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Differential
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abortion, spontaneous

abstinence syndrome

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

acute necrotizing encephalitis

addiction, heroin

advances in neurology

adverse drug reaction

agenesis of aqueduct of Sylvius

agenesis of corpus callosum

Aicardi-Goutieres syndrome

Aicardi's syndrome

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

Angelman syndrome

angiotensin-converting enzyme, inhibitors

anticoagulant, complications of

anticoagulant, treatment

antiviral agents

aphasia, conduction

aqueduct of Sylvius, stenosis

aqueductal stenosis

ataxia, cerebellar

attention deficit disorder with hyperactivity

autoimmune epilepsy

autonomic dysfunction

Bannayan-Riley-Ruvalcaba syndrome

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavior, combative

behavioral disorder

blue tongue virus

bone marrow transplantation

brainstem, atrophy

burst suppression pattern, electroencephalogram

cafe au lait spots

calcification, intracranial

calcification, periventricular

Canavan's disease

carcinoma of lung

CAT scan, abnormal

cataracts, congenital

central nervous system, infection of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hypoplasia

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, intrauterine

cerebrovascular accident, neonatal

chilbran skin lesions

choreoathetosis

chorioretinitis

chromosomal abnormality

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

cocaine, intrauterine exposure

Cockayne's syndrome

cognitive delay

cold hands sign

congenital birth defects

congenital heart disease

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, non CNS

contractures, joint

cornea, opacification in infancy-causes of

cornea, opacity of

corpus callosum

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, thinning

cortical blindness

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cry, high-pitched

cultured skin fibroblasts

cyst, parenchymal

cyst, porencephalic

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

cytosine arabinoside

Dandy Walker malformation

deafness, congenital

deep gray nuclei

degenerative diseases of CNS

dementia, childhood

dentate nuclei, lesion of

depression, psychotic

dermatoglyphics

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

differential diagnosis

digits, abnormal

disability, neurological

drug abuse, toxic screen In

drug withdrawal

dural sinus thrombosis

dysostosis multiplex

dystonia, children

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

encephalitis, brainstem

encephalitis, viral

encephalopathy, metabolic

endoscopic surgery

epicanthal folds

epidemiology of neurology

epidermal nevus syndrome

episodic disorders

ethics in neurology

ethylmalonic aciduria

ethylmalonic encephalopathy

evoked potentials

exome sequencing

eye movement, disorders of

facial anomalies

facial appearance, abnormal

facial asymmetry

facial expression abnormality

facial nerve palsy

facial weakness

failure to thrive

feeding disorder

fetal alcohol syndrome

fluorescene in situ hybridization

fontanel, bulging

frontal bossing

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

glioblastoma multiforme(astrocytoma Gr.III)

Gowers maneuver

growth retardation

Guillain Barre syndrome

head circumference

head circumference and brain development

hemorrhage, intracranial, newborn

hepatosplenomegaly

herpes labialis

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

herpes simplex encephalitis, infancy and childhood

herpes simplex encephalitis, prognosis of

herpes simplex encephalitis, recurrent

herpes simplex encephalitis, treatment of

herpes simplex myelitis

herpes simplex virus

herpes simplex virus infection, immunosuppressed patient

herpes simplex virus infection, newborn

herpes simplex virus, human nervous system and

herpes simplex virus, localization of

herpes simplex virus, malignancy with

herpes simplex virus, pathogenesis of

herpes simplex virus, pathology of

herpes simplex, neurocutaneous lesions in

herpes, genital

holoprosencephaly

human immunodeficiency virus type 1

Hurler's syndrome

hydranencephally

hydrocephalus, congenital

hydrocephalus, non-communicating(obstructive)

hydrocephalus, treatment of

hydroxyglutaric aciduria

hyperhomocysteinemia

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypoglycorrhachia

hypomyelination

hypopigmentation of skin

hypoplastic left heart syndrome

hypotonia, infants

immunofluorescent exam of CSF cells

immunosuppression

in situ hybridization

inborn errors of metabolism

inclusion bodies, intranuclear

infantile spasm

infection, recurrent

infectious mononucleosis

influenza A virus

insect repellent

intellectual deficit

intellectual deterioration

intelligence quotient

interferon alpha

interferon inducer

intracranial hemorrhage

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

iododeoxyuridine

klippel feil syndrome

laughing, pathologic

learning disability, in children

lens, dislocation of

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

lid abnormalities

life expectancy

limbic encephalitis

long bone lesion

low birth weight

lymphadenopathy

lymphocytic choriomeningitis

lysosomal storage disease

lysosomes, abnoral

malformation, CNS, congenital

malnutrition and brain development

meningitis, aseptic

meningitis, carcinomatous

meningoencephalitis

mental retardation

mental status, abnormal

metabolic disorder, primary

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

midline defect in children

Miller-Dieker syndrome

molecular genetics

molybdenum cofactor deficiency

monoamines, brain

movement disorder

movement disorder, hyperkinetic

multiple sclerosis

multiple system atrophy

muscle weakness

muscular dystrophy

muscular dystrophy, congenital

muscular dystrophy, LAMA2

myelomeningocele

nasal bridge, wide

nasal stuffiness

nausea and vomiting

neonatal abstinence syndrome

neonatal infection, viral

neoplasm, primary intracerebral

neoplasm, primary of CNS

neural tube defect

neurocutaneous disease

neurofibromatosis 1

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

neurologic signs

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuroophthalmology

neuropathology, brain

neuropathy, peripheral

nutritional deficiency

nystagmus, monocular

opportunistic infection

optic atrophy, infants

optic nerve, hypoplasia of

optic nerve, lesion of

optic neuropathy

organoid nevus syndrome

palatal myoclonus

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

pediatric neurology

penis, pigmented macules

personality change

pheochromocytoma

philtrum, tented

photosensitivity, skin

pigmentary retinopathy

pigmented macules

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

polyinosinic cytidic acid(poly IC)

polyps, gastrointestinal tract

postural abnormality

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

pupil, abnormality in neurologic disorders

pyramidal tract dysfunction

radiation therapy, CNS treatment and complications with

radiation, ionizing

radiation, ionizing, intrauterine

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

remote effect of cancer on the nervous system

respiratory failure

retinal degeneration

Rett's syndrome

Rosenthal fibers

rubella syndrome

scoliosis, neurologic association with

seizure, children

seizure, intractable

seizure, neonatal

seizure, psychomotor-temporal lobe

seizure, withdrawal

sensorineural hearing loss

septo-optic dysplasia

sexually transmitted disease

shunt procedure, ventricular

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

skull x-ray, bony defect on

spastic diplegia

speech disorder

speech disorder, childhood

speech, absence of

speech, delayed development of

spongy degeneration of brain

startle reaction

status epilepticus

stereotyped behavior

steroid therapy, CNS treatment and complications with

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

subdural hematoma

subdural hematoma, neonates and infants

subtemporal decompression

sulfite oxidase deficiency

superior sagittal sinus thrombosis

symmetric brain lesions

teeth, wide-spaced

teratogenesis, viral

teratogenic drugs

thrombocytopenia

tongue, protrusion of

toxoplasmosis, CNS

transplacental virus infections

travel, foreign

treatment of neurologic disorder

trigeminal neuralgia

ultrasonography

ultrasonography, head, fetus-neonate

urine test for metabolic disorders

varicella zoster virus

ventriculostomy

vertebral anomalies

viral infection

viral infection, CNS

Virchow-Robin spaces, dilated

visual evoked response

visual tracking

vomiting, episodic

vomiting, recurrent

white matter disease

whole genome sequencing

wide based gait

xeroderma pigmentosa

yawning movements

Zika virus infection

Showing articles 300 to 350 of 18584 << Previous Next >>

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

Acquired Stuttering
Neurol 28:1159-1165, Helm,N.A.,et al, 1978

Adult Onset of the Dandy-Walker Syndrome
Arch Neurol 35:672-674, Lipton,H.L.,et al, 1978

Intracranial Neoplasms in Infants
Arch Neurol 35:533, Farwell,J.R.,et al, 1978

Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome
Arch Neurol 35:337, Brumback,R.A.,et al, 1978

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

Adverse Effects on Offspring of Maternal Alcohol Abuse During Pregnancy
NEJM 297:528, Ouellette,E.M.,et al, 1977

Neurological Stuttering-A Clinical Entity
et al. , JNNP 40:699977., Quinn,P.T., 1977

Progressive Focal Deficit with Porencephaly
Arch Neurol 34:154, Leahy,W.R.,et al, 1977

Normal Pressure Hydrocephalus
In Wells C. E. Dementia 2nd Ed, F. A. Davis Co, Phila, P. 69-92, Katzman,R., 1977

School Failure & Deafness After"Silent"Congenital Cytomegalovirus Infection
NEJM 295:468, Hanshaw,J.B.,et al, 1976

Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients
Medicine 55:467, Knox,D.L.,et al, 1976

Neurologic Disorders in Renal Failure (1st of Two Parts)
NEJM 294:143, Raskin,N.H.,et al, 1976

The Thyroid Gland:Its Relationship to Neurology
In Handbook of Clin Neurol, Vinken & Bruyn (Ed) , North Holland Publ Co, Amsterdam 27:255, Greene,R., 1976

Catecholamines & Neurologic Diseases
NEJM 293:274, Moskowitz,M.A.,et al, 1975

Sequelae of Central Nervous System Interovirus Infections
NEJM 293:1, 1975. ; 3975., Sells,C.J.,et al, 1975

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Case Records of MGH-NEJM 290:273
1974 Subacute Sclerosing Panencephalitis., , 1974

Case Records of MGH-Polycythemia
Carotid Occlusion & Cerebral Infarcts, NEJM 291:96674., , 1974

Infiltration of the Leptomeninges by Systemic Cancer:a Clinical & Pathologic Study
Arch Neurol 30:122, Olson,M.E.,et al, 1974

Sarcoidosis of the Central Nervous System
JNNP 36:1024, Douglas,A.C.,et al, 1973

Corneal Opacification in Infancy
MCV Quart 8:230, Ching,F., 1972

Thromboangiitis Obliterans Cerebri
Edited by, Vinken, E. , Handbook Clinical Neurol 12:3842., Bernsmeier,A.&Held,K., 1972

Homonymous Hemioptic Hypoplasia
Br J Ophthalmol 56:537, Hoyt,W.F.,et al, 1972

Microcephaly & Mental Retardation
Am J Dis Child 119:128, Martin,H.P., 1970

Abnormal Head Size, In Neurology In Pediatrics
(Ed) , 1970 Year Book Med. Publishers, p. 61., Bray,P.F., 1970

Benign Intracranial Cyst, In Neurosurgery of Infancy & Childhood
(Ed) , 1969, Charles C. Thomas p. 179., Matson,D.D., 1969

Benign Intracranial Hypertension
Pediatr Clin North Am 14:819-830, Greer,M., 1967

Thalamic Tumors
J Neurosurg 24:505, Cheek,W.R.,et al, 1966

Neuro CPC of MGH
Congenital Toxoplasmosis Involving CNS, NEJM 269:369-3741963., , 1963

Microcephaly
Arch Dis Child 37:623-627, Davies,H.,et al, 1962

Neurology & Psychiatry Section-Year book of Pediatrics
Pediatr Abstract p. 406-449., , 1850

Reversible Leukoencephalopathy and Parkinsonism Due to CNS Involvement in Cryoglobulinemia
Neurol 106:e214622, German,A.,et al, 2026

A 41-Year-Old Man with Steroid-Responsive Hemiparesis
Neurol 106:e214088, Obaidi,Z.A.,et al, 2026

Zorevunersen in Children and Adolescents with Dravet Syndrome
NEJM 394:969-982, Laux,L.,et al, 2026

Niemann-Pick Type C Disease
www.UpToDate.com, Nov, Schiffmann, R., 2026

Association of Changes in Activity Patterns with Brain Atrophy and Disability Progression in People with Multiple Sclerosis
Neurol 106:e214678, e214742, Fitzgerald,K.C.,et al, 2026

A 49-Year-Old Man with Meningoencephalitis and Persistent Altered Mental Status
Neurol 106:e214777, Hariswar,P.T.,et al, 2026

Unilateral Primary Angiitis of the Central Nervous System: A Rare and Under-Recognized Entity
AJNR 47:589-595, Rai,P.,et al, 2026

Deep Venous Dural Arteriovenous Fistula Mimicking Progressive Dementia
Stroke 57:e180-181, Langlois-Therien,T.,et al, 2026

Status Epilepticus After Carotid Endarterectomy:An Illustrative Case of Cerebral Hyperfusion Syndrome
Stroke 57:e188-191, Reuter,P.,et al, 2026

Cerebral Amyloid Angiopathy
NEJM 394:1836-1845, Greenberg,S.M., 2026

Autoimmune Encephalitis as Treatment-Responsive Cause of Rapidly Progressive Dementia
Neurol 106:e214933, van Steenhoven,R.W.,et al, 2026

A 32-Year-Old Woman with Progressive Vision Loss and Confusion
Neurol 106:e214988, Kumar,A.B.,et al, 2026

Wearable Technology and Its Role in Neurologic Care, Emerging Issues in Neurology
Neurol 106:e214802, Benish,S.M.,et al, 2025

Trident Sign in GFAP-Associated Meningoencephalomyelitis
Neurol 106:e214566, Mallett,N.S.,et al, 2025

Melas Syndrome
Stat PearlsPubl Jan 25, Pia,S. & Lui,F., 2025

Acromegaly
NEJM 393:1926-1939, Giustina,A. & Colao,A.,, 2025

Neuropathologic Changes in People with Essential Tremor With Dementia
Neurol 105:e214310, Wainman,E.,et al, 2025

Myelin Oligodendrocyte Glycoprotein Antibody - Associated Cerebral Cortical Encephalitis: A Case Report Highlighting Diagnostic Challenges and Therapeutic Implications
Front Immunol 16:1619807, Liu,M. & Li, D., 2025

Showing articles 300 to 350 of 18584 << Previous Next >>