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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 850 to 900 of 1214 << Previous Next >>

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

Clinicopath Conf
Motor Neuron Disease, Progressive-Muscular-Atrophy Type, Case 43-1992, NEJM 327:1298-130592., , 1992

The Use of Magnetic Resonance Imaging in Diagnosing Infantile Neuroaxonal Dystrophy
Neurol 43:110-113, Tanabe,Y.,et al, 1992

Serum Antibodies to L-Type Calcium Channels in Patients with Amyotrophic Lateral Sclerosis
NEJM 327:1721-1728, 17521992., Smith,R.G.,et al, 1992

MRI and SPECT in Amyotrophic Lateral Sclerosis, Demonstr of Upper Motor Neurone Invol by Neuroimaging
Neuroradiology 34:389-393, Udaka,F.,et al, 1992

A Controlled Trial of Tacrine in Alzheimer's Disease
JAMA 268:2523-2529, 25641992., Farlow,M.,et al, 1992

Absence of Cyme Borreliosis Among Patients with Presumed Bell's Palsy
Arch Neurol 49:940-943, Kuiper,H.,et al, 1992

Deprenyl Effects of Levodopa Pharmacodynamics, Mood, and Free Radical Scavenging
Neurol 42:541-544, Baronti,F.,et al, 1992

Psychiatric Disturbances in Metachromatic Leukodystrophy
Arch Neurol 49:401-406, Hyde,T.M.,et al, 1992

Immunodiagnosis of Neurocysticercosis
Arch Neurol 49:633-636, Ramos-Kuri,M.,et al, 1992

Release of Superoxide Dismutase Into CSF as a Marker of Brain Lesion in Acute Cerebral Infarction
Stroke 23:515-518, Strand,T.&Marklund,S.L., 1992

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Motor Neurone Disease
BMJ 304:459-460, Norris,F.H., 1992

Motor Neurone Disease:A Hospice Perspective
BMJ 304:471-473, O'Brien,T.,et al, 1992

Decreased Glutamate Transport by the Brain and Spinal Cord in Amyotrophic Lateral Sclerosis
NEJM 326:1464-1468, 14931992., Rothstein,J.D.,et al, 1992

Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
Neurol 42:1488-1492, Applebaum,J.S.,et al, 1992

Amyotrophic Lateral Sclerosis and Lymphoma:Bone Marroe Examination and Other Diagnostic Tests
Neurol 42:1101-1102, Rowland,L.P.,et al, 1992

Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
Ann Neurol 32:404-407, Boylan,K.B.&Cornblath,D.R., 1992

Genetic Diagnosis of Gaucher's Disease
Lancet 339:889-892, Mistry,P.K.,et al, 1992

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992

Surgical Treatment of Cervical Spondylotic Myelopathy:Time for a Controlled Trial
Neurol 42:5-13, Rowland,L.P., 1992

Complications of Acute Stroke
Lancet 339:721-724, Oppenheimer,S.&Hachinski,V., 1992

Myelopathy Associated with Human T Cell Lymphotropic Virus Type 1 in a White European Native to England
BMJ 305:453, Ali,A.&Rudge,P., 1992

Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings
Ann Neurol 31:64-68, Perlman,J.M.&Argyle,C., 1992

Nervous System Lyme Borreliosis-Revisited
Arch Neurol 49:102-107, Finkel,M.J.&Halperin,J.J., 1992

Phenytoin and Carbamazepine Decrease Oral Bioavailability of Praziquantel
Neurol 42:492-496, Bittencourt,P.R.M.,et al, 1992

Progressive Neuropathy & Recurrent Myoglobinuria in a Child with Long-chain 3-Hydroxyacylcoenzyme A Dehydrogenase Defic
J Pediatr 118:744-746, Dionisi,C.,et al, 1991

Pick's Disease:A Case Clinically Resembling Amyotrophic Lateral Sclerosis
Neurol 41:1831-1833, Sam,M.,et al, 1991

Wilson Disease:Clinical Presentation, Treatment, and Survival
Ann Int Med 115:720-726, Stremmel,W.,et al, 1991

Parental Sex Effect in Familial Amyotrophic Lateral Sclerosis
Neurol 41:1292-1294, Leone,M., 1991

Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
NEJM 324:1381-1384, 1430-14321991., Siddique,T.,et al, 1991

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

Clinicopath Conf
Hepatic Encephalopathy in a 40-Year-Old Woman, Am J Med 90:374-3801991., , 1991

Lymphoma, Motor Neuron Diseases, and Amyotrophic Lateral Sclerosis
Ann Neurol 29:78-86, Younger,D.S.,et al, 1991

Glucosephosphate Isomerase as a CSF Marker for Leptomeningeal Metastasis
Neurol 41:395-398, Newton,H.B.,et al, 1991

The Evaluation of Patients with Human Immunodeficiency Virus-Related Disorders and Brain Mass Lesions
Arch Int Med 151:1381-1384, Cimino,C.,et al, 1991

Clinicopath Conf
Thrombotic Thrombocytopenic Purpura, Case 30-1991, NEJM 325:265-273991., , 1991

Clinicopath Conf
CA of Lung, DIC, Marantic Endocarditis, Multiple CVA's, Case 36-1991, NEJM 325:714-726., , 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Tacrine in Alzheimer's Disease
Lancet 337:989-992, Eagger,S.A.,et al, 1991

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

Lyme Neuroborreliosis:Diagnostic Assay for Intrathecal Synthesis of Borrelia Burgdorferi-Specific IgG, A, and M
Ann Neurol 30:197-205, Hansen,K.&Lebech,A., 1991

A Case of Herpes Zoster Myelitis:Positive Magnetic Resonance Imaging Finding
Eur Neurol 31:164-167, Hwang,Y.M.,et al, 1991

Olfactory Impairment in Motor Neuron Disease:A Pilot Study
JNNP 54:927-928, Elian,M., 1991

Subacute, Reversible Motor Neuron Disease
Neurol 41:1541-1544, Tucker,T.,et al, 1991

Stroke-Like Syndrome, Mineralizing Microangiopathy, and Neuroaxonal Dyst with Intrathecal Methotrexate
Neurol 41:1847-1848, Phanthumchinda,K.,et al, 1991

Progressive Motor Neuron Disease Associated with Electrical Injury
Muscle & Nerve 14:977-980991., Sirdofsky,M.D.,et al, 1991

Late Onset Globoid Cell Leukodystrophy
JNNP 54:1011-1012, Grewal,R.P.,et al, 1991

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Anomalous Molecular Form of Acetylcholinesterase in CSF in Histologically Diagnosed Alzheimer's Disease
Lancet 337:447-450, Navaratnam,D.S.,et al, 1991

Showing articles 850 to 900 of 1214 << Previous Next >>