Neudle.com: "dystonia children"

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abscess, intracerebral

abscess, intracranial

abscess, retropharyngeal

abscess, sphenoid sinus

acetazolamide

aciduria

acrocyanosis

advances in neurology

adverse drug reaction

agitation

Aicardi-Goutieres syndrome

algorithm

alpha-fetoprotein

alveolar hypoventilation

ammonia

AMPA receptor antibodies

aneurysm

aneurysm, intracranial

angiography, cerebral

angiography, posterior fossa

anorexia

anti basal ganglia antibodies

anti GQ1b IgG antibody

anticholinergic drugs

anti-dopamine 2 receptor antibody

anxiety

aortic valve, lesion of

apraxia of eye movements

arteriovenous malformation

arteriovenous malformation, brainstem

arteriovenous malformation, cerebral

arylsulfatase A

ataxia

ataxia telangiectasia

atlanto-axial subluxation

atypical

auditory evoked brainstem potentials

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

Babinski sign

bacterial infection

basal ganglia

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

benign essential tremor

biopterin deficiency

biotin

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

brainstem, hemorrhage, primary

brainstem, lesion of

brainstem, vascular malformation of

calcification, intracranial

carcinoembryonic antigen

carcinoma

cardiomyopathy

cardiopulmonary bypass

carotid artery occlusion, neck

CAT scan

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CAT scan, contrast enhanced

CAT scan, isodense lesion with acute hemorrhage

cataracts

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cavernous hemangioma

cavernous sinus, syndrome

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar degeneration

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cerebellar hemorrhage

cerebellar lesion

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cerebellar pontine angle tumor

cerebral cortex

cerebral cortical atrophy

cerebral palsy

cerebral vasculature, calcification

cerebral venous thrombosis

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cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, young adult

cervical spine

channelopathy

chilbran skin lesions

children

chiropractic manipulation

chiropractic manipulation, neurologic complications with

chromosomal abnormality

chronic progressive external ophthalmoplegia

cisterna magna

Clinical Pathologic Conference(C.P.C.)

cranial nerve palsies

cranial neuropathy, multiple

C-reactive protein, elevated

crying

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

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dementia, childhood

demyelinating disease

dentate nuclei, lesion of

depression

developmental milestones, loss of

developmental retardation

diabetes mellitus

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diet

differential diagnosis

diurnal variation

donut sign

dopa responsive dystonia

dopamine receptor, D2

down-beat nystagmus

drooling

drug induced neurologic disorders

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dural sinus thrombosis

dying

dysarthria

dyskinesia

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dyskinesia, causes of

dyskinesia, drug induced

dysphagia

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dystonia

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dystonia, cervical

dystonia, children

dystonia, delayed onset

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, focal

dystonia, painful

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dystonia, treatment of

dystonic reaction, acute

DYT1 mutation

ear, pain in

echocardiogram

electroencephalogram, abnormalities of

encephalitis lethargica

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, etiology

encephalitis, paraneoplastic

encephalitis, viral

encephalopathy

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

episodic neurologic deficits

epsilon sarcoglycan gene

exercise-induced neurologic dysfunction

extrapyramidal

eye movement, disorders of

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

frontal lobe, pathologic signs of

fungal infection, CNS

gait disorder

galactorrhea

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gaze palsy

gaze palsy, supranuclear

gene

gene mutation

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

Gilles de la Tourette syndrome

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

growth retardation

Hallervorden Spatz disease

hands, fisted

head injury

head injury, pediatric

hepatolenticular degeneration(Wilson's disease)

Huntington's chorea, genetic counselling

Huntington's disease, children

hydrocephalus

hyperpyrexia, CNS disorder causing

iatrogenic neurologic disorders

imbalance

immunodeficiency

immunosuppression

immunosuppressive agents

immunotherapy

inborn errors of metabolism

intellectual deterioration

interferon alpha

internal cerebral vein

internet

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracranial hemorrhage

intracranial pressure, increased

jugular foramen syndrome

Kearns-Sayre syndrome

ketogenic diet

L-dopa

Leber's hereditary optic neuropathy

leg spasms

leg spasms, painful

Leigh's disease

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia

leukodystrophy

leukoencephalopathy

level of consciousness, decreased

limbic encephalitis

lipid storage disorder of CNS

liver disease

lumbar puncture

lymphoma

malformation, vascular

malformation, vascular, cerebral

mastoiditis

MELAS syndrome

memory, impairment of

meningismus

meningitis

mental retardation

mental status, abnormal

MERRF syndrome

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methylmalonic acidemia

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoclonal antibodies

morphine

mortality

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, treatment of

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR

MRI, paramagnetic effect

multiple sclerosis, differential diagnosis of

multiple system atrophy

mycoplasma

mycoplasma pneumoniae

myopathy, mitochondrial

nasal stuffiness

neck pain

neoplasm, posterior fossa

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-infants

nerve biopsy

nerve conduction studies

neurocutaneous disease

neuroendocrinology

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neuropathy, peripheral

neurotomy

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neurotoxin

next-generation sequencing

Niemann-Pick disease

NMDA antagonists

nystagmus

nystagmus, congenital

nystagmus, dissociated

nystagmus, infancy

nystagmus, monocular

nystagmus, vertical

obsessive-compulsive disorder

occipital lobe, lesion of

ocular motility, disorders of

otitis, neurologic complications with

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, juvenile

Parkinson disease, treatment of

Parkinsonism syndrome

pathology

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

pediatric opioid use associated neurotoxicity

personality change

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleural effusion

poison, neurologic problems with

POLG1 gene

poliomyelitis

polycythemia, primary

pons, lesion of

pontine glioma

posterior fossa, arteriovenous malformation

posterior fossa, lesion of

posterior fossa, signs of

potassium channel antibodies

practice guidelines

precipitating factors

prenatal

primary episodic ataxia

primary familial brain calcification

procyclidine

progeria

prognosis

progressive neurologic disorder

prolactin, elevated

proptosis

proptosis, unilateral

pseudohypoparathyroidism

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

ptosis

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

radiation hypersensitivity

remote effect of cancer on the nervous system

respirator

restless leg syndrome

retinitis pigmentosa

retinopathy

reversible neurologic disorder

sensorineural hearing loss

serologic testing

serologic testing, false negative

seronegative

sexual behavior, disorder of

short stature

sinemet

sinusitis

skin, lesions in neurologic disorders

sleep pathology and physiology

speech disorder, childhood

spinal cord, neoplasm

spinal cord, neoplasm, infants and children

spinal muscular atrophy

splenomegaly

spongy degeneration of brain

startle reaction

stereotaxic surgery

steroid

steroid therapy, CNS treatment and complications with

stimulation, deep brain

stimulation, deep brain, bilateral

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

subarachnoid hemorrhage

substantia nigra

subtraction of x-rays

suck, poor

suicide

sural nerve

symmetric brain lesions

syringomyelia

tardive dyskinesia

tardive dyskinesia, treatment of

thalamus, infarction of

thalamus, lesion of-bilateral

torticollis, acute infectious

torticollis, benign paroxysmal

torticollis, familial

torticollis, infants and children

torticollis, ocular

toxins, nervous system

treatment of neurologic disorder

tremor

tremor, postural

trigeminal neuralgia

trinucleotide repeats

tripping

tyrosine hydroxylase deficiency

valvulopathy

viral infection

viral infection, CNS

visual evoked response

visual impairment

walking

walking frame

walking, difficulty with

Showing articles 0 to 50 of 3064 Next >>

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

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Torticollis in a Child with Otalgia
BMJ 378:e070608, Sarathi, C.I.P.,et al, 2022

Clinical and Radiologic Features of Pedicatric Opioid Use-Associated Neurotoxicity with Cerebellar Edema (POUNCE) Syndrome
Neurol 94:710-712, Kim, D.D. & Prasad, A.N., 2020

A Young Generalized Dystonia Patient with Globus-Pallidus-Specific Lesion
Ann Neurol 88:637-638, Wu, H.,et al, 2020

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

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Treatable Bilateral Striatal Lesions Related to Anti-Dopamine 2 Receptor
Neurol 91:98-101, Marques-Matos, C.,et al, 2018

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

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 2017

A Demure Teenager and Her Dystonic Foot
Neurol 89:e71-e75, Cullinane, P.W.,et al, 2017

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

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease
JAMA Neurol 73:668-674, Martikainen, M.H.,et al, 2016

Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
JNNP 86:774-781, Van Egmond, M.E.,et al, 2015

Inherited Metabolic Diseases of the Nervous System, Biopterine Deficiency
Adams & Victors Principles of Neurology, Chp 37, pg 951, Ropper, A.H.,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, Subacute Necrotizing Encephalopathy (Leigh Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 996, Ropper, A.H.,et al, 2014

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

Dopa-Responsive Dystonia Revisited
Arch Neurol 69:1558-1562, Tadic, V.,et al, 2012

MRI in Methylmalonic Acidemia
Neurol 74:e14, Bindu, P.S.,et al, 2010

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

Pneumonias Link With the Head and Neck
Lancet 376:388, Mariotti,P., et al, 2010

Huntingtons Disease
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 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

N-Methyl-D-Aspartate Receptor Antibodies in Pediatric Dyskinetic Encephalitis Lethargica
Ann Neurol 66:704-709, Dale,R.,et al, 2009

The Expanding Phenotype of GLUT1-Deficiency Syndrome
Brain & Dev 31:545-552, Brockmann,K., 2009

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

Poststreptococcal Dystonia With Bilateral Striatal Enlargement: MR Imaging and Spectroscopic Findings
AJNR 29:1276-1278, Kendi,A.T.K.,et al., 2008

Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
Brain 130:2484-2493, Jen, J.C.,et al, 2007

Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
NEJM 355:831-839, Case 26-2006, 2006

Dopamine-Responsive Dystonia
eMedicine (Apr), Nikhar,N.K., 2006

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Dystonia and Chorea in Acquired Systemic Disorders
JNNP 65:436-445, Janavs,J.L.&Aminoff,M.J., 1998

Long-Term Follow-Up of Levodopa Responsiveness in Generalized Dystonia
Arch Neurol 55:1320-1323, Dewey,R.B.,et al, 1998

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Ependymomas of the Posterior Cranial Fossa:CT and MRI Findings
Neuroradiology 37:238-243, Tortori-Donati,P.,et al, 1995

Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
J Pediatr 123:242-247, Kelly,D.A.,et al, 1993

Quadriplegia after Chiropractic Manip in Infant with Congen Torticollis by a Spinal Cord Astrocy
J Pediatr 120:266-269, Shafrir,Y.&Kaufman,B.A., 1992

The Sit-up Test:An Alternative Clinical Test for Evaluating Pediatric Torticollis
Pediatrics 90:612-615, Caputo,A.R.,et al, 1992

Focal Dystonia Secondary to Cavernous Angioma of Basal Ganglia, Case Report & Review of Literature
Neurosurg 31:1108-1112, Lorenxana,L.,et al, 1992

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

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

Magnetic Resonance Imaging in Pathologically Proven Hallervorden-Spatz Disease
Neurol 39:440-442, Schaffert,D.A.,et al, 1989

Tetrabenazine Therapy of Dystonia, Chorea, Tics, & Other Dyskinesias
Neurol 38:391-394, Jankovic,J.&Orman,J., 1988

Vascular Malformations of the Posterior Fossa, Clinical & Radiologic Features
Arch Neurol 44:965-969, Silber,M.H.,et al, 1987

Arteriovenous Malformation Presenting as Hemidystonia
Neurol 36:1590-1593, Friedman,D.I.,et al, 1986

Hemidystonia:A Report of 22 Patients & a Review of the Literature
JNNP 48:650-657, Pettigrew,L.C.&Jankovic,J., 1985

Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
Case 7-1984, NEJM 310:445-4551984., , 1984

Showing articles 0 to 50 of 3064 Next >>