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Neurology Specific Literature Search

Differential
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abscess, intracerebral

acoustic nerve, vestibular division of

acoustic neurinoma

acquired immunodeficiency syndrome

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

Alexanders disease

alternating hemiplegia

alternating hemiplegia of childhood

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, early onset

Alzheimer's disease, familial

Alzheimer's disease, familial, late onset

Alzheimer's disease, pathogenesis

Alzheimer's disease, risk factors in

Alzheimer's disease, treatment of

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

amyloid beta protein

amyloid plaques

amyotrophic lateral sclerosis

anaplastic large cell lymphoma

anemia, hemolytic

anesthesia, general

aneurysm, intracranial, screening for

Angelman syndrome

angiofibroma, facial

angiomyolipomas

animal exposure

anterior horn cell disease

anterior tibial muscle weakness

antibiotic prophylaxis

antibodies to voltage-gated calcium channels

anticonvulsants

anticonvulsants, selection of

antiviral agents

apolipoprotein E

aromatic amino acid decarboxylase deficiency

arrhythmia, cardiac

arteriovenous malformation, cerebral

arthrogryposis multiplex

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, truncal

ataxic-dystonia syndromes

atrioventricular block

attention deficit disorder with hyperactivity

autoimmune basal ganglia encephalitis

autoimmune disease

automatic implantable cardioverter-defibrillator

autonomic dysfunction

azidodeoxythymidine

bacterial infection

bacterial infection, CNS

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavior, combative

behavioral disorder

biologic markers

biotinidase deficiency

bitemporal visual field defect

bladder dysfunction

brachial neuritis

brachial plexus

brachial plexus neuropathy

brachial plexus neuropathy, familial

brain biopsy, negative

brainstem, atrophy

brainstem, lesion of

burning paresthesia

cafe au lait spots

calcification, gyral

calcification, intracranial

calf hypertrophy

Canavan's disease

candida albicans

carcinoma of pancreas

CAT scan, abdomen

CAT scan, abnormal

CAT scan, chest

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, muscle

cavernous hemangioma

Central America

central core disease

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellum, neoplasms of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema, origin and treatment

cerebral edema, vasogenic

cerebral embolism

cerebral palsy, etiology

cerebral palsy, work up

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, beta-D-glucan

cerebrospinal fluid, biochemical markers of CNS tumors

cerebrospinal fluid, childhood

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, proteincytologic dissociation

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, cryptogenic

cerebrovascular accident, familial occurrence

cerebrovascular accident, multiple

cerebrovascular accident, silent

cerebrovascular accident, young adult

cerebrovascular disease

ceruloplasmin, serum

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chewing, impaired

chloride channel dysfunction

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cingulate gyrus

Clinical Pathologic Conference(C.P.C.)

clinical trials

clubbing of fingers

clubfoot as related to neurologic disease

cobalamin C deficiency

collagen vascular disease

coma, sudden onset

compression neuropathy

compression neuropathy, recurrent

conduction block

confidentiality

congenital malformation

congenital myasthenic syndromes

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

conjunctival biopsy

contractures, joint

controversies in neurology

corpus callosum

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical ribbon sign

cranial nerve enhancement

cranial nerve tumor

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cultured skin fibroblasts

cyst, benign intracranial

cyst, cortical parenchyma

cyst, parenchymal

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental abnormality of brain

developmental disability

developmental evaluation

developmental retardation

diabetes mellitus

diagnostic criteria

dichlorphenamide

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

disease modifying agents

distal muscle atrophy

distal muscle weakness

diurnal variation

dopa responsive dystonia

dopaminergic dysfunction

double-cortex syndrome

drug induced neurologic disorders

dysdiadochokinesia

dystonia musculorum deformens

dystonia, children

dystonia, etiology of

dystonia, painful

dystroglycanopathies

dystrophin associated proteins

eating disorder

Ehlers-Danlos syndrome

Ehlers-Danlos syndrome, classification

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, inflammatory disease

electron microscopy

Emery-Dreifuss muscular dystrophy

emotional lability

encephalitis, autoimmune

encephalitis, diagnosis of

encephalitis, viral

encephalitis, viral-causes of

encephalopathy, acute

encephalopathy, progressive

endolymphatic sac tumors

endovascular therapy

epidemiology of neurology

esophageal varices

ethics in neurology

evoked potentials

executive dysfunction

exercise intolerance

exome sequencing

eye movement, disorders of

Fabry's disease

facial appearance, abnormal

facial expression abnormality

facial weakness

facial weakness, bilateral

failure to thrive

fatal familial insomnia

feeding disorder

fibroma, ungual

fine motor function, impaired

fingerprint bodies

fistula, arterio-venous, pulmonary

foot drop, bilateral

fourth ventricle, compression

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

fundus, abnormality of

funduscopic exam

fungal infection

fungal infection, CNS

gangliosidosis GM1

gangliosidosis GM2

gastrointestinal bleeding

Gaucher's disease

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

giant axonal neuropathy

glioblastoma multiforme(astrocytoma Gr.III)

glioma, low-grade

gliomatosis cerebri

globus pallidus, lesion of, bilateral

glucocerebrosidase

GLUT1 deficiency syndrome

glycogen storage disease

gram positive cocci

growth hormone deficiency

growth retardation

Guillain Barre syndrome

gyrus, abnormal

headache, awakening with

headache, positional

headache, progressive

heart block, complete

helminthic infection of CNS

hemangioblastoma

hemianopia, homonymous

hemiparesis, transient

hemoglobin abnormality, neurologic complications of

hemophagocytic lymphohistiocytosis

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herniation syndromes, intracranial

hexosaminidase-A

high arched feet

high arched palate

histochemistry of muscle

history of neurology

human herpesvirus 6

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's chorea, presymptomatic detection of

hydrocephalus, non-communicating(obstructive)

hyperammonemic encephalopathy

hyperhomocysteinemia

hyperkalemic periodic paralysis

hypoalbuminemia

hypoglycorrhachia

hypogonadism, hypogonadotropic

hypokalemic periodic paralysis

hypopigmentation of skin

hypotonia, causes of

hypotonia, infants

immunodeficiency

immunohistochemistry

immunosuppressive agents

in situ hybridization

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

inclusion body myositis

infantile spasm

insular cortex, lesion

intellectual deficit

intellectual deterioration

interstitial pulmonary fibrosis

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial pressure, increased

intranasal medication

intrauterine infection

intrauterine infection, viral

intravenous drug abuse

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

joint hypermobility

Kayser-Fleischer ring

Kearns-Sayre syndrome

Krabbe's disease

lactic acidemia

Lafora's disease

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

leg spasms, painful

leg weakness, bilateral

Legius syndrome

Leigh's disease

Lesch-Nyhan syndrome

leukoencephalopathy

leukoencephalopathy with calcification and cysts

level of consciousness, decreased

lid abnormalities

life expectancy

lipid storage disorder of CNS

liver function enzymes

lung-brain syndromes

lymphadenopathy

lymphangiomyomatosis

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, screening for

malignant hyperpyrexia

marche a petits pas

McArdle's disease

McLeod syndrome

medulloblastoma

memory, impairment of

meningeal enhancement

meningeal sarcomatosis

meningitis, basilar

meningitis, candida

meningitis, chronic

meningitis, fungal

meningitis, leptospira

meningitis, neutrophilic

meningoencephalitis

mental retardation

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

methylmalonic acidemia

microhemorrhage, intracerebral

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Miller-Dieker syndrome

Mini Mental Status Examination

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

molecular genetics

molecular markers

mononeuropathy, recurrent

motor neuron disease

movement disorder

moyamoya, adult

MRI, angiography

MRI, blooming effect

MRI, contrast enhanced

MRI, diffusion weighted

MRI, mass effect on

MRI, nodular enhancement

MRI, spinal cord

MRI, target sign

multiple sclerosis

muscle atrophy, progressive

muscle diseases, characteristics of

muscle hypertrophy

muscle phosphorylase deficiency

muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, neurogenic hypothesis of

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelin protein zero gene

myelitis, longitudinal

myeloneuropathy

myoclonic jerks

myoclonus, epilepsy

myopathy, centronuclear

myopathy, distal

myopathy, distal Laing

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, mitochondrial

myopathy, proximal

myopathy, vacuolar

myotonia congenita

myotonia dystrophica

myotonia dystrophica, classification

myotonia dystrophica, type 2

nasal bridge, wide

nausea and vomiting

nemaline rod myopathy

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, peripheral nerve

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-surgical treatment of

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

nerve biopsy, indication

nerve conduction studies

nerve hypertrophy

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination, focal

neurologic practice

neurologic signs

neurologic testing

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal migration disorder

neuroophthalmology

neuropathology, brain

neuropathy, amyloid

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, peripheral

neuropathy, recurrent

neuropathy, work up for

newborn, evaluation of

next-generation sequencing

Niemann-Pick disease

night blindness

numbness, extremity

obsessive-compulsive disorder

ocular motility, disorders of

oculogyric crisis

oculopharyngeal muscular dystrophy

oligodendroglioma

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, hereditary

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

ornithine transcarbamylase deficiency

orthostatic hypotension

ovarian dysgenesis

overlap syndrome

owl's eye sign of spinal cord

pacemaker, cardiac-transvenous

paraparesis, familial spastic

paraparesis, spastic

parasitic infection, CNS

Parkinson disease

Parkinson disease, etiology of

Parkinson disease, familial

Parkinson disease, pathogenesis of

Parkinson disease, treatment of

Parkinsonism syndrome

paroxysmal neurologic deficits

patient information and support

percussion induced muscle contraction

periodic paralysis

peripheral blood smear

Perrault syndrome

personality change

pheochromocytoma

philtrum, tented

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pleural effusion

polyglucosan body disease

polymerase chain reaction

polyneuropathy, familial

pons, lesion of

positive sharp waves

posterior fossa, lesion of

postural abnormality

potassium channel dysfunction

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

presenilin-1 gene

presenilin-2 gene

prevention of neurologic disorders

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

proximal muscle atrophy

proximal myotonic myopathy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychotic behavior

ptosis, bilateral

pulmonary embolism

pupil, dilated and fixed, bilateral

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quality of life

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

ragged-red fibers

rapidly fatal neurologic illness

recombinant DNA

renal cell carcinoma

respiratory failure

respiratory tract infection

retina, abnormal

retinal hamartoma

retinal hemangioma

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

rhabdomyoma, cardiac

rhabdomyosarcoma of heart

root lesion, nerve

Rosenthal fibers

saccadic eye movements, abnormal

salivation, excessive

scotoma, central

sedimentation rate, elevated

seizure, laughing as manifestation

seizure, paradoxical

seizure, treatment of

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

shunt procedure, ventricular

shunt procedure, ventricular-complications of

sickle cell disease

skin, darkening of

skin, hyperextensible

skin, lesions in neurologic disorders

skin, translucent

sleep pathology and physiology

slit lamp examination

small vessel disease

sodium channel dysfunction

spastic paraplegia, type 7

speech disorder

speech, absence of

spinal cord degeneration

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, intramedullary

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 6

spinocerebellar degeneration

spirochete infection

spongy degeneration of brain

SPRED1 mutation

status epilepticus

striatal encephalitis

strokelike episodes

subarachnoid hemorrhage

subependymal nodules

substantia nigra

survival motor neuron gene

symmetric brain lesions

systemic illness

T cell lymphoma

tandem gait, ataxic

Tay-Sachs disease

telangiectases, retinal

temper tantrums

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

thalamus, lesion of

thalamus, lesion of-bilateral

thalassemia/mental retardation syndrome

thiazide diuretic

thrombocytopenia

tomaculous neuropathy

tongue, protrusion of

travel, foreign

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trichopoliodystrophy

trientine dihydrochloride

trinucleotide repeats

tuber, cortical

tuberous sclerosis

tuberous sclerosis, screening for

tumefactive lesion

ultrasonography, head

ultrasonography, head, fetus-neonate

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

urinary catecholamines

urinary urgency

urine test for metabolic disorders

vestibular migraine

viral infection

viral infection, CNS

vision loss, sequential

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual impairment

visual loss, progressive

visual loss, slow

visual loss, transient

visual obscurations, transient

visuospatial disturbance

vitamin E deficiency

Von Hippel Lindau

Von Hippel Lindau, carrier

Von Hippel Lindau, screening protocol for

walking, delayed

walking, difficulty with

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

Western immunoblot test

Whipple's disease

white matter disease

white matter disease, unilateral

whole genome sequencing

wide based gait

winging of scapula

wound healing, poor

X-linked bulbospinal neuronopathy

x-linked intellectual deficit

x-linked mental retardation

Zika virus infection

Showing articles 1400 to 1450 of 1775 << Previous Next >>

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

Normal Caudate Glucose Metabolism in Persons at Risk for Huntington's Disease
Arch Neurol 44:254-257, Young,A.B.,et al, 1987

Reduced Cerebral Glucose Metabolism in Asymptomatic Subjects at Risk for Huntington's Disease
NEJM 316:357-362, Mazziotta,J.C.,et al, 1987

Effective Strategy for Prenatal Prediction of Duchenne & Becker Muscular Dystrophy
Lancet 2:1294-1296, Forrest,S.M.,et al, 1987

Ocular Complications of Tangier Disease
Am J Med 83:991-994, Pressley,T.A.,et al, 1987

Prediction of Cerebral Palsy in Very Low Birthweight Infants:Prospective Ultrasound Study
Lancet 2:593-596, Graham,M.,et al, 1987

MR Imaging in a Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 11:1057-1058, Tanfani,G.,et al, 1987

Cervicomedullary Compression in Young Patients with Achondroplasia:Value of Neurologic & Respiratory Eval
J Pediatr 110:522-530, Reid,C.S.,et al, 1987

The Autosomal Dominant Form of"Pure"Familial Spastic Paraplegia:Clinical Findings & Linkage Analysis of a Pedigree
Neurol 37:910-915, Boustany,R.M.N.,et al, 1987

MR Imaging of Pelizaeus-Merzbacher Disease
J Comput Assist Tomogr 11:591-593, Penner,M.W.,et al, 1987

Magnetic Resonance Imaging in Pelizaeus-Merzbacher Disease
Neuroradiology 29:403-405, Journel,H.,et al, 1987

Neurofibromatosis
Editorial, Lancet 1:663-6641987., , 1987

Renal Cell Carcinoma in von Hippel-Lindau Syndrome
Am J Med 82:236-238, Malek,R.S.,et al, 1987

Adrenoleukodystrophy:Dietary Oleic Acid Lowers Hexacosanoate Levels
Ann Neurol 21:230-231, 232-2391987., Rizzo,W.B.,et al, 1987

A New Dietary Therapy for Adrenoleukodystrophy:Biochemical & Preliminary Clinical Results in 36 Patients
Ann Neurol 21:230-231, 240-2491987., Moser,A.B.,et al, 1987

Familial Occurrence of Spontaneous Dissection of the Internal Carotid Artery
Stroke 18:246-251, Mokri,B.,et al, 1987

Cerebral Amyloid Angiopathy, A Critical Review
Stroke 18:311-324, Vinters,H.V., 1987

Hereditary Neuropathy with Liability to Pressure Palsies
In Handbk of Clin Neurol, Elsevier Sci Publ Co, NY 51:551-562987., Cherry,S.&Mayer,R.F., 1987

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
McGraw-Hill Book Co, NY, p1251986., Munsat,T.L., 1986

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

Familial Hyperlipidemia in Stroke in the Young
Stroke 17:1142-1145, Bansal,B.C.,et al, 1986

Huntington's Disease, Pathogenesis & Management
NEJM 315:1267-1276, Martin,J.B.&Gusella,J.F., 1986

Computed Tomography of Familial Pineoblastoma
J Comput Assist Tomogr 10:32-33, Peyster,R.G.,et al, 1986

Inherited Multiple Meningiomas:A Clinical, Pathological & Cytogenetic Study of an Affected Family
JNNP 49:362-368, Battersby,R.D.E.,et al, 1986

On Heredity, Twins, & Parkinson's Disease
Ann Neurol 19:409-411, Duvoisin,R.C., 1986

Parkinson's Disease in Monozygotic Twins
Ann Neurol 19:405-408, Jankovic,J.&Reches,A., 1986

Monozygotic Twins with Parkinson's Disease
Ann Neurol 19:402-405, Koller,W.,et al, 1986

Infantile Bilateral Striatal Necrosis, Clinicopathological Classification
Arch Neurol 43:677-680, Mito,T.,et al, 1986

Familial Amyloidosis with Cranial Neuropathy & Corneal Lattice Dystrophy
Neurol 36:432-435, Darras,B.T.,et al, 1986

Familial Association of Intracranial Aneurysms & Multiple Congenital Anomalies
Arch Neurol 43:30-33, Berg,H.W.M.,et al, 1986

Chronic Demyelinating Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Ann Neurol 20:89-91, Argov,Z.,et al, 1986

Recurrent Cerebral Infarctions in Two Brothers with Antiphospholipid Antibodies that Block Coagulation Reactions
Stroke 17:98-102, Jacobson,D.M.,et al, 1986

Cerebrospinal Fluid Findings in Healthy Siblings of Multiple Sclerosis Patients
Neurol 36:727-729, Duquette,P.&Charest,L., 1986

Alzheimer's Disease
NEJM 314:964-973, Katzman,R., 1986

Narcolepsy & Immunity
BMJ 292:359-360, Parkes,J.D.,et al, 1986

Autosomal Dominant Osteosclerosis Associated with Familial Spinal Canal Stenosis
Neurol 36:687-692, Yasuda,Y.,et al, 1986

Adynamia Episodica & Paralysis Periodica Paramyotonica
Neurol 36:682-686, Ricker,K.,et al, 1986

Neurological Manifestations in Xeroderma Pigmentosum
Ann Neurol 20:70-75, Mimaki,T.,et al, 1986

Successful Treatment with Tocainide of Recessive Generalized Congenital Myotonia
Ann Neurol 19:501-504, Streib,E.W., 1986

Familial Adult Motor Neuron Disease:Amyotrophic Lateral Sclerosis
Neurol 36:511-517, Mulder,D.W.,et al, 1986

Myasthenia Gravis in Identical Twins
Neurol 36:78-80, Murphy,J.&Murphy,S.F., 1986

Clinicopathological Conference
Paget's Disease of Bone, Giant-Cell Reparative Granuloma, Case 1-1986, NEJM 314:105-11386., , 1986

Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986

Location of the Gene for X-Linked Spinal Muscular Atrophy
Neurol 36:1595-1598, Fischbeck,K.H.,et al, 1986

Transketolase Abnormality in Tolazamide-Induced Wernicke's Encephalopathy
Neurol 36:1508-1510, Mukherjee,A.B.,et al, 1986

Ornithine Transcarbamylase Deficiency-A Cause of Bizarre Behavior in a Man
NEJM 315:744-747, DiMagno,E.P.,et al, 1986

Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
Neurol 36:1424-1428, Nygaard,T.C.&Duvoisin,R.C., 1986

Familial Long Thoracic Nerve Palsy:A Manifestation of Brachial Plexus Neuropathy
Neurol 36:1251-1253, Phillips,L.H., 1986

Bone-Marrow Transplantation for Neurovisceral Storage Disorders
Editorial, Lancet 2:788-7891986., , 1986

Showing articles 1400 to 1450 of 1775 << Previous Next >>