Neudle.com: neonatal screening genetic neurologic disorders

Differential
(Click to cross reference)

abdominal protrusion

abscess, intracerebral

acetylcholinesterase deficiency

achilles tendon, enlarged

acid maltase deficiency

acromicria

ACTH

activated protein C resistance

acyl CoA dehydrogenase deficiency

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

agenesis of corpus callosum

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, preclinical

Alzheimer's disease, risk factors in

Alzheimer's disease, visual variant

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

anemia

anesthesia, general

aneurysm

aneurysm, intracranial

aneurysm, intracranial, familial

angiofibroma, facial

angiography, cerebral

angiomyolipomas

ankle reflex, absent

ankle, swelling of

anterior horn cell disease

antibiotic prophylaxis

antibiotics

antibiotics, neurologic complications with

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, effectiveness

anticonvulsants, selection of

anticonvulsants, teratogenicity of

antiphospholipid antibodies

antiviral agents

anxiety

aphasia

aphasia, progressive, primary

aphasia, transcortical

aphasia, transcortical-sensory

apolipoprotein E

APP gene

apraxia

apraxia, constructional

arteriovenous malformation

arteriovenous malformation, cerebral

arteriovenous malformation, multiple

arteriovenous malformation, pulmonary

asymmetric crying facies

asymptomatic

ataxia

ataxia telangiectasia

ataxic-dystonia syndromes

atrioventricular block

attention deficit disorder with hyperactivity

atypical

auditory and vestibular pathways

autism

autism, screening for

autistic behavior

autoimmune disease

automobile accidents

autonomic dysfunction

autonomic nervous system

autosomal dominant leukodystrophy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery stenosis

basilar impression

behavior, combative

behavioral disorder

benign familial neonatal convulsions

biologic markers

biotin deficiency

biotinidase deficiency

bladder dysfunction

bleeding disorder

blindness

blood dyscrasias, neurologic findings with

body odor

bone biopsy

bone marrow transplantation

brachial neuritis, acute

brachial neuritis, bilateral

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brain biopsy, negative

brain biopsy, stereotaxic

brain purpura

brainstem, atrophy

brainstem, infarction of

burst suppression pattern, electroencephalogram

cachexia

CAG repeats

calcification, gyral

calcification, intracranial

cardiac surgery, hypothermia and circulatory arrest for

cardiac surgery, neurologic complications with

cardiomyopathy

cardiovascular disease

caribbean

carotid artery occlusion, bilateral

CAT scan, emission, abnormal

CAT scan, isodense lesion with acute hemorrhage

caudate nucleus, atrophy

cavernous hemangioma

Central America

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebellum, disease of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, carotid origin

cerebral infarction

cerebral infarction, hemorrhagic

cerebral infarction, subcortical

cerebral palsy

cerebral palsy, etiology

cerebral palsy, risk factors

cerebral palsy, work up

cerebral peduncle

cerebral vasculature

cerebral vasculature, calcification

cerebral venous infarction

cerebral venous thrombosis

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, cryptogenic

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, intrauterine

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, nonarterial territory

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, work up for

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, surgical treatment of

ceruloplasmin, serum

channelopathy

Charcot-Marie-Tooth

chenodeoxycholic acid

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

choroid plexus, abnormality of

choroid plexus, cyst

chromosomal abnormality

cingulate island sign

claustrum

cleft lip

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

coagulopathy

coat-hanger pain

Coats plus

cobalamin C deficiency

collagen vascular disease

color vision

color vision, impaired

congenital birth defects

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, non CNS

congenital myasthenic syndromes

controversies in neurology

copper deficiency

cornea, abnormal

corpus callosum

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical blindness, transient

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

Cree leukoencephalopathy

Creutzfeldt-Jakob disease, genetic

cry, abnormal

cryopyrin-associated periodic syndrome

cryptorchidism

Cuba

cultured skin fibroblasts

cyanosis

cyst

cyst, peritumoral

cyst, benign intracranial

cyst, cortical parenchyma

cyst, neoplastic cerebellum

cyst, parenchymal

cyst, porencephalic

cystinuria

cytomegalovirus infection

degenerative diseases of CNS

Dejerine-Sottas syndrome

dementia, age at onset

dementia, childhood

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

descending paralysis

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

diamond on quadriceps

diet

differential diagnosis

difficulty climbing stairs

disability, neurological

disease modifying agents

disorientation

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

down-beat nystagmus

Dravet syndrome

dropped head syndrome

drug abuse

drug interactions

dural sinus thrombosis

dystonia, etiology of

dystonia, painful

dystrophin

ear, abnormal

ears of the Lynx MR sign

ears, low set

echocardiogram

echocardiogram, transesophageal

eczema

Ehlers-Danlos syndrome

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, inflammatory disease

electroencephalogram, monitoring, continuous

electroencephalogram, periodic complexes

electroencephalogram, video monitoring with

electromyogram

electron microscopy

electrophoretic pattern, serum

electroretinograph

embolism, paradoxical

Embryonal tumors

Emery-Dreifuss muscular dystrophy

encephalopathy, acute

encephalopathy, acute necrotizing

encephalopathy, acute necrotizing of childhood

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

endocarditis, prophylaxis

endolymphatic sac tumors

enzyme treatment

enzyme, defect

enzyme, induction

enzyme, muscle disease

ependymoma

epicanthal folds

epidemic

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

evidence-based research

executive dysfunction

exercise

exercise intolerance

exome sequencing

extracorporeal membrane oxygenation

eye movement, disorders of

Fabry's disease

face, elongated

facial anomalies

facial appearance, abnormal

facial weakness, bilateral

facioscapulohumeral syndrome

fatal familial insomnia

fatigue

fatty acid, elevated plasma content

fibrinolytic agents, contraindications

fibroma, ungual

fibromuscular dysplasia

fine motor function, impaired

finger nose finger test

finger tapping

fingers, abnormal

fistula, arterio-venous, pulmonary

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frataxin

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal balding

frontal bossing

frontotemporal dementia, behavioral variant

fundus, abnormality of

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

geniculate body, lateral

Gerstmann-Straussler-Scheinker disease

GFAP gene

glaucoma

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucose level, serum

glucose tolerance test, abnormal

GLUT1

GLUT1 deficiency syndrome

glycine

glycogen storage disease

Guillain Barre syndrome

gynecomastia

gyrus, abnormal

Hallervorden Spatz disease

hallucination

hallucination, visual

hearing loss, bilateral

hearing loss, sudden, unilateral

hemangioma, leptomeningeal

hemangioma, skin

hemianopia

hemianopia, homonymous

hemianopia, transient

hemiparesis

hemiparesis, transient

hemiplegia

hemiplegia, congenital

hemoglobin abnormality, neurologic complications of

hemophagocytic lymphohistiocytosis

hemorrhage, intracranial, newborn

hemorrhage, periventricular

hemorrhagic diathesis

hepatic encephalopathy

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herniated disc, thoracic

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

huntingtin

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's chorea, late onset

Huntington's chorea, misdiagnosis of

Huntington's chorea, presymptomatic detection of

Huntington's chorea, sporadic form

Huntington's disease, children

hydrocephalus

hydrocephalus, congenital

hyperglycinemia, nonketotic

hyperhomocysteinemia

hyperpigmentation of skin

hypertrophic cardiomyopathy

hypertrophic intracranial pachymeningitis

hypocalcemia

hypodontia

hypogammaglobulinemia

hypoglycorrhachia

hypogonadism

hypogonadism, hypogonadotropic

hypopigmentation of skin

hyporeflexia

hyposmia

hypotelorism

hypotension, neurologic causes of

hypotension, systemic

hypothermia

hypothyroidism

hypothyroidism, congenital

hypoxic encephalopathy

hypoxic-ischemic leukoencephalopathy

hypsarrhythmia

iatrogenic neurologic disorders

implantable cardioverter defibrillator

impulsivity

inappropriate behavior

inattention

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

incoordination

infant, evaluation of

inflexibility, mental

insomnia

insulin resistance

intellectual deficit

intellectual deterioration

intelligence quotient

intelligence testing in children

internal capsule

internet

interstitial pulmonary fibrosis

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, young adult

intracranial hemorrhage

intranasal medication

intrauterine

intrauterine growth retardation

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intraventricular hemorrhage

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

klippel feil syndrome

Krabbe's disease

KRIT1 gene

kyphoscoliosis, neurologic causes of

learning disability, in children

Leber's hereditary optic neuropathy

leg spasms

leg spasms, painful

leg weakness, bilateral

leucine-rich repeat kinase 2 gene

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

lid

lid abnormalities

lid closure, weakness of

life expectancy

limb-girdle weakness

linear lesion

lipid storage disorder of CNS

lissencephaly

livedo reticularis

liver disease

liver function enzymes

lysosomal storage disease

macrocephaly

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

masseter muscle weakness

McLeod syndrome

meconium staining

medical-legal aspects of neurology

medulla oblongata

medulla oblongata, atrophy

medulla oblongata, lesion of

medulla oblongata, neoplasm of

medulloblastoma

melanomatosis, primary malignant

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis

meningitis, aseptic

meningitis, basilar

meningitis, carcinomatous

meningitis, CSF cell count-normal

meningitis, leptospira

meningocele

meningoencephalitis

mental retardation

mental retardation, familial

mental status, abnormal

MERRF syndrome

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

methylmalonic acidemia

Mexican

microangiopathy, brain

microcephaly

microdontia

microhemorrhage, intracerebral

microspherophakia

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery territory infarction

middle cerebral artery, occlusion of

miglustat

migraine

migraine, hemiplegic

migratory lesion pattern

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

molecular genetics

molybdenum cofactor deficiency

mongolism

monoclonal antibodies

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, false negative

MRI, fetal

MRI, gradient-echo

MRI, gyral enhancement

MRI, hypointense signal foci on

MRI, muscle

MRI, negative

MRI, optic nerve

MRI, paramagnetic effect

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

MRS

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle pain

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

mutism

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, distal weakness

myasthenia gravis, familial incidence of

myasthenia gravis, infantile and juvenile

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, neonatal

myasthenia gravis, seronegative

myasthenia gravis, treatment of

myasthenic syndrome

myelin protein zero gene

myelopathy, chronic progressive

myeloproliferative disorder

myoclonus, stimulus sensitive

myoglobinuria

myokymia

myopathy

myopathy, drug-induced

myopathy, genetic

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, metabolic

myopathy, mitochondrial

myotonia dystrophica, classification

myotonia dystrophica, type 2

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, peripheral nerve

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-treatment of

nephritis

nerve conduction studies

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neural tube defect

neuroaxonal leukodystrophy

neuroblastoma

neurocutaneous disease

neurodegeneration with brain iron accumulation

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic practice

neurologic signs

neurologic testing

neuromuscular junction

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, classification of

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, sensory

neuropathy, work up for

newborn, evaluation of

next-generation sequencing

Notch3 gene, false negative

numbness, extremity

nusinersen

nystagmus

nystagmus, gaze-evoked

nystagmus, monocular

nystagmus, rotary

nystagmus, vertical

obsessive-compulsive disorder

occipital lobe, infarction

occipital lobe, lesion of

ocular dysmetria

ocular motility, disorders of

oculodentodigital dysplasia

old age, neurology of

omeprazole

ophthalmoplegia

ophthalmoplegia, progressive external

opisthotonus

optic ataxia

optic atrophy

optic atrophy, bilateral

optic chiasm, enlarged

optic disc edema

optic glioma

optic nerve, compression of

optic nerve, enhancement

optic nerve, enlarged

optic nerve, hypoplasia of

optic nerve, lesion of

optic neuritis

optic neuritis, bilateral

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

optical coherence tomography

oral contraceptives

organomegaly

ornithine transcarbamylase deficiency

orthostatic hypotension

osteogenesis imperfecta

osteoporosis

otosclerosis

ovarian dysgenesis

ovarian insufficiency

pacemaker, cardiac-transvenous

pain, increased response

paraparesis, familial spastic

paraparesis, familial spastic, classification

paresthesias, lower extremity

Parkinson disease

Parkinson disease, atypical

Parkinson disease, dystonia with

Parkinson disease, familial

Parkinson disease, juvenile

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

past pointing

pathology

patient in waiting

patient information and support

pectus carinatum

pectus excavatum

Pelizaeus Merzbacher

percussion induced muscle contraction

peripheral blood smear

peripheral nerve, lesion of

periventricular leukomalacia

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

poison, neurologic problems with

POLG1 gene

POLR3B

polycythemia, primary

polyglucosan body

polyglucosan body disease

polyhydramnios

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polyneuropathy

Pompe's disease of glycogen storage

pons, lesion of

port wine nevus

portal caval shunt

post hemorrhagic hydrocephalus

posterior cerebral artery territory infarction

posterior cortical atrophy

posterior fossa, lesion of

postoperative neurologic complications

postural abnormality

practice guidelines

precipitating factors

preclinical

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

premature infant, problems in

prenatal

prenatal diagnosis by amniocentesis

presenilin-1 gene

presenilin-2 gene

prethrombotic state

prevention of neurologic disorders

primary episodic ataxia

primary familial brain calcification

primary thrombocythemia

progressive myoclonic epilepsy

progressive neurologic disorder

prolactin, elevated

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

protein C deficiency

protein S deficiency

proteinuria

proton pump inhibitors

proximal muscle atrophy

proximal myotonic myopathy

pseudobulbar palsy

pseudohypoparathyroidism

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

pulmonary hypertension

pulmonary stenosis

pupil

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, dilated, episodic

pyramidal tract

pyramidal tract dysfunction

pyridoxine

pyridoxine deficiency

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, progressive

quadriplegia, transient

quality of life

radiculopathy

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

reaction time

real-time quaking-induced conversion

respiratory tract infection

reversible neurologic disorder

rhabdomyosarcoma of heart

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

riboflavin

rigidity

risk factors

risk-benefit assessment

saccadic eye movements, abnormal

salivation, excessive

scoliosis, neurologic association with

scotoma, central

screaming

screening

sedimentation rate, elevated

seizure

seizure, children

seizure, complications following

seizure, crying as manifestation of

seizure, diagnosis of

seizure, drug resistance

seizure, drug-induced

seizure, injury following

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, pregnancy

seizure, pyridoxine dependent

seizure, teenager

seizure, tonic-clonic

seizure, treatment of

seizure, workup of

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

shoulder-girdle wasting

single photon emission computed tomography

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

skull bone, thickening

sleep pathology and physiology

slit lamp examination

small vessel disease

small vessel disease, cerebral

SMN1 gene

SNCA duplication

sodium channel dysfunction

somnolence

South America

Southern immunoblot test

spastic ataxia

spastic diplegia

spastic paraplegia, type 11

spasticity

speech disorder

speech disorder, childhood

speech, absence of

speech, delayed development of

speech, loss of

spinal cord, compression of

spinal cord, lesion of

spinal cord, neoplasm

spinal muscular atrophy

spinal muscular atrophy, classification

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 2

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spinocerebellar degeneration

spirochete infection

splenium of corpus callosum

splenomegaly

spondylolysis

spontaneous remission

stem cell transplantation

steppage gait

stereotyped behavior

steroid therapy, CNS treatment and complications with

stiff legs

straight sinus

stress, emotional

striatonigral degeneration

striatonigral degeneration, infantile

striopallidodentate calcifications, familial idiopathic

strokelike episodes

Sturge-Weber syndrome

subarachnoid hemorrhage

sudden infant death syndrome

suicide

sulfite oxidase deficiency

superior sagittal sinus thrombosis

symmetric brain lesions

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

teeth, number of in infants

telangiectases

telangiectases, retinal

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

testicular enlargement

tetrahydrobiopterin

thalamus, lesion of

thalamus, lesion of-bilateral

tissue plasminogen activator, intravenous

tongue, fasciculations of

tonic foot response

topiramate

transient ischemic attack

transient neurologic deficit

transplacental virus infections

transverse smile

travel, foreign

treatment of neurologic disorder

trinucleotide repeats

tuberous sclerosis, screening for

tumefactive lesion

tumor suppressor gene

twins

tyrosine hydroxylase deficiency

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

ultrasonography, nerve

unconsciousness

unconsciousness, transient

undiagnosed

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

urine test for metabolic disorders

venous thrombosis, non-cerebral

ventricular enlargement

vibratory sensation, abnormal

violent behavior

viral infection

viral infection, CNS

vision loss, sequential

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual acuity, decreased, monocular

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visuospatial disturbance

Von Hippel Lindau, screening protocol for

von Hippel-Lindau, screening

walking, difficulty with

walking, difficulty with in dark

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

web sites

weight loss

wheelchair

whistle, inability to

white matter disease

white matter disease, subcortical

white matter disease, unilateral

whole genome sequencing

wide based gait

winging of scapula

Wolff-Parkinson-White syndrome

Wood's light

word-finding difficulty

workup

writing

xanthoma, tendon

X-linked bulbospinal neuronopathy

x-linked hydrocephalus

x-linked intellectual deficit

x-linked mental retardation

Zika virus infection

Showing articles 250 to 300 of 25411 << Previous Next >>

Benign Familial Neonatal Convulsions:Evidence for Clinical and Genetic Heterogeneity
Ann Neurol 29:469-473, Ryan,S.G.,et al, 1991

Attitudes of Mothers to Neonatal Screening for Duchenne Muscular Dystrophy
BMJ 300:1112, Smith,R.A.,et al, 1990

Periventricular-Intraventricular Hemorrhage Sonographic Localization in Low Birth Weight Infants
Pediatrics 85:1027-1032, Krishamoorthy,K.,et al, 1990

Neurofibromatosis and Other Disorders Among Children with CNS Tumors and Their Families
Neurol 39:487-492, Baptiste,M.,et al, 1989

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
Lancet 2:425-427, Greenberg,C.R.,et al, 1988

CT in Ceroid Lipofuscinosis
Neurol 37:1025-1026, Dunn,D.W., 1987

Childhood Stroke Associated with Protein C or S Deficiency
J Pediatr 111:562-564, Israels,S.J.&Seshia,S.S., 1987

Mendelian Etiologies of Stroke
Ann Neurol 22:175-192, Natowicz,M.&Kelley,R.I., 1987

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
Ann Neurol 18:614-617, Wolf,B.,et al, 1985

Benign Familial Neonatal Seizures
E. , Arch Neurol 37:47-48980., Pettit,R., 1980

Familial Vascular Malformation or Chance Occurrence
Neurol 28:98, Barre,R.G.,et al, 1978

Mirror Movements after Childhood Hemiparesis
Neurol 28:1152-1158, Woods,B.T.,et al, 1978

Clinical Syndromes of Myasthenia in Infancy & Childhood
Arch Neurol 35:97, Fenichel,G.M., 1978

Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue
(Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972

Clinical Study of Nine Patients with ReNU Syndrome
, Okamoto,N.,et al,

Ribbon-Like Sign in Convexity Subarachnoid Hemorrhage
Ann Neurol 99:881-882, Liu,S-X.,et al, 2026

Severe Myotonic Crisis Resembling Malignant Hyperthermia
Neurol 104:e213497, Wadhwani,A.R.,et al, 2025

Spectrum of Intracranial Hemorrhages in Cerebral Venous Thrombosis, A Pictorial Case Series and Review of Pathophysiology and Management
Neurologist 30:45-51, Jha,S.,et al, 2025

A 26-Year-OldWoman with Headache and Eosinophilia
Neurol 104:e213434, Goh,W.G.W.,et al, 2025

Ribbon-Like Cortical Calcifications in Hereditary Cerebral Hemorrhage With Amyloidosis-Dutch Type
Neurol 106:e214464, Chen,Y.,et al, 2025

A 59-Year-Old Man with Acute-Onset Encephalopathy and Aphasia
Neurol 105:e214299, Gutierrez-Abizuri,C.,et al, 2025

In Utero MR Imaging for Fetuses with Small Head Sizes Without Intracranial Abnormalities Detected on Ultrasonography
AJNR 46:1917-1924, Griffiths,P.D.,et al, 2025

AAV9-Mediated Gene Therapy for Infantile-Onset Pompes Disease
NEJM 392:2438-2446, 2477, Ma,X.,et al, 2025

Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
Neurol 104:e213636, Chanda,G.,et al, 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

RNF213 Polymorphisms in Intracranial Artery Dissection
Genes doi.org/10.3390/genesis 15060725, Zedde,M.,et al, 2024

Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
Neurol 103:e209844, Dhawan,A.,et al, 2024

Pomalidomide for Epistaxis in Hereditary Hemorrhagic Telangiectasia
NEJM 391:1015-1027, Al-Samkari,H.,et al, 2024

A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
Neurol 103:e209796, Bouchart,J.,et al, 2024

Vascular Malformations of the Central Nervous System
www.UptoDate.Com, March, Singer,R.J.,et al, 2024

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024

A 24-Year-Old Man with Spastic Ataxia and Hypodontia
JAMA Neurol 81:658-659, Marien,L.,et al, 2024

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

Cavernous Maliformations of the Central Nervous System
NEJM 390:1022-1028, Smith,E.R., 2024

Primary Brain Tumours in Adults
Lancet 402:1564-1579, van den Bent,M.,et al, 2023

Unpacking the CNS Manifestations of Epstein-Barr Virus:An Imaging Perspective
AJNR 44:1002-1008, Soni,N.,et al, 2023

Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
Neurol 101:e1884-e1892, van der Veen,S.,et al, 2023

Hereditary Hemorrhagic Telangiectasia, Clinical Presentations, and Management
Stroke 54:e512-e515, Silveira,L.,et al, 2023

Focusing on the Eye Signs of Alport Syndrome in a 40-Year-Old Man Who Previously Had a Kidney Transplant and Hearing Loss
Lancet 401:e2, Kovalchuk,B. & Khoramnia,R., 2023

Paroxysmal Exercise-Induced Dyskinesias Due to Pyruvate Dehydrogenase Deficiency
Neurol 101:46-49, deGusmao,C.M.,et al, 2023

Current and Emerging Issues in Wilsons Disease
NEJM 389:922-938, Roberts,E.A. & Schilsky, M.L., 2023

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

A 36-Year-Old Man With Asymmetric Muscle Weakness
Neurol 99"1057-1061, Harada,Y.,et al, 2022

Infantile and Childhood Hydrocephalus
NEJM 387:2067-2073, Whitehead,W.E.&Weiner,J.L., 2022

Clinical Manifestations and Diagnosis of Listeria Monocytogenes Infection
UptoDate Aug, Gelfand, M.S.,et al, 2022

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022

Spontaneous Intracerebral Hemorrhage
NEJM 387:1589-1596, Sheth, K.N., 2022

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