Neudle.com: "speech disorder childhood"

Differential
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aciduria

acquired immunodeficiency syndrome

acrocyanosis

acute ataxia of childhood

acute cerebellar ataxia

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

advances in neurology

affect, inappropriate

Africa

aggression

agitation

Aicardi-Goutieres syndrome

akinetic mute

alcohol

alcohol intolerance

alcohol, neurologic complications with

alcoholism

alopecia

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alveolar hypoventilation

angiitis, granulomatous of CNS

ankle, swelling of

anomic aphasia

anorexia

antibiotics, neurologic complications with

anxiety

aphasia

aphasia, children

aphasia, classification of

aphasia, recovery from

ataxia telangiectasia

attention deficit disorder with hyperactivity

attention span

atypical

audiologic test to localize site of pathology

audiology

auditory dominance

auditory processing, impaired

autism

autoantibodies

autoimmune disease

autonomic dysfunction

Babinski sign

basal ganglia

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

bifid uvula

biotin

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

bone marrow transplantation

brain biopsy, stereotaxic

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

Brown-Vialetto-Van Laere syndrome

bruxism

burning feet

burning feet, differential diagnosis of

CAG repeats

calcification, intracranial

CAT scan, angiography

CAT scan, dense artery sign

catatonia

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 disease, eye movement disorder in

cerebellar hypoplasia

cerebellum, disease of

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral dominance

cerebral embolism

cerebral embolism, mechanical extraction

cerebral palsy

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

Chagas'disease

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chilbran skin lesions

chromosomal abnormality

chromosome 15

chromosome 7

cirrhosis

cirrhosis, causes of childhood

cleft palate

Clinical Pathologic Conference(C.P.C.)

congenital bilateral perisylvian syndrome

congenital myasthenic syndromes

corpus callosum, infarction of

corpus callosum, lesion of

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

crying

crying, pathologic

cultured skin fibroblasts

cyanide poison

cytomegalic inclusion disease

cytomegalovirus infection

degenerative diseases of CNS

demyelinating disease

dense basilar artery sign

dense middle cerebral artery sign

dentate nuclei

dentate nuclei, lesion of

depression

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty climbing stairs

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

diplegia, atonic

diplegia, spastic cerebral

diplopia

disconnection syndrome

doll's head maneuver

dopa responsive dystonia

dysequilibrium syndrome

dyskinesia

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, children

dystonia, laryngeal

dystonia, painful

dystonia, treatment of

dystrophin

DYT1 mutation

echolalia

EDTA(ehtylenediamine tetraacetic acid)

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, sleep

electromyogram

electron microscopy

ELISA

embolism, paradoxical

embolism, vertebral-basilar artery

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, etiology

encephalitis, viral

encephalopathy

encephalopathy, acute

encephalopathy, metabolic

encephalopathy, parainfectious

encephalopathy, progressive

endovascular therapy

enuresis

enzyme, defect

epidemiology of neurology

epilepsia partialis continua

epileptic encephalopathy

epsilon sarcoglycan gene

equinovarus

exome sequencing

eye movement, disorders of

eyedness

face, inexpressive

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial weakness

facial weakness, bilateral

fetal alcohol syndrome

fetus

fever

fine motor function, impaired

finger nose finger test

fingerprint bodies

fish

fluctuate

fluorescene in situ hybridization

folic acid

footedness

frontal lobe, pathologic signs of

fucosidosis

fungal infection, CNS

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Hallervorden Spatz disease

hallucination

hallucination, visual

head injury, pediatric

hearing problems in children

heavy metal intoxication

hemiparesis, transient

hemiplegia

hemisensory loss

hepatitis

hepatolenticular degeneration(Wilson's disease)

human immunodeficiency virus type 1

hydrocephalus

hydroxyglutaric aciduria

hyperactivity

hyperintense vessel sign

hyperkalemia

hyperosmolality

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hyperreflexia

hypertension

hypertonia

hypokinetic left ventricle

hyponatremia

hypopigmentation of skin

hyporeflexia

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

incoordination

industrial neurologic disorders

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

Kayser-Fleischer ring

klippel feil syndrome

konzo

lactic acidemia

Landau-Kleffner syndrome

language

language delay

language development, neurologic basis of

language disorders in children

laughing, pathologic

L-dopa

learning disability

learning disability, in children

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

level of consciousness, decreased

liver disease

liver function enzymes

locked-in syndrome

Lyme disease

Lyme disease, children

lymphoma involving CNS

lysosomal storage disease

macrocephaly

macrognathia

magnetic source image

magnetoencephalography

malabsorption syndrome

manganese intoxication

maple syrup urine disease

marche a petits pas

masked facies

medulla oblongata, neoplasm of

medulloblastoma

megalencephaly

megalencephaly, idiopathic

memory, defect of recent

memory, impairment of

meningismus

meningitis

meningitis, aseptic

meningitis, CSF cell count-normal

meningitis, recurrent

meningoencephalitis

mental retardation

mental status, abnormal

MERCI trial

MERS

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

midline defect in children

migraine

mirror writing

misdiagnosis

mitochondrial disease

molecular genetics

monoclonal antibodies

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR, hyperintense vessels

MRI, functional

MRI, negative

MRI, paramagnetic effect

MRI, pelvis

MRI, serial

MRI, T1 weighted high signal foci

MRS

muscle cramp

muscle stiffness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, central nervous system abnormality

muscular dystrophy, Duchenne

mutism

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, familial incidence of

myelinolysis, extrapontine

neoplasm, posterior fossa

neoplasm, primary of CNS

neoplasm, primary of CNS-children

nerve biopsy

nerve conduction studies

neurofibromatosis 1

neurologic complications

neurologic complications of, burns

neurologic complications of, surgery

neurologic disease, diagnoses of

neurologic examination, focal

neurologic testing

neuromuscular junction

neuronal ceroid-lipofuscinosis

neuropathology

neuropathology, brain

neuropathy

neuropathy, hereditary peripheral

non-dominant hemisphere

nonverbal

nystagmus

nystagmus, rotary

nystagmus, spontaneous

opened mouth

operculum syndrome

operculum syndrome, bilateral

osmotic demyelination syndrome

palatal myoclonus

palatopharyngeal incompetence

paralysis, acute areflexic

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, spastic

paraplegia

paresthesias

parietal lobe, syndromes of

Parkinson disease

Parkinson disease, freezing phenomena in

Parkinsonism syndrome

paroxysmal neurologic deficits

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

polyneuropathy, uremic

pons, infarction of

pons, lesion of

positional head-hanging test

postural abnormality

precipitating factors

pregnancy, neurologic complications in

prenatal

prevention of neurologic disorders

prognathism

prognosis

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

psychosis

psychosis, childhood

psychosocial aspects

psychosomatic disease

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

quadriparesis

quadriplegia

reading disorder, acquired

recurrent

release phenomena

remote effect of cancer on the nervous system

renal transplantation

renal tubular acidosis

respirations in CNS disease

respirator

restless leg syndrome

reticulum cell sarcoma

reversible neurologic disorder

reversible splenial lesion syndrome

review article

rhabdomyolysis

rheumatic brain disease

rheumatic fever

rheumatic heart disease

riboflavin transporter deficiency

rubella encephalitis, progressive

saccadic eye movements, abnormal

salivation, excessive

seizure, advice to parents and teachers regarding

seizure, children

seizure, focus

seizure, psychosocial aspects of

seizure, recurrent

seizure, surgical treatment of

seizure, treatment of

seizure, workup of

sexual behavior, disorder of

sign language

skin, biopsy

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

speech disorder, childhood

speech disorder, non aphasic

speech lateralization

speech therapy

speech, delayed development of

spinocerebellar ataxia

spinocerebellar ataxia type 7

splenium of corpus callosum

splenomegaly

spongy degeneration of brain

stimulation, deep brain

stimulation, deep brain, bilateral

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

stuttering

stuttering following CVA

subdural hematoma

substantia nigra

suck, poor

symmetric brain lesions

temporal lobe, lesion

temporal lobe, lesion, bilateral

tongue, impaired movements of

tongue, protrusion of

tonic foot response

tonic spasms

torticollis

toxoplasmosis, acquired

toxoplasmosis, CNS

transient neurologic deficit

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, intention

trinucleotide repeats

tuberculosis, miliary

tyrosine hydroxylase deficiency

upgaze, paralysis of

uremia

uremic encephalopathy

uremic twitching

uric acid, low

urine test for metabolic disorders

very long chain fatty acids

vestibulopathy

vibratory sensation, abnormal

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual impairment

visual loss

visual loss, progressive

visual loss, slow

vitamin supplementation

vitiligo

Vogt-Koyanagi-Harada syndrome

voice, abnormality of

Wada test

walking frame

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

weight loss

welder

Wernicke's aphasia

Wernicke's encephalopathy

word-finding difficulty

workup

wrist drop

writing

Showing articles 0 to 50 of 17745 Next >>

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Manganese Accumulation in the Brain
NEJM 389:1320, Sherman,S.V., 2023

Pediatric Parainfectious Encephalitis Associated with COVID-19
Neurol 96:541-544, Gaughan, M.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Wilson Disease
NIDDK Oct2018, , 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

An 11-year-old Boy with Language Disorder and Epilepsy
Neurol 86:e48-e53, Dong, L. & Zhou, X., 2016

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

Cyclical Konzo Epidemics and Climate Variability
Ann Neurol 77:371-380, Oluwole, O.S.A., 2015

Identifying and Managing Common Childhood Language and Speech Impairments
BMJ 350:h2318, Reilly, S.,et al, 2015

A 32-year-old Woman with Right-Sided Numbness and Word-Finding Difficulties
Neurol 83:e98-e102, Busza, A.,et al, 2014

Degenerative Diseases of the Nervous System, Dystonia Musculorum Deformans
Adams & Victors Principles of Neurology, Chp 39, pg 1099, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Central Pontine Myelinolysis and other Patterns of Osmotic Demyelination
Adams & Victors Principles of Neurology Chp 40, pg 1149, Ropper, A.H.,et al, 2014

Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Mercury
Adams & Victors Principles of Neurology Chp 43, pg 1223, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Acute Cerebellitis (Acute Ataxia of Childhood)
Adams & Victors Principles of Neurology, Chp 33, pg 754, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Progressive Rubella Panencephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 766, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 996, Ropper, A.H.,et al, 2014

Gait Freezing and Speech Disturbance in Parkinsons Disease
Neurol Sci 35:357-363, Park,H.K.,et al, 2014

Cognitive Delay in a 7-year-old Girl
Neurol 81: e148-e150, Cachia, D. & Stine, C., 2013

Clinicopathologic Conference, Acute Ischemic Stroke due to Basilar Artery Embolism. Patent Foramen Ovale
NEJM 367:1450-1460, Case 31-2012, 2012

Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012

Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study
Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012

Folic Acid Supplements in Pregnancy and Severe Language Delay in Children
JAMA 36:1566-1573, Roth, C.,et al, 2011

Late onset autism and anti-NMDA-receptor encephalitis
Lancet 378:98;378, Creten, C.,et al, 2011

Profound Deafness in Childhood
NEJM 363:1438-1450, Kral,A.,et al, 2010

Clinical and Radiological Features of Rotavirus Cerebellitis
AJNR 31:1591-1595, Takanashi,J.,et al, 2010

Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
Ann Neurol 66:11-18,1, Florance,N.R.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008

Age and High-Dose Methotrexate are Associated to Clinical Acute Encephalopathy in FRALLE 93 Trial for Acute Lymphoblastic Leukemia in Children
Leukemia 21:238-247, Dufourg, M.N.,et al, 2007

Magnetoencephalography (MEG) and Magnetic Source Imaging (MSI)
The Neurologist 10:138-153, Wheless,J.W.,et al, 2004

MR Brain Imaging of Fucosidosis Type I
AJNR 22:777-780, Galluzzi,P.,et al, 2001

A Six-Year-Old Girl with Tick paralysis
NEJM 342:90-94, Felz,M.W.,et al, 2000

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Neurodevelopmental Dysfunction Among Nonreferred Children with Idiopathic Megalencephaly
J Pediatr 131:320-324, Sandler,A.D.,et al, 1997

Clinicopath Conf
Granulomatous Angiitis of CNS, Case 33-1995, NEJM 333:1135-1143995., , 1995

Brainstem Tumors in Patients with Neurofibromatosis Type 1:A Distinct Clinical Entity
Neurol 45:1897-1902, Molloy,P.T.,et al, 1995

Functional Dysphonia
BMJ 311:1039-1040, Wilson,J.A.,et al, 1995

The Landau-Kleffner Syndrome
Arch Dis Child 72:386-387, Appleton,R.E., 1995

Speech Motor Control Disorder after HIV Infection
Neurol 44:2187-2189, Lopez,O.L.,et al, 1994

Showing articles 0 to 50 of 17745 Next >>