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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 2300 to 2350 of 3218 << Previous Next >>

Distal Vacuolar Myopathy with Complete Heart Block
Arch Neurol 45:698-699, Krendel,D.A.,et al, 1988

Outcome from Coma After Cardiopulmonary Resuscitation:Relation to Seizures & Myoclonus
Neurol 38:401-405, Krumholz,A.,et al, 1988

Relationship of Penile Brachial Pressure Index to Myocardial Infarction & Cerebrovascular Accidents in Older Men
Am J Med 84:445-448, Morley,J.E.,et al, 1988

Guillain-Barre Syndrome Following Campylobacter Jejuni Enteritis, Report of Three Cases & Review of the Lit
Arch Int Med 148:739-741, Sovilla,J.Y.,et al, 1988

Neuromuscular Diseases Associated with Human Immunodeficiency Virus Infection
Ann Neurol 23:S38-S48, Dalakas,M.C.&Pezeshkpour,G.H., 1988

Severe Polymyositis-Like Syndrome Associated with Zidovudine Therapy of AIDS & ARC
NEJM 318:708, Bessen,L.J.,et al, 1988

Limited Relapse in Guillain-Barre Syndrome after Plasma Exchange
Arch Neurol 45:314-315, Ropper,A.H.,et al, 1988

Cardiovascular Autonomic Dysfunction in Guillain-Barre Syndrome, Therapeutic Implications of Swan-Ganz Monitoring
Arch Neurol 45:115-117, Dalos,N.P.,et al, 1988

Lyme Disease & Its Neurologic Complications
Arch Neurol 45:99-104, Finkel,M.F., 1988

Amyotrophic Lateral Sclerosis, Recent Advances in Pathogenesis & Therapeutic Trials
Arch Neurol 45:189-202, Mitsumoto,H.,et al, 1988

The Natural History of Motoneuron Loss in Amyotrophic Lateral Sclerosis
Neurol 38:409-413, Munsat,T.L.,et al, 1988

Use of Composite Scores (Megascores) to Measure Deficit in Amyotrophic Lateral Sclerosis
Neurol 38:405-408, Andres,P.L.,et al, 1988

Morphologic Changes in the Muscles of Patients with Postpoliomyelitis Neuromuscular Symptoms
Neurol 38:99-104, Dalakas,M.C., 1988

Dialysis Myelopathy:Quardiparesis Due to Extradural Amyloid of B2 Microglobulin Origin
BMJ 296:752-753, Allain,T.J.,et al, 1988

Pure Trigeminal Motor Neuropathy
BMJ 296:209-210, Lie-Gan,C., 1988

Deep Branch Ulnar Neuropathy Due to Giant Cell Tumor:Report of a Case
Neurol 38:327-329, Rafecas,J.C.,et al, 1988

Serum Antibodies to GM1 Ganglioside in Amytrophic Lateral Sclerosis
Neurol 38:1457-1461, Pestronk,A.,et al, 1988

Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988

A Creutzfeldt-Jakob Like Syndrome Due to Lithium Toxicity
JNNP 51:120-123, Smith,S.J.M.&Kocen,R.S., 1988

Myoclonus During Combined Tricyclic Antidepressant and Lithium Treatment
J Clin Psychopharmacol 8:446-447, Devanand,D.P.,et al, 1988

Amyotrophic Lateral Sclerosis Presenting with Sleep Hypopnea Syndrome
Chest 93:1309-1312, Carre,P.C.,et al, 1988

Creutzfeldt-Jakob Disease without Periodic Sharp Wave Complexes:A Clinical, EEG, and Path Study
Neurol 38:1056-1060, Zochodne,D.W.,et al, 1988

Headaches in Pregnancy
Semin Neurol 8:187-192, Reik,L., 1988

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

Syndrome De Gougerot Sjogren Primitif Avec Polymyosite Necrosante:Effet Favorable de L'Hydroxychloroquine
Rev Neurol 143:147-148, Ponge,T.,et al, 1987

Bilateral Retrobulbar Optic Nerve Infarctions After Blood Loss & Hypotension, A Clinicopath Case Study
Ophthalmol 94:1577-1584, Johnson,M.W.,et al, 1987

Computed Tomography and Magnetic Resonance Imaging in the Diagnosis of Inflammatory Disease of the Optic Nerve
Surv Ophthalmol 31:352-355, McCrary,J.A.,et al, 1987

Cholesterol Crystal Embolization:A Review of 221 Cases in the English Literature
Angiology 38:769-784, Fine,M.J.,et al, 1987

Iodinated Contrast Agents in Myasthenia Gravis
Neurol 37:1400-1402, Frank,J.H.,et al, 1987

The Association of Stroke & Coronary Heart Disease:A Population Study
Mayo Clin Proc 62:1077-1083, 1158-11601987., Dexter,D.D.,et al, 1987

Transient Traumatic Quadriplegia
Editorial, Lancet 1:8441987., , 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Current Status of Thyrotropin-Releasing Hormone Therapy in Amyotrophic Lateral Sclerosis
Comm. on Health Care Issues, Amer Neuro Assoc, Ann Neurol 22:541-54387., , 1987

A Rating Scale for Amyotrophic Lateral Sclerosis:Description & Preliminary Experience
Ann Neurol 22:328-333, Appel,V.,et al, 1987

Late Denervation in Patients with Antecedent Paralytic Poliomyelitis
NEJM 317:7-12, Cashman,N.R.,et al, 1987

Motor Neuron Disease in the US, 1971 & 1973-1978:Patterns of Mortality & Associated Conditions at Time of Death
Neurol 37:1339-1343, Leone,M.,et al, 1987

Clinincopath Conf
Progressive Muscular Atrophy & Diabetic Neuromuscular Disease, Case 21-1987, NEJM 316:1326-13357., , 1987

Acute Lead Poisoning in Two Users of Illicit Methamphetamine
JAMA 258:510-511, Allcott,J.V.,et al, 1987

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

Colchicine Myopathy & Neuropathy
NEJM 316:1562-1568, Kuncl,R.W.,et al, 1987

Clinicopath Conf
Kearns-Sayre Syndrome (Oculocraniosomatic Neuromuscular Disease with Mitochondrial Myopathy) , Case, 4-1,NEJM 317:493-501,1987., 1987

Minimal Thyroid Ophthalmopathy
Neurol 37:1803-1808, Spector,R.H.&Carlisle,J.A., 1987

Neuropathologic & Clinical Features of Parkinson's Disease in Alzheimer's Disease Patients
Neurol 37:754-760, Ditter,S.M.&Mirra,S.S., 1987

Parkinson's Disease & Myasthenia Gravis:Adverse Effect of Trihexyphenidyl on Neuromuscular Transmission
Neurol 37:832-833, Ueno,S.,et al, 1987

Familial Recurrent Bell's Palsy with Ocular Motor Palsies
Neurol 37:1369-1371, Aldrich,M.S.,et al, 1987

Diagnosis of Thoracic Outlet Syndrome, Value of Sensory & Motor Conduction Studies & Quantitative EMG
Arch Neurol 44:1161-1163, Smith,T.&Trojabor,W., 1987

Hereditary Motor & Sensory Neuropathy, X-Linked:A Half Century Follow-Up
Neurol 37:1460-1465, Rozear,M.P.,et al, 1987

Symptomatic Atlantoaxial Dislocation in Down's Syndrome
Ann Neurol 21:606-609, Chaudhry,V.,et al, 1987

Pretended Paralysis Requiring Artificial Ventilation
BMJ 294:961-962, Hopkins,A.&Clarke,C., 1987

Showing articles 2300 to 2350 of 3218 << Previous Next >>