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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 700 to 750 of 1214 << Previous Next >>

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Interferon Treatment for Multiple Sclerosis:Autoimmune Complications May be Lethal
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More on Reflex Sympathetic Dystrophy Syndrome Following Air-Bag Inflation
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Lamotrigine-Associated Anticonvulsant Hypersentivitiy Syndrome
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Loss of Vision in Gaucher's Disease and Its Reversal by Enzyme-Replacement Therapy
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Tolcapone for Parkinson's Disease
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Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
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Postpartum Coma
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An Analysis of Extended Survival in Patients with Amyotrophic Lateral Sclerosis Treated with Riluzole
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Magnetic Resonance Imaging of Muscle in Amyotrophic Lateral Sclerosis
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Wobbly Handwriting
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Gabapentin Does Not Interact with a Contraceptive Regimen of Norethindrone Acetate and Ethinyl Estradiol
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HIV-Protease Inhibitors
NEJM 338:1281-1292, Flexner,C., 1998

Permanent Visual Loss and Cerebrovascular Accidents in Giant Cell Arteritis: Predictors and Response to Treatment
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Intravascular Malignant Lymphomatosis with Neurologic Presentation: Factors Facilitating Antemortem Diagnosis
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Flail Arm Syndrome: A Distinctive Variant of Amyotrophic Lateral Sclerosis
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COMT Inhibition with Tolcapone Reduces the"Wearing Off"Phenomenon & Levodopa Requirements in Fluctuating Parkinsonisn Pts
JNNP 63:421-428, Baas,H.,et al, 1997

Tolcapone Improves Motor Function in Parkinsonian Pts with the"Wearing Off"Phenomenon
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Entacapone Improves Motor Fluctuations in Levodopa-Treated Parkinson's Dis Pts
Parkinson Study Group, Ann Neurol 42:747-7551997., , 1997

Multifocal Motor Neuropathy, Serum IgM Anti-GM1 Ganglioside Antibodies Detected Using Linkage of GM1 to ELISA Plates
Neurol 49:1289-1292, Pestronk,A.&Choksi,R., 1997

Adult-Onset Krabbe Disease with Mutation in the Galactocerebrosidase Gene, MRI of Corticospinal Tract Demyelin
Neurol 49:1392-1399, Satoh,J.-I.,et al, 1997

ALS & Severe Cervical Spondylotic Myelopathy in Pt with a Posterior Fossa Archnoid Cyst:Diag Dilemma
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Laboratory Evaluation in the Diagnosis of Lyme Disease
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CSF Findings in Children with Lyme Disease-Associated Facial Nerve Palsy
Arch Pediatr Adolesc Med 151:1224-1228, 11831997., Belman,A.L.,et al, 1997

Serum Angiotensin-Converting Enzyme in Multiple Sclerosis
Arch Neurol 54:1012-1015, Constantinescu,C.S.,et al, 1997

Donepezil (Aricept) for Alzheimer's Disease
The Medical Letter 39:53-54, , 1997

A Controlled Trial of Selegiline, Alpha-Tocopherol, or Both as Treatment for Alzheimer's Disease
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A Case of Acute Monocytic Ehrlichiosis with Prominent Neurologic Signs
Neurol 48:1619-1623, Grant,A.C.,et al, 1997

Adult-Onset Krabbe's Disease in Siblings with Novel Mutations in the Galactocerebrosidase Gene
Ann Neurol 41:111-114, Bernardini,G.L.,et al, 1997

Clinicopath Conf
Genetic Hemochromatosis, Micronodular Cirrhosis of Liver, Case 10-1997, NEJM 336:939-94797., , 1997

Drug Treatment of Alzheimer's Disease, Raise Clinical and Ethical Problems
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Prognosis in Familial ALS:Progr & Surv in Pts with glu100gly & ala4val Mutations in Cu, Zn Superoxide Dismutase
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High Signal Intensity on T1 Weighted MRI of Anterolateral Column of Spinal Cord of Amyotrophic lateral Sclerosis
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ALS Standard of Care Consensus
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Effect of Noninvasive Positive-Pressure Ventilation on Survival in Amyotrophic Lateral Sclerosis
Ann Int Med 127:450-453, Aboussouan,L.S.,et al, 1997

Practice Advisory on the Trtm of ALS with Riluzole
Quality Standards Subcommittee of the AAN, Neurol 49:657-6591997., , 1997

Motor Neuron Syndromes in Cancer Patients
Ann Neurol 41:722-730, 7031997., Forsyth,P.A.,et al, 1997

Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
Neurol 49:400-409, McGeer,P.L.,et al, 1997

Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
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Lymphoproliferative Disorders and Motor Neuron Disease:An Update
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Tolcapone in Stable Parkinson's Disease:Efficacy and Safety of Long-Term Treatment
Neurol 49:665-671, Waters,C.H.,et al, 1997

Vascular Effects of Statins in Stroke
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Extrapyramidal Side Effects with Low-Dose Risperidone
Can J Psychiatry 42:325-325, Brown, E.S., 1997

Three Get Ready
Arch Neurol 53:1222-1223, Goldblatt,D., 1996

Motor Neuron Disease, Lymphoproliferative Disease, and Bone Marrow Biopsy
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Immunoassays Fail to Detect Antibodies Against Neuronal Calcium Channels in Amyotrophic Lateral Sclerosis Serum
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Nonsystemic Vasculitic Mononeuropathy Multiplex, Cryoglobulinemia, and Hepatitis C
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Diagnosis of Creutzfeldt-Jakob Disease in Two-Dimensional Gel Electrophoresis of Cerebrospinal Fluid
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Clinicopath Conf
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Showing articles 700 to 750 of 1214 << Previous Next >>