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abdominal distention

acid maltase deficiency

acid maltase deficiency, adult

acute intermittant porphyria

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

alcoholic polyneuropathy

anesthesia, general

aneurysm, thoracic aortic

anterior horn cell disease

anticonvulsants

antineurofascin antibodies

aortic wall, thickened

arrhythmia, cardiac

arterial dissection, aorta

arterial dissection, wall thickness

arteritis, temporal

autoimmune disease

autonomic dysfunction

bacterial infection

botulinum toxin

brachial neuritis, acute

bulging of biceps

calf hypertrophy

cardiovascular disease

CAT scan, abnormal

CAT scan, angiography

CAT scan, emission, abnormal

CAT scan, metrizamide

CAT scan, muscle

CAT scan, myelogram with

cauda equina, enhancement

cauda equina, lesion of

cavernous sinus

cavernous sinus, lesion of

central nervous system, infection of

cerebellar lesion

cerebral ischemia

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular disease, cardiovascular disease with

cerebrovascular disease, risk factors in

Charcot-Marie-Tooth

chewing movements

chewing, impaired

chromosomal abnormality

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

CLOVES syndrome

clubfoot as related to neurologic disease

congenital malformation

congenital myopathy

congestive heart failure

contactin associated protein like 1 antibodies

contractures, joint

coronary artery disease

corticotropin level

corticotropin-releasing factor

cortisol, elevated

cranial nerve enlargement

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

Cushing's syndrome

cysticercosis, cerebral

cysticercosis, disseminated

cysticercosis, intraventricular

cysticercosis, miliary

deep gray nuclei

Dejerine-Sottas syndrome

delay in diagnosis

denervation of muscle

dentate nuclei, lesion of

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diamond on quadriceps

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

distal muscle atrophy

distal muscle weakness

dysferlinopathy

dysplasia of C.N.S.

dysthyroid ocularmyopathy

dystonia, post traumatic

dystrophin associated proteins

echocardiogram, LVH

edema, periorbital

electrocardiogram, abnormal

electrocardiogram, LVH

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

encephalopathy, progressive

entrapment neuropathy

eosinophilic fasciitis

epidermal nevus syndrome

extraocular muscle enlargement

facial hair, excessive

facial pain, atypical

facial weakness

facial weakness, bilateral

failed medical management

feeding disorder

fine motor function, impaired

fistula, arterio-venous, carotid-cavernous

fistula, arterio-venous, dural

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

giant cell arteritis

Gowers maneuver

Graves ophthalmopathy

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

headache, bilateral

headache, temporal

hemiatrophy, congenital

hemidiaphragm, paralysis of

hemihypertrophy, congenital

hemihypertrophy, facial

hemimegalencephaly

hereditary myopathy with early respiratory failure

high arched feet

hyperthyroidism

hypomelanosis of Ito

hypopigmentation of skin

IgG4-related disease

inability to sit up

infantile spasm

intellectual deficit

intrinsic hand muscles, wasting of

Isaacs syndrome

Kobberling-Dunnigan syndrome

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lacrimal gland enlargement

laminectomy, cervical

laminectomy, lumbar

learning disability

learning disability, in children

left ventricular dilatation

leg weakness, unilateral

leukocyte enzyme abnormality

life expectancy

limb hypertrophy

limb-girdle weakness

liver function enzymes

lumbosacral plexopathy

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignant hyperpyrexia

masseter muscle hypertrophy

maxillary nerves

meconium staining

mental retardation

mental status, abnormal

metabolic alkalosis

molecular genetics

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy chronic inflammatory demyelinating

motor neuron disease

movement disorder

MRI, angiography

MRI, contrast enhanced

MRI, cranial nerves

MRI, hypointense signal foci on

MRI, lumbosacral plexus

MRI, optic nerve

MRI, peripheral nerve

MRI, spinal cord

MRI, vessel wall

MRI, vessel wall enhancement

multimodal neuroimaging

multiple myeloma

muscle atrophy, focal

muscle atrophy, progressive

muscle hypertrophy

muscle hypertrophy, congenital

muscle stiffness

muscle swelling

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, female occurrence of

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

myeloradiculopathy

myocardial infarction

myopathy, amyloid

myopathy, focal

myopathy, hereditary

myopathy, metabolic

myopathy, monomelic

myopathy, quadriceps

myopathy, vacuolar

myositis, ocular

myotonia congenita

nausea and vomiting

neoplasm, hormone producing, ectopic

neoplasm, metastatic to muscle

neoplasm, metastatic to orbit

neoplasm, peripheral nerve

nephrotic syndrome

nerve conduction studies

nerve enlargement

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neuritis, causes of

neuritis, heavy metals causing

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurologic disease, diagnoses of

neurologic examination

neurologic history

neurologic signs

neuroophthalmology

neuropathy, amyloid

neuropathy, ataxic

neuropathy, autoimmune

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, medication induced

neuropathy, onion bulb

neuropathy, peripheral

night blindness

node of Ranvier

nodopathy, autoimmune

ophthalmic artery

optic chiasm, enlarged

optic nerve sheath enhancement

optic nerve, compression of

optic nerve, enlarged

optic nerve, lesion of

optic neuropathy

optic neuropathy, bilateral

orbit, cellulitis of

orbit, inflammation in

orbit, lesions of

orbit, meningioma of

orbit, neoplasms of

orbit, pseudotumor of

paresthesias, feet

paresthesias, lower extremity

PAS positive material in the brain

percussion induced muscle contraction

perineuritis, optic

peripheral nerve, lesion of

peroxisomal disease

plasma cell dyscrasia

polyneuropathy, chronic idiopathic

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic relapsing

polyneuropathy, familial

post polio syndrome

postural abnormality

prenatal diagnosis by amniocentesis

progressive neurologic disorder

proximal muscle atrophy

pseudohypertrophy

pulmonary embolism

pyramidal tract

Refsum's disease

respiratory failure

retinitis pigmentosa

rhabdomyosarcoma

rhabdomyosarcoma of orbit

rippling muscle disease

root lesion, nerve

sarcoglycanopathy

scalp tenderness

sciatic neuropathy

sensorineural hearing loss

shoulder, elevation

sinuses, diseases of

skin, lesions in neurologic disorders

speech disorder, childhood

speech, delayed development of

spinal accessory nerve

spinal cord, compression of

spinal cord, neoplasm

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, intermediate form

spinal stenosis

spinal stenosis, familial

startle reaction

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

subcutaneous nodules

superior ophthalmic vein

survival motor neuron gene

symmetric brain lesions

systemic illness

telangiectases, retinal

temporal artery

temporalis muscle enhancement

temporalis muscle hypertrophy

temporalis muscle swelling

thalamus, lesion of-bilateral

tongue, enlarged

tongue, weakness

tram-track sign

transient ischemic attack

treatment of neurologic disorder

trigeminal nerve

trigeminal nerve, abnormality of

trigeminal nerve, hypertrophy

trigeminal nerve, lesion of

trigeminal neuralgia

ultrasonography, nerve

urinary frequency

vasculitis, large vessel

vertebral artery wall thickness

vision, blurred

visual acuity, decreased

visual fields, constricted

weakness, generalized

weakness, progressive

weakness, proximal

white matter disease

winging of scapula

Showing articles 1950 to 2000 of 3218 << Previous Next >>

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

Clinical Use of Botulinum Toxin
National Institutes of Health Consensus Develop Conf Stmt, Nov 12-14, 1990, Arch Neurol 48:1294-1298, 199, 1991

Peripheral Neuropathy in a Cohort of HIV Infected Patients, Incidence & Relationship to Nervous System Dysfunction
Arch Neurol 48:1273-1274, Hall,C.D.,et al, 1991

Fatigue and Myalgia in AIDS Patients
Neurol 41:1603-1607, Miller,R.G.,et al, 1991

Pancuronium-Induced Prolonged Neuromuscular Blockade
Crit Care Med 19:1583-1587, Rossiter,A.,et al, 1991

Myopathy and Prolonged Neuromuscular Blockade after Lung Transplant
Crit Care Med 19:1580-1582, 14571991., Subramony,S.H.,et al, 1991

Prolonged Paralysis after Treatment with Neuromuscular Junction Blocking Agents
Crit Care Med 19:1125-1131, Gooch,J.L.,et al, 1991

Central Nervous System Infarction Related to Cocaine Abuse
Stroke 22:1320-1325, Daras,M.,et al, 1991

Etiology of Motor or Sensory Stroke:The Predictive Value of Clinical and Radiological Features
Ann Neurol 30:519-525, Chimowitz,M.I.,et al, 1991

CT patterns of Intracranial Hemorrhage Complicating Thrombolytic Therapy for Acute Myocardial Infarction
Radiology 181:555-559, Uglietta,J.P.,et al, 1991

Optic Nerve Sheath Hemorrhage
In Walsh & Hoyt's Clinical Neuro-ophthalmology, Williams & Wilkins, Baltimore, Vol4, p. 2082-2085, 2, 52-2454, 19Miller, N. R., 1991

Complete Ophthalmoplegia as a Complication of Acute Corticosteroid-and Pancuronium-Associated Myopathy
Neurol 41:921-922, Sitwell,L.D.,et al, 1991

Lotus Footdrop:Sciatic Neuropathy in the Thigh
Neurol 41:605-606, Vogel,C.M.,et al, 1991

Mitochondrial Dysfunction in Multiple Symmetrical Lipomatosis
Ann Neurol 29:566-569, Berkovic,S.F.,et al, 1991

Acquired Factor VIII Deficiency and Polyradiculoneuropathy
NEJM 324:1139, Garland,L.,et al, 1991

The Spectrum of Lissencephaly:Report of Ten Patients Analyzed by Magnetic Resonance Imaging
Ann Neurol 30:139-146, Barkovich,A.J.,et al, 1991

MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease
Neuroradiology 33:181-182, Johnsen,D.E.,et al, 1991

Clinical & Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Ref to Growth & Renal Function
NEJM 324:1318-1325, Charnas,L.R.,et al, 1991

Neonatal Opiate Abstinence Syndrome in Term and Preterm Infants
J Pediatr 118:933-937, Doberczak,T.M.,et al, 1991

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

Encephalomyelopathy as an Idiosyncratic Reaction to Carbamazepine:A Case Report
Neurol 41:760-761, Smith,C.R., 1991

Muscle Carnitine Deficiency in Patients Using Valproic Acid
J Pediatr 118:646-649, Shapira,Y.&Gutman,A., 1991

Myasthenia Gravis Unmasked by Cocaine Abuse
NEJM 325:892, Berciano,J.,et al, 1991

Gemfibrozil-Induced Myopathy
Arch Int Med 151:1873-1874, Magarian,G.J.,et al, 1991

Cholesterol-Lowering Agent Myopathy (CLAM)
Neurol 41:1159-1160, London,S.F.,et al, 1991

Staphylococcal Pyomyositis in Patients Infected by the Human Immunodeficiency Virus
Am J Med 90:595-600, Schwartzman,W.A.,et al, 1991

Pyomyositis in Patients with the Human Immunodeficiency Virus:An Unusual Form of Disseminated Bacterial Infection
Am J Med 91:129-136, Widrow,C.A.,et al, 1991

Pyomyositis Presenting as Rapidly Progressive Generalized Weakness
Neurol 41:944-945, Felice,K.,et al, 1991

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

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

Diagnosis of Thymoma in Myasthenics Using Anti-Striated Muscle Antibodies:Predictive Value & Gain in Diagnostic Certainty
Neurol 41:520-524, Lanska,D.J., 1991

Clinical and Electrophysiological Aspects of Acute Paralytic Disease of Children and Young Adults in Northern China
Lancet 338:593-597, McKhann,G.M.,et al, 1991

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

Aggravation of Myasthenia Gravis by Erythromycin
J Pediatr 119:155-156, Absher,J.R.&Bale,J.F., 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

Management of Injuries Due to Chemical Weapons
BMJ 302:129-130, Murray,V.S.G.&Volans,G.N., 1991

Prognosis and Prognostic Factors of Retinal Infarction:A Prospective Cohort Study
BMJ 302:499-504, Hankey,G.J.,et al, 1991

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

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

Eosinophilia-Myalgia Syndrome Associated with Ingestion of L-Tryptophan:Muscle Biopsy Findings in 4 Patients
Neurol 41:319-321, Hollander,D.&Adelman,L.S., 1991

Inflammatory Demyelinating Polyneuropathy in a Child with Symptomatic Human Immunodeficiency Virus Infection
J Pediatr 118:242-245, Raphael,S.A.,et al, 1991

Continuous Muscle Fiber Activity, Peripheral Neuropathy, and Thymoma
Ann Neurol 29:215-218, Garcia-Merino,A.,et al, 1991

Depletion of Muscle Mitochondrial DNA in AIDS Patients with Zidovudine-Induced Myopathy
Lancet 337:508-510, Arnaudo,E.,et al, 1991

Hashimoto's Encephalopathy:A Steroid-Responsive Disorder Associated with High Anti-Thyroid Antibody Titers-Report of 5 Cases
Neurol 41:228-233, Shaw,P.J.,et al, 1991

Myelopathic Neurosarcoidosis:Diagnostic Value of Enhanced MRI
Neurol 41:150-151, Sauter,M.K.,et al, 1991

Treatment of Guillain-Barre Syndrome with Anti-T Cell Monoclonal Antibodies
JNNP 54:51-54, Feasby,T.E., 1991

Showing articles 1950 to 2000 of 3218 << Previous Next >>