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Differential
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abdominal distention

abdominal reflex, absent

abducens nerve paralysis

abscess, intracerebral

aceruloplasminemia

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome myelopathy

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

acute disseminated encephalomyelitis

acute disseminated encephalomyelitis, multiphasic

acute respiratory distress syndrome

addiction, heroin

Addison's disease

adrenomyeloneuropathy

adult polyglucosan body disease

adverse drug reaction

agenesis of corpus callosum

Aicardi-Goutieres syndrome

alcohol intolerance

altered states of consciousness

alternating rapid movement

Alzheimer's disease

amyloid plaques

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anemia, megaloblastic

aneurysm, vertebral basilar system

angiitis, granulomatous of CNS

ankle reflex, absent

antecedent illness

anterior horn cell disease

anterior tibial muscle weakness

anti GQ1b IgG antibody

anticholinergic drugs

anticoagulant, complications of

anticoagulant, treatment

antiviral agents

Argyll Robertson pupil

arm swing, reduced

Arnold Chiari malformation

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atherosclerosis, generalized

atherosclerosis, premature

atrioventricular block

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

azidodeoxythymidine

B 12 deficiency

Babinski sign in new born

bacterial infection

bacterial infection, CNS

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavior modification

behavioral disorder

Behcet's syndrome

Bell's phenomenon

Bickerstaff's brainstem encephalitis

bladder dysfunction

bone marrow biopsy

brain biopsy, false negative

brain biopsy, stereotaxic

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, infarction of

brainstem, ischemia

brainstem, lesion of

brainstem, neoplasms of

brucellosis, nervous system involvement with

Brudzinski's sign

bulbar palsy, progressive

burning paresthesia

calcification, intracranial

CAT scan, abnormal

CAT scan, emission, abnormal

CAT scan, metrizamide

CAT scan, myelogram with

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar hemangioma

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral folate deficiency syndrome

cerebral infarction

cerebral peduncle

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure increased

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, vascular territory involved

cerebrovascular disease

ceruloplasmin, serum

cervical spondylosis

Chaddock's sign

Charcot-Marie-Tooth

cherry red spot

cherry red spot-myoclonus syndrome

chilbran skin lesions

chorea, causes of

chorea, familial

choreoathetosis

chorioretinitis

choroid plexus, tumor of

chromosomal abnormality

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

coccidioidomycosis

comprehension, impaired

compression fracture

concentration, impaired

congenital bilateral perisylvian syndrome

congenital malformation

congenital malformation, non CNS

controversies in neurology

convergence, impaired

conversion reaction

copper deficiency

corneomandibular reflex

corpus callosum

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

critical care unit

crying, pathologic

cryptococcal meningitis

cyst, epidermoid of CNS

cytomegalic inclusion disease

decompressive spinal cord surgery

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

Dejerine's sign

Dejerine-Sottas syndrome

delay in diagnosis

dementia, childhood

dementia, familial

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei, lesion of

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

digiti quinti sign

disability, neurological

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

Dravet syndrome

dropped head syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, children

dystonia, focal

dystonia, treatment of

ears of the Lynx MR sign

electrical sensation

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

emergencies, neurologic

emergencies, neurosurgical

emotional lability

Emperor's clothes syndrome

empyema, epidural-spinal

encephalitis lethargica

encephalitis, brainstem

encephalitis, viral

encephalopathy, acute

encephalopathy, Hashimoto's

encephalopathy, progressive

enzyme, muscle disease

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

evoked potentials

executive dysfunction

exome sequencing

eye movement, disorders of

face, numbness of

facial anomalies

facial weakness

facial weakness, bilateral

failure to thrive

FARS2 deficiency

fatal familial insomnia

feeding disorder

ferritin, elevated

fetal alcohol syndrome

fine motor function, impaired

finger nose finger test

fingers, abnormal

Fisher's syndrome

flaccid paralysis

folic acid deficiency

fragile-X syndrome

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

gag reflex, depressed

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastric partitioning

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

giant axonal neuropathy

girdle sensation

glioblastoma multiforme(astrocytoma Gr.III)

glioma, low-grade

gliomatosis cerebri

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamate dehydrogenase deficiency

glutamic acid decarboxylase, antibody

granular osmiphilic material

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

headache, positional

headache, recurrent

headache, severe

heel-knee-shin test

hematoma, epidural-spinal

hemiplegia, progressive

hemosiderosis of CNS, superficial

hepatosplenomegaly

herniated disc, cervical

hexosaminidase-A

high arched feet

hip flexor weakness

history of neurology

Hodgkin's disease

Hoffmann's sign

homocysteine, serum

human immunodeficiency virus type 1

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, exvacuo

hypereosinophilic syndrome(HES)

hyperhomocysteinemia

hyperparathyroidism

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypersegmented polys

hyperthyroidism

hypoglycorrhachia

hypoglycorrhachia, causes of

hypomyelination

hypothalamus, disturbance of

hypotonia, infants

imbalance, postural

immunosuppression

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic intranuclear

incontinence, fecal

initiative, lack of

intellectual deficit

intellectual deterioration

interferon alpha

internal capsule

internuclear ophthalmoplegia

interobserver agreement

intrinsic hand muscles, wasting of

iron, serum, low

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

jaw jerk, abnormal

Krabbe's disease

lactic acidemia

lacunar infarction

laminectomy, cervical

laminectomy, lumbar

language disorder in adults

laughing, pathologic

left-right orientation

leg spasms, painful

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy

level of consciousness, decreased

Lhermitte's sign

life expectancy

lipid storage disorder of CNS

locked-in syndrome

loss of sympathy

lymphadenopathy

lymphadenopathy, hilar

lymphoma involving CNS

lysosomal storage disease

magnetic stimulation

magnetic stimulation, brain

malformation, CNS, congenital

malformation, vascular

manganese intoxication

meconium staining

mediastinum, lymph-node biopsy

mediastinum, mass of

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningeal gliomatosis

meningitis, actinomycotic

meningitis, aseptic

meningitis, bacterial

meningitis, blastomyces

meningitis, brucellosis

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, chronic benign lymphocytic

meningitis, cladosporium

meningitis, coenurosis

meningitis, CSF cell count-normal

meningitis, cysticercosis

meningitis, echinococcal

meningitis, eosinophilic

meningitis, fungal

meningitis, helminthic

meningitis, histoplasma

meningitis, leptospira

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, neutrophilic

meningitis, nocardia

meningitis, paracoccidioides

meningitis, pneumococcal

meningitis, post myelography

meningitis, recurrent

meningitis, syphilitic

meningitis, toxoplasma

meningoencephalitis

meningoencephalitis, toxoplasma

mental retardation

mental retardation, familial

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, late-infantile

methylmalonic acid, serum

methylmalonic acidemia

midbrain, lesion of

middle cerebellar peduncle, lesion

mitochondrial disease

molecular genetics

Montreal cognitive assessment

motor dysfunction

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, psychogenic

movement disorder, treatment of

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, contrast enhanced, high dose

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, gradient-echo

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, hypointense signal foci on

MRI, linear enhancement

MRI, nodular enhancement

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

multinucleated giant cell

multiple sclerosis

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple system atrophy

muscle atrophy, progressive

muscle weakness

mycoplasma pneumoniae

myelitis, longitudinal

myelitis, post infectious

myelitis, transverse

myelogram, cervical

myeloneuropathy

myelopathy hand

myelopathy, chronic progressive

myelopathy, vacuolar

myeloradiculopathy

myoclonic jerks

myoclonus, epilepsy

nausea and vomiting

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-treatment of

nerve conduction studies

nerve root hypertrophy

neuroendocrinology

neurofibrillary degeneration

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology, brain

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, peripheral

neuropathy, sensory

neuropsychiatry

next-generation sequencing

nutritional deficiency

nystagmus, gaze-evoked

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

ocular dysmetria

ocular motility, disorders of

oculogyric crisis

old age, neurology of

operculum syndrome, bilateral

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

optic chiasm, enlarged

optic nerve, enlarged

optic nerve, lesion of

optic neuropathy

oral contraceptives

orthostatic hypotension

osteomyelitis, spinal

pain, interscapular

palmomental response

palpebromandibular synkinesia

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, flaccid

paraparesis, spastic

paraplegia, in flexion

paraplegia, progressive

parathyroid adenoma

paresthesias, feet

paresthesias, hands

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, asymmetric onset

Parkinson disease, hemiparesis in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, postencephalitic

Parkinson disease, tremor, absence of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic disorder

PAS positive material in the brain

pathologic reflex

patient information and support

pediatric neurology

perivascular enhancement

pernicious anemia

Persistent postural-perceptual dizziness

personality change

pharyngeal sensation

photic sneeze reflex

pituitary stalk

pituitary stalk, lesion of

pleocytosis of cerebrospinal fluid

polyglucosan body

polyglucosan body disease

polyneuropathy, familial

pons, infarction of

pons, lesion of

position sensation, abnormal

posterior column disease

posterior inferior cerebellar artery syndrome

posterior leukoencephalopathy syndrome

postictal neurologic deficits

postural abnormality

precipitating factors

precocious puberty

premature infant

prenatal diagnosis by amniocentesis

primary lateral sclerosis

progressive encephalomyelitis with rigidity syndrome

progressive myoclonic epilepsy

progressive neurologic disorder

proprioception, abnormal

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

pure dysarthria

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis, progressive

radiation therapy, CNS treatment and complications with

Raynaud's phenomenon

reflex, cutaneous

release phenomena

repetition, impaired

respiratory dyskinesias

respiratory failure

respiratory tract infection

retinal degeneration

retinal detachment

retinal exudates

retinitis pigmentosa

reversible neurologic disorder

rubella encephalitis, progressive

saccadic eye movements, abnormal

saddle anesthesia

sarcoidosis, CNS

scalp tenderness

scleroderma, neurologic involvement with

sea-blue histiocytes

sedimentation rate, elevated

seizure, children

seizure, familial

seizure, febrile

seizure, hysterical

seizure, intractable

seizure, neonatal

seizure, tonic-clonic

selective serotonin reuptake inhibitors

sensory loss, cutaneous

serologic testing

serotonin norepinephrine reuptake inhibitors

severe acute respiratory syndrome

single photon emission computed tomography

skin, lesions in neurologic disorders

skin, temperature difference

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

sodium channel dysfunction

somatosensory evoked potentials

spastic diplegia

spastic paraplegia, type 11

spastic paraplegia, type 7

speech disorder

speech disorder, childhood

speech, loss of

spinal cord, compression of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal stenosis

spinal stenosis, familial

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spinocerebellar degeneration

spongy degeneration of brain

spontaneous remission

startle myoclonus

startle reaction

status epilepticus

steroid therapy, CNS treatment and complications with

stooped posture

striatonigral degeneration

striatonigral degeneration, infantile

striopallidodentate calcifications, familial idiopathic

subarachnoid hemorrhage

subdural effusion

substantia nigra

superior cerebellar artery infarction

superior sagittal sinus thrombosis

symmetric brain lesions

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

Tay-Sachs disease

temporal lobe, lesion

temporal lobe, lesion, bilateral

testicular enlargement

thalamus, lesion of

thalamus, lesion of-bilateral

tone, muscle, increased

tongue, fasciculations of

tongue, impaired movements of

tonic foot response

toxoplasmosis, acquired

toxoplasmosis, CNS

transient neurologic deficit

transilumination of skull

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trinucleotide repeats

unconsciousness

upgaze, paralysis of

urinary frequency

urinary incontinence

urinary retention

urinary urgency

vaccination, neurologic complications with

valsalva maneuver

ventricular enlargement

vertigo, episodic

vibratory sensation, abnormal

viral infection

viral infection, CNS

visual acuity, decreased

visual evoked response

visual fields, constricted

vitamin deficiency

vitamin E deficiency

Vogt-Koyanagi-Harada syndrome

walking, delayed

walking, difficulty with

Wallerian degeneration

watershed infarcts

weakness, generalized

weakness, progressive

weaning from respirator, failure to

white matter disease

white matter disease, periventricular

wide based gait

x-linked mental retardation

x-ray, thoracic spine

Showing articles 50 to 100 of 1808 << Previous Next >>

CMT with Pyramidal Features
Neurol 60:696-699, Vucic,S.,et al, 2003

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Dysarthria in Acute Ischemic Stroke
Neurol 56:1021-1027, Urban,P.P.,et al, 2001

Brainstem Gliomas in Adults: Prognostic Factors and Classification
Brain 124:2528-2539, Guillamo,J.-S.,et al, 2001

Presence of Diarrhea and Absence of Tendon Xanthomas in Patients With Cerebrotendinous Xanthomatosis
Arch Neurol 57:520-524, Verrips,A.,et al, 2000

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Clinical Correlates of Vascular Parkinsonism
Arch Neurol 56:98-102, Winikates,J.&Jancovic,J., 1999

Disequilibrium in Patients with Atherosclerosis; Relevance of Pontine Ischemic Rarefaction
Neurol 51:570-573, Kwa,V.I.H.,et al, 1998

MR of Childhood Metachromatic Leukodystrophy
AJNR 18:733-738, Kim,T.S.,et al, 1997

Neurological Signs and Frontal White Matter Lesions in Vascular Parkinsonism
Stroke 28:965-969, Yamanouchi,H.&Nagura,H., 1997

Cognitive and Brain Magnetic Resonance Imaging Findings in Adrenomyeloneuropathy
Ann Neurol 40:675-678, Edwin,D.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

The Babinski Sign:100 Years On
BMJ 313:1029-1030, Ditunno,J.F.&Bell,R., 1996

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Pharyngeal Sensation and Gag Reflex in Healthy Subjects
Lancet 345:487-488, Davies,A.E.,et al, 1995

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,et al, 1995

Asymmetrical Skin Temperature in Ischemic Stroke
Stroke 26:1543-1547, Korpelainen,J.T.,et al, 1995

Plantar Responses after Epileptic Seizures
Neurol 44:2191-2193, Walczak,T.S.&Rubinsky,M., 1994

Clinicopath Conf
Mycoplasma Pneumoniae Infection, Case 42-1994, NEJM 331:1437-1444994., , 1994

Spontaneous Palpebromandibular Synkinesia:A Localizing Clinical Sign
Ann Neurol 35:222-228, Pullicino,P.M.,et al, 1994

The Motor Disorder of Multiple System Atrophy
JNNP 56:1239-1242, Quinn,N.P.&Marsden,C.D., 1993

Congenital Bilateral Perisylvian Syndrome:Study of 31 Patients
Lancet 341:608-612, Kuzniecky,R.,et al, 1993

Extrapyramidal Signs and Other Neurologic Findings in Clinically Diagnosed Alzheimer's Dis, A Community-Based Study
Arch Neurol 50:51-56, Funkenstein,H.H.,et al, 1993

The Photic Sneeze Reflex:Literature Review and Discussion
Neurol 43:868-871, Whitman,B.W.&Packer,R.J., 1993

The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
Neurol 43:2167-2169, Kayden,H.J., 1993

MRI and SPECT in Amyotrophic Lateral Sclerosis, Demonstr of Upper Motor Neurone Invol by Neuroimaging
Neuroradiology 34:389-393, Udaka,F.,et al, 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992

Idiopathic Hemiparetic Parkinsonism, A Syndrome Distinct from Idiopathic Parkinsonism
Lancet 339:149-150, DeKeyser,J.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

The Sensitivity of Transcranial Cortical Magnetic Stimulation in Detecting Pyramidal Tract Lesions in Clin Definite MS
Neurol 41:566-569, Mayr,N.,et al, 1991

Idiopathic Myelopathies with White Matter Vacuolation in Non-AIDS Patients
Human Pathol 22:816-824, Kamin,S.S.&Petito,C.K., 1991

Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
Neurol 41:174-181, Nygaard,T.G.,et al, 1991

Magnetic Stimulation of the Motor Cortex in Cervical Spondylosis
Neurol 41:75-80, deNoordhout,A.M.,et al, 1991

Neurologic Aspects of Cobalamin Deficiency
Medicine 70:229-245, Healton,E.B.,et al, 1991

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

Selective Involvement of the Pyramidal Tract on Magnetic Resonance Imaging in Primary Lateral Sclerosis
Neurol 40:1799-1800, Marti-Fabregas,J.&Pujol,J., 1990

Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy
Ann Neurol 27:103-106, Goutieres,F.,et al, 1990

Neurological Findings in Alzheimer's Disease and Normal Aging
Arch Neurol 47:625-627, Glasko,D.,et al, 1990

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989

Spinal Cord Pathology in Pediatric Acquired Immunodeficiency Syndrome
Neurol 39:227-235, Dickson,D.W.,et al, 1989

The Acquired Immunodeficiency Syndrome (AIDS) Dementia Complex
Ann Int Med 111:400-410, Ho,D.D.,et al, 1989

Familial Idiopathic Striopallidodentate Calcifications
Neurol 39:381-385, Ellie,E.,et al, 1989

Clinicopath Conf
Chronic Osteomyelitis of Spine, with Intervertebral Diskitis (T3-T4) & Epidural Abscess (Staph Aureu, ) , Cas9,NEJM 320:1610-1618,1989., 1989

Primary Lateral Sclerosis in a Child
Neurol 39:1530-1532, Grunnet,M.L.,et al, 1989

Demyelinating Diseases
In Rowlands Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 749, Sibley,W.A.,et al, 1989

Subacute Combined Degeneration of the Spinal Cord
In Rowland's, Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 691, Mancall,E.L., 1989

Showing articles 50 to 100 of 1808 << Previous Next >>