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abdominal distention
acanthocytosis
acquired immunodeficiency syndrome
adrenoleukodystrophy
advances in neurology
adverse drug reaction
agammaglobulinemia
alcoholism
aminoacidopathies
anterior tibial muscle weakness
anticonvulsants
anticonvulsants, selection of
aphasia
areflexia
arrhythmia, cardiac
aspirin
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
autoimmune disease
azidodeoxythymidine
basal ganglia, calcification of
basal ganglia, infarction
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
blindness
blindness, sudden
botulism
brain biopsy
brainstem, lesion of
bulbar palsy
cachexia
calcification, intracranial
carcinoma
cardiomegaly
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, disappearing lesion on
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
CAT scan, muscle
CAT scan, xenon-enhanced
cataracts
cataracts, congenital
cause of death
central core disease
central nervous system, infection of
cerebellar ataxia, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral blood flow
cerebral cortical atrophy
cerebral edema, cytotoxic
cerebral embolism
cerebral embolism, cardiac origin
cerebral glucose metabolism
cerebral infarction
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
children
chromosomal abnormality
chronic progressive external ophthalmoplegia
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
coenzyme Q10
coenzyme Q10 deficiency
coma
congenital birth defects
congenital myopathy
consanguinity
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
deafmute
deafness
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, rapidly progressive
dentatorubral-pallidoluysian atrophy
depression
developmental retardation
diabetes mellitus
diarrhea
differential diagnosis
diplopia
distal muscle weakness
dizziness
DNA probes
drug induced neurologic disorders
dwarfism
dyschromatopsia
dysphagia
dyspnea
dyspraxia
dystonia
Ekbom's Syndrome
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electronystagmography
electroretinograph
encephalomyopathy
encephalopathy
encephalopathy, progressive
enzyme, defect
epilepsia partialis continua
evoked potentials
exercise
exercise intolerance
extraocular muscle atrophy
extraocular muscle lesion
eye closure
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
falling
false negative
familial
fatigue
fever
fibrillations
foot drop
foot ulcer, neuropathic
Friedreich's ataxia
fundus, abnormality of
gadolinium
gait disorder
gargoylism
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gene
gene mutation
gene therapy
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
glaucoma
gonadal dysgenesis
growth retardation
Hallervorden Spatz disease
Hallgren's syndrome
headache
headache, sudden onset of
hearing loss
heart block
hemianopia
hemianopia, homonymous
hemianopia, transient
hemiparesis
hepatic failure
hepatomegaly
heralding manifestation
herpes simplex encephalitis
herpes simplex encephalitis, differential diagnosis of
hirsutism
histochemistry of muscle
human immunodeficiency virus type 1
Huntington's chorea
Hurler's syndrome
hydrocephalus
hypocalcemia
hypomagnesemia
hypoparathyroidism
hypoparathyroidism, idiopathic
hypophonia
hypothyroidism
hypotonia
ileus, paralytic
imbalance
impulsivity
inclusion bodies
inclusion bodies, intranuclear
inclusion body myositis
intellectual deficit
intellectual deterioration
intelligence quotient
intestinal pseudoobstruction
ischemic exercise test
Kearns-Sayre syndrome
keratoconus
lactate
lactic acidemia
Lafora's disease
laminar necrosis, cortical
Laurence-Moon-Bardet-Biedl syndrome
Leber's hereditary optic neuropathy
leg numbness
leg weakness, bilateral
Leigh's disease
lenticular nucleus, lesion of, bilateral
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
lid closure, weakness of
life expectancy
lipoma of skin
lipomatosis
lipomatosis, multiple symmetrical
lordosis
macular degeneration
malaise
malformation, CNS, congenital
MELAS syndrome
Melkersson's syndrome
memory, impairment of
mental retardation
MERRF syndrome
microangiopathy, brain
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
mimics
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
mitochondrial recessive ataxic syndrome
MNGIE syndrome
molecular genetics
mortality
motor neuron disease
movement disorder
MRI
MRI pattern
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, muscle
MRI, serial
MRS
mucopolysaccharidoses
muscle atrophy, progressive
muscle biopsy
muscle biopsy, extraocular
muscle cramp
muscle pain
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
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, drug-induced
myopathy, inclusion body
myopathy, inclusion body, hereditary
myopathy, mitochondrial
myopathy, proximal
myopathy, toxic
myopathy, vacuolar
myopia
myotonia
myotonia dystrophica
nausea and vomiting
neck weakness
negative
nemaline rod myopathy
neoplasm, primary of CNS
nephrotic syndrome
neuritis
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
neurons
neuroophthalmology
neuropathology
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, hereditary peripheral
neuropathy, peripheral
next-generation sequencing
night blindness
normal
nystagmus
obesity
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
optic atrophy, hereditary
optic disc edema
optic nerve
optic nerve, compression of
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, hereditary
orbicularis oculi muscle
orbit, lesions of
pain
pain, abdominal
pancytopenia
paraparesis
paraparesis, spastic
Parkinsonism syndrome
periodic paralysis
peroxisomal disease
personality change
pes cavus
pigmentary retinopathy
PLEDs
PLEDs, bilateral independent
PLEDs, etiology of
POLG1 gene
polydactyly
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymyalgia rheumatica
polymyositis
polyneuropathy
prognosis
progressive infantile poliodystrophy
progressive myoclonic epilepsy
progressive neurologic disorder
prostigmine
proteinuria
proximal muscle atrophy
pseudomyasthenia
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychosis
psychosis, acute
ptosis
ptosis, bilateral
ragged-red fibers
rapidly progressing neurologic illness
refractive errors
Refsum's disease
renal failure
research
respiratory tract infection
retina, abnormal
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
Reye's syndrome
Reye's syndrome, adult
RFLPs
rhabdomyolysis
Romberg's sign
schizophrenia
screening
seizure
seizure, focal
seizure, paradoxical
seizure, treatment of
sensorineural hearing loss
sensory loss
seronegative
short stature
single photon emission computed tomography
sore throat
Southern immunoblot test
spasticity
Spielmeyer Vogt syndrome
spinal muscular atrophy
spinocerebellar degeneration
spongy degeneration of brain
standing difficulty
Stephens syndrome
strokelike episodes
succinate dehydrogenase deficiency
symmetric brain lesions
systemic illness
tapetoretinal degeneration
temporal lobe, lesion
thalamus, lesion of-bilateral
transverse smile
treatment of neurologic disorder
trinucleotide repeats
undiagnosed
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
visual loss, progressive
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weaning from respirator, failure to
web sites
weight loss
wheelchair
whistle, inability to
white matter disease
white matter disease, pattern
wide based gait
winging of scapula
workup
Showing articles 700 to 750 of 1110 << Previous Next >>

Clinical Follow-Up and Immunogenetic Studies of 32 Patients with Eosinophilia-Myalgia Syndrome
Lancet 337:1071-1074, Kaufman,L.D.,et al, 1991

Late Effects of Paralytic Poliomyelitis in Olmsted County, Minnesota
Neurol 41:501-507, Windebank,A.J.,et al, 1991

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

Polymyositis after Ciguatera Toxin Exposure
Arch Neurol 48:874-877, Stommel,E.W.,et al, 1991

Colchicine-Induced Myopathy and Neuropathy
Neurol 41:943, Younger,D.S.,et al, 1991

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

Legionella Myositis
Neurol 41:750-752, Warner,C.L.,et al, 1991

Rickettsial Meningitis and Encephalitis
Arch Int Med 151:1753-1757, Silpapojakul,K.,et al, 1991

Treatment of Dermatomyositis with Intravenous Gammaglobulin
Am J Med 91:169-172, Lang,B.A.,et al, 1991

Efficacy of Intravenous Gammaglobulin Therapy in Chronic Refactory Polymyositis & Dermatomyositis:20 Adult Patients
Am J Med 91:162-168, Cherin,P.,et al, 1991

The Idiopathic Inflammatory Myopathies and Their Treatment
JNNP 54:285-287, Walton,J., 1991

Magnetic Resonance Imaging Shows Specific Abnormalities in the MELAS Syndrome
Neurol 41:1043-1046, Matthews,P.M., 1991

Necrotizing Myopathy with Pipestem Capillaries, Microvasc Depos
Neurol 41:936-939, Emslie-Smith,A.M.&Engel,A.G., 1991

Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation
NEJM 325:1673-1681, Rousseau,F.,et al, 1991

Response to Treatment with Antihistamines in a Family with Myotonia Congenita
Lancet 337:28-30, Hughes,E.F.&Wilson,J., 1991

Eosinophilia-Myalgia Syndrome, A Clinical Case Series of 21 Patients
Arch Int Med 151:533-537, Philen,R.M.,et al, 1991

Congenital Monomelic Hypertrophy with Progressive Myopathy
Arch Neurol 48:107-110, Shukla,A.,et al, 1991

Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
NEJM 324:364-369, 4111991., Haller,R.G.&Lewis,S.F., 1991

Polymyositis Mediated by T Lymphocytes that Express the y/8 Receptor
NEJM 324:877-881, Hohlfeld,R.,et al, 1991

Neurodegenerative Diseases of Childhood:MR and CT Evaluation
J Comput Assist Tomogr 15:210-222, Mirowitz,S.A.,et al, 1991

Lisch Nodules in Neurofibromatosis Type I
NEJM 324:1264-1266, 1283-12851991., Lubs,M-L.E.,et al, 1991

Diagnostic Tests for Choreoacanthocytosis
Neurol 41:1000-1006, Feinberg,T.E.,et al, 1991

Cervical Dystonia:Clinical Findings and Associated Movement Disorders
Neurol 41:1088-1091, Jankovic,J.,et al, 1991

Myopathy Associated with Ketoconazole Treatment
Am J Dis Child 145:970-971, Garty,B-Z.,et al, 1991

Cramp-Fasciculation Syndrome:A Treatable Hyperexcitable Peripheral Nerve Disorder
Neurol 41:1021-1024, Tahmoush,A.J.,et al, 1991

Poliomyelitis-Like paralysis During Recovery from Acute Bronchial Asthma:Possible Etiology and Risk Fators
Pediatrics 88:276-279, Shahar,E.M.,et al, 1991

Prognosis in AZT Myopathy
Neurol 41:1181-1184, Chalmers,A.C.,et al, 1991

Myopathy in Human Immunodeficiency Virus-Infected Children Receiving Long-Term Zidovudine Therapy
J Pediatr 119:152-155, Walter,E.B.,et al, 1991

Kearns-Sayre Syndrome Presenting as Renal Tubular Acidosis
Neurol 40:1761-1763, Eviatar,L.,et al, 1990

Improved Molecular-Genetic Diagnosis of Leber's Hereditary Optic Neuropathy
NEJM 323:1488-1489, Johns,D.R., 1990

Graves Orbitopathy:Correlation of CT and Clinical Findings
Radiology 177:675-682, Nugent,R.A.,et al, 1990

Eosinophilia-Myalgia Syndrome (L-Tryptophan-Associated Neuromyopathy)
Neurol 40:1793-1796, Turi,G.K.,et al, 1990

L-Tryptophan-Induced Eosinophila-Myalgia Syndrome and Myopathy
Neurol 40:1629-1630, Sagman,D.L.&Melamed,J.C., 1990

New Muscle Power Test in Neuromuscular Disease
Am J Dis Child 144:1083-1087, Tirosh,E.,et al, 1990

Magnetic Resonance Imaging in MELAS Syndrome
Neuroradiology 32:168-171, Rosen,L.,et al, 1990

Myopathy and Rhabdomyolysis Associated with Lovastatin-Gemfibrozil Combination Therapy
JAMA 264:71-75, Pierce,L.R.,et al, 1990

Peripheral Neuropathy in the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Neurol 40 1035-1040, Smith,B.E.&Dyck,P.J., 1990

The Clinical Spectrum of the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Ann Int Med 113:124-134, Martin,R.W.,et al, 1990

L-Tryptophan-Associated Eosinophilic Perimyositis, Neuritis, and Fasciitis
Medicine 69:187-199, Kaufman,L.D.,et al, 1990

Autosomal Dominant Cramping Disease
Arch Neurol 47:810-812, Ricker,K.&Moxley,R.T., 1990

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

MR Findings in Patients with Subacute Necrotizing Encephalomyelopathy (Leigh Syndrome)
AJR 154:1269-1274, Medina,L.,et al, 1990

Progressive Myopathy in Hyperkalemic Periodic Paralysis
Arch Neurol 47:1013-1017, Bradkey,W.G.,et al, 1990

Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
Ann Neurol 27:448-449, Katafuchi,Y.,et al, 1990

Attitudes of Mothers to Neonatal Screening for Duchenne Muscular Dystrophy
BMJ 300:1112, Smith,R.A.,et al, 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
Neurol 40:671-676, Speer,M.C.,et al, 1990

Myopathy with Human Immunodeficiency Virus Type I (HIV-1) Infection:HIV-1 or Zidovudine?
Ann Int Med 113:492-493, Till,M.&MacDonell,K., 1990

Human Immunodeficiency Virus Assoc Myopathy:Immunocytochemical Ident of an HIV Antigen (gp41) in Muscle Macrophages
Ann Neurol 28:579-582, Chad,D.A.,et al, 1990

Neurosarcoidosis:Signs, Course and Treatment in 35 Confirmed Cases
Medicine 69:261-276, Chapelon,C.,et al, 1990



Showing articles 700 to 750 of 1110 << Previous Next >>