Neudle.com: myopathy metabolic

Neurology Specific Literature Search

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

antiviral agents

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

basilar artery stenosis

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

bent spine syndrome

biological warfare

black toenail sign

blindness, sudden

blood dyscrasias, neurologic findings with

bone marrow suppression

bone marrow transplantation

brainstem, dysfunction

brainstem, lesion of

bright tongue sign

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 cortex

cerebral cortical atrophy

cerebral glucose metabolism

cerebral ischemia

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

chromosomal abnormality

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

diagnostic criteria

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

encephalomalacia

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 screening

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

gyrus, abnormal

Hallervorden Spatz disease

headache, sudden onset of

heavy metal intoxication

hemianopia, transient

heralding manifestation

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

laminar necrosis, cortical

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

meningeal enhancement

meningitis, leukemic

meningoencephalopathy

mental retardation

mental status, abnormal

mesial temporal lobe

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 lesion location

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, gyral enhancement

MRI, gyral swelling

MRI, hypointense signal foci on

MRI, T1 weighted high signal foci

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

next-generation sequencing

night blindness

nitrogen mustard

numbness, extremity

occipital lobe, lesion of

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 in waiting

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

Pompe's disease, infantile

position sensation, abnormal

postural abnormality

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

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

respiratory tract infection

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

spontaneous remission

standing difficulty

startle reaction

status asthmaticus

steroid therapy, CNS treatment and complications with

stiff man syndrome

stooped posture

storage disease of CNS

strokelike episodes

subarachnoid hemorrhage

sweating, abnormality of

symmetric brain lesions

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

transient neurologic deficit

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

whole genome sequencing

winging of scapula

Showing articles 1350 to 1400 of 1936 << Previous Next >>

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

Agenesis of the Corpus Callosum:A Marker for Inherited Metabolic Disease
Neurol 39:847-848, Kolodny,E.H., 1989

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

Randomised Double Blind Controlled Trial of Cyclosporin in Multiple Sclerosis
JNNP 52:559-565, Rudge,P.,et al, 1989

Diagnosis of Gerstmann-Straussler Syndrome in Familial Dementia with Prion Protein Gene Analysis
Lancet 2:15-17, Collinge,J.,et al, 1989

Dorsal Radiculopathy Resulting from Podophyllin Toxicity
Neurol 39:607-608, Gorin,F.,et al, 1989

AIDS and the Nervous System
JAMA 261:2396-2399, Dalakas,M.,et al, 1989

Zidovudine-Associated Myopathy
Am J Med 86:814-818, Gertner,E.,et al, 1989

HTLV-I Polymyositis in a Patient Also Infected with the Human Immunodeficiency Virus
NEJM 320:992-995, Wiley,C.A.,et al, 1989

Computeritis, Who's Responsible When PCs Make Employees Sick?
Infoworld 11:51-54, Flynn,L., 1989

The Chronic Fatigue Syndrome-One Entity or Many?
NEJM 319:1726-1728, Swartz,M.N., 1989

Aseptic Meningitis Complicating Adult Kawasaki Disease:Case Report and Review of the Literature
Am J Med 87:106-110, McIlroy,M.A.,et al, 1989

Flaccid Quadriparesis Associated with Yersinia Enterocolitis-Induced Hypokalemia
Arch Int Med 149:1193-1194, Orman,R.A.&Lewis,J.B., 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

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Busulphan and Phenytoin
Ann Int Med 111:1049-1050, Grigg,A.P.,et al, 1989

Trichloroethylene Cranial Neuropathy:Is It Really a Toxic Neuropathy or Does It Activate Latent Herpes Virus?
JNNP 52:297-303, Cavanaugh,J.B.&Buxton,P.H., 1989

Taxol Produces a Predominantly Sensory Neuropathy
Neurol 39:368-373, Lipton,R.B.,et al, 1989

Hemorrhagic Shock and Encephalopathy:Clinical, Pathologic, and Biochemical Features
J Pediatr 114:194-203, Levin,M.,et al, 1989

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene
Neurol 39:1277-1280, Gospe,S.M.,et al, 1989

Eosinophilia-Myalgia Syndrome-New Mexico
JAMA 262:3116, Belvins,W.L.,et al, 1989

MR Findings in Methotrexate-Induced CNS Abnormalities
AJR 153:1283-1288, Ebner,F.,et al, 1989

Opsoclonus and Hyperosmolar Stupor
Neurol 39:1401-1402, Weissman,B.,et al, 1989

Decreased Phenytoin Levels in Patients Receiving Chemotherapy
Am J Med 87:505-510, Grossman,S.A., 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Life-Threatening Cranial Dystonia Following Trihexyphenidyl Withdrawal
Movement Disorders 4:349-353, Gimenez-Roldan,S.,et al, 1989

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

Antecollis in Parkinsonism
Lancet 1:1320-1321, Jorens,P.G.,et al, 1989

Human Leptospirosis-A Review of 50 Cases
Infection 17:10-14, Lecour,H.,et al, 1989

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Trauma-Triggered Migraine:An Explanation for Common Neurological Attacks after Mild Head Injury
J Neurosurg 68:181-188, Haas,D.C.&Lourie,H., 1988

The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
Brain 111, 577-5961988., O'Neill,J.H.,et al, 1988

Myopathy and Cystine Storage in Muscles in a Patient with Nephropathic Cystinosis
NEJM 392:1461-1464, Gahl,W.A.,et al, 1988

Inborn Errors of Metabolism in Children Referred with Reye's Syndrome, A Changing Pattern
JAMA 260:3167-3170, 3178-31801988., Rowe,P.C.,et al, 1988

Paraplegia and Quadriplegia after Intrathecal Chemotherapy
Arch Phys Med Rehabil 69:1054-1056, Werner,R.A., 1988

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

Neurologic Complications of Bone marrow Transplantation
In Neurol Complic of Transplants, Neurologic Clinics, 6:377-378988., Davis,D.G.&Patchell,R.A., 1988

The Reversible Dementias:Do They Reverse?
Ann Int Med 109:476-486, Clarfield,A.M., 1988

Cyclosporin Neurotoxicity in Cardiac Transplant Recipients
JNNP 51:1434-1437, Lane,R.J.M.,et al, 1988

Successful Treatment of Ciguatera Fish Poisoning with Intravenous Mannitol
JAMA 259:2740-2742, Palafox,N.A.,et al, 1988

Successful Chemotherapy for Recurrent Malignant Oligodendroglioma
Ann Neurol 23:360-364, Cairncross,J.G.&Macdonald,D.R., 1988

Treatment Response in Malignant Optic Glioma of Adulthood
Neurol 38:1071-1074, Albers,G.W.,et al, 1988

Overuse Syndrome:A Muscle Biopsy Study
Lancet 1:905-908, Dennett,X.&Fry,H.J.H., 1988

Perinatal Brain Damage:Predictive Value of Metabolic Acidosis & The Apgar Score
BMJ 297:24-27, Ruth,V.J.&Raivio,K.O., 1988

The Neuromuscular Manifestations of Human Immunodeficiency Virus Infections
Arch Neurol 45:1084-1088, Lange,D.J.,et al, 1988

Genetic Markers for Neurofibromatosis
Editorial, Lancet 2:719-7201988., , 1988

Dysphagia in Inclusion Body Myositis
JNNP 51:1542-1545, Wintzen,A.R.,et al, 1988

Suxamethonium Myalgia
Editorial, Lancet 2:945-9461988., , 1988

Showing articles 1350 to 1400 of 1936 << Previous Next >>