Neudle.com: metabolic myopathy

Differential
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abdominal distention

abdominal muscle paralysis

abducens nerve paralysis

abscess, intracerebral

acetazolamide

acid maltase deficiency

acid maltase deficiency, adult

acoustic nerve

acquired immunodeficiency syndrome

activities of daily living scale

acyl CoA dehydrogenase deficiency

adrenoleukodystrophy

advances in neurology

adverse drug reaction

alcohol

alcohol intolerance

alcohol, heart involvement with

alcohol, neurologic complications with

alcoholism

alkylating agents

alpha glucosidase

altered states of consciousness

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

anemia

aneurysm

aneurysm, intracranial

ankle, swelling of

anterior horn cell disease

anterior tibial muscle weakness

arthrogryposis multiplex

ascending paralysis

asparginase

aspartate aminotransferase

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

azidodeoxythymidine

Babinski sign

BAL

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

blood dyscrasias, neurologic findings with

bone marrow suppression

bone marrow transplantation

brainstem, dysfunction

brainstem, lesion of

bulbar palsy

burning paresthesia

calcification, intracranial

calf hypertrophy

caloric testing

camptocormia

cancer, cerebrovascular accident complicating patients with

canned food

carbon monoxide poisoning

carbon monoxide poisoning, chronic

carnitine deficiency myopathy

CAT scan

CAT scan, abnormal

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, muscle

cataracts

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

Chvostek sign

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

coenzyme Q10

coenzyme Q10 deficiency

congestive heart failure

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

cytokines

deafness

DEET

degenerative diseases of CNS

delay in diagnosis

delirium

dementia

dementia, rapidly progressive

developmental milestones, loss of

developmental retardation

diabetes mellitus

diaphragmatic paralysis

diarrhea

differential diagnosis

difficulty climbing stairs

diphtheria

diplopia

distal muscle atrophy

distal muscle weakness

dropped head syndrome

drowsiness

drug induced neurologic disorders

electrocardiogram, abnormal

electromyogram

electron microscopy

electronystagmography

electroretinograph

emergencies, medical

emergencies, neurologic

encephalitis

encephalitis, autoimmune

encephalomyopathy

encephalopathy

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

enzyme treatment

enzyme, defect

enzyme, muscle disease

enzyme, serum

eosinophilia

epidemiology of neurology

epilepsia partialis continua

episodic disorders

episodic neurologic deficits

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 pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

Fazio-Londe's disease

feeding disorder

fever

fibrillations

fingernails, abnormal

fundus, abnormality of

gag reflex, depressed

gait disorder

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastroenteritis

gastrointestinal motility

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

hallucination

hand weakness

headache

headache, sudden onset of

hearing loss

heart block

heavy metal intoxication

hemianopia

hemianopia, transient

histochemistry of muscle

human immunodeficiency virus type 1

hypoparathyroidism, idiopathic

hypophonia

hyporeflexia

hypotension, systemic

hypoxic encephalopathy

iatrogenic neurologic disorders

ileus, paralytic

imbalance

immune checkpoint inhibitors

immune-related adverse events

immunologic disease

immunosuppression

immunosuppressive agents

immunotherapy

impotence

impulsivity

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

insecticides

intellectual deficit

intellectual deterioration

intelligence quotient

intestinal pseudoobstruction

intracerebral hemorrhage

ipecac

ipilimumab

ischemic exercise test

Kearns-Sayre syndrome

klippel feil syndrome

Korsakoff's psychosis

Kugelberg-Welander syndrome

kyphosis

lactic acidemia

lactic dehydrogenase(LDH)

Lafora's disease

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

leg swelling

leg weakness, bilateral

Leigh's disease

lens, dislocation of

leukemia

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

level of consciousness, decreased

lid closure, weakness of

life expectancy

limb-girdle weakness

lipid storage disorder of CNS

lipid storage myopathy

liver disease

liver function enzymes

lordosis

low back pain

lymphopenia

lysosomal storage disease

McArdle's disease, adult onset

memory, impairment of

meningismus

meningitis

meningitis, leukemic

meningoencephalopathy

mental retardation

mental status, abnormal

metabolic disorder, primary

metallic taste

methotrexate

methylhydrazine derivatives

microcephaly

migraine

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

molybdenum cofactor deficiency

monoamine oxidase inhibitors

MRI, disappearing lesion on

MRI, hypointense signal foci on

MRI, muscle

MRI, serial

mucopolysaccharidoses

multiple organ failure

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle spasm

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

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

myotonia, treatment of

nemaline rod myopathy

neonatal screening, genetic neurologic disorders

neoplasm, hormone producing, ectopic

neoplasm, metastatic

neoplasm, metastatic to CNS

nephrotic syndrome

nerve agents

nerve biopsy

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

neurons

neuroophthalmology

neuropathology

neuropathology, peripheral nerves

neuropathy

neuropathy, acute

neuropathy, ataxia, retinitis pigmentosa

neuropathy, diabetic

neuropathy, diphtheritic

neuropathy, hereditary peripheral

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, peripheral

newborn, evaluation of

occupational neurologic disorders

ocular motility, disorders of

ocular myopathy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, total

organ transplantation

orthopnea

orthostatic hypotension

paramyotonia congenita

paraparesis

paraspinal muscle

paraspinal muscle weakness

patient information and support

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

peroxisomal disease

personality change

phosphorylase b kinase deficiency

pigmentary retinopathy

plasmapheresis

pleocytosis of cerebrospinal fluid

pleural effusion

poison, mercury

poison, neurologic problems with

poison, organophosphate

POLG1 gene

poliomyelitis

polymerase chain reaction

polymyalgia rheumatica

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, critically ill

Pompe's disease of glycogen storage

porphyria

position sensation, abnormal

postpartum

postural abnormality

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

procarbazine

prognosis

progressive neurologic disorder

proprioception, abnormal

proteinuria

proximal muscle atrophy

pruritus

pseudomyotonia

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pulmonary function tests

pulmonary hypertension

pulmonary infiltrates

quadriparesis

quadriparesis, acute

quadriparesis, progressive

quadriplegia

quadriplegia, transient

radionuclide imaging, heart

ragged-red fibers

rapidly progressing neurologic illness

rash

recurrent

recurrent laryngeal nerve paralysis

reversible neurologic disorder

second wind phenomena

sensorineural hearing loss

sensory symptoms

sensory testing

sensory testing, quantitative

short stature

skin, lesions in neurologic disorders

sleep pathology and physiology

sodium channel dysfunction

sodium valproate

sodium valproate, toxicity

somatosensory evoked potentials

Southern immunoblot test

spasticity

spinal cord, compression of

spinal cord, metastasis to

spinal muscular atrophy

spinocerebellar degeneration

spongy degeneration of brain

steroid therapy, CNS treatment and complications with

stiff man syndrome

stooped posture

strokelike episodes

subarachnoid hemorrhage

suicide

sweating, abnormality of

systemic illness

tachycardia

tapetoretinal degeneration

taxol

Tay-Sachs disease

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thirst

thrombocytopenia

tinnitus

tone, muscle, increased

toxins, nervous system

transverse smile

treatment of neurologic disorder

Unverricht-Lundborg disease

urine test in toxic screen

urine, dark

Usher's syndrome

vaccination, neurologic complications with

vecuronium

vinblastine

vincristine neurotoxicity

walking, difficulty with

weakness, fluctuating

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weight loss

Werdnig-Hoffman disease

wheelchair

whistle, inability to

Showing articles 1700 to 1750 of 1908 << Previous Next >>

Cerebral Reticulum Cell Sarcoma
Arch Neurol 36:727, DeCoul,A.A.W.,et al, 1979

Creatine Phosphokinase MB Band In Oculopharyngeal Muscular Dystrophy
(Letter) NEJM 301:270979., Diskin,C.J., 1979

Extraocular Muscle Biopsy in Chronic Progressive External Ophthalmoplegia
Ann Neurol 6:326-339, Ringel,S.P.,et al, 1979

Acute Generalized Polyneuropathy Accompanying Lithium Poisoning
Ann Neurol 6:360-362, Brust,J.C.M.,et al, 1979

Sciatic Nerve Entrapment by Pentazocine-Induced Muscle Fibrosis, A Case Report
Arch Neurol 36:723-724, Rousseau,J.J.,et al, 1979

Phenytoin Hypersensitivity:38 Cases
Neurol 29:1480-1485, Harunda,F., 1979

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Muscle Fiber-Type Disproportion
Arch Neurol 35:823-826, Eisler,T.,et al, 1978

HLA-B8 in Polymyositis
NEJM 298:1260, Behan,W.M.H.,et al, 1978

Malignant Optic Gliomas in Adults
Arch Neurol 35:731-735, Harper,C.G.,et al, 1978

Disulfiram Neuropathy
Arch Neurol 35:658-660, Moddel,G.,et al, 1978

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Possible Biochemical Basis of Memory Disorder in Alzheimer Disease
Ann Neurol 3:471, Smith,C.M.,et al, 1978

Malignant Hyperthermia & Central Core Disease in a Child with Congenital Dislocating Hips
Arch Neurol 35:189, Eng,G.D.,et al, 1978

Adult Onset Nemaline Myopathy
Neurol 28:1306-1309, Brownell,A.K.W.,et al, 1978

Isolated Trigeminal Sensory Neuropathy:Early Manifestation of Mixed Connective Tissue Disease
Neurol 28:1286-1289, Searles,R.P.,et al, 1978

Nemaline (Rod) Myopathy:The Need for Histochemical Evaluation of Affected Families
Ann Neurol 4:37, Bender,A.N.,et al, 1978

Inclusion Body Myositis:A Distinct Variety of Idiopathic Inflammatory Myopathy
Neurol 28:8, Carpenter,S.,et al, 1978

Jamaica Ginger Paralysis
Arch Neurol 35:530, Morgan,J.P.,et al, 1978

Chlordecone Intoxication in Man
Neurol 28:626, Taylor,J.R.,et al, 1978

Transient Cerebral Dysfunction Following Chemotherapy for Osteogenic Sarcoma
Ann Neurol 3:441, Allen,J.C.,et al, 1978

Glycine Encephalopathy
NEJM 298:687, Ch'ien,L.T., 1978

Abnor CT Scans of Brain in Asympt. Chil with Acute Lymph. Leuk. after Prophy. Treat of CNS with Radia & Intrathe Chemo
NEJM 298:815, Peylan-Ramu,N.,et al, 1978

Perhexiline Neuropathy:A Clinicopathological Study
Ann Neurol 3:259, Said,G., 1978

Polyneuropathy From Inhalation of N2O Cartridges Through a Whipped-cream Dispenser
Neurol 28:485, Sahenk,Z.,et al, 1978

Neuropathy Following Abuse of Nitrous Oxide
. et al, Neurol 28:504978., Layzer,R.B., 1978

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978

The Cherry-red Spot-Myoclonus Syndrome
Ann Neurol 3:234, Rapin,I.,et al, 1978

Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978

The Muscular Pain-fasciculation Syndrome
Neurol 28:1105-1109, Hudson,A.J.,et al, 1978

Quinine Sulfate for Pain in the Guillain-Barre Syndrome
Ann Neurol 4:386-387, Nixon,R.A., 1978

Systemic Membrane Defect in the Proximal Muscular Dystrophies
NEJM 299:841-846, Pickard,N.A.,et al, 1978

Prolonged Encephalopathy with Arsenic Poisoning
Neurol 28:853-855, Freeman,J.W.,et al, 1978

Acute & Chronic Progressive Encephalopathy Due to Gasoline Sniffing
Neurol 28:507-510, Valpey,R.,et al, 1978

Progressive Dialysis Encephalopathy
Ann Neurol 4:199-204, Lederman,R.J.,et al, 1978

Toluene Optic Neuropathy
Ann Neurol 4:390, Keane,J.R., 1978

Adult-onset GM2 Gangliosidosis
Neurol 28:1117-1123, O'Neill,B.,et al, 1978

Computerised Tomography in Severe Methanol Intoxication
BMJ 2:929-930, Aquilonius,S-M.,et al, 1978

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

Intrathecal Methotrexate Causing Paraplegia in a Middle-Aged Woman
Acta Haemat 60:59-60, Weiss,S.,et al, 1978

Encephalomyelopathy Following Intrathecal Methotrexate Treatment in a Child with Acute Leukemia
Cancer 41:1211-1215, Skullerud,D.,et al, 1978

Neuromuscular Diseases that Affect the Eye
International Ophthal Clx 18:103, Black,J., 1978

Cis-diamminedichloroplatinum (II) , A New Anticancer Drug
Ann Int Med 86:803-812, Rozencweig,M.,et al, 1977

Pellagra
In Brain's Diseases of the Nervous System, 8th Ed. 1977, p 849-851, Oxford University Press., , 1977

Persistent Cerebellar Ataxia after Exposure to Toluene
Ann Neurol 2:440, Boor,J.W.,et al, 1977

Clinical Pathological Conference
Dermatomyositis, Case Record, 33-1977, NEJM 297:37877., , 1977

Alternating Proptosis
Arch Neurol 34:642, Keane,J.R., 1977

Ophthalmoplegia as a Sign of Metabolic Disease in the Newborn
Neurol 27:971, MacDonald,J.T.,et al, 1977

Neonatal Ophthalmoplegia with Microfibers:A Reversible Myopathy
Neurol 27:974, Hanson,P.A.,et al, 1977

Showing articles 1700 to 1750 of 1908 << Previous Next >>