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acid maltase deficiency

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

ACTH, ectopic syndrome of

acute intermittant porphyria

Addison's disease

adult polyglucosan body disease

advance directives

advances in neurology

adverse drug reaction

alcoholic polyneuropathy

alpha-fetoprotein

alveolar hypoventilation

Alzheimer's disease

aminoacidopathies

amyloid angiopathy, cerebral

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, childhood

amyotrophic lateral sclerosis, cluster

amyotrophic lateral sclerosis, complications with

amyotrophic lateral sclerosis, conjugal

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, hospitalization

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, myasthenic syndrome with

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, post-encephalitic

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, sensory symptoms in

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis, work up

amyotrophic lateral sclerosis-like syndrome

aneurysm, cavernous sinus

aneurysm, internal carotid artery

animal exposure

ankle reflex, preserved

ankylosing spondylitis

anterior horn cell disease

anterior interosseous neuropathy

anterior spinal artery infarction

anterior tibial muscle weakness

anti citrullinated antibody

anti Hu antibody

antibodies to voltage-gated calcium channels

anticonvulsants

antiviral agents

aphasia, progressive, primary

apraxia of eye movements

arrhythmia, cardiac

arterial dissection

arterial dissection, aorta

arterial dissection, vertebral

arthrogryposis multiplex

ascending paralysis

asthma, poliomyelitis-like syndrome with

ataxia telangiectasia

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

athetosis, causes of

atlanto axial dislocation, congenital

autoimmune disease

autonomic dysfunction

axonal degeneration

basal ganglia, calcification of

basal ganglia, lesion of

behavioral disorder

Bence Jones protein

benign congenital hypotonia

biologic markers

bitemporal visual field defect

bladder dysfunction

bone marrow biopsy

botulinum toxin

botulinum toxin, complications of

brachial amyotrophic diplegia

brachial neuritis

brainstem, infarction of

brainstem, lesion of

bright tongue sign

Brown Sequard syndrome

Brugada syndrome

bulbar palsy, acute

bulbar palsy, childhood

bulbar palsy, progressive

calcification, intracranial

calcium channel dysfunction

calf hypertrophy

carbon monoxide poisoning

carcinoembryonic antigen

carcinoma of breast

carcinoma of lung

carpo-pedal spasm

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

cavernous sinus, syndrome

central core disease

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar vermis

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral peduncle

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, young adult

cerebrovascular disease, cardiovascular disease with

cervical collar

cervical osteoarthritis

cervical osteophyte

cervical spine injury

cervical spine injury, treatment of

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

Charcot-Marie-Tooth

chest x-ray, abnormal

chewing, impaired

Chinese paralytic syndrome

chorea, Sydenham's

choreoathetosis

chromosomal abnormality

chronic polyneuritis, children

chronic progressive external ophthalmoplegia

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

cluster, geographic

cold temperature

compression neuropathy

conduction block

congenital heart disease

congenital myopathy

congestive heart failure

controversies in neurology

conversion reaction

cortical hand knob

cost effectiveness

coxsackievirus, myopathy with

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

crying, pathologic

Cushing's syndrome

cycad seed flour

cyclophosphamide

degenerative diseases of CNS

Dejerine-Sottas syndrome

delay in diagnosis

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

denervation of muscle

denervation potentials

dentatorubral-pallidoluysian atrophy

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic mononeuropathy

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

differential diagnosis

difficulty climbing stairs

diplegia, atonic

diplegia, brachial

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

dropped head syndrome

drug interactions

electrical injury of nervous system

electrical sensation

electrocardiogram, abnormal

electromyogram, decremental response

electron microscopy

electrophoretic pattern, serum

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, central European

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalomyeloneuritis

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, post anoxic

endocarditis, subacute bacterial

enterovirus infection of CNS

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

ethics in neurology

evidence-based research

evoked potentials

exercise intolerance

extremity, cold

eye movement, disorders of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fasciculation, benign

fatigable chewing

Fazio-Londe's disease

fine motor function, impaired

finger weakness

flaccid paralysis

flail arm syndrome

flu-like illness

football neurologic injuries

fragile-X syndrome

Friedreich's ataxia

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontotemporal dementia, behavioral variant

F-wave response

gag reflex, depressed

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastrectomy, neurologic complications following

gastrostomy, percutaneous endoscopic

gaze palsy, horizontal

gaze palsy, supranuclear

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glycogen storage disease

GM1 ganglioside

GM1 ganglioside antibodies

granular atrophy, cerebral cortex

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

Gulf War syndrome

hallucination, auditory

handlebar palsy

Hand-Schuller-Christian disease

health insurance

heavy metal intoxication

hemifacial atrophy

hemiplegia, progressive

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

heterochromia iridis

highly active antiretroviral therapy

history of neurology

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

Horner's syndrome

Horner's syndrome, etiologies of

human immunodeficiency virus type 1

human T-lymphotropic virus type I(HTLV-I)

Huntington's chorea

hyperadrenalism

hyperinsulinism

hyperparathyroidism

hyperpigmentation of skin

hyperthyroidism

hypogammaglobulinemia

hypoglycemic coma

hypokalemic alkalosis

hypokalemic periodic paralysis

hypoparathyroidism

hypotension, systemic

hypothalamus, disturbance of

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

immune complexes

immunodeficiency

immunoelectrophoresis, serum

immunohistochemistry

immunologic disease

immunosuppression

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, ubiquitin

inclusion body myositis

incontinentia pigmenti

infant, evaluation of

infantile neuronal degeneration

infantile tremor syndrome

inflexibility, mental

intellectual deficit

intellectual deterioration

intermittent positive pressure breathing

internal capsule

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Isaacs syndrome

islet cell tumor

Jackson's syndrome

Jakob-Creutzfeldt disease

jaw closure weakness

jaw jerk, abnormal

juvenile distal and segmental muscular atrophy

Kearns-Sayre syndrome

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

laboratory values, normal

lactic acidemia

laminectomy, cervical

laughing, pathologic

lead and the nervous system

Leber's hereditary optic neuropathy

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

leukemia, neurologic findings assoc.with

leukoencephalopathy

level of consciousness, decreased

Lewy body disease, diffuse

Lhermitte's sign

lid closure, weakness of

life expectancy

life support, withdrawal of

life support, withholding of

life sustaining treatment

limbic encephalitis

locked-in syndrome

lumbar puncture

lymphadenopathy

lymphadenopathy, hilar

lymphoma involving CNS

lysosomal storage disease

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

Man-In-The-Barrel syndrome

masseter muscle wasting

masseter muscle weakness

median neuropathy

medical-legal aspects of neurology

memory, defect of recent

memory, impairment of

mental retardation

mental status, abnormal

metabolic disorder, primary

Millard Gubler syndrome

minimally conscious state

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve lesion

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy, motor

Motor Band Sign

motor neuron disease

motor neuron disease, juvenile form

motor neuron disease, misdiagnosis

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, extrapyramidal

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, functional

MRI, gradient-echo

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

multiple myeloma

multiple sclerosis

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle hypertrophy

muscle relaxant

muscle stiffness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, neurogenic hypothesis of

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, treatment of

myasthenic crisis

myasthenic syndrome

myelitis, longitudinal

myelitis, transverse

myelogram, cervical

myeloneuropathy

myelopathy, ischemic

myelopathy, carcinomatous

myelopathy, chronic progressive

myelopathy, necrotizing

myelopathy, radiation induced

myeloradiculitis

myeloradiculopathy

myocardial infarction

myocardial injury

myopathy, carcinomatous

myopathy, centronuclear

myopathy, distal

myopathy, mitochondrial

myopathy, neurogenic hypothesis of

myopathy, quadriceps

myopathy, thyroid disease causing

myotonia congenita

myotonia dystrophica

myxedema, neurologic manifestations of

N-acetyl-L-aspartic acid

narcotic analgesics

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve conduction studies

nerve conduction studies, motor

nerve growth factor

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurogenic bladder

neurogenic vs.myopathic atrophy

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, incurable

neurologic evaluation

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal migration disorder

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, acute

neuropathy, amyloid

neuropathy, bicycle

neuropathy, diabetic

neuropathy, diphtheritic

neuropathy, hereditary peripheral

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, short-fiber

neuroprotective agents

neurotransmitter

newborn, evaluation of

next-generation sequencing

NMDA antagonists

nystagmus, primary position of gaze

nystagmus, rotary

occupational neurologic disorders

occupational neuropathies

ocular motility, disorders of

old age, neurology of

olivary degeneration, hypertrophic

Onufrowicz nucleus

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, total

Oppenheim muscular dystrophy

optic neuropathy

otitis, neurologic complications with

owl's eye sign of spinal cord

pain, increased response

pain, management of chronic

palatal myoclonus

palliative care

paralysis, acute

paralysis, acute areflexic

paralysis, asymmetric

paralysis, use-related

paraneoplastic ganglionopathy

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, flaccid

paraparesis, spastic

paraproteinemia

paraspinal muscle

parathyroid adenoma

paratrigeminal syndrome

Parkinson disease

Parkinson disease, motor neuron disease with

Parkinson disease, treatment of

Parkinsonism syndrome

Parkinsonism-dementia complex

paroxysmal neurologic deficits

patient information and support

periodic paralysis

periodic paralysis, thyrotoxic

peripheral vascular disease

peroneal muscle atrophy, causes of

peroxisomal disease

persistent vegetative state

personality change

pheochromocytoma

phrenic nerve pacemaker

physical activity

physical therapy

physician assisted suicide

pigmentary retinopathy

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

poliomyelitis, provocation

poliomyelitis-like illness

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

positive sharp waves

post polio syndrome

posterior fossa, differential diagnosis of lesions of

posterior inferior cerebellar artery syndrome

posterior interosseous neuropathy

practice guidelines

pregnancy, neurologic complications in

prevention of neurologic disorders

primary aldosteronism

primary lateral sclerosis

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

proprioception, abnormal

proximal muscle atrophy

pseudoathetosis

pseudobulbar palsy

pseudohypertrophy

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary embolism

pulmonary function tests

pupil, abnormality in neurologic disorders

pyramidal tract

pyramidal tract dysfunction

quadriceps atrophy

quadriceps weakness

quality of life

rabies, nervous system involvement with

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, salivary gland

ragged-red fibers

rapidly progressing neurologic illness

recombinant DNA

Refsum's disease

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

repetitive nerve stimulation

respiratory arrest

respiratory depression

respiratory failure

respiratory tract infection

retinitis pigmentosa

retrograde axonal flow

reverse split hand sign

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

risk-benefit assessment

Roussy Levy syndrome

saccadic eye movements, abnormal

salivation, excessive

scoliosis, neurologic association with

segmental demyelination

seizure, children

seizure, treatment of

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory symptoms

sensory testing

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum alanine aminotransferase

shell fish poisoning

shoulder, subluxation

single photon emission computed tomography

skin, lesions in neurologic disorders

sleep pathology and physiology

Smell Identification Test

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

speech disorder

speech, loss of

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, infarction of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, intramedullary

spinal cord, pathologic exam 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 degeneration

sports medicine, neurology of

standing difficulty

stem cell tourism

stem cell transplantation

stereotyped behavior

sternocleidomastoid muscle

stiff man syndrome

subacute myelo-opticoneuropathy(S.M.O.N.)complex

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

subdural hematoma

superoxide dismutase

survival motor neuron gene

syphilis, neurologic complications with

tandem gait, ataxic

temporal lobe, atrophy

temporalis muscle wasting

tensilon test, false positive

testicular atrophy

thalamus, lesion of

thoracic outlet syndromes

thrombophlebitis

thyrotropin-releasing hormone

tick-borne encephalitis

Tolosa Hunt syndrome

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

treatment of neurologic disorder

tremor, postural

triangle of Guillain and Mollaret

tricresylphosphate

trinucleotide repeats

Trousseau's sign

tuberous sclerosis

ulnar nerve, deep palmar branch of

ulnar neuropathy

unconsciousness

unconsciousness, episodic

unconsciousness, transient

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

venous thrombosis, non-cerebral

vestibular function, tests of

viral infection

viral infection, CNS

viral isolation

visual field defect

vitamin E deficiency

Waldenstrom's macroglobulinemia

walking, difficulty with

watershed infarcts

weakness, acute

weakness, fatiguable

weakness, generalized

weakness, infant

weakness, progressive

weaning from respirator, failure to

Weber's syndrome

Werdnig-Hoffman disease

West Nile fever

whistle, inability to

white matter disease

winging of scapula

word-finding difficulty

X-linked bulbospinal neuronopathy

Showing articles 1450 to 1500 of 7468 << Previous Next >>

Respiratory Muscle Function and Ventilatory Control in Patients with Myotonic Dystrophy
Q J Med 202:205-226, Serisier,D.E.,et al, 1982

Necrotizing Myopathy Associated with Steroid Therapy, Report of Two Cases
Pathology 14:435-438, Ojeda,V.J., 1982

Hypersomnia Associated with Alveolar Hypoventilation in Myotonic Dystrophy
Neurol 31:1336-1337, Hansotia,P.,et al, 1981

Changes in the Basal Ganglia Following Cyanide Poisoning
J Comput Assist Tomogr 5:755-756, Finelli,P.F., 1981

Use of Radiologic Modalities in Coccidioidal Meningitis
Arch Int Med 141:75-78, Stadalnik,R.C.,et al, 1981

Meningeal Gliomatosis:A Review of 12 Cases
Ann Neurol 8:605-608, Young,W-k.A.,et al, 1980

Poliomyelitis-like Syndrome Associated with Asthma
Arch Neurol 37:52-53, Wheeler,S.D.,et al, 1980

Juvenile Muscular Atrophy Localized to Arms
Arch Neurol 37:297-299, Singh,N.,et al, 1980

Electrocardiogram Abnormalities in Carriers of Duchenne Muscular Dystrophy
Neurol 30:497-501, Lane,R.J.M.,et al, 1980

Echocardiographic Evaluation of Cardiac Abnormalities in Duchenne's Dystrophy & Myotonic Muscular Dystrophy
Arch Neurol 37:273-277, Reeves,W.C.,et al, 1980

Horner Syndrome with Causalgia
Neurol 30:534-535, Bernad,P.G.,et al, 1980

Multiple Vertebral Hemangiomas Resembling Metastases with Spinal Cord Compression
Arch Neurol 37:247-248, Zito,G.,et al, 1980

Unusual Effects of Metrizamide Lumbar Myelography
Arch Neurol 37:588-589, Kelley,R.E.,et al, 1980

Demyelinating Radiculopathy in the Kearns-Sayre Syndrome:A Clinicopathological Study
Ann Neurol 8:373-380, Groothuis,D.R.,et al, 1980

Clinical Aspects of CNS Cysticercosis
Arch Int Med 140:1309-1313, Shanley,J.D.,et al, 1980

Acne Fulminans with Inflammatory Myopathy
Neurol 8:67-69, Noseworthy,J.H.,et al, 1980

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

Computerised Tomography as an Indication of Long-Term Outcome After Acute Carbon Monoxide Poisoning
Lancet 1:783-784, Sawada,Y.,et al, 1980

Acute Carbon Monoxide Poisoning:Computed Tomography of the Brain
AJNR 1:399-402, Kim,K.S.,et al, 1980

Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979

Deficiency of Arylsulfatase B in 2 Brothers Aged 40 & 38 Years (Maroteaux-Lamy Syndrome, Type B)
Ann Neurol 6:315-325, Pilz,H.,et al, 1979

Muscular Dystrophy in Six Young Girls
Neurol 29:1486-1491, Hazama,R.,et al, 1979

Creatine Phosphokinase MB Band In Oculopharyngeal Muscular Dystrophy
(Letter) NEJM 301:270979., Diskin,C.J., 1979

Extraocular Muscle Biopsy in Chronic Progressive External Ophthalmoplegia
Ann Neurol 6:326-339, Ringel,S.P.,et al, 1979

Chronic Progressive Myelopathy:Investigation with CSF Electrophoresis, Evoked Potentials, & CT Scan
Ann Neurol 6:419-424, Patty,D.W.,et al, 1979

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

Lymphocyte Capping in Muscular Dystrophy
Neurol 29:1419-1421, Hauser,S.L.,et al, 1979

Basal Ganglia Calcification in Kearns-Sayre Syndrome
Arch Neurol 36:711-713, Robertson,W.C.Jr., 1979

Acute Anterior Myelitis Complicating West Nile Fever
Arch Neurol 36:172-173, Gadoth,N.,et al, 1979

Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
Neurol 29:448-457, Chen,J.R.,et al, 1979

Progressive Myelopathy Due to Extramedullary Hematopoiesis:Case Report & Review of the Literature
Ann Neurol 5:485-489, Stahl,S.M.,et al, 1979

Computed Tomography in a Verified Case of Tuberculous Meningitis
Neurol 29:384-386, Arimitsu,T.,et al, 1979

Familial Chorea & Myoclonus Epilepsy
Neurol 28:913-919, Takahata,N.,et al, 1978

Peripheral Neuropathy in Myotonic Dystrophy
Arch Neurol 35:741-745, Olson,N.D.,et al, 1978

Deformed Erythrocytes in Muscular Dystrophies
Neurol 28:842-844, Grassi,E.,et al, 1978

Erythrocyte Metabolism in Muscular Dystrophy
Arch Neurol 35:592-595, Danon,M.J.,et al, 1978

Alteration in Erythrocyte Membrane Structure in Duchenne Muscular Dystrophy
Ann Neurol 4:253-256, Wakayama,Y.,et al, 1978

Systemic Membrane Defect in the Proximal Muscular Dystrophies
NEJM 299:841-846, Pickard,N.A.,et al, 1978

Pineal Tumors
Arch Neurol 35:736-740, Donat,J.F.,et al, 1978

Medical Implications of Computed Tomography ("Cat scanning")
NEJM 298:255, Abrams,H.L.,et al, 1978

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Kearns-Sayre Syndrome & Hypoparathyroidism
Ann Neurol 3:455, Pellock,J.M.,et al, 1978

Central Nervous System Lesions in Childhood Leukemia
Neurol 28:678, Crosley,C.J.,et al, 1978

The Cervical Myelopathy Associated with Rheumatoid Arthritis:Analysis of 32 Patients, with Two Post-mortem Cases
Ann Neurol 3:144, Nakano,K.K.,et al, 1978

Jamaica Ginger Paralysis
Arch Neurol 35:530, Morgan,J.P.,et al, 1978

Cerebral Cysticercosis
Neurol 28:838-842, Latovitzki,N.,et al, 1978

Hypoglossal Nerve Palsy in Infectious Mononucleosis
Neurol 28:844-847, DeSimone,P.A.,et al, 1978

Clinical Pathological Conference
Meningitis, listeria monocytogenes, Case Record 40-1978, NEJM 299:819-82678., , 1978

Cervical Myelopathy Due to Ossification of the Posterior Longitudinal Ligament
Arch Neurol 35:33, Murakami,N., 1978

Tuberculous Meningitis
Br J Hos Med Nov. 1977, p. 436., , 1977

Showing articles 1450 to 1500 of 7468 << Previous Next >>