Neudle.com: muscle enzymes

Differential
(Click to cross reference)

abdominal muscle paralysis

acid maltase deficiency

acid maltase deficiency, adult

aciduria

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

bacterial infection, CNS

BAL

basal cistern

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

Borrelia burgdorferi infection

brachial neuritis

brachial plexus neuropathy

bradykinesia

brain atrophy

brain biopsy

brain biopsy, false negative

brain natriuretic peptide

calcification, lymph node

calf hypertrophy

California

campylobacter infection

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 atrophy, secondary

cerebellar degeneration

cerebellar infarction

cerebellar lesion

cerebellar vermis

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, oligoclonal IgG in

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

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

D-dimer

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

disability, neurological

distal muscle atrophy

distal muscle weakness

dizziness

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

facial nerve palsy, recurrent

femoral artery catheterization

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

gram negative rod

granulomatous disease

growth retardation

grunting

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, sensory

Guillain Barre syndrome, variant forms of

guinea pigs

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

headache, retro-orbital

hearing loss

hearing loss, unilateral

heart block

heart block, complete

heart murmur

heart rhythm

heavy metal intoxication

hematuria, microscopic

hemiparesis

hemoglobin abnormality, neurologic complications of

hemoglobinuria

hemolytic-uremic syndrome

hemophilia

hemorrhagic diathesis

hepatic encephalopathy

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

Legionella pneumophilia

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

lumbosacral plexopathy

lumbosacral plexus

lumbosacral plexus, neuritis

Lyme disease

lymphadenopathy

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

precipitating factors

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

pulmonary infiltrates

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

sensory loss

seroconversion

serologic testing

serologic testing of cerebrospinal fluid

seronegative

serum alanine aminotransferase

serum gamma glutamyl transferase

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

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

trigeminal neuropathy

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 100 to 150 of 3508 << Previous Next >>

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

Peripheral Source of MB Band of Creatine Kinase in Alcoholic Rhabdomyolysis
JAMA 244:580-582, Siegel,A.J., 1980

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Insulin-Induced Weakness in Hypokalemic Myopathy
Ann Neurol 6:139-140, Ruff,R.L., 1979

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

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

Serum LDH-5 in Carriers of Duchenne Muscular Dystrophy
Neurol 29:239-241, Burt,D.,et al, 1979

Elevated Skeletal-Muscle Enzymes During Quinidine Therapy
NEJM 300:1218, Weiss,M.,et al, 1979

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

Fatal Infantile Form of Muscle Phosphorylase Deficiency
Neurol 28:1124-1129, DiMauro,S.,et al, 1978

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

The Adult Form of Acid Maltase (a-1, 4-Glucosidase) Deficiency
Ann Neurol 1:276, Karpati,G.,et al, 1977

Clofibrate-Induced Muscle Damage with Myoglobinuria & Cardiomyopathy
NEJM 296:942, Smals,A.G.H., 1977

Electrocardiographic Changes & Myocardial Damage in Patients with Acute Cerebrovascular Accidents
Stroke 8:448, Dimant,J.,et al, 1977

Drug Therapy of Parkinsonism
NEJM 295:814, Bianchine,J.R., 1976

Adult Toxoplasmosis Presenting as Polymyositis & Cerebellar Ataxia
Ann Int Med 82:367, Greenlee,J.,et al, 1975

Complains of Muscle Weakness
Patient Care Clinical Concepts, 21, 1970 Jan., , 1970

The Use of Serum Lactate Dehydrogenase Isoenzymens in the Diagnosis of Muscle Disease
Neurol 19:26, Hooshmard,H.,et al, 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:527, Meadows,J.C.,et al, 1969

Contributions of Serum Enzymes & Isozymes to the Diagnosis of Myocardial Injury
Med Concept of CVD 36:43, Cohen,L., 1967

A Spectrum of Myopathy Associated with Alcoholism (I. Clinical & Laboratory Features)
Ann Int Med 67:481, Perkoff,G.T.,et al, 1967

Contributions of Serum Enzymes to the Diagnosis of Myocardial Injury
Med Concepts of CVD 36:49, , 1967

Congenital Zika Syndrome
NEJM 394:e2, Bacin,F. & Montenegro,M.A., 2026

Progressive Quadriparesis and Falls in a 66-Year-Old Man With Longstanding Human Immunodeficiency Virus
Neurol 106:e214621, Ong,B.A. & Carlson,A.K., 2026

Clinical Insights Into CASPR1 and CASPR1/Contactin1 Com-lex Autoimmune Nodopathies
Neurol 106:e214403, Paramasivan,N.K.,et al, 2026

Polymyalgia Rheumatica
NEJM 394:1097-1109, Dejaco,C.,et al, 2026

A 67-Year-Old Man with Exercise Intolerance nd Progressive Weakness
Neurol 106:e214830, Gosset,A.,et al, 2026

A 35-Year-Old Man with Recurrent Asymmetric Lumbosacral and Cervical Plexopathy
Neurol 106:e214910, Tayade,K.S., et al, 2026

A 35-Year-Old Patient with Rapidly Progressive Ascending Weakness Leading to Loss of Brainstem Reflexes
Neurol 106:e218059, Lyons,H.J.,et al, 2026

A Woman with Parkinson Disease, Dyskinesia, Rhadomyolysis, Subcutaneous Emphysema, and Pneumomediastinum
Neurol 106:e218064, Iqbal,M.M.,et al, 2026

A 55-Year-Old Man with Rapidly Progressive Weakness and Numbness
Neurol 106:e218063, Li,X.,et al, 2026

An 81-Year-Old Woman with Chronic Isolated Neck Extensor Weakness
Neurol 106:e218060, Chen,J.,et al, 2026

Inflammatory Myopathies
NEJM 394:1925-1938, AllenBach,Y. & Benveniste,O., 2026

Melas Syndrome
Stat PearlsPubl Jan 25, Pia,S. & Lui,F., 2025

A 16-Year-Old Adolescent Boy with Ophthalmoplegia and Unilateral Ptosis
Neurol 105:e214430, Lu,Y.,, 2025

A 5-Year-Old Boy with Subacute and Refractory Myoclonus
Neurol 106:e214457, Park,P.S.,et al, 2025

A 62-Year-Old Man with Progressive Limb Weakness, Involuntary Movements, and HyperCKemia
JAMA Neurol 82L:1286-1287, Liu,Y.,et al, 2025

A 32-Year-Old Woman Presenting with Thunderclap Headache in the Third Trimester
Neurol 105:e214029, Kuczynski,A.M. & Kingston,W.S., 2025

Cervical Radiculopathy Due to Vertebral Artery Dissection
Neurol 105:e214090, Guadalupi,P.,et al, 2025

A 73-Year-Old Man With Progressive Proximal Muscle Weakness and Binocular Diplopia
Neurol 105:e214173, Wold,K.J.,et al, 2025

A Woman with Subacute Progression of Distal Upper Extremity Weakness
Neurol 105:e214212, Zhao,A.J.,et al, 2025

Clinicopathologic Features, Pathogenesis, and Treatment of Monoclonal Gammopathy-Associated Myopathies
Neurol 105:213101, Soontrapa,P.,et al, 2025

Atypical Diabetic Neuropathies
BMJ 390:e081109, McCray,B.A.,et al, 2025

A 59-Year-Old Man with Acute-Onset Encephalopathy and Aphasia
Neurol 105:e214299, Gutierrez-Abizuri,C.,et al, 2025

A 38-Year-Old Man With Involuntary Jerk-Like Movements and Ataxia
Neurol 105:e214381, Gomez,A.C.et al, 2025

Tiger Man Sign in Sarcoid Myopathy
Neurol 105:e214323, Sun,Q.,et al, 2025

Intercostal Muscle Wasting is the Clue to a Diagnosis of Diabetic Thoracic Radiculopathy
Neurol 105:e214290, Lau,T.M. & Coebergh,J.A., 2025

Imaging Findings in Giant Cell Arteritis:Dont Turn a Blind Eye to the Obvious!
AJNR 46:457-464, Bathla,G.,et al, 2025

A 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
Neurol 104:e213495, Alsabah,A-A.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

Showing articles 100 to 150 of 3508 << Previous Next >>