Neudle.com: inclusion body myopathy

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abdominal protrusion

abortion, spontaneous

acquired immunodeficiency syndrome

advances in neurology

adverse drug reaction

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, misdiagnosis

ANA

animal exposure

anorexia

anterior horn cell disease

anterior interosseous neuropathy

anti Ku antibody

anti NT5C1A

anticardiolipin antibodies

antiphospholipid antibodies

antisynthetase syndrome

arthrogryposis multiplex

aspiration

asymptomatic

atrioventricular block

basal ganglia, lesion of

basal ganglia, lesion, bilateral

cardiovascular disease

carpal tunnel syndrome

central nervous system, infection of

cerebellar lesion

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, multiple

cerebrovascular accident, young adult

cerebrovascular disease

Clinical Pathologic Conference(C.P.C.)

cognition

collagen vascular disease

coma

common variable immunodeficiency

compression neuropathy

confusion

congenital myopathy

congestive heart failure

contractures, joint

controversies in neurology

cortical blindness

cost effectiveness

creatine phosphokinase(CPK)elevated

cricopharyngeal dysfunction

cricopharyngeal myotomy

cyclophosphamide

cyclosporine

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, frontotemporal

Dengue fever

dermatomyositis

dermatomyositis, childhood

diabetes mellitus

difficulty climbing stairs

distal muscle atrophy

distal muscle weakness

drug induced neurologic disorders

dyskinesia

dysphagia

dyspnea

dystrophic calcification

electroencephalogram, abnormalities of

electromyogram

electron microscopy

encephalitis

encephalitis, eastern equine

encephalitis, viral

encephalopathy

endemic area

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

evidence-based research

Fazio-Londe's disease

fever

fibrillations

finger flexor weakness

gag reflex, depressed

gait, waddling

gammaglobulin therapy, intravenous

gender

gene

gene mutation

genetic neurologic disorders

genetic testing

Guillain Barre syndrome

heavy metal intoxication

hepatitis

hepatitis C virus

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

human immunodeficiency virus type 1

hyperreflexia

hypertension

hyporeflexia

idiopathic inflammatory myopathy

immunodeficiency

immunologic disease

immunology and the nervous system

immunomodulation

immunosuppressive agents

inability to stand on tiptoes

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

intellectual deficit

interstitial pulmonary fibrosis

intrinsic hand muscles, wasting of

Kugelberg-Welander syndrome

leg weakness, bilateral

leg weakness, unilateral

lenticular nucleus, lesion of, bilateral

lid closure, weakness of

memory, impairment of

mitochondrial disease

mitochondrial encephalomyopathy

mixed connective tissue disease

multiple sclerosis, treatment of

muscle atrophy, progressive

muscle biopsy

muscle pain

muscle strength, testing

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, pattern

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

myasthenia gravis

myasthenia gravis, etiology of

myasthenia gravis, treatment of

myasthenic syndrome

myasthenic syndrome, treatment of

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inclusion body, hereditary

myopathy, inflammatory

myopathy, mitochondrial

myopathy, necrotizing

myopathy, necrotizing, autoimmune

myopathy, necrotizing, immune-mediated

myopathy, quadriceps

myopathy, steroid induced

myositis, eosinophilic

myositis, focal

myositis, fungal

myositis, granulomatous

nerve conduction studies

neurofibrillary degeneration

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neurons

neuropathology

neuropathy

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, vasculitic, systemic

old age, neurology of

ophthalmoplegia

Paget's disease

paraspinal muscle

paraspinal muscle weakness

Parkinsonism syndrome

partial thromboplastin time, prolonged

patient information and support

periodic paralysis

pleocytosis of cerebrospinal fluid

pneumonia

poison, mercury

poison, neurologic problems with

poliomyelitis-like illness

polymyositis

polyneuropathy, chronic inflammatory demyelinating

positive sharp waves

posterior interosseous neuropathy

practice guidelines

prevention of neurologic disorders

prognosis

progressive neurologic disorder

proximal muscle atrophy

radiation therapy, total body

rash

Raynaud's phenomenon

remote effect of cancer on the nervous system

research

respiratory failure

respiratory tract infection

scleroderma, neurologic involvement with

sclerosis, bone

seizure

seizure, intractable

seizure, intractable, treatment of

seizure, treatment of

serologic testing

serologic testing of cerebrospinal fluid

short stature

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

spinal cord, lesion of

standing difficulty

steppage gait

steroid

steroid therapy, CNS treatment and complications with

stiff man syndrome

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

thalamus

thalamus, lesion of

thalamus, lesion of-bilateral

thoracic outlet syndromes

thrombocytopenia

treatment of neurologic disorder

tremor

tricresylphosphate

trigeminal neuropathy

twins

ulnar neuropathy

Venereal Disease Research Laboratory test

weakness, generalized

weakness, progressive

weight loss

Werdnig-Hoffman disease

West Nile fever

wheelchair

workup

Showing articles 1600 to 1650 of 2809 << Previous Next >>

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Bilateral Brachial Plexus Neuritis Following Parvovirus B19 and Cytomegalovirus Infection
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Erroneous Diagnosis Corrected After 28 Years
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Confirmation of Linkage of Oculopharyngeal Muscular Dystrophy to Chromosome 14q11. 2-q13
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Clinical Genetic Analysis of Parkinson's Disease in the Contursi Kindred
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Psychiatric Features in Diffuse Lewy Body Disease:A Clinicopath Study Using Alzheimer's & PD Groups
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Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
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Acute Myopathy of Intensive Care:Clinical, Electromyographic, and Pathological Aspects
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Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
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Diagnostic Guidelines in Central Nervous System Whipple's Disease
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Differentiation of Central Nervous System Lesions in AIDS Patients Using Positron Emission Tomography (PET)
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Idiopathic Dysautonomia Treated with Intravenous Gammaglobulin
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Herpes Encephalitis is a Disease of Middle Aged & Elderly People:PCR for Detection of HSV in CSF of 516 Pts with Encephalitis
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Body Temperative in Acute Stroke:Relation to Stroke Severity, Infarct Size, Mortality, and Outcome
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Acute Meningitis with a Negative Gram's Stain:Clinical and Management Outcomes in 171 Episodes
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Wernicke's Encephalopathy After Vertical Banded Gastroplasty for Morbid Obesity
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Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
Lancet 347:582-584, Sewry,C.A.,et al, 1996

Acute Rectus Muscle Palsy in Children as a Result of Orbital Myositis
J Pediatr 128:230-233, Pollard,F.,et al, 1996

Ocular Manifestations of AIDS
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Intraorbital Wooden Foreigh Body:CT and MR Appearance
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Bent Spine Syndrome
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Meningitis, Vasculitis, and Cerebritis Caused by CNS Histoplasmosis:Radiologic-Pathologic Correlation
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Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
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Chronic Lymphocytic Leukemia and the Central Nervous System:A clinical and Pathological Study
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Evaluating Contrast-Enhancing Brain Lesions in Patients with AIDS by Using Positron Emission Tomography
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Neurological Sequelae of Cyanide Intoxication-The Patterns of Clinical MRI & Pet Findings
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Evidence for Cardioembolic Stroke in a Case of Kearns-Sayre Syndrome
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Complementary Positron Emission Tomographic Studies of the Striatal Dopaminergic System in Parkinson's Disease
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Early Differential Diagnosis of Parkinson's Disease with F-flurodeoxyglucose and Positron Emission Tomography
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Recurrent Brainstem Encephalitis Associated with Herpes Simplex Virus Type 1 DNA in Cerebrospinal Fluid
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Primary Prevention of Stroke
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Arch Int Med 31:146-148, Puchhammer-Stockl,E.,et al, 1995

Neurologic Manifestations in Children with Lyme Disease
Pediatrics 96:1053-1056, Bingham,P.M.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Cerebrospinal Fluid
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Fever in Acute Stroke Worsens Prognosis:A Prospective Study
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Effects of Surgically Induced Weight Loss on Idiopathic Intracranial Hypertension in Morbid Obesity
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Apolipoprotein E Allele E4, Dementia, and Cognitive Decline in a Population Sample
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Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
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Clinical/Metabolic Correlations in Multiple System Atrophy, A PET Study
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Amyloidosis Causing A Progressive Myopathy
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Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995

Showing articles 1600 to 1650 of 2809 << Previous Next >>