Neudle.com: "cerebellar atrophy secondary"

Differential
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abdominal contractions

abdominal distention

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

acquired immunodeficiency syndrome, infants and children

ACTH, ectopic syndrome of

Adies pupil

adverse drug reaction

agitation

alcohol

alcohol intoxication

alcohol, blood level of

alcohol, heart involvement with

alcohol, neurologic complications with

alcoholic polyneuropathy

alcoholic withdrawal states, DT's, convulsions, etc.

alcoholism

alpha-fetoprotein

alternating rapid movement

amenorrhea

amnesia

amphiphysin antibodies

amyloid plaques

anatomy of

anemia

aneurysm, intracranial

angiography, cerebral

anti mGluR1 encephalitis

antibodies to voltage-gated calcium channels

anticonvulsants, untoward effects of

antithyroid antibodies

antiviral agents

aphasia

apraxia of eye movements

areflexia

Arnold Chiari malformation

arthralgia

ataxia

ataxia telangiectasia

auditory evoked brainstem potentials

autoantibodies

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autonomic dysfunction

autonomic neuropathy

axonal spheroid

basal ganglia, calcification of

brainstem, infarction of

calcification, intracranial

calcium channel dysfunction

CAR syndrome

carcinoembryonic antigen

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, pelvis

cataracts

cataracts, congenital

cauda equina, enhancement

celiac disease, adult

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar pontine angle tumor

cerebellar vermis

cerebellitis

cerebellitis, autoimmune

cerebellum

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral vasculature

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, prevention of

chemotherapy, CNS treatment and complications with

chromosomal abnormality

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

cognition

collapsin response mediator protein 5 IgG

coma

compression neuropathy

confusion

consanguinity

contactin associated protein like 2 antibodies

controversies in neurology

corpus callosum, lesion of

cough

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cytosine arabinoside

deafness

degenerative diseases of CNS

dementia, frontotemporal

dementia, presenile

demyelinating disease

dentate nuclei, lesion of

depression

dermatomyositis

developmental abnormality of brain

developmental retardation

differential diagnosis

dilantin

dilantin, factors influencing metabolism of

dilantin, serum level

down-beat nystagmus, primary position of gaze

DPPX

DPPX, antibodies, encephalitis

drooling

drug induced neurologic disorders

dyssynergia cerebellaris myoclonica

dystonia

echolalia

ectatic basilar artery

electrical injury of nervous system

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, paraneoplastic

encephalopathy

enzyme, defect

eosinophilia

epidemiology of neurology

extraocular muscle lesion

eye movement, disorders of

face, numbness of

facial appearance, abnormal

familial hemiplegic migraine

familial periodic ataxia

fatigue

fetal alcohol syndrome

fever

fine motor function, impaired

finger nose finger test

foam cells

foot deformity

fourth ventricle, enlargement of

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

Friedreich's ataxia, late onset

frontotemporal dementia, behavioral variant

gadolinium

gait disorder

gammaglobulin therapy, intravenous

ganglionitis

gangliosidosis GM2

gastroenteritis

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

gaze palsy

gaze palsy, horizontal

gene

gene mutation

genetic linkage

genetic neurologic disorders

genetic testing

Gerstmann-Straussler-Scheinker disease

gliadin antibodies

globus pallidus, lesion of

glutamic acid decarboxylase, antibody

growth hormone deficiency

growth retardation

Guillain Barre syndrome

gynecomastia

Hallervorden Spatz disease

hemianopia, transient

hemifacial spasm

hemiparesis

hemiplegia

hepatic encephalopathy

heralding manifestation

highly active antiretroviral therapy

histochemistry

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

hot cross bun sign

human immunodeficiency virus type 1

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

hydrocephalus

hydroxytryptophan L-5(L-5 HTP)

hyperactivity

hypercalcemia

hyperesthesia

hyperpigmentation of skin

hypogonadism, hypogonadotropic

hypokalemia

hypokalemic alkalosis

hypomyelination

hyponatremia

hypothalamus, damage to

hypothyroidism

hypotonia

imbalance

immune reconstitution inflammatory syndrome

immunocompetent

immunodeficiency

immunologic disease

immunology and the nervous system

intellectual deterioration

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal biopsy

intestinal pseudoobstruction

irritability

isoniazid

Jakob-Creutzfeldt disease

JC virus

Korsakoff's psychosis

lactic acidemia

laughing, pathologic

leg numbness

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

level of consciousness, decreased

limbic encephalitis

lymphadenopathy

lymphoma

lymphoma involving CNS

malabsorption

malabsorption syndrome

malformation, CNS, congenital

malignancy screen

malignancy, occult

Marchiafava-Bignami disease

Marinesco-Sjogren syndrome

mediastinum, mass of

MELAS syndrome

memory, defect of recent

memory, impairment of

meningitis

mental retardation

mental status, abnormal

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

MNGIE syndrome

monoclonal antibodies

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, abnormal, seizure causing

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

multiple system atrophy

muscle biopsy

muscle pain

muscle weakness

muscle weakness, proximal

mutism

myasthenia gravis, paraneoplastic

myelopathy, carcinomatous

myelopathy, necrotizing

myopathy, mitochondrial

myopia

Native Americans

nausea and vomiting

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

nephrotic syndrome

nerve conduction studies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neurocutaneous disease

neuroendocrinology

neuroleptic malignant syndrome

neurologic complications

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic signs

neuromuscular junction

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronopathy

neuronopathy, sensory

neuropathy, paraneoplastic

neuropathy, peripheral

next-generation sequencing

Niemann-Pick disease

NMDA antagonists

NMDA receptors

nutritional deficiency

nystagmus

nystagmus, gaze-evoked

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

occipital lobe, infarction

occipital lobe, lesion of

ocular dysmetria

ocular flutter

ocular motility, disorders of

old age, neurology of

onconeural antibodies

ophthalmoplegia

opsoclonus

opsoclonus-myoclonus syndrome

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

parietal lobe, lesion of

Parkinson disease

Parkinsonism syndrome

parotid gland neoplasm

pathology

pellagra

pelvic mass

peripheral nerve, lesion of

pes cavus

photosensitivity, skin

pigmentary retinopathy

pitfalls

pituitary, lesion of

plasmapheresis

pleocytosis of cerebrospinal fluid

POLG1 gene

polymerase chain reaction

polymyositis

polyneuropathy, chronic inflammatory demyelinating

pons, atrophy

pons, infarction of

pons, lesion of

positional head-hanging test

posterior fossa, lesion of

posterior inferior cerebellar artery syndrome

prion disease

progeria

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive pallidum atrophy

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

ptosis

pupil, abnormality in neurologic disorders

pupil, tonic

Purkinje cell

pursuit eye movements, abnormal

pyramidal tract dysfunction

quadriplegia

radiation hypersensitivity

ragged-red fibers

Ramsay Hunt syndrome

rapidly progressing neurologic illness

rash

reading disorder, acquired

Red flags

reflex, brainstem

remission

remote effect of cancer on the nervous system

renal failure

respiratory depression

reticulum cell sarcoma

reversible splenial lesion syndrome

saccadic eye movements, abnormal

screening

sedimentation rate, elevated

seizure

seizure, children

seizure, withdrawal

sensorineural hearing loss

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

spasticity

speech disorder

speech disorder, non aphasic

spinal cord, injury of

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 2

spinocerebellar ataxia type 5

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spinocerebellar ataxia type 8

spinocerebellar degeneration

splenium of corpus callosum

splenomegaly

staphylococcal protein A column therapy

subarachnoid hemorrhage

syphilis, neurologic complications with

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of-bilateral

thiamine

thyroiditis

titubation

transglutaminase antibodies

transient ischemic attack

treatment of neurologic disorder

trinucleotide repeats

ubiquitination

urinary gonadotropin

vertebral-basilar insufficiency

vibratory sensation, abnormal

viral infection

viral infection, CNS

viral infection, CNS, treatment of

vision, failure of in childhood

visual evoked response

visual impairment

visual loss

vitiligo

voice, abnormality of

walking frame

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weaning from respirator, failure to

weight loss

Wernicke's encephalopathy

Western immunoblot test

Showing articles 0 to 50 of 3624 Next >>

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

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

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

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

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

Imaging Review of Paraneoplastic Neurologic Syndromes
AJNR 41:2176-2187, Madhavan, A.A.,et al, 2020

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
Neurol 87:e56-e57, Saini, A.G.,et al, 2016

A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
JAMA Neurol 73:1494-1495, Hughes, A.J.C.,et al, 2016

Diseases of the Nervous System Caused by Nutritional Deficiency, "Alcoholic" Cerebellar Degeneration
Adams & Victors Principles of Neurology Chp 41, pg 1178, Ropper, A.H.,et al, 2014

Alcohol and Alcoholism
Adams & Victors Principles of Neurology Chp 42, pg 1186, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Cerebellar Degeneration
Adams & Victors Principles of Neurology, Chp 39, pg 1105, Ropper, A.H.,et al, 2014

Paraneoplastic Neurological Syndromes
Clin Exp Immunol 175:336-348, Leypoldt, F. & Wandinger, K.-P., 2014

Transglutaminase 6 Antibodies in the Diagnosis of Gluten Ataxia
Neurol 80:1740-1745, Hadjivassilou, M.,et al, 2013

Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
NEJM 368:1992-2003, Margolin, D.,et al, 2013

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Spectrum of Paraneoplastic Disease Associated With Lymphoma
Neurol 76:705-710, Briani,C.,et al, 2011

JC Virus Infection of the Brain
AJNR 31:1564-1576, Bag,A.K.,et al, 2010

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

Sjogren Syndrome: Neurologic Complications
www.Medlink.com,Jan, Roman,G.C., 2010

Paraneoplastic Syndromes Affecting Brain and Cranial Nerves
UpToDate May 2009, Dalmau,J. &Rosenfeld,M., 2009

A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
Neurol 72:1262-1276, DiMauro,S.,et al, 2009

The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
Eur J Neurol 16:513-516, Lee, Y.-C.,et al, 2009

Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
J Neuro-Ophthalmol 28:58-68, Ko,M.W.,et al, 2008

Auto-Immune Cerebellar Ataxia with Anti-GAD Antibodies Accompanied by De Novo Late-Onset Type 1 Diabetes Mellitus
Diabetes Metab 34:386-388, Bayreuther,C.,et al, 2008

Downbeat Nystagmus: Aetiology and Comorbidity in 117 Patients
JNNP 79:672-677, Wagner,J.N.,et al, 2008

Anti-Ma and Anti-Ta Associated Paraneoplastic Neurological Syndromes: 22 Newly Diagnosed Patients and Review of Previous Cases
JNNP 79:767-773,742, Hoffmann,L.A.,et al, 2008

JC Viral Infection-Related Cerebellar Degeneration as the First Manifestation of AIDS
Eur Neurol 59:205-207, Shin,H.-W.,et al, 2008

Clinicopath Conf., Paraneoplastic Cerebellar Degeneration Due to Anti-Yo Antibodies From Breast Cancer
NEJM 356:612-620, Case 4-2007, 2007

JC Virus Granule Cell Neuronopathy: A Novel Clinical Syndrome Distinct from Progressive Multifocal Leukoencephalopathy
Ann Neurol 57:576-580, Koralnik,I.J.,et al, 2005

Leukoencephalopathy with Ataxia, Hypodontia, and Hypomyelination
Neurol 64:1461-1464, Wolf,N.I.,et al, 2005

Late-Onset Friedreich Ataxia
Arch Neurol 62:1865-1869, Bhidayasiri,R.,et al, 2005

Late-Onset Cerebellar Ataxia with Hypogonadism and Muscle Coenzyme Q10 Deficiency
Neurol 62:818-820, Gironi,M.,et al, 2004

Ipsilateral Thalamic MRI Abnormality in an Epilepsy Patient
Neurol 58:641-644, Nagasaka,T.,et al, 2002

Gluten Sensitivity as a Neurological Illness
JNNP 72:560-563, Hadjivassiliou,M.,et al, 2002

Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10
Arch Neurol 59:1285-1290, Grewal,R.P.,et al, 2002

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
Neurol Sci 23:145-151, Vianello,M.,et al, 2002

Ataxia Associated with Hashimotos Disease: Progressive Non-Familial Adult Onset Cerebellar Degeneration with Autoimmune Thyroiditis
JNNP 71:81-87, Selim, M. and Drachman, D.A., 2001

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Clinical and MRI Findings in Spinocerebellar Ataxia Type 5
Neurol 53:1355-1357, Stevanin,G.,et al, 1999

Paraneoplastic Syndromes
Arch Neurol 56:405-408, Dalmau,J.O.&Posner,J.B., 1999

Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
Lancet 352:1582-1585, Hadjivassiliou,M.,et al, 1998

Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 1998

Neuroradiological Features of Six Kindreds with MELAS tRNA(Leu) A3243G Point Mutation: Implications for Pathogenesis
JNNP 65:233-240, Sue,C.M.,et al, 1998

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997

Clinicopath Conf
Hodgkin's Disease, Paraneoplastic Cerebellar Degeneration, Case 21-1997, NEJM 337:115-12297., , 1997

Showing articles 0 to 50 of 3624 Next >>