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abdominal distention

acquired immunodeficiency syndrome

adrenoleukodystrophy

advances in neurology

adverse drug reaction

agammaglobulinemia

aminoacidopathies

anterior tibial muscle weakness

anticonvulsants

anticonvulsants, selection of

antiviral agents

arrhythmia, cardiac

ataxia, cerebellar

ataxia, progressive

autoimmune disease

azidodeoxythymidine

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion, bilateral

basilar artery stenosis

Bassen-Kornzweig syndrome

black toenail sign

blindness, sudden

brainstem, lesion of

calcification, intracranial

CAT scan, abnormal

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, gyral swelling

CAT scan, muscle

CAT scan, xenon-enhanced

cataracts, congenital

central core disease

central nervous system, infection of

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebral blood flow

cerebral cortex

cerebral cortical atrophy

cerebral edema, cytotoxic

cerebral embolism

cerebral embolism, cardiac origin

cerebral glucose metabolism

cerebral infarction

cerebral ischemia

cerebro hepato renal syndrome

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cherry red spot-myoclonus syndrome

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

coenzyme Q10 deficiency

congenital birth defects

congenital myopathy

cornea, abnormal

corpus callosum, lesion of

cortical blindness

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cricopharyngeal bar

cultured skin fibroblasts

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, rapidly progressive

dentatorubral-pallidoluysian atrophy

developmental retardation

diabetes mellitus

diagnostic criteria

differential diagnosis

difficulty climbing stairs

distal muscle weakness

drug induced neurologic disorders

dyschromatopsia

Ekbom's Syndrome

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

electroretinograph

encephalomalacia

encephalomyopathy

encephalopathy, progressive

epilepsia partialis continua

evoked potentials

exercise intolerance

extraocular muscle atrophy

extraocular muscle lesion

eye movement, disorders of

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failure to thrive

foot ulcer, neuropathic

Friedreich's ataxia

fundus, abnormality of

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic counselling

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

gonadal dysgenesis

growth retardation

gyrus, abnormal

Hallervorden Spatz disease

Hallgren's syndrome

headache, sudden onset of

hemianopia, homonymous

hemianopia, transient

hepatic failure

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

histochemistry of muscle

human immunodeficiency virus type 1

Huntington's chorea

Hurler's syndrome

hypoparathyroidism

hypoparathyroidism, idiopathic

iatrogenic neurologic disorders

ileus, paralytic

inclusion bodies

inclusion bodies, intranuclear

inclusion body myositis

intellectual deficit

intellectual deterioration

intelligence quotient

intestinal pseudoobstruction

ischemic exercise test

Kearns-Sayre syndrome

lactic acidemia

Lafora's disease

laminar necrosis, cortical

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukocyte enzyme abnormality

leukoencephalopathy

lid closure, weakness of

life expectancy

lipomatosis, multiple symmetrical

macular degeneration

malformation, CNS, congenital

Melkersson's syndrome

memory, impairment of

meningeal enhancement

mental retardation

mesial temporal lobe

microangiopathy, brain

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migratory lesion pattern

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molecular genetics

motor neuron disease

movement disorder

MRI lesion location

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, gyral enhancement

MRI, gyral swelling

MRI, linear enhancement

MRI, T1 weighted high signal foci

mucopolysaccharidoses

muscle atrophy, progressive

muscle biopsy, extraocular

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, ocular

myasthenia gravis, seronegative

myasthenic syndrome

myoclonic jerks

myoclonus, epilepsy

myopathy, centronuclear

myopathy, drug-induced

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, mitochondrial

myopathy, proximal

myopathy, toxic

myopathy, vacuolar

myotonia dystrophica

nausea and vomiting

nemaline rod myopathy

neoplasm, primary of CNS

nephrotic syndrome

neuroendocrinology

neurogenic vs.myopathic atrophy

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathy, ataxia, retinitis pigmentosa

neuropathy, hereditary peripheral

neuropathy, peripheral

next-generation sequencing

night blindness

occipital lobe, infarction

occipital lobe, lesion of

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculopharyngeal muscular dystrophy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

optic atrophy, hereditary

optic disc edema

optic nerve, compression of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

orbicularis oculi muscle

orbit, lesions of

pain, abdominal

paraparesis, spastic

Parkinsonism syndrome

periodic paralysis

peroxisomal disease

personality change

pigmentary retinopathy

PLEDs, bilateral independent

PLEDs, etiology of

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polymyalgia rheumatica

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

proximal muscle atrophy

pseudomyasthenia

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychosis, acute

ptosis, bilateral

ragged-red fibers

rapidly progressing neurologic illness

refractive errors

Refsum's disease

respiratory tract infection

retina, abnormal

retinal degeneration

retinitis pigmentosa

Reye's syndrome

Reye's syndrome, adult

seizure, paradoxical

seizure, treatment of

sensorineural hearing loss

single photon emission computed tomography

Southern immunoblot test

Spielmeyer Vogt syndrome

spinal muscular atrophy

spinocerebellar degeneration

spongy degeneration of brain

spontaneous remission

standing difficulty

Stephens syndrome

strokelike episodes

succinate dehydrogenase deficiency

symmetric brain lesions

systemic illness

tapetoretinal degeneration

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of-bilateral

transient neurologic deficit

transverse smile

treatment of neurologic disorder

trinucleotide repeats

Unverricht-Lundborg disease

upgaze, paralysis of

Usher's syndrome

viral infection, CNS

visceral neuropathy

vision, failure of in childhood

visual acuity, decreased

visual field defect

visual fields, constricted

visual loss, progressive

walking, difficulty with

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

whistle, inability to

white matter disease

white matter disease, pattern

whole genome sequencing

wide based gait

winging of scapula

Showing articles 500 to 550 of 1133 << Previous Next >>

Recurrent Strokes in a 34-Year-Old Man
Lancet 350:560, Chinnery,P.F.,et al, 1997

Obstetric Aspects in Women with FSH Muscular Dystrophy, Limb-Girdle Musc Dyst, & Cogen Myopathies
Arch Neurol 54:888-894, Rudnik-Schoneborn,S.,et al, 1997

A 9-Year-Old With Fever and Severe Muscle Pains
Lancet 349:1666, Punda-Polic,V.,et al, 1997

Treatment of Inflammatory Myopathies
Muscle & Nerve 20:651-664997., Mastaglia,F.L.,et al, 1997

Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy
Neurol 48:1227-1234, Eymard,B.,et al, 1997

Magnetic Resonance Imaging of the Forearm as a Diagnostic Aid in Pts with Sporadic Inclusion Body Myositis
Neurol 48:863-866, Sekul,E.A.,et al, 1997

Steroid Myopathy in Cancer Patients
Neurol 48:1234-1238, Batchelor,T.T.,et al, 1997

Clinicopath Conf
Acute Critical-Illness Myopathy, with Loss of Myosin Filaments, ? Induced by Steroid, Case 11-1997,, EJM 379-1088,1997., 1997

Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9
Ann Neurol 41:432-437, Ikeuchi,T.,et al, 1997

Painful Proximal Diabetic Neuropathy:Inflammatory Nerve Lesions and Spontaneous Favorable Outcome
Ann Neurol 41:762-770, Said,G.,et al, 1997

Clinicopath Conf
Skeletal-Muscle Infarction Associated with Diabetes Mellitus, Case 29-1997, NEJM 337:839-845997., , 1997

Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
Arch Neurol 54:1226-1229, Roses,A.D., 1997

Clinicopath Conf
Rocky Mountain Spotted Fever with Meningoencephalomyelitis, Vasculitis and Focal Myocarditis, Case 3, -17,NEJM 337:1149-1156,1997., 1997

Acute Corticosteroid Myopathy in Intensive Care Patients
Muscle & Nerve 20:1371-1380997., Hanson,P.,et al, 1997

Hemiparetic Acute Myopathy of Intensive Care Progressing to Triplegia
Arch Neurol 54:1420-1422, Sun,D.Y.,et al, 1997

Thrombotic Thrombocytopenic Purpura:A Treatable Cause of Childhood Encephalopathy
J Pediatr 130:313-316, Lawlor,E.R.,et al, 1997

Few Psychological Consequences of Presymptomatic Testing for Huntington Disease
Lancet 349:4, Bundey,S., 1997

The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
JAMA 277:832-836, Post,S.G.,et al, 1997

Botulinum Toxin Treatment of Muscle Cramps, A Clinical & Neurophysiological Study
Ann Neurol 41:181-186, Bertolasi,L.,et al, 1997

Evaluation of Neuromuscular Symptoms in Veterans of the Persian Gulf War
Neurol 48:4-12, Amato,A.A.,et al, 1997

Is There a Gulf War Syndrome? Searching for Syndromes by Factor Analysis of Symptoms
JAMA 227:215-222, 2591997., Haley,R.W.,et al, 1997

Self-Reported Exposure to Neurotoxic Chemical Combinations in the Gulf War:A Cross-Sectional Epidemiologic Study
JAMA 227:231-237, 2591997., Haley,R.W.&Kurt,T.L., 1997

Evaluation of Neurologic Function in Gulf War Veterans:A Blinded Case-Control Study
JAMA 227:223-230, 2591997., Haley,R.W.,et al, 1997

Proximal Myotonic Myopathy with MRI White Matter Abnormalities of the Brain
Neurol 48:33-37, Hund,E.,et al, 1997

Mutations in the Sarcoglycan Genes in Patients with Myopathy
NEJM 336:618-624, Duggan,D.J.,et al, 1997

The Muscular Dystrophies-Clarity or Chaos
NEJM 336 650-651, Dubowitz,V., 1997

MELAS Presenting as Migraine Complicated by Stroke:Case Report
Neuroradiology 39:781-784, Ohnok,IK.,et al, 1997

Inclusion Body Myositis:Clinical and Pathological Boundaries
Ann Neurol 40:581-586, Amato,A.A.,et al, 1996

Distal WEakness in Dystrophin-Deficient Muscular Dystrophy
Muscle & Nerve 19:1608-1610996., Felice,K.J., 1996

Practice Parameter:Genetic Testing Alert
Pract Comm Genet Testing Task Force AAN, Neurol 47:1343-13441996., , 1996

Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
Ann Neurol 40:829-840, Levy-Lahad,E.&Bird,T.D., 1996

Clozapine-Induced Myotoxicity in Patients with Chronic Psychotic Disorders
Neurol 47:1518-1523, Scelsa,S.N.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Linomide Reduces the Rate of Active Lesions in Relapsing-Remitting Multiple Sclerosis
Neurol 47:895-900, Anderson,O.,et al, 1996

Angiotropic Large-Cell Lymphoma with Peripheral Nerve & Skeletal Muscle Involvement:Early Diagnosis & Treatment
Neurol 47:1009-1011, Levin,K.H.&Lutz,G., 1996

AAEM Case Report#13:Diabetic Amyotrophy
Muscle & Nerve 19:939-945996., Chokroverty,S.&Sander,H.W., 1996

Critical Illness Myopathy and Neuropathy
Lancet 347:1579-1582, Latronico,N.,et al, 1996

Motor Neuropathy Due to Docetaxel and Paclitaxel
Neurol 47:115-118, Freilich,R.J.,et al, 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Cerebral Infarction Associated with Kearns-Sayre Syndrome-Related Cardiomyopathy
Neurol 46:826-828, Provenzale,J.M.,et al, 1996

Inclusion Body Myositis
JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996

Acute Type II Myofiber Atrophy in Critical Illness
Neurol 46:819-821, 6001996., Gutman,L.,et al, 1996

Muscle is Electrically Inexcitable in Acute Quadriplegic Myopathy
Neurol 46:731-736, 6001996., Rich,M.M.,et al, 1996

Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
Neurol 47:579-580, El-Schahawi,M.,et al, 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Mushroom Myopathy
Muscle & Nerve 19:790-792996., Gonzalez,J.,et al, 1996

Isolated Neck Extensor Myopathy:A Common Cause of Dropped Head Syndrome
Neurol 46:917-921, Katz,J.S.,et al, 1996

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

Showing articles 500 to 550 of 1133 << Previous Next >>