Neudle.com: myopathy metabolic

Differential
(Click to cross reference)

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

basilar artery stenosis

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

blood dyscrasias, neurologic findings with

bone marrow suppression

bone marrow transplantation

brainstem, dysfunction

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 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

chromosome 11

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

diagnostic criteria

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

emtricitabine

encephalitis

encephalitis, autoimmune

encephalomalacia

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

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 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

hallucination

hand weakness

headache

headache, sudden onset of

hearing loss

heart block

heavy metal intoxication

hemianopia

hemianopia, transient

heralding manifestation

hexosaminidase-A

hip flexor weakness

hirsutism

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

laminar necrosis, cortical

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

meningeal enhancement

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, diffusion weighted

MRI, disappearing lesion on

MRI, gyral enhancement

MRI, gyral swelling

MRI, hypointense signal foci on

MRI, muscle

MRI, serial

MRI, T1 weighted high signal foci

MRS

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

next-generation sequencing

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

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

Pompe's disease, infantile

porphyria

position sensation, abnormal

postpartum

postural abnormality

precipitating factors

preclinical

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

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

respiratory tract infection

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

spontaneous remission

steroid therapy, CNS treatment and complications with

stiff man syndrome

stooped posture

storage disease of CNS

strokelike episodes

subarachnoid hemorrhage

suicide

sweating, abnormality of

symmetric brain lesions

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

transient neurologic deficit

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

white matter disease

whole genome sequencing

winging of scapula

workup

wrist drop

Showing articles 1250 to 1300 of 1936 << Previous Next >>

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

A Glossary of What is Available
Chemical Weapons, Biological Weapons, USA Today, p. 3A, Feb 8., , 1991

The Treamtent of Primary Malignant Brain Tumours
JNNP 54:101-103, 182-1831991., Whittle,I.R.&Gregor,A., 1991

Response to Treatment with Antihistamines in a Family with Myotonia Congenita
Lancet 337:28-30, Hughes,E.F.&Wilson,J., 1991

N-Isopropyl-p- (123I) Iodoamphetamine SPECT in MELAS Syndrome:Comparison with CT & MR Imaging
J Comput Assist Tomogr 15:77-82, Satoh,M.,et al, 1991

Eosinophilia-Myalgia Syndrome, A Clinical Case Series of 21 Patients
Arch Int Med 151:533-537, Philen,R.M.,et al, 1991

Necrotizing Myopathy with Pipestem Capillaries, Microvasc Depos
Neurol 41:936-939, Emslie-Smith,A.M.&Engel,A.G., 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

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

Skeletal Muscle Pathology in AIDS:An Autopsy Study
Muscle & Nerve, 13:508-51590., Wrzolek,M.A.,et al, 1990

Eosinophilia-Myalgia Syndrome (L-Tryptophan-Associated Neuromyopathy)
Neurol 40:1793-1796, Turi,G.K.,et al, 1990

L-Tryptophan-Induced Eosinophila-Myalgia Syndrome and Myopathy
Neurol 40:1629-1630, Sagman,D.L.&Melamed,J.C., 1990

New Muscle Power Test in Neuromuscular Disease
Am J Dis Child 144:1083-1087, Tirosh,E.,et al, 1990

Myopathy with Human Immunodeficiency Virus Type I (HIV-1) Infection:HIV-1 or Zidovudine?
Ann Int Med 113:492-493, Till,M.&MacDonell,K., 1990

Human Immunodeficiency Virus Assoc Myopathy:Immunocytochemical Ident of an HIV Antigen (gp41) in Muscle Macrophages
Ann Neurol 28:579-582, Chad,D.A.,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

Adjuvant Chemotherapy for Primary Lymphoma of the Central Nervous System
Arch Neurol 47:1113-1116, Chamberlain,M.C.&Levin,V.A., 1990

Kearns-Sayre Syndrome Presenting as Renal Tubular Acidosis
Neurol 40:1761-1763, Eviatar,L.,et al, 1990

Clinicopath Conf
Acute Febrile Neutrophilic Dermatosis (Sweet's Syndrome) , Case 30-1990, NEJM 323:254-2630., , 1990

Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, and Intestinal Pseudo-Obstruction:POLIP Syndrome
Ann Neurol 28:349-360, Simon,L.T.,et al, 1990

Attitudes of Mothers to Neonatal Screening for Duchenne Muscular Dystrophy
BMJ 300:1112, Smith,R.A.,et al, 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
Neurol 40:671-676, Speer,M.C.,et al, 1990

Fluctuating MR Images with Mitochondrial Encephalopathy, Lactic Acidosis, Stroke-Like Syndrome (MELAS)
Neuroradiology 32:77, Abe,K.,et al, 1990

Korsakoff's Syndrome
Editorial, Lancet 336:912-9131990., , 1990

Clioquinol (lodochlorhydrozyquin
Vioform) and Iodoquinol (Diiodohydrozyquin) :Blindness and Neuropathy, Pediatrics 86:797-7980., , 1990

Irregular Breathing
In Internal Medicine, Little, Brown & Co, Boston, 3rd Ed, p. 573-574, Cherniack,N.S., 1990

Acute Mental Status Changes in Children with Systemic Cancer
Pediatrics 85:353-360, DiMario,F.J.&Packer,R.J., 1990

Primary CNS Lymphoma:Combined Treatment with Chemotherapy and Radiotherapy
Neurol 40:80-86, DeAngelis,L.M.,et al, 1990

Scleroderma, fasciitis, and Eosinophilia Associated with the Ingestion of Tryptophan
NEJM 322:874-881, 9261990., Silver,R.M.,et al, 1990

Association of the Eosinophilia-Myalgia Syndrome with the Ingestion of Tryptophan
NEJM 322:869-873, 9261990., Hertzman,P.A.,et al, 1990

Genetic Testing for Huntington's Disease
BMJ 300:1089-1090, Harper,P.,et al, 1990

Cyclosporine-Related Central Nervous System Toxicity in Cardiac Transplantation
NEJM 323:420-421, Hughes,R.L., 1990

Reversal of Prolonged Isoniazid-Induced Coma by Pyridoxine
Arch Int Med 150:1751-1753, Brent,J.,et al, 1990

Prevention of Cisplatin Neurotoxicity with an ACTH (4-9) Analogue in Patients with Ovarian Cancer
NEJM 322:89-94, 126-1271990., Gerritsen Van Der Hoop,R.,et al, 1990

Cortical Blindness During Chemotherapy:Clinical, CT, and MR Corrlations
J Comput Assist Tomogr 14:262-266, Heran,F.,et al, 1990

White Matter Dementia in Chronic Toluene Abuse
Neurol 40:532-534, Filley,C.M.,et al, 1990

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

Isopropyl Alcohol Intoxication
Arch Neurol 47:322-324, Rich,J.,et al, 1990

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990

Clinicopath Conf
Eosinophilic Fasciitis, Case Study 4-1990, NEJM 322:252-261, 93190., , 1990

Development of Diffuse Fasciitis with Eosinophilia During L-Tryptophan Treatment:Elevated Type I Collagen Gene
Ann Int Med 112:344-351, Varga,J.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Septic Encephalopathy
Arch Int Med 150:443-449, Mizock,B.A.,et al, 1990

Night-Time Nasal Ventilation in Neuromuscular Disease
Lancet 335:579-582, Heckmatt,J.Z.,et al, 1990

Mitochondrial Encephalomyopathy (MELAS) with Mental Disorder, CT, MRI and SPECT Findings
Neuroradiology 32:74-76, Suzuki,T.,et al, 1990

Myopathy and Rhabdomyolysis Associated with Lovastatin-Gemfibrozil Combination Therapy
JAMA 264:71-75, Pierce,L.R.,et al, 1990

Peripheral Neuropathy in the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Neurol 40 1035-1040, Smith,B.E.&Dyck,P.J., 1990

Showing articles 1250 to 1300 of 1936 << Previous Next >>