Neudle.com: muscular dystrophy enzyme elevation in

Differential
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acquired immunodeficiency syndrome

acyl CoA dehydrogenase deficiency

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

atrioventricular block

Babinski sign

bladder dysfunction

blood dyscrasias, neurologic findings with

cardiovascular disease

carnitine deficiency myopathy

cathartic

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clofibrate

coenzyme Q10 deficiency

complications

congestive heart failure

contractures, joint

creatine kinase

creatine phosphokinase isoenzyme elevation

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

delay in diagnosis

dermatomyositis

developmental retardation

diagnostic criteria

difficulty climbing stairs

distal muscle atrophy

distal muscle weakness

DNA probes

drug induced neurologic disorders

dysphagia

dystrophic calcification

dystrophin

eating disorder

electrocardiogram, abnormal

enzyme, muscle disease

fine motor function, impaired

genetic neurologic disorders

genetic screening

genetic testing

glycogen debranching enzyme deficiency

glycogen storage disease

human immunodeficiency virus type 1

hypocalcemia

hypoglycemia

hypokalemia

hypoparathyroidism, idiopathic

hyporeflexia

imbalance

immunologic disease

immunosuppressive agents

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies

inclusion body myositis

insulin

ischemic exercise test

Jewish

Kearns-Sayre syndrome

Kugelberg-Welander syndrome

lactic dehydrogenase(LDH)

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

leukocyte enzyme abnormality

leukodystrophy

leukoencephalopathy

lipid lowering agent

lipid storage disorder of CNS

liver function enzymes

Lowe's syndrome

MELAS syndrome

MERRF syndrome

metachromatic leukodystrophy

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle pain

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle strength, testing

muscle tenderness

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

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, hypokalemic

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, vacuolar

myositis

neck weakness

neonatal screening, genetic neurologic disorders

nerve biopsy

nerve conduction studies

neurogenic bladder

neurologic complications of, surgery

neurologic disease, diagnoses of

neuropathy

neuropathy, ataxia, retinitis pigmentosa

neuropathy, sensory

oculopharyngeal muscular dystrophy

ophthalmoplegia, progressive external

phosphorylase b kinase deficiency

polyglucosan body

polyglucosan body disease

polymyositis

prenatal diagnosis by amniocentesis

prognosis

progressive neurologic disorder

serum glutamic oxaloacetic transaminase

serum glutamic pyruvic transaminase

short stature

skin, lesions in neurologic disorders

spasticity

speech disorder, childhood

speech, delayed development of

spinal muscular atrophy

spinal muscular atrophy, adult onset

toxoplasmosis, muscle

treatment of neurologic disorder

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

wheelchair

white matter disease

Showing articles 1150 to 1200 of 1300 << Previous Next >>

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Acute Thallium Poisoning, Toxicological & Morphological Studies of the Nervous System
Ann Neurol 10:38-44, Davis,L.E.,et al, 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Phenytoin-Induced Methadone Withdrawal
Ann Int Med 94:349-351, Tong,T.G.,et al, 1981

Preservation of the Phrenic Motorneurons in Werdnig-Hoffman Disease
Ann Neurol 9:506-510, Kuzuhara,S.,et al, 1981

Deprenyl in Parkinson Disease
Neurol 31:19-23, Eisler,T.,et al, 1981

An Ultramicroscopic Study of Skin & Conjunctival Biopsies in Chronic Neuro. Disorders of Childhood
Ann Neurol 9:163-173, Arsenio-Nunes,M.L.,et al, 1981

Infection of Collagenase in the Treatment of Herniated Lumbar Disk
JAMA 245:730-732, Sussman,B.J.,et al, 1981

Interaction Between Estrogen & Dilantin In A Menopausal Woman
NEJM 304:788-789, Notelovitz,M.,et al, 1981

The Reflex Sympathetic Dystrophy Syndrome (RSDS)
Am J Med 70:23-30, Kozin,F.,et al, 1981

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Gross Demonstration of Atrophic Cauda Equina Roots in Motor Neuron Disease, An Improved Method
Arch Neurol 37:394, Meneses,A., 1980

Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
NEJM 303:377-380, Hirschhorn,R.,et al, 1980

Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
Ann Neurol 8:317-324, Steiman,G.S.,et al, 1980

Interaction Between Carbamazepine & Warfarin
BMJ 280:1415-1416, Ross,J.R.Y.,et al, 1980

Abetalipoproteinemia, Report of Two Cases & Review of Therapy
Arch Neurol 37:659-662, Illingworth,D.R.,et al, 1980

Management of Hypoventilation in Motor Neuron Disease Presenting with Respiratory Insufficiency
Ann Neurol 7:188-191, Sivak,E.D.,et al, 1980

Juvenile Muscular Atrophy Localized to Arms
Arch Neurol 37:297-299, Singh,N.,et al, 1980

Horner Syndrome with Causalgia
Neurol 30:534-535, Bernad,P.G.,et al, 1980

Sensory Neuropathy Associated with Primary Biliary Cirrhosis, Histologic & Morphometric Studies
Arch Neurol 37:84-87, Charron,L.,et al, 1980

Diagnosis of Infatile Neuroaxonal Dystrophy by Skin Biopsy
Ann Neurol 7:377-379, Wisniewski,K.,et al, 1980

Familial Tapetorentinal Degeneration & Epilepsy
Arch Neurol 36:544-546, Cohan,S.L.,et al, 1979

Reye's Syndrome in the Adult Patient
Am J Med 67:672-678, Atkins,J.N.,et al, 1979

Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

Lidase Treatment of Spinal Cord Transected Rats
Ann Neurol 6:78-79, Kowalski,T.F.,et al, 1979

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

Valproic Acid, Review of a New Antiepileptic Drug
Arch Neurol 36:393-398, Bruni,J.,et al, 1979

Subacute Motor Neuronopathy:A Remote Effect of Lymphoma
Ann Neurol 5:271-287, Schold,S.C.,et al, 1979

Reduction of Angiotensin-Converting Enzyme in Substantia Nigra in Early-Onset Schizophrenia
NEJM 300:502-503, Arregui,A.,et al, 1979

Enzyme Treatment of Spinal Cord Transected Rats
Ann Neurol 5:203-206, Feringa,E.R.,et al, 1979

Acute Hepatic Failure Associated with the Use of Sodium Valproate
NEJM 300:962-966, Suchy,F.J.,et al, 1979

Presenile Dementia With Motor Neuron Disease in Japan, A New Entity
Arch Neurol 36:592-593, Mitsuyama,Y.,et al, 1979

Amyotrophic Lateral Sclerosis With Ophthalmoplegia; A Cliniocopathologic Study
Arch Neurol 36:615-617, Harvey,D.G.,et al, 1979

Remission of a Syndrome Indistinguishable from Motor Neuron Disease after Resection of Bronchial Carcinoma
BMJ 2:176-177, , 1979

Clinical Pathological Conference
Amyotrophic Lateral Sclerosis, Case Record 46-1979, NEJM 301:1104-1111979., , 1979

Idiopathic Hypoparathyroidism:A Cause of Fits in the Elderly
BMJ l:1460, Graham,K.,et al, 1979

Basal Ganglia Calcification in Kearns-Sayre Syndrome
Arch Neurol 36:711-713, Robertson,W.C.Jr., 1979

Efficacy of Radionuclide Scanning in Patients with Lung Cancer
JAMA 242:2855-2857, Kelly,R.J.,et al, 1979

Use of the ECG in the Diagnosis of Childhood Spinal Muscular Atrophy
Arch Neurol 36:317-318, Russman,B.S.,et al, 1979

Spirometry in Amyotrophic Lateral Sclerosis
Arch Neurol 36:74-80, Fallat,R.J.,et al, 1979

Age & Cerebrospinal-Fluid Protein in Motor-Neuron Disease
NEJM 300:437-438, Guiloff,R.J.,et al, 1979

Double-Blind Study of Modified Neurotoxin in Motor Neuron Disease
Neurol 29:77-81, Tyler,H.R., 1979

Spinocerebellar Degeneration:Hexosaminidase A & B Deficiency in Two Adult Sisters
Neurol 29:380-384, Oonk,J.G.W.,et al, 1979

Multiple Molecular Forms of Arylsulfatase in Different Forms of Metachromatic Leukodystrophy (MLD)
Neurol 29:16-20, Farrell,D.F.,et al, 1979

Spinal Cord Compression by Extramedullary Hemopoietic Tissue in Pyruvate-Kinase-Deficiency-Caused Hemolytic Anemia
Neurol 29:510-513, Rutgers,M.J.,et al, 1979

Juvenile Amaurotic Idiocy (Neuronal Ceroid Lipofuscinosis) & Lymphocyte Fingerprint Profiles
Ann Neurol 4:531-536, Baumann,R.J.,et al, 1978

Distal Chronic Spinal Muscular Atrophy Involving the Hands
JNNP 41:653-658, O'Sullivan,D.J.,et al, 1978

Amyotrophic Lateral Sclerosis
Arch Neurol 35:638-642, Rosen,A.D., 1978

Showing articles 1150 to 1200 of 1300 << Previous Next >>