

fontanel, bulging

food-borne infection

fracture, long bone

frontal lobe, pathologic signs of

fundus, abnormality of

fungal infection, CNS

gag reflex, depressed

gammaglobulin therapy, intravenous

gangliosidosis GM1

gangliosidosis GM2

gastroenteritis

gastrointestinal motility

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

Gitelman's syndrome

gliomatosis cerebri

globus pallidus

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

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

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, visual

headache, sudden onset of

headache, vascular

hearing loss, bilateral

hearing loss, sudden, bilateral

heavy metal intoxication

hemianopia, transient

hemiparesis, transient

hemolytic-uremic syndrome

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

herpes simplex virus

herpes virus infection

hexosaminidase-A

hip flexor weakness

histochemistry of muscle

homocysteine, serum

human immunodeficiency virus type 1

hydroxychloroquine

hydroxyglutaric aciduria

hyperammonemic encephalopathy

hyperamylasemia

hyperbaric oxygen

hyperglycinemia

hyperglycinemia, nonketotic

hyperhomocysteinemia

hyperosmotic coma

hypertensive encephalopathy

hypoglycemic coma

hypokalemic paralysis

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

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

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intracytopasmic

inclusion body myositis

industrial neurologic disorders

infant, evaluation of

infantile spasm

infection, recurrent

insect repellent

intellectual deficit

intellectual deterioration

internal capsule

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial pressure, increased

intrathecal chemotherapy

intrinsic hand muscles, wasting of

iododeoxyuridine

ischemic exercise test

Jakob-Creutzfeldt disease

jaw contractures

Kayser-Fleischer ring

Kearns-Sayre syndrome

keratoconjunctivitis

klippel feil syndrome

Korsakoff's psychosis

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

Lafora's disease

laminar necrosis, cortical

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

lens, dislocation of

leukemia, neurologic findings assoc.with

leukemia, prophylactic treatment of CNS

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, toxic

level of consciousness, decreased

lid closure, weakness of

life expectancy

limb-girdle weakness

limbic encephalitis

lipid storage disorder of CNS

lipid storage myopathy

liver function enzymes

liver transplantation

Lowe's syndrome

lumbosacral plexopathy

lumbosacral plexus

lumbosacral plexus, lesion of

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

lysosomes, abnoral

malformation, CNS, congenital

malignant hyperpyrexia

manganese intoxication

McArdle's disease

meconium staining

melanoma, malignant

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, bacterial

meningitis, basilar

meningitis, chronic

meningitis, leukemic

meningoencephalopathy

mental retardation

mental status, abnormal

mental status, abnormal, acute

metabolic acidosis

metabolic alkalosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

methylglutaconic aciduria

methylhydrazine derivatives

methylmalonic acid, serum

methylmalonic acidemia

microangiopathic hemolytic anemia

microangiopathy, brain

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mild cognitive impairment

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoamine oxidase inhibitors

mononeuropathy multiplex

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI lesion location

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, false negative

MRI, gyral swelling

MRI, high signal foci on

MRI, hypointense signal foci on

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

multiple organ failure

multiple sclerosis

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle hypertrophy

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle relaxant

muscle stiffness

muscle strength, testing

muscle twitching

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, facioscapulohumeral

muscular dystrophy, limb-girdle

mussel poisoning

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenic crisis

myasthenic syndrome

myelitis, longitudinal

myeloneuropathy

myelopathy, tract-specific

myelopathy, vacuolar

myoclonic encephalopathy of infancy

myoclonic jerks

myoclonus, action

myoclonus, epilepsy

myoclonus, stimulus sensitive

myopathy, acute

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

myotonic discharges

nasal bridge, wide

nausea and vomiting

nemaline rod myopathy

neoplasm, hormone producing, ectopic

neoplasm, metastatic

neoplasm, metastatic to CNS

neoplasm, metastatic to lumbosacral plexus

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplastic angioendotheliosis

nephrocalcinosis

nephrotic syndrome

nerve conduction studies

nerve conduction studies, sensory

neuraminidase deficiency

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

neurologic testing

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathy, acute

neuropathy, diabetic

neuropathy, diphtheritic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, painful

neuropathy, peripheral

neuropathy, sensory

neuropathy, toxic

neurotoxicity, acute

neurotransmitter

newborn, evaluation of

next-generation sequencing

nitrogen mustard

numbness, ascending

numbness, extremity

numbness, generalized

nutritional deficiency

nystagmus, rotary

occipital lobe, lesion of

occupational neurologic disorders

occupational neuropathies

ocular motility, disorders of

oculogyric crisis

old age, neurology of

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic chiasm, enlarged

optic nerve, enlarged

optic neuropathy

organ transplantation

ornithine transcarbamylase deficiency

orthostatic hypotension

oxalosis, primary

pain, abdominal

paralysis, acute

paralysis, acute areflexic

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive material in the brain

pediatric neurology

pericardial effusion

periodic paralysis

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

pernicious anemia

peroxisomal disease

personality change

phenylketonuria

phosphorylase b kinase deficiency

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleural effusion

poison, mercury

poison, neurologic problems with

poison, organophosphate

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, critically ill

polyneuropathy, uremic

Pompe's disease of glycogen storage

Pompe's disease, infantile

pons, lesion of

position sensation, abnormal

posterior column disease

posterior leukoencephalopathy syndrome

postural abnormality

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progressive multifocal leucoencephalopathy

progressive neurologic disorder

prolactin, elevated

proprioception, abnormal

proximal muscle atrophy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis, cause of

ptosis, bilateral

pulmonary edema

pulmonary embolism

pulmonary function tests

pulmonary hypertension

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis, acute

quadriparesis, progressive

quadriplegia, transient

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapidly progressing neurologic illness

recurrent laryngeal nerve paralysis

release phenomena

remote effect of cancer on the nervous system

renal failure, acute

renal transplantation

repetitive nerve stimulation

respiratory arrest

respiratory failure

respiratory paralysis, pharmacologic

respiratory tract infection

restless leg syndrome

reticulum cell sarcoma

retinal degeneration

reverse straight leg raising test

reversible neurologic disorder

salivation, excessive

sarcoidosis, CNS

Schilder's disease

scoliosis, neurologic association with

second wind phenomena

sedimentation rate, elevated

seizure, children

seizure, drug-induced

seizure, intractable

seizure, intractable, treatment of

seizure, neonatal

seizure, treatment of

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory loss, glove-stocking

sensory symptoms

sensory testing

sensory testing, quantitative

serum lipase, elevated

shell fish poisoning

skin, lesions in neurologic disorders

sleep pathology and physiology

slow virus infection of CNS

sodium channel dysfunction

sodium valproate

sodium valproate, toxicity

speech disorder

speech disorder, childhood

speech, loss of

speech, unintelligible

spinal cord, compression of

spinal cord, lesion of

spinal cord, metastasis to

spinal muscular atrophy

splenium of corpus callosum

spongy degeneration of brain

spontaneous remission

standing difficulty

staphylococcal protein A column therapy

startle myoclonus

startle reaction

status asthmaticus

status epilepticus

status epilepticus, nonconvulsive

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulant drugs

stooped posture

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

subarachnoid hemorrhage

subdural hematoma

sulfite oxidase deficiency

superior sagittal sinus thrombosis

sweating, abnormality of

symmetric brain lesions

sympathomimetic drugs

syphilis, diagnosis and treatment

systemic illness

systemic lupus erythematosus

Tay-Sachs disease

temporal lobe, lesion

temporal lobe, lesion, bilateral

terrorist attack

tetrahydrobiopterin

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine deficiency

thrombocytopenia

thrombotic microangiopathy

tone, muscle, increased

tongue, enlarged

tongue, weakness

toxic encephalopathy

toxic oil syndrome

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

transient neurologic deficit

transverse smile

treatment of neurologic disorder

tremor, intention

tremor, postural

tricresylphosphate

Trousseau's sign

tyrosine hydroxylase deficiency

uncal herniation

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

uremic encephalopathy

uremic twitching

urinalysis, abnormal

urinary frequency

urine test for metabolic disorders

urine test in toxic screen

vaccination, neurologic complications with

vibratory sensation, abnormal

vincristine neurotoxicity

violent behavior

viral infection

viral infection, CNS

visual acuity, decreased

vitamin deficiency

vocal cord paralysis

walking, difficulty with

weakness, acute

weakness, chronic

weakness, episodic

weakness, fluctuating

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weakness, rapidly progressive

Werdnig-Hoffman disease

Wernicke's encephalopathy

Whipple's disease

whistle, inability to

white matter disease

whole genome sequencing

wide based gait

winging of scapula

x-linked mental retardation

Showing articles 100 to 150 of 18701 << Previous Next >>

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

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

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

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

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

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

Encephalopathy from Abuse of Bismuth Subsalicylate (Popto-Bismol)
Neurol 43:1265, Jungreis,A.C.&Schaumburg,H.H., 1993

Life-Threatening Organophosphate-Induced Delayed Polyneurop in Child After Accidental Chlorpyrifos Ingest
J Pediatr 122:658-660, Aiuto,L.A.,et al, 1993

Brain Imaging in Late-Onset CM2 Gangliosidosis
Neurol 43:2055-2058, Streifler,J.Y.,et al, 1993

Differential Diagnosis of Guillain-Barre Synd, In Guillain-Barre Synd
Thieme Med Publ, Ch 3, p 42993., Parry,G.J., 1993

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

Ifosfamide-Induced Nonconvulsive Status Epilepticus
Arch Neurol 50:1104-1105, Wengs,W.J.,et al, 1993

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Persistent Paralysis in Critically Ill Patients after Long-Term Administration of Vecuronium
NEJM 327:524-528, Segredo,V.,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

Aluminium Intoxication in Undialysed Adults with Chronic Renal Failure
JNNP 55:697-700, Russo,L.S.,et al, 1992

Nerve Agents:A Review
Neurol 42:946-950, Gunderson,C.H.,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

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

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

Progressive Neuropathy & Recurrent Myoglobinuria in a Child with Long-chain 3-Hydroxyacylcoenzyme A Dehydrogenase Defic
J Pediatr 118:744-746, Dionisi,C.,et al, 1991

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

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

Management of Injuries Due to Chemical Weapons
BMJ 302:129-130, Murray,V.S.G.&Volans,G.N., 1991

Infant Botulism:A Review of 12 Years'Experience at the Children; s Hosp of Phila
Pediatrics 87:159-165, Schreiner,M.S.,et al, 1991

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,et al, 1990

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

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

Paralytic Shellfish Poisoning:A Case Report and Serial Electrophysiologic Observations
Neurol 40:1310-1312, Long,R.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

Cardioembolic Stroke in Primary Oxalosis with Cardiac Involvement
DiPasquale. G. , et al, Stroke 20:1403-14069., , 1989

Infectious and Toxic Syndromes from Fish and Shellfish Consumption, A Review
Arch Int Med 149:1735-1740, Estaugh,J.&Shepherd,S., 1989

Motoneuron Disease:A Disorder Secondary to Solvent Exposure?
Lancet 1:73-76, 82-831989., Hawkes,C.H.,et al, 1989

Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
Neurol 39:252-257, Brown,G.K.,et al, 1989

Agenesis of the Corpus Callosum and Gyral Malformations are Frequent Manifestations of Nonketotic Hyperglycinemia
Neurol 39:817-820, Dobyns,W.B., 1989

Busulphan and Phenytoin
Ann Int Med 111:1049-1050, Grigg,A.P.,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

A Creutzfeldt-Jakob Like Syndrome Due to Lithium Toxicity
JNNP 51:120-123, Smith,S.J.M.&Kocen,R.S., 1988

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

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

Neurologic Manifestations of AIDS
Medicine 66:407-437, McArthur,J.C., 1987

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

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

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

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