Neudle.com: cerebellar ataxia children

Differential
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acetazolamide

aciduria

acute ataxia of childhood

acute cerebellar ataxia

advances in neurology

aggression

alcohol intolerance

alpha-fetoprotein

alternating rapid movement

Alzheimer's disease

AMPA receptor antibodies

amyotrophic lateral sclerosis

aneurysm, vertebral basilar system

Angelman syndrome

angiography, cerebral

angiography, posterior fossa

angiotensin-converting enzyme

aniridia

ankle reflex, absent

anti GQ1b IgG antibody

anticonvulsants

anticonvulsants, effectiveness

anxiety

apraxia of eye movements

areflexia

Arnold Chiari malformation

arterial dissection

arterial dissection, intracranial

arterial dissection, ruptured

arterial dissection, vertebral

ataxia telangiectasia

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

Babinski sign

bacterial infection

bacterial infection, CNS

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

behavioral disorder, acute

blindness

blood dyscrasias, neurologic findings with

brachycephaly

brainstem, atrophy

brainstem, dysfunction

brainstem, glioma in children

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

CAG repeats

calcification, intracranial

carcinoembryonic antigen

CAT scan, emission, abnormal

CAT scan, pelvis

cataplexy

cataracts

cataracts, congenital

cauda equina, enhancement

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar pontine angle

cerebellar pontine angle tumor

cerebellar vermis

cerebellitis

cerebellitis, autoimmune

cerebellum, neoplasms of

cerebral cortical atrophy

cerebral edema

cerebral folate deficiency syndrome

cerebral palsy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, red cells in

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, prognosis in

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

cerebrovascular disease, surgical treatment of

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clonus

coenzyme Q10

coenzyme Q10 deficiency

corpus callosum, thinning

counterimmunoelectrophoresis

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

degenerative diseases of CNS

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatitis herpetiformis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

drug induced neurologic disorders in children

electroencephalogram, abnormalities of

electromyogram

electron microscopy

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis, postinfectious

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

finger nose finger test

fingerprint bodies

fish

Fisher's syndrome

fluorescene in situ hybridization

folic acid

folic acid deficiency

foot deformity

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

fragile-X syndrome

Friedreich's ataxia

fundus, abnormality of

gait disorder

gait, spastic

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

Gillespie syndrome

glioblastoma multiforme(astrocytoma Gr.III)

glutamic acid

glutamic acid decarboxylase, antibody

gluten ataxia

gluten sensitivity

gluten-free diet

granulomatous disease

growth hormone

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, variant forms of

headache, sudden onset of

hearing loss

heel-knee-shin test

hemosiderosis of CNS, superficial

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

HLA

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

huntingtin

Huntington's chorea

hydroxyglutaric aciduria

hypertension, cerebrovascular disease with

hypopigmentation of skin

hyporeflexia

hypothalamus

hypothalamus, disturbance of

hypotonia

hypotonia, infants

hypoxia

iatrogenic neurologic disorders

imbalance

immunization, neurologic complications with

immunodeficiency

immunosuppression

immunotherapy

inborn errors of metabolism

inclusion bodies

incoordination

infection

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

intracranial pressure, increased

intrathecal medication

iris, abnormal

irritability

Jakob-Creutzfeldt disease

learning disability, in children

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukemia

leukodystrophy

limbic encephalitis

lipid storage disorder of CNS

lymphoma

lysosomal storage disease

Marinesco-Sjogren syndrome

masked facies

mediastinum, mass of

memory, impairment of

meningismus

meningitis

meningoencephalitis, mumps

meningovascular syphilis

mental retardation

mental status, abnormal

metabolic disorder, primary

microcephaly

microdontia

middle cerebellar peduncle

middle cerebellar peduncle, lesion, bilateral

migraine

migraine, children

misdiagnosis

mitochondrial disease

molecular genetics

monoclonal antibodies

mortality

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

MRI, negative

MRI, serial

multiple sclerosis

multiple system atrophy

mycoplasma pneumoniae

myelinolysis, extrapontine

neoplasm, posterior fossa

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-treatment of

nephrotic syndrome

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neurocutaneous disease

neuroendocrinology

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neuronal ceroid-lipofuscinosis

nystagmus, hereditary

nystagmus, periodic

nystagmus, rotary

ocular motility, disorders of

oculodentodigital dysplasia

ophelia syndrome

ophthalmoplegia

opsoclonus

opsoclonus-myoclonus syndrome

optical coherence tomography

oral ulcerations

oscillopsia

osmotic demyelination syndrome

Parkinsonism syndrome

parotitis

paroxysmal neurologic deficits

past pointing

pathology

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

personality change

piperazine

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

Poretti-Boltshauser syndrome

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

progeria

prognathism

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

Refsum's disease

remote effect of cancer on the nervous system

renal failure

respiratory failure

respiratory tract infection

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, tonic-clonic

seizure, treatment of

sensorineural hearing loss

serologic testing

serologic testing, false negative

seronegative

short stature

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

smiling

sodium channel dysfunction

spastic ataxia

spasticity

speech disorder

speech disorder, childhood

speech, delayed development of

speech, loss of

spinal cord

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinocerebellar degeneration

splenomegaly

spongy degeneration of brain

startle myoclonus

status epilepticus

steroid

steroid therapy, CNS treatment and complications with

strabismus

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

subarachnoid hemorrhage

subarachnoid hemorrhage, recurrent

symmetric brain lesions

syndactyly

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

tongue, protrusion of

topiramate

torticollis

toxins, nervous system

transient ischemic attack

treatment of neurologic disorder

trinucleotide repeats

vertebral-basilar insufficiency

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual impairment

visual loss

visual loss, progressive

visual loss, slow

Von Hippel Lindau

walking, difficulty with

X-linked bulbospinal neuronopathy

Showing articles 50 to 100 of 4221 << Previous Next >>

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Acute Cerebellar Ataxia Associated With Epstein-Barr Virus Infection
JAMA 243:148-149, Cleary,T.G.,et al, 1980

Mycoplasma Antibody in Guillain-Barre Syndrome & Other Neurological Disorders
Ann Neurol 7:108-112, Goldschmidt,B.,et al, 1980

Fusiform Basilar Artery Aneurysm in a Child
Neurol 29:1045-1049, Read,D.,et al, 1979

Hereditary Paroxysmal Ataxia:Response to Acetazolamide
Neurol 28:1259-1264, Griggs,R.C.,et al, 1978

Peperazine Neurotoxicity:"Worm Wobble"
BMJ 792, 1971 Dec., Parsons,A.C., 1971

Brain Stem Tumors of Childhood & Adolescence
Am J Dis Child 119:465-472, Panitch,H.S.,et al, 1970

Ataxia In Childhood
Dev Med Child Neurol 10:388-389, Wilson,J., 1968

Cerebellar Ataxia in Children
Handout & References., Gilbert,J.J., 1850

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

Recurrent Rhombencephalitis Associatedwith Anti-GAD65 Antibody
Neurol 102:e208040, Alferes,A.R.,et al, 2024

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

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

Occult Breast Cancer with Anti-Ri Antibody Positivity and Pontine Hot Cross Bun Sign
JAMA Neurol 80:207-208, Liu,Y.,et al, 2023

Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023

An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
Neurol 101:e570-e575, Rodrigo-Gisbert,M.,et al, 2023

Wernekinck Commissure Syndrome
Radiopaedia doi.org/10.53347/rlD-85274, Aug, Deng,F.,et al, 2023

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

A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023

Shrimp Sign in Ataxic Cerebellar Progressive Multifocal Leukoencephalopathy
Neurol 101:918-919, Varela,F.J.,et al, 2023

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

A Dizzy Architect
Neurol 98:543-549, Scutelnic, A.,et al, 2022

A 57-Year-Old Man with Stepwise Progressive Paraparesis, Sensory Loss, Urinary Retention, and Constipation
Neurol 98:e555-e560, Alkabie, S.,et al, 2022

A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
Neurol 98:e669-e674, Sakoda, M.,et al, 2022

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

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

A 71-Year-Old Man with Horizontal Gaze Palsy, Anarthria, and Quadriparesis
Neurol 96:1146-1150, Cheema, I.,et al, 2021

A 65-Year-Old Woman with Tremor
Neurol 97:e1257-e1261, Ye, J.,et al, 2021

Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
NEJM 385:1317-1325, Case 30-2021, 2021

A 13-Year-Old Boy with Subacute-Onset Spastic Gait
JAMA Neurol 78:e1-e2, Xie, N.,et al, 2021

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

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

Progressive Ataxia and Doenbeat Nystagmus in an Adult
JAMA Neurol 78:1018-10019, Fernandez, A.C.,et al, 2021

A Vertebral Artery Halo Sign Indicates Giant Cell Arteritis Affecting the Posterior Circulation of the Brain
Lancet 397:e6, Lambrechts, R.A.,et al, 2021

Clinicopathologic Conference, HIV Type 2 Infection & Cerebral Toxoplasmosis
NEJM 383:859-866, Case 27-2020, 2020

Pediatric Leigh Syndrome
Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020

An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
Neurol 95:e1760-e1763, Brigham, E.,et al, 2020

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

Bithalamic Lesions
Stroke 51:e355-e358, Chen, P.M.,et al, 2020

Clinical features, prognostic factors, and antibody effects in anti-mGluR1 encephalitis
Neurol 95:e3012-e3025, Spatola, M.,et al, 2020

Clinicopathologic conference, Vitamin D deficiency
NEJM 383:2462-2470, Case 39-2020, 2020

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 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
Neurol 94:e1664-e1669, Han, F.,et al, 2020

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020

Showing articles 50 to 100 of 4221 << Previous Next >>