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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 2700 to 2750 of 3218 << Previous Next >>

Eosinophilic Myositis, An Unusual Cause of Pseudotumor & Eosinophilia
JAMA 246:70-71, Agrawal,B.L.,et al, 1981

Labetalol-induced Toxic Myopathy
BMJ 282:1824-1825, Teicher,A.,et al, 1981

Lipid Storage Myopathy:Successful Treatment with Propranolol
BMJ 282:1997-1999, Martyn,C.,et al, 1981

Myopathy Induced by Rifampicin
BMJ 283:105-106, Jenkins,P.,et al, 1981

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Atlanto-Axial Instability in Children with Down Syndrome
Pediat Radiol 10:129-132, Pueschel,S.M.,et al, 1981

Plasmapheresis in the Treatment of Four Cases of Guillain-Barre Syndrome (acute form)
Ital. J Neurol Sci 4:331-3361981., Zerbi,D.,et al, 1981

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,et al, 1981

Primary Lateral Sclerosis
Arch Neurol 38:630-633, Beal,M.F.,et al, 1981

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981

Biotin Deficiency:An Unusual Complication Of Parenteral Alimentation
NEJM 304:820-823, Mock,D.M.,et al, 1981

Post-encephalitic Parkinsonism:Current Experience
JNNP 44:670-676, Rail,D.,et al, 1981

Chronic Focal Polymyositis in the Adult
JNNP 44:419-425, Bharucha,N.E.,et al, 1981

Plasmapheresis in Idiopathic Inflammatory Myopathy Experience With 35 Patients
Arch Neurol 38:544-552, Dau,P.C., 1981

Bilateral Vocal Cord Paralysis in a Patient With Familial Hypertrophic Neuropathy
Arch Neurol 38:532, Johnson,J.A.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Encephalopathy in Infants & Children With Chronic Renal Disease
Arch Neurol 38:656-658, Foley,C.M.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Cephaloridine Encephalopathy
BMJ 283:409-410, Taylor,R.,et al, 1981

Pattern Reversal Visual Evoked Potentials
Arch Neurol 38:739-741, Bird,T.D.,et al, 1981

Procainamide-Induced Myasthenia-like Weakness in a Patient with Peripheral Neuropathy
Arch Neurol 38:378-379, Niakan,E.,et al, 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Neurologic Manifestations in Macroglobulinemia
In Vinken PJ, Bruyn GW, Eds, Handbook of Clin Neurol, Vol 39, North-Holland Publ Co, p. 189, Abramsky,O., 1980

Guillain-Barre-Like Polyneuropathy after Renal Transplant, Possible Association with Cytomegalovirus Infection
Arch Neurol 37:784, Bale,J.F.,et al, 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Acute Rhabdomyolysis Associated With An Echovirus 9 Infection
Arch Int Med 140:1671-1672, Josselson,J.,et al, 1980

Ciguatera Fish Poisoning in Miami
JAMA 244:254-258, Lawrence,D.N.,et al, 1980

Management of Cerebral Embolism of Cardiac Origin
Stroke 11:433-442, Easton,J.D.,et al, 1980

Phencyclidine:The New American Street Drug
Editorial, BMJ 281:1511-15121980., , 1980

Valproic Acid
NEJM 302:661-666, Brown,T.R., 1980

Clonazepam Treatment of Insomnia Due to Sleep Myoclonus
Arch Neurol 37:119-120, Oshtory,M.A.,et al, 1980

Peripheral Source of MB Band of Creatine Kinase in Alcoholic Rhabdomyolysis
JAMA 244:580-582, Siegel,A.J., 1980

Neurologic Prognosis after Cardiopulmonary Arrest:III. Seizure Activity
Neurol 30:1292-1297, Snyder,B.D.,et al, 1980

Mitral Valve Prolapse & Ophthalmoplegia:A Progressive, Cardioneurologic Syndrome
Ann Int Med 92:735-741, Darsee,J.R.,et al, 1980

Lobar Cerebral Hemorrhages:Acute Clinical Syndromes in 26 Cases
Ann Neurol 8:141-147, Ropper,A.H.,et al, 1980

Phencyclidine Abuse Mimicking Head Injury
JAMA 243:2323-2324, Corales,R.L.,et al, 1980

A pedigree of Amyotrophic Chorea With Acantho-cytosis
Arch Neurol 37:514-517, Kito,S.,et al, 1980

Diagnosis & Treatment, Physiologic & Pathologic Tremors
Ann Int Med 93:460-465, Jankovic,J.,et al, 1980

Lafora Disease:Diagnosis by Liver Biopsy
Ann Neurol 8:409-415, Nishimura,R.N.,et al, 1980

Motor Neuropathy Associated with Cimetidine
BMJ 281:974-975, Walls,T.J.,et al, 1980

Masticatory Spasm in Facial Hemiatrophy
Ann Neurol 7:585-587, Kaufman,M.D., 1980

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

Pathogenesis of Papilloedema & Raised Intra-cranial Pressure in Guillain-Barre Syndrome
BMJ 281:1393-1394, Reid,A.C.,et al, 1980

Guillain-Barre Syndrome in Recipients of A/New Jersey Influenza Vaccine
JAMA 243:2490-2494, Marks,J.S.,et al, 1980

Fatal Guillain-Barre Syndrome after the National Influenza Immunization Program
Neurol 30:929-933, Keenlyside,R.A.,et al, 1980

Arrhythmic Complications in the Guillain-Barre Syndrome
Arch Int Med 140:1053-1055, Greenland,P.,et al, 1980

Guillain-Barre Syndrome:Is There a Role for Plasma-pheresis
Neurol 30:1112, Asbury,A.,et al, 1980

Influenzal Acute Myositis in the Elderly
Neurol 30:877-878, Congy,F.,et al, 1980

Myositis, Myoglobinemia, & Myoglobinuria Associated With Enterovirus Echo 9 Infection
Arch Neurol 37:457-458, Jehn,U.W.,et al, 1980

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

Showing articles 2700 to 2750 of 3218 << Previous Next >>