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acquired immunodeficiency syndrome

acute ataxia of childhood

acute cerebellar ataxia

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

advances in neurology

affect, inappropriate

Aicardi-Goutieres syndrome

alcohol intolerance

alcohol, neurologic complications with

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alveolar hypoventilation

anemia, hemolytic

Angelman syndrome

angiitis, granulomatous of CNS

ankle, swelling of

antibiotics, neurologic complications with

aphasia, children

aphasia, classification of

aphasia, recovery from

apraxia, speech

arylsulfatase A

ascending paralysis

ataxia telangiectasia

ataxia, acute onset

ataxia, cerebellar

ataxia, progressive

ataxia, sensory

ataxia, truncal

attention deficit disorder with hyperactivity

audiologic test to localize site of pathology

auditory dominance

auditory processing, impaired

autoimmune disease

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

behavior, combative

behavioral disorder

Benedict's solution test

benign essential tremor

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

blood brain barrier

bone marrow transplantation

botulinum toxin

brain biopsy, stereotaxic

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

Brown-Vialetto-Van Laere syndrome

burning feet, differential diagnosis of

calcification, intracranial

calf hypertrophy

carpo-pedal spasm

CAT scan, abnormal

CAT scan, angiography

CAT scan, dense artery sign

celiac disease, adult

Central America

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar lesion

cerebellar mutism

cerebellar vermis

cerebellum, disease of

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral dominance

cerebral embolism

cerebral embolism, mechanical extraction

cerebral palsy, associated problems with

cerebral palsy, pure ataxic

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chilbran skin lesions

chorea, Sydenham's

choreoathetosis

chromosomal abnormality

cirrhosis, causes of childhood

Clinical Pathologic Conference(C.P.C.)

cochlear implant

cognitive delay

congenital bilateral perisylvian syndrome

congenital myasthenic syndromes

conjunctival biopsy

contractures, joint

conversion reaction

corpus callosum, infarction of

corpus callosum, lesion of

cortical blindness

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

crying, pathologic

cultured skin fibroblasts

cytomegalic inclusion disease

cytomegalovirus infection

deafness, congenital

decerebrate posture

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, childhood

dementia, presenile

demyelinating disease

dense basilar artery sign

dense middle cerebral artery sign

dentate nuclei, lesion of

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diagnostic criteria

dialysis dementia

dichotic hearing

differential diagnosis

difficulty climbing stairs

dinitrophenylhydrazine(D.N.P.H.)reaction

diplegia, atonic

diplegia, spastic cerebral

disconnection syndrome

disease modifying agents

doll's head maneuver

dopa responsive dystonia

dysdiadochokinesia

dysequilibrium syndrome

dyskinesia, buccal lingual facial

dysplasia of C.N.S.

dystonia musculorum deformens

dystonia, children

dystonia, laryngeal

dystonia, painful

dystonia, treatment of

EDTA(ehtylenediamine tetraacetic acid)

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, sleep

electron microscopy

embolism, paradoxical

embolism, vertebral-basilar artery

emotional lability

encephalitis, autoimmune

encephalitis, etiology

encephalitis, viral

encephalopathy, acute

encephalopathy, metabolic

encephalopathy, parainfectious

encephalopathy, progressive

endovascular therapy

epidemiology of neurology

epilepsia partialis continua

epileptic encephalopathy

epsilon sarcoglycan gene

exome sequencing

eye movement, disorders of

face, inexpressive

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial weakness

facial weakness, bilateral

failure to thrive

FARS2 deficiency

feeding disorder

ferric chloride test

fetal alcohol syndrome

fine motor function, impaired

finger nose finger test

fingerprint bodies

fluorescene in situ hybridization

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frontal lobe, pathologic signs of

fungal infection, CNS

gastroenteritis

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

Gowers maneuver

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Hallervorden Spatz disease

hallucination, visual

head circumference

head injury, pediatric

headache, vascular

hearing problems in children

heavy metal intoxication

heel-knee-shin test

hemiparesis, transient

hemisensory loss

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

human immunodeficiency virus type 1

hydroxyglutaric aciduria

hyperintense vessel sign

hyperosmolality

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypokinetic left ventricle

hypopigmentation of skin

hypotonia, infants

iatrogenic neurologic disorders

immunodeficiency

immunosuppression

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

industrial neurologic disorders

infection, recurrent

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

interferon alpha

intestinal biopsy

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intracranial pressure, increased

joint hypermobility

Kayser-Fleischer ring

klippel feil syndrome

lactic acidemia

Landau-Kleffner syndrome

language development, neurologic basis of

language disorders in children

laughing, pathologic

learning disability

learning disability, in children

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukoencephalopathy

level of consciousness, decreased

lipid storage disorder of CNS

liver function enzymes

locked-in syndrome

Lyme disease, children

lymphoma involving CNS

lysosomal storage disease

magnetic source image

magnetoencephalography

malabsorption syndrome

manganese intoxication

maple syrup urine disease

marche a petits pas

medulla oblongata, neoplasm of

medulloblastoma

megalencephaly, idiopathic

memory, defect of recent

memory, impairment of

meningitis, aseptic

meningitis, CSF cell count-normal

meningitis, recurrent

meningoencephalitis

mental retardation

mental status, abnormal

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

midbrain, atrophy

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

midline defect in children

mitochondrial disease

molecular genetics

monoclonal antibodies

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR, hyperintense vessels

MRI, functional

MRI, paramagnetic effect

MRI, T1 weighted high signal foci

muscle stiffness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, central nervous system abnormality

muscular dystrophy, Duchenne

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, familial incidence of

myelinolysis, extrapontine

myoclonic dystonia

myoclonic jerks

myoclonus, action

neoplasm, posterior fossa

neoplasm, primary of CNS

neoplasm, primary of CNS-children

nerve conduction studies

neurofibromatosis 1

neurologic complications

neurologic complications of, burns

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic testing

neuromuscular junction

neuronal ceroid-lipofuscinosis

neuropathology, brain

neuropathy, hereditary peripheral

neuropathy, painful

neuropathy, sensory

neurotoxicity, acute

Niemann-Pick disease

NMDA antagonists

non-dominant hemisphere

nystagmus, rotary

nystagmus, spontaneous

operculum syndrome

operculum syndrome, bilateral

ophthalmoplegia

osmotic demyelination syndrome

ovarian insufficiency

palatal myoclonus

palatopharyngeal incompetence

paralysis, acute

paralysis, acute areflexic

paraparesis, familial spastic

paraparesis, spastic

parietal lobe, syndromes of

Parkinson disease

Parkinson disease, freezing phenomena in

Parkinsonism syndrome

paroxysmal neurologic deficits

patent foramen ovale

Penumbra System

peroxisomal disease

personality change

phenylketonuria

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

polyneuropathy, uremic

pons, infarction of

pons, lesion of

positional head-hanging test

postural abnormality

precipitating factors

pregnancy, neurologic complications in

prevention of neurologic disorders

progressive neurologic disorder

prolactin, elevated

protozoan infection

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

psychosis, childhood

psychosocial aspects

psychosomatic disease

ptosis, bilateral

pulmonary infection

pure word deafness

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

reading disorder, acquired

release phenomena

remote effect of cancer on the nervous system

renal transplantation

renal tubular acidosis

respirations in CNS disease

restless leg syndrome

reticulum cell sarcoma

retina, abnormal

retinal detachment

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

reversible splenial lesion syndrome

rheumatic brain disease

rheumatic fever

rheumatic heart disease

riboflavin transporter deficiency

rubella encephalitis, progressive

saccadic eye movements, abnormal

salivation, excessive

sea-blue histiocytes

seizure, advice to parents and teachers regarding

seizure, children

seizure, laughing as manifestation

seizure, psychosocial aspects of

seizure, recurrent

seizure, surgical treatment of

seizure, treatment of

seizure, workup of

sexual behavior, disorder of

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

spastic diplegia

spastic dysphonia

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech lateralization

speech, delayed development of

speech, loss of

speech, pressured

spinocerebellar ataxia

spinocerebellar ataxia type 7

splenium of corpus callosum

spongy degeneration of brain

startle reaction

stereotaxic surgery

stereotyped behavior

stimulation, deep brain

stimulation, deep brain, bilateral

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

stuttering following CVA

subdural hematoma

substantia nigra

symmetric brain lesions

systemic illness

tandem gait, ataxic

teeth, wide-spaced

temporal lobe, lesion

temporal lobe, lesion, bilateral

teratoma, ovarian

testicular enlargement

thrombus, mural

tongue, impaired movements of

tongue, protrusion of

tonic foot response

toxoplasmosis, acquired

toxoplasmosis, CNS

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trinucleotide repeats

Trousseau's sign

trypanosoma cruzi

tuberculosis, miliary

tyrosine hydroxylase deficiency

upgaze, paralysis of

uremic encephalopathy

uremic twitching

urine test for metabolic disorders

very long chain fatty acids

vibratory sensation, abnormal

violent behavior

viral infection

viral infection, CNS

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual impairment

visual loss, progressive

visual loss, slow

vitamin supplementation

Vogt-Koyanagi-Harada syndrome

voice, abnormality of

walking, difficulty with

weakness, fatiguable

weakness, generalized

weakness, progressive

Wernicke's aphasia

Wernicke's encephalopathy

white matter disease

wide based gait

word-finding difficulty

x-linked intellectual deficit

x-linked mental retardation

Showing articles 250 to 300 of 18064 << Previous Next >>

Cyclic Vomiting Syndrome in Children
AJGH 2:doi:10.33552/AJGH.2020, Al-Ansari, N., 2020

Human Parechovirus Meningoencephalitis: Neuroimaging in the Era of Polymerase Chain Reaction-Based Testing
AJNR 40:1418-1421, Sarma, A.,et al, 2019

Central Nervous System Infections Due to Coccidioidomycosis
J Fungi 5:2-12, Jackson, N.R.,et al, 2019

Treatment Approaches for MOG-Ab-Associated Demyelination in Children
Curr Treat Options Neurol 21:2, Hacohen, Y. & Banweil, B., 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

Long-Term Treatment Effect in Cerebrotendinous Xanthomatosis Depends on Age at Treatment Start
Neurol 92:e83-e95, Stelten, B.M.L.,et al, 2019

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

A 61-Year-Old Woman with Acute Onset Dysgraphia
Neurol 92:e386-e391, Smith, L.R.,et al, 2019

Toxic Diffuse Isolated Cerebellar Edema from Over-the-Counter Health Supplements
Neurol 92:965-966, Kim, D.D.,et al, 2019

A Teenager with Persistent Headache
Neurol 92:e1526-e1531, Hu, Y.,et al, 2019

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

Bobblehead-Doll Syndrome
NEJM 380:e5, Sacks, C.A., 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

Clinicopathologic Conference, Pernicious Anemia (Vitamin B12 Deficiency)
NEJM 380:665-674, Case 5-2019, 2019

Fibromuscular Dysplasia and Its Neurologic Manifestations
JAMA Neurol 76:217-226, Touze, E.,et al, 2019

A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
Neurol 92:486-492, Lau, K.H.V.,et al, 2019

Management of Stroke in Neonates and Children
Stroke 50:e51-e96, Ferriero, D.M.,et al, 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

Clinical Characteristics and Outcomes of Methamphetamine-Associated Intracerebral Hemorrhage
Neurol 93:e1-e7, Swor, D.E.,et al, 2019

Case 27-2019:A 16-Year-Old Girl with Head Trauma During a Sailboat Race
CPC,Concussion,Benign Paroxysmal Positional Vertigo, Case 27-2019, NEJM 381:863-871, Iaccarino,M.A.,et al, 2019

Childhood Primary Angiitis of the Central Nervous System
www.UptoDate.com, Dec, Twilt, M. & Benseler, S., 2019

Acute Treatment of Migraine in Children and Adolescents
Neurol 93:487-499, Oskoui, M.,et al, 2019

Pharmacologic Treatment for Pediatric Migraine Prevention
Neurol 93:500-509, Oskoui, M.,et al, 2019

Rapidly Progressive Vision Loss in a Patient with Breast Cancer
JAMA 322:1098-1099, Izzo, M.C.,et al, 2019

Recurrent Epistaxis in an Adolescent
BMJ 367:I5393, McLaren, O. & Ronan, N., 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Postraumatic Stress Disorder and Risk for Stroke in Young and Middle-Aged Adults
Stroke 50:2996-2003, Rosman, L.,et al, 2019

Acute Rheumatic Fever: Clinical Manifestations and Diagnosis
www.UptoDate.com, Oct, Steer, A. & Gibofsky, A., 2019

Reversible Cerebral Vasoconstriciton Syndrome
www.UptoDate.com, June, Singhal, A., 2019

When MRI is a Clue in Episodic Ataxia
Neurol 93:e2074-e2075, Dhawan, S.R.,et al, 2019

Orofacial Dyskinesia in a Young Man
JAMA Neurol 76:1517-1518, Tian, X.,et al, 2019

Acute Paraplegia in a Healthy Child
BMJ 367:L6257, Haque, A.K.M.,et al, 2019

Lyme Myelopathy:Case Report and Literature Review of a Rare But Treatable Disorder
Mult Scler Relat Disord 29:1-6, Kaiser,E.A.,et, 2019

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
Pediatr Emer Care 35:e67-e69, Kartal,A., 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Cerebral Sinovenous Thrombosis as a Compliction of Otitis Media
Clin Case Rep 7:186-188, Salloum,S. and Bezer,K., 2019

Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
Pract Neurol 18:201-210, Khadilkar,S.V.,et al, 2018

Pediatric HIV Infection: Classification, Clinical Manifestations, and Outcome
www.UptoDate.com, June, Gillespie, S.L., 2018

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,et al, 2018

Pontine Tegmental Cap Dysplasia in a Neonate
Neuol 91:e2100-e2101, Bilgin, N.,et al, 2018

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Use of Newer Disease-Modifying Therapies in Pediatric Multiple Sclerosis in the US
Neurol 91:e1778-e1787, Krysko, K.M.,et al, 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Hearing and Vision Loss in an Older Man
JAMA Neurol 75:1439-1440, Ho, V.M.,et al, 2018

Trial of Fingolimod Versus Interferon Beta-1a in Pediatric Multiple Sclerosis
NEJM 379:1017-1027, Chitnis, T.,et al, 2018

Distinctive Imaging in a Paucisymptomatic Child with Leukodystrophy
Neruol 91:e1368-e1369, Sharawat, I.K.,et al, 2018

Childhood Seizures After Phototherapy
Pediatrics 142:e20180648, Newman, T.B.,et al, 2018

Facial Myokymia and Myorhythmia in Anti-IgLON5 Disease
Neurol 91:e1659, Vetter, E.,et al, 2018

Showing articles 250 to 300 of 18064 << Previous Next >>