Neudle.com: "muscle enzymes"

Differential
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abdominal muscle paralysis

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

activities of daily living scale

addiction, heroin-neurologic complications with

adenosine deaminase deficiency

adult polyglucosan body disease

advances in neurology

adverse drug reaction

agitation

alcohol, neurologic complications with

altered states of consciousness

alveolar hypoventilation

aminoacylase 1 deficiency

amyloid

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, treatment of

ANA

anemia

anemia, hemolytic

anemia, megaloblastic

aneurysm

angina pectoris

angiography, neurologic complications with

angiokeratoma

angiotensin-converting enzyme

anterior horn cell disease

anti signal recognition particle antibody

anticholinergic drugs

anticoagulant, complications of

anticonvulsants

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

antihistamines

antiphospholipid antibodies

antithyroid antibodies

aromatic amino acid decarboxylase deficiency

aspartate aminotransferase

atherosclerosis, generalized

athetosis

atrial fibrillation

atrial myxoma

atrioventricular block

autism

autoantibodies

autoimmune disease

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

behavioral disorder

biotin deficiency

biotinidase deficiency

blood dyscrasias, neurologic findings with

bone age

bone demineralization

bone marrow infarction

bone marrow necrosis

bone marrow suppression

bone marrow transplantation

bradykinesia

brain atrophy

brain biopsy

brain biopsy, false negative

brain natriuretic peptide

calcification, lymph node

cardiac surgery, neurologic complications with

cardiac tumor

cardiomegaly

cardiomyopathy

cardiovascular disease

carnitine deficiency myopathy

CAT scan, emission, abnormal

cataracts

catatonia

cathartic

cauda equina, lesion of

CD4 counts

central nervous system, infection of

central nuclei, muscle

cerebellar infarction

cerebellar lesion

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction, hemorrhagic

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, complications with

cerebrovascular accident, multiple

cerebrovascular accident, prognosis in

cerebrovascular accident, seizure with

cerebrovascular disease, cardiovascular disease with

ceruloplasmin, serum

chelation therapy

chemosis

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest pain

chest x-ray, abnormal

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clofibrate

cogwheel rigidty

coinfection

collagen vascular disease

coma

complications

confusion

congenital infection, CNS

congenital infection, viral

congenital myopathy

congestive heart failure

conjunctival injection

conjunctivitis

consanguinity

contractures, joint

coronary artery bypass

corpus callosum, infarction of

corpus callosum, lesion of

cough

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine kinase

creatine phosphokinase isoenzyme elevation

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

critical care unit

cry, abnormal

cultured skin fibroblasts

cytochrome c oxidase, deficiency

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

decerebrate posture

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dentate nuclei

dentate nuclei, lesion of

depression

dermatitis

dermatomyositis

developmental disability

developmental milestones, loss of

developmental retardation

diaphragmatic paralysis

diarrhea

diet

differential diagnosis

difficulty climbing stairs

dilantin

dilantin, hypersensitivity to

diplopia

distal muscle atrophy

distal muscle weakness

DNA probes

DNA sequencing

dopa responsive dystonia

doxycycline

drooling

dropped head syndrome

drug abuse

drug induced neurologic disorders

dyskinesia, buccal lingual facial

dystrophic calcification

dystrophin

eating disorder

echocardiogram

echocardiogram, transesophageal

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

embolism, atheromatous

embolism, cholesterol

emergencies, neurologic

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, etiology

encephalitis, viral

encephalomyelitis

encephalopathy

encephalopathy, acute

encephalopathy, Hashimoto's

encephalopathy, neonatal

encephalopathy, progressive

enzyme, muscle disease

enzyme, serum

eosinophilia

eosinophilia-myalgia syndrome

epidemiology of neurology

epistaxis

Epstein-Barr virus

Epstein-Barr virus, negative

extraocular muscle enlargement

extraocular muscle lesion

eye movement, disorders of

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

femoral artery catheterization

femoral neuropathy

fever

fibrillations

fine motor function, impaired

fingernails, abnormal

fundus, abnormality of

gammaglobulin therapy, intravenous

gangliosidosis GM1

gangliosidosis GM2

gastroenteritis

gastrointestinal bleeding

genetic diagnosis, prenatal

genetic neurologic disorders

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glycine

glycogen debranching enzyme deficiency

glycogen storage disease

glycoprotein

Gowers maneuver

granulomatous disease

growth retardation

grunting

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

guinea pigs

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

headache, retro-orbital

hearing loss

hearing loss, unilateral

heart block

heart murmur

heavy metal intoxication

hematuria, microscopic

hemiparesis

hemoglobin abnormality, neurologic complications of

hemoglobinuria

hemolytic-uremic syndrome

hemophilia

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatitis

hepatitis B virus

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatomegaly

hepatosplenomegaly

herniation syndromes, intracranial

heterophile antibody test

histochemistry of muscle

HMGcoA reductase inhibitors

hoarseness

homosexual

human granulocytic anaplasmosis

human immunodeficiency virus type 1

human immunodeficiency virus type 1, acute infection

hyperparathyroidism, secondary

hyperphosphatasia

hyperreflexia

hypersegmented polys

hypersensitivity reaction

hypertension

hypertensive encephalopathy

hypertonia

hypertrophic intracranial pachymeningitis

hypokalemic paralysis

hypomyelination

hyponatremia

hypoparathyroidism

hypoparathyroidism, idiopathic

hyporeflexia

hypothalamus

hypothalamus, disturbance of

hypothalamus, lesion of

hypotonia

hypotonia, infants

hypoxia

iatrogenic neurologic disorders

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, intracytopasmic

inclusion body myositis

infection

infection, recurrent

infectious mononucleosis

insulin

intellectual deficit

intellectual deterioration

interferon

interferon antibodies

interferon beta 1-a

interferon beta 1-b

intracerebral hemorrhage

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral

iritis

iron, brain

irritability

ischemic exercise test

Kayser-Fleischer ring

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic dehydrogenase(LDH)

L-dopa

L-dopa, drug interactions with and side effects of

L-dopa, potentiators of

learning disability

learning disability, in children

leg weakness, bilateral

leukocyte enzyme abnormality

level of consciousness, decreased

life expectancy

limbic encephalitis

lipid lowering agent

lipid storage disorder of CNS

livedo reticularis

liver biopsy

liver disease

liver function enzymes

lymphadenopathy, cervical

lymphadenopathy, hilar

lymphadenopathy, paraaortic

lymphocytic choriomeningitis

lymphocytosis

lymphoma

lymphoma involving CNS

lymphopenia

lysosomal storage disease

memory, impairment of

meningeal enhancement

meningitis, leptospira

meningitis, neutrophilic

meningitis, plasma cell

meningitis, recurrent

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

methylmalonic acid, serum

microcephaly

microhemorrhage, intracerebral

migraine, seizures in

mimics

misdiagnosis

mitochondrial disease

mitoxantrone

molecular genetics

monoamine oxidase inhibitors

mononeuropathy

mononeuropathy multiplex

movement disorder, extrapyramidal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, false negative

MRI, gradient-echo

MRI, hypointense signal foci on

MRI, muscle

MRI, negative

MRI, orbit

MRI, paramagnetic effect

MRI, pelvis

MRI, spine

MRI, sulcal hyperintensity

MRI, susceptibility weighted

MRS

multinucleated giant cell

multiple sclerosis

multiple sclerosis, treatment of

muscle atrophy, progressive

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle spasm

muscle stiffness

muscle strength, testing

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, insidious onset of

muscle weakness, intermediate onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, central nervous system abnormality

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

myelitis, longitudinal

myelomalacia

myeloneuropathy

myelopathy

myocardial infarction

myocardial infarction, acute

myopathy, centronuclear

myopathy, critically ill

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, genetic

myopathy, hypocalcemic

myopathy, hypokalemic

myopathy, inflammatory

myopathy, metabolic

myopathy, necrotizing

myopathy, necrotizing, autoimmune

necrotizing granuloma

negative

neonatal infection, viral

neonatal screening, genetic neurologic disorders

neoplastic angioendotheliosis

nephritis

nerve biopsy

nerve conduction studies

neuraminidase deficiency

neuritis, heavy metals causing

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neuromuscular disease, electrodiagnosis of

neuropathology

neuropathy

neuropathy, painful

neuropathy, peripheral

nonsteroidal anti-inflammatory drug

nutritional deficiency

nystagmus

occupational neurologic disorders

oculogyric crisis

oculopharyngeal muscular dystrophy

optic chiasm, enlarged

optic disc edema

optic nerve

optic nerve, enlarged

optic nerve, lesion of

paralysis, acute areflexic

paraparesis

paraparesis, spastic

parasitic infection

parasitic infection, CNS

paraspinal muscle

paraspinal muscle weakness

Parkinson disease, on-off phenomena in

Parkinson disease, treatment of

Parkinsonism syndrome

PAS positive

PAS positive material in the brain

peripheral blood smear

peripheral blood smear, abnormal

phosphorylase b kinase deficiency

photophobia

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymyositis

polyneuropathy

Pompe's disease of glycogen storage

position sensation, abnormal

positive sharp waves

postural abnormality

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

pressure sores

prevention of neurologic disorders

procyclidine

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

prolactin, elevated

proprioception, abnormal

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

ptosis, unilateral

pulmonary embolism

pulmonary function tests

pulmonary hypertension

pyloric stenosis

pyramidal tract

pyridoxine

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

rapidly progressing neurologic illness

remote effect of cancer on the nervous system

reserpine and reserpine like drugs

respirator

respiratory distress syndrome, neurologic status with

respiratory failure

reticulum cell sarcoma

Sabin-Feldman dye test

scoliosis, neurologic association with

screening

second wind phenomena

sedimentation rate

sedimentation rate, elevated

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

serum alanine aminotransferase

serum glutamic oxaloacetic transaminase

serum glutamic pyruvic transaminase

serum lipase, elevated

serum sickness

severe acute respiratory syndrome

sex reassignment surgery

sexual behavior, disorder of

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

small for dates infant, problems in

speech disorder, childhood

speech, delayed development of

spinal cord

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spirochete infection

splenectomy

splenomegaly

spongy degeneration of brain

steroid therapy, CNS treatment and complications with

stiff joints

stuporous

subarachnoid hemorrhage

subcutaneous nodules

sudden death

sweating

sweating, abnormality of

symmetric brain lesions

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

tone, muscle, increased

toxoplasma complement fixation test

toxoplasma gondii

toxoplasmosis, acquired

toxoplasmosis, CNS

toxoplasmosis, muscle

transgender

travel history

travel, foreign

treatment of neurologic disorder

tremor

tremor, intention

trientine dihydrochloride

tripping

troponin T

tumor necrosis factor inhibitor

type 2 muscle fiber

typhus, murine

tyrosine

tyrosine hydroxylase deficiency

tyrosinemia

ultrasonography, head

urinary tract infection

urine test for metabolic disorders

urine test in toxic screen

vision, blurred, monocular

visual acuity, decreased

visual acuity, decreased, monocular

visual evoked response

visual impairment

visual loss

visual loss, sudden-unilateral

visual loss, transient

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

Western immunoblot test

Showing articles 0 to 50 of 3066 Next >>

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
Neurol 100:1025-1031, Sharma,V. & Soto,O, 2023

Extrapulmonary Manifestations of Sarcoidosis
Rheum Dis Clin North Am 39:277-297, Rao,D.A. & Dellaripa,P.F., 2023

Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023

Babesiosis: Clinical Manifgestations and Diagnosis
www.UptoDate.com, Oct, Krause,P.J. & Vannier,E.G., 2022

Clinicopathologic Conference, Systemic Primary Amyloidosis
NEJM 384:363-372, Case 3-2021, 2021

Clinicopathologic Conference, Acute human immunodeficiency virus type 1
NEJM 385:641-648, Case 24-2021, 2021

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

Progressive Proximal Weakness in a 61-Year-Old Man
Neurol 98:122-127, Yu, M.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Muscle Stiffness, Gait Instability, and Liver Cirrhosis in Wilsons Disease
Lancet 396:990, Kronlage, C.,et al, 2020

Clinicopathologic conference, Vitamin D deficiency
NEJM 383:2462-2470, Case 39-2020, 2020

Clinicopathologic Conference, Statin-Associated Autoimmune Myopathy
NEJM 381:275-283, Case 22-2019, 2019

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

A Headache of a Diagnosis
NEJM 379:475-479, Stern,R.M.,et al, 2018

Clinical Pathologic Conference, West Nile Virus Encephalitis
NEJM 377:1878-1886, Case 34-2017, 2017

Long-Term Benefit of Enzyme Replacement Therapy in Pompe Disease
Neurol 89:2365-2373, Kuperus, E.,et al, 2017

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017

A Case of Fulminant Encephalopathy in a 69-year-old Woman
Neurol 89:e109-e114, Lamotte, G. and Williams, C, 2017

A 37-Year-Old Man with Multiple Cranial Neuropathies
Neurol 86:e66-e70, OLoghlen, S.,et al, 2016

A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness
Neurol 86:e190-e194, McIntosh, P. & Karam, C., 2016

Mouse Infestation Likely Source of Lymphocytic Choriomeningitis in Teen
MMWR 65:248-249, Rostad, C.A. & Pickering, L.K., 2016

Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
NEJM 370:1830-1841, Case 14-2014, 2014

The Acquired Metabolic Disorders of the Nervous System, Hashimoto Encephalopathy (Steroid Responsive Encephalopathy Syndrome)
Adams & Victors Principles of Neurology Chp 40, pg 1155, Ropper, A.H.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Sarcoidosis
Adams & Victors Principles of Neurology, Chp 32, pg 721, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
Adams & Victors Principles of Neurology, Chp 37, pg 957, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Galactosemia
Adams & Victors Principles of Neurology, Chp 37, pg 951, Ropper, A.H.,et al, 2014

Clinicopatholic Conference, Acute Infection with Hepatitis B Virus
NEJM 368:1239-1245, Case 10-2013, 2013

Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
NEJM 366:1626-1633, Case 13-2012, 2012

Clinical Findings and Diagnosis in Human Granulocytic Anaplasmosis: A Case Series from Massachusetts
Mayo Clin Proc 87:233-239, Weil, A.A.,et al, 2012

Clinicopathologic Conference, Cystoisospora Belli Enteritis and HIV Infection
NEJM 365:2306-2316, Case 38-2011, 2011

Infectious Mononucleosis in Adults and Adolescents
UpToDate, May, Aronson,M.D. & Auwaerter,P.G., 2011

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

Clinicopath Conf, Acute HIV-1 Infection
NEJM 360:1540-1548, Case 11-2009, 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
Ann Neurol 66:11-18,1, Florance,N.R.,et al, 2009

A 46-Year-Old Woman With Severe Weakness Following Acute Respiratory Distress Syndrome
Neurol 68:1529-1535, Waclawik,A.J.,et al, 2007

Neurological Findings in Aminoacylase 1 Deficiency
Neurol 68:2151-2153, Sass,J.O.,et al, 2007

Clinicopath Conf., Left Atrial Myxoma with Systemic Embolization
NEJM 357:1137-1145, Case 28-2007, 2007

Glycogen-Storage Disease Type II
eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006

Clinicopath Conf, Human Granulocytic Ehrlichiosis
NEJM 352:1358-1364, Case 10-2005, 2005

Underappreciated Statin-Induced Myopathic Weakness Causes Disability
Neurorehabil Neural Repair 19:259-263, Dobkin,B.H., 2005

Mitoxantrone Treatment of Multiple Sclerosis
Neurol 63(Suppl 6):S28-S32, Cohen,B.A. &Mikol,D.D., 2004

Aromatic L-Amino Acid Decarboxylase Deficiency
Neurol 62:1058-1065, Pons,R.,et al, 2004

Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003

Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
Neurol 60:1413-1417, Pearl,P.L.,et al, 2003

Polymyositis and Dermatomyositis
Lancet 362:971-982, Dalakas,M.C.&Hohlfeld,R., 2003

Cardiac Troponin Levels Following Monitored Epileptic Seizures
Neurol 60:1690-1692, Woodruff,B.K.,et al, 2003

The Neurological Masquerade of Intravascular Lymphomatosis
Arch Neurol 59:439-443, Beristain,X.&Azzarelli,B., 2002

Showing articles 0 to 50 of 3066 Next >>