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abductor pollicis brevis

abscess, intracerebral

abscess, intracranial

abscess, vertebral

accomodation, abnormal

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, infants and children

acute disseminated encephalomyelitis

adolescent medicine

advances in neurology

adverse drug reaction

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alcohol intolerance

alcohol intoxication

alcohol, neurologic complications with

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alternating rapid movement

alternating rapid movement, impaired

amaurosis fugax

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, complications with

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anemia, hemolytic

anemia, megaloblastic

anesthesia, general

aneurysm, abdominal aortic

aneurysm, intracranial, screening for

angiography, cerebral

angiography, neurologic complications with

angiotensin-converting enzyme, inhibitors

angular gyrus syndrome

ankle reflex, absent

ankle, swelling of

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

anti citrullinated antibody

antibiotic prophylaxis

anticoagulant, complications of

anticoagulant, treatment

anticoagulant, treatment in CVD

anticonvulsants

anticonvulsants, selection of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antiviral agents

apraxia, constructional

arrhythmia, cardiac

arterial dissection

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arteriovenous malformation

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arthrogryposis multiplex

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atrial fibrillation

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attention deficit disorder with hyperactivity

autoimmune disease

automobile accidents

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

B 12 deficiency

bacterial infection

Balint's syndrome

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basement membrane

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basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

behavioral disorder

Bence Jones protein

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blinking, reduced

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Borrelia burgdorferi infection

botulinum toxin

botulinum toxin, complications of

brachial neuritis

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brachial plexus, lesion of

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, lesion of

Brown-Vialetto-Van Laere syndrome

burning paresthesia

calcification, intracranial

calf hypertrophy

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cardiac catheterization, neurologic complications

cardiovascular disease

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carotid artery stenosis

carpal tunnel syndrome

CAT scan, abnormal

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celiac disease, adult

central cord syndrome

central core disease

central nervous system, infection of

cerebellar atrophy, primary

cerebellar degeneration

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cerebellar lesion

cerebellum, disease of

cerebral cortical atrophy

cerebral dominance

cerebral embolism

cerebral embolism, artery to artery

cerebral embolism, cardiac origin

cerebral embolism, carotid origin

cerebral infarction

cerebral infarction, small, deep

cerebral peduncle

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, red cells in

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, incidence of

cerebrovascular accident, location of

cerebrovascular accident, mimics

cerebrovascular accident, young adult

ceruloplasmin, serum

cervical collar

cervical myelopathy

cervical spine abnormality

cervical spondylosis

Charcot-Marie-Tooth

cheiralgia paresthetica

chelation therapy

chest x-ray, abnormal

chiasmal syndromes

cholesterol, HDL

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

Cockayne's syndrome

cognition, slowed

cogwheel rigidty

coin lesion on chest X-ray

cold hands sign

cold temperature

collagen vascular disease

collateral circulation

compartment syndrome

compartment syndrome, medial brachial fascial

compression fracture

compression neuropathy

conduction block

congenital deformities

congenital heart disease

congenital infection, CNS

congenital malformation

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

contractures, joint

contraindications

contrast agents, neurotoxicity of

controversies in neurology

convergence, impaired

cornea, abnormal

cornea, opacity of

Cornelia de Lange syndrome

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, infarction of

corpus callosum, lesion of

corpus callosum, thinning

cortical hand knob

cortical hand knob infarct

cortical infarction

cortical infarction, small

cortical topography

cortical vein thrombosis

cortical wrist drop

costoclavicular syndrome

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

Craniosynostosis

crawl regression

C-reactive protein, elevated

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cryopyrin-associated periodic syndrome

cyclophosphamide

cyst, perineural

cytomegalovirus infection

cytomegalovirus infection, congenital

Dawson's fingers

decision analysis

deep gray nuclei

delay in diagnosis

dementia, familial

dementia, frontotemporal

dementia, rapidly progressive

demyelinating disease

denervation of muscle

denervation potentials

dental procedure, neurologic complications with

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diamond on quadriceps

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

digital neuropathy

digiti quinti sign

digits, abnormal

digits, shortened

diplegia, brachial

disability rating scale, neurological

disability, neurological

disc space infection

disc space narrowing

dislocated hip, congenital

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

diurnal variation

dopa responsive dystonia

drug induced neurologic disorders

dural sinus thrombosis

dysdiadochokinesia

dysostosis multiplex

dystonia, children

dystonia, focal

dystonia, treatment of

dystrophic calcification

electrical sensation

electrical stimulation, spinal nerves

electrocardiogram, abnormal

electroencephalogram, abnormalities of

embolism, paradoxical

embolism, septic

Emery-Dreifuss muscular dystrophy

emotional lability

empyema, epidural-spinal

encephalomyelitis

encephalopathy, progressive

endocarditis, neurologic manifestations with

endocarditis, prophylaxis

endocarditis, subacute bacterial

endocarditis, treatment of

endovascular therapy

entrapment neuropathy

enzyme, muscle disease

eosinophilia-myalgia syndrome

eosinophilic fasciitis

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

episodic neurologic deficits

epistaxis, recurrent

erythema migrans

esophageal reflux

esophageal varices

evoked potentials

exome sequencing

extremity, cold

eye movement, disorders of

eyebrows, abnormal

face, numbness of

facial appearance, abnormal

facial nerve palsy

facial weakness

facial weakness, bilateral

failed medical management

failure to thrive

FARS2 deficiency

feeding disorder

fetal movements, reduced

fibrinolytic agents, contraindications

fine motor function, impaired

finger flexor weakness

finger nose finger test

finger numbness

finger swelling

finger weakness

fingernails, abnormal

fingernails, white

fingers, abnormal

fingers, painful

fistula, arterio-venous

fistula, arterio-venous, pulmonary

folic acid deficiency

foot drop, bilateral

fracture, long bone

Friedreich's ataxia

frontotemporal dementia, behavioral variant

gait, festinating

gamma amino butyric acid

gammaglobulin therapy, intravenous

gastroenteritis

gastrointestinal bleeding

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann syndrome

girdle sensation

glutamic acid decarboxylase, antibody

Gowers maneuver

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Hallgren's syndrome

handcuff neuropathy

headache, positional

headache, progressive

heart block, complete

heavy metal intoxication

heel-knee-shin test

hematocrit, neurologic complications with elevation of

hematuria, gross

hematuria, microscopic

hemianopia, homonymous

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herniated disc, central

herniated disc, cervical

herniated disc, thoracic

high arched feet

histochemistry of muscle

Horner's syndrome

human immunodeficiency virus type 1

human immunodeficiency virus type 1, false positive

human immunodeficiency virus type 2

Hurler's syndrome

hyperamylasemia

hyperhidrosis, palmar

hyperhomocysteinemia

hyperpigmentation of skin

hypersegmented polys

hypertensive crisis

hypertensive encephalopathy

hypoglycorrhachia

hypomyelination

hypoparathyroidism

hypoproteinemia

hypoprothrombinemia

hypothalamus, damage to

hypothalamus, lesion of

hypotonia, infants

iatrogenic neurologic disorders

imbalance, postural

immune reconstitution inflammatory syndrome

immunoelectrophoresis, serum

immunohistochemistry

immunomodulation

immunosuppression

immunosuppressive agents

imperforate anus

implantable cardioverter defibrillator

inability to stand on tiptoes

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

inclusion body myositis

infection, recurrent

influenza A virus

influenza B virus

injection neuropathy

intellectual deficit

intellectual deterioration

internuclear ophthalmoplegia, unilateral

interosseous muscles

interstitial pulmonary fibrosis

intestinal biopsy

intracerebral hemorrhage

intracerebral hemorrhage, young adult

intracranial hypertension, benign

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

jaw contractures

jaw jerk, abnormal

joint hypermobility

juvenile distal and segmental muscular atrophy

Kayser-Fleischer ring

Kearns-Sayre syndrome

kinesia paradoxica

Krabbe's disease

kyphoscoliosis, neurologic causes of

labyrinth, disorder of

labyrinthitis, acute

lactic dehydrogenase(LDH)

lateral cutaneous nerve of forearm

Laurence-Moon-Bardet-Biedl syndrome

left-right orientation

leg weakness, bilateral

lens, dislocation of

leukoencephalopathy, differential diagnosis

Lewy body disease, diffuse

Lhermitte's sign

life expectancy

life support, withdrawal of

limb-girdle weakness

liver function enzymes

liver transplantation

low birth weight

lumbrical muscles

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, paraaortic

lymphocytic interstitial pneumonitis

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

malabsorption syndrome

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, screening for

malformation, Vein of Galen

malignant hyperpyrexia

malignant hypertension

Man-In-The-Barrel syndrome

marche a petits pas

Marfan syndrome

marfanoid skeletal abnormalities

median nerve, lesion of

median nerve, palmar cutaneous branch of

median neuropathy

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, chronic

meningitis, CSF cell count-normal

meningitis, leptospira

meningoencephalitis

mental retardation

mental status, abnormal

methylmalonic acid, serum

microangiopathy, brain

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery territory infarction

middle cerebral artery, emboli to

middle cerebral artery, occlusion of

mitochondrial disease

mitral valve prolapse

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monomelic amyotrophy

mononeuropathy multiplex

mononeuropathy, sensory

monoparesis, focal

motor neuron disease

movement disorder

movement disorder, extrapyramidal

moyamoya, adult

MRI, angiography

MRI, brachial plexus

MRI, CAT scan compared to

MRI, complications with

MRI, contraindications

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, punctate pattern

MRI, spinal cord

MRI, T1 weighted fat suppression

MRI, venography

mucopolysaccharidoses

multiple myeloma

multiple sclerosis

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle spasm, paraspinal

muscle stiffness

muscle strength, testing

muscle tenderness

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, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, congenital, Ullrich

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, familial incidence of

myasthenia gravis, limb-girdle

myasthenic syndrome

mycotic aneurysm

myeloma, osteosclerotic

myeloneuropathy

myelopathy hand

myelopathy, chronic progressive

myocardial biopsy

myocardial infarction

myoclonic jerks

myopathy, autoimmune

myopathy, distal

myopathy, distal, vacuolar

myopathy, hypocalcemic

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, quadriceps

myopathy, vacuolar

myositis ossificans, progressive

myositis, acute of childhood

myositis, ocular

myositis, post infectious

myotonia dystrophica

myotonic discharges

nausea and vomiting

nephrogenic systemic fibrosis

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve enlargement

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neural tube defect

neuritis, heavy metals causing

neurocutaneous disease

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurolymphomatosis

neuromuscular disease, electrodiagnosis of

neuronal migration disorder

neuronopathy, sensory

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

numb clumsy hands syndrome

numbness, extremity

nystagmus, direction fixed

nystagmus, rotary

nystagmus, spontaneous

occupational neurologic disorders

occupational neuropathies

ocular myopathy

oculodentodigital dysplasia

old age, neurology of

opportunistic infection

opportunistic infection, CNS

optic atrophy, bilateral

optic nerve, lesion of

optic neuropathy

orange peel appearance of skin

orbit, lesions of

osteolytic lesion, causes of

osteomyelitis, spinal

overlap syndrome

pacemaker, cardiac-transvenous

pain, abdominal

pain, interscapular

palliative care

Pallister-Hall syndrome

paracentral lobule

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, spastic

paraproteinemia

paresthesias, feet

paresthesias, hands

Parkinson disease

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinsonism syndrome

paroxysmal nonkinesigenic dyskinesia

patient information and support

pectus excavatum

pericardial effusion

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

periventricular leukomalacia

pernicious anemia

personality change

photosensitivity, skin

physical therapy

pigmentary retinopathy

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pleural effusion

polycythemia, secondary

polymerase chain reaction

polymerase chain reaction, false negative

polymyalgia rheumatica

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

pons, lesion of

portal caval shunt

position sensation, abnormal

positive sharp waves

posterior column disease

posterior cortical atrophy

posterior fossa

posterior fossa, lesion of

posterior interosseous neuropathy

postural abnormality

practice guidelines

precentral gyrus

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

primary intracranial hypotension

prisoners of war, neurologic complications in

progressive multifocal leucoencephalopathy

progressive neurologic disorder

prolactin, elevated

proprioception, abnormal

proximal muscle atrophy

pseudohypertrophy

pseudomedian nerve palsy

pseudoperipheral palsy

pseudoradial nerve palsy

pseudoretinitis pigmentosa

pseudoulnar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

ptosis, unilateral

pulmonary infiltrates

pupil, ectopic-congenital

pure motor stroke

pursuit eye movements, abnormal

pyramidal tract dysfunction

quadriceps atrophy

quadriceps weakness

quality of life

radial nerve, palsy of

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

Raynaud's phenomenon

real-time quaking-induced conversion

recruitment, reduced

reflex sympathetic dystrophy

reflex sympathetic dystrophy, children

remote effect of cancer on the nervous system

renal failure, acute

renal tubular acidosis

repetitive nerve stimulation

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retinal detachment

retinitis pigmentosa

Rett's syndrome

reverse split hand sign

rhabdomyosarcoma

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

riboflavin transporter deficiency

rigid spine syndrome

rippling muscle disease

Rolandic artery

root lesion, nerve

saccadic eye movements, abnormal

salivation, excessive

sarcoglycanopathy

scalenus anticus syndrome

scleroderma, neurologic involvement with

scoliosis, neurologic association with

sedimentation rate

sedimentation rate, elevated

seizure, children

seizure, neonatal

seizure, treatment of

sensorimotor stroke

sensorineural hearing loss

sensory loss, asymmetric

sensory loss, cortical

sensory loss, pseudoradicular

sensory loss, truncal

sensory symptoms

sensory testing, quantitative

serologic testing

serologic testing, false negative

shoulder, numbness

shoulder, pain in

simultanagnosia

single photon emission computed tomography

Sjogren's syndrome

skin, discoloration

skin, hyperextensible

skin, lesions in neurologic disorders

skin, temperature difference

skin, thickened

skin, wrinkling in warm water

skull x-ray, abnormal

small vessel disease

sodium valproate

spastic diplegia

speech disorder

speech disorder, childhood

Spielmeyer Vogt syndrome

spinal cord, cervical

spinal cord, compression of

spinal cord, compression, epidural abscess causing

spinal cord, lesion of

spinal cord, vascular malformation of

spinocerebellar ataxia

spinocerebellar ataxia type 7

spirochete infection

splenium of corpus callosum

splinter hemorrhages

spontaneous muscle activity

spontaneous remission

sports medicine, neurology of

square wave jerks

standing difficulty

startle myoclonus

stereotyped behavior

steroid therapy, CNS treatment and complications with

stiff man syndrome

stooped posture

strokelike episodes

subarachnoid hemorrhage

subconjunctival hemorrhage

subcortical U fibers

superior sagittal sinus thrombosis

swallow evaluation

sweating, abnormality of

symmetric brain lesions

sympathetic block

sympathetic nervous system

systemic illness

systemic juvenile idiopathic arthritis

tandem gait, ataxic

Tangier's disease

teeth, abnormal

telangiectases, retinal

thalamus, lesion of

thalamus, lesion of-bilateral

thoracic outlet syndromes

thrombocytopenia

tongue, swelling

toxic encephalopathy

toxic oil syndrome

toxoplasmosis, CNS

transient ischemic attack

travel, foreign

treatment of neurologic disorder

tremor, intention

tremor, postural

tremor, resting

trigeminal nerve, lesion of

trigeminal neuropathy

trinucleotide repeats

type 1 muscle fiber

type 2 muscle fiber

tyrosine hydroxylase deficiency

ulcers, fingertip

ulnar nerve, compression of

ulnar neuropathy

ultrasonography, nerve

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urine test for metabolic disorders

urine test in toxic screen

Usher's syndrome

vertebral erosion

vibratory sensation

vibratory sensation, abnormal

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

visual evoked response

visual field defect

visual fields, confrontation-color

visual fields, confrontation-finger

visual fields, constricted

visual loss, progressive

visuospatial disturbance

vitamin deficiency

voice, abnormality of

Walker-Warburg syndrome

walking, delayed

walking, difficulty with

weakness, congenital

weakness, generalized

weakness, progressive

weakness, proximal

white matter disease

wide based gait

winging of scapula

word-finding difficulty

WORLD spelling test

x-linked mental retardation

x-ray, cervical spine

Showing articles 150 to 175 of 175 << Previous

Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
P. D. , et al, Muscle & Nerve 10:114-120, , 1987

Vertigo and Dizziness
In Diseases of the Nervous System, Asbury, A. K. , et al, W B Saunders, p. 561, Brandt,T., 1986

Clinicopath. Conference
Acquired Immunodeficiency Syndrome, Rhabdomyosarcoma, with Extensive Metastases, Case 9-1986, NEJM 3, 4:620,1986., 1986

Central Nervous System Infections Associated with Hereditary Hemorrhagic Telangiectasia
Am J Med 77:86-92, Press,O.L.W.,et al, 1984

Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship
Neurol 33:267-277, Stein,S.A.,et al, 1983

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Fibrodysplasia Ossificans Progressiva, The Clinical Features & Natural Hx of 34 Pts
J Bone Joint Surg 64B:76-83, Connor,J.M.&Evans,D.A.P., 1982

Confrontation Visual Field Techniques in the Detection of Anterior Visual Pathway Lesions
Ann Neurol 10:28-34, Trobe,J.D.,et al, 1981

Finger Wrinkling after Immersion in Water
BMJ 281:586-587, Alvarez,G.,et al, 1980

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

Skin Wrinkling on Immersion of Hands
Arch Neurol 36:113-114, Braham,J.,et al, 1979

Emery-Dreifuss Muscular Dystrophy
Ann Neurol 5:111-117, Rowland,L.P.,et al, 1979

Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978

Polyneuropathy, Skin Hyperpigmentation, Edema, & Hypertrichosis in Localized Osteosclerotic Myeloma
Neurol 27:675, Iwashita,H.,et al, 1977

Neurologic Aspects of Hereditary Hemorrhagic Telangiectasia
Arch Neurol 34:101, Adams,H.P.,et al, 1977

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

Rigid Spine Syndrome:A Type I Fiber Myopathy
Arch Neurol 34:119, Seay,A.R.,et al, 1977

Neuro Complica of Coeliac Disease & Trop Sprue, Neurology of GI Disease
1974, Major Problems in Neurology V-3, W. B. Saunders Co, Ltd., Pallis,C.A.&Lewis,P.D., 1974

Neurologic Manifest. of Infective Endocarditis:A Review
Stroke 4:958, Greenlee,J.E.,et al, 1973

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Syndromes of Central Motor Disorder
in Vinken, P. J. , Bruyn, G. W. , ed. , Handbook of Clinical Neurology, Vol. 1, North-Holland Publ C, , Amsterdam, 19Rondot, P., 1969

Surgical Anatomy of the Hand
Clinical Symposia,Ciba 21:66-109, Lampe,E.W., 1969

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968

Neurological Disorders Associated with Adult Celiac Disease
Brain 89:683, Cooke,W.T.,et al, 1966

The Cornelia de Lange Syndrome
J Pediatr 63:1000-1020, Ptacek,L.J., 1963

Electric Shocks and Weakness of the Right Hand in a Young Man:Hirayama Disease
, Witiw,C.D.&OToole,J.E.,

Showing articles 150 to 175 of 175 << Previous