Neudle.com: "tremor cerebellar"

Differential
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abdominal contractions

abdominal x-ray

acoustic nerve

acoustic nerve, vestibular division of

acquired immunodeficiency syndrome

acute ataxia of childhood

acute cerebellar ataxia

addiction, heroin

addiction, heroin-neurologic complications with

Adies pupil

adverse drug reaction

agitation

agranulocytosis

akathisia

alcohol, neurologic complications with

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

alcoholism

Alexanders disease

Alexanders disease, adult onset

alien hand syndrome

alopecia

altered states of consciousness

alternating rapid movement

anterior horn cell disease

anterior tibial muscle weakness

anti IgLON5

anti La antibody

anti mGluR1 encephalitis

anti Ro antibody

anti Yo antibody

antiarrhythmic drugs

anticonvulsants, untoward effects of

antidepressant

antineurofascin antibodies

antithyroid antibodies

apraxia of eye movements

aqueduct of Sylvius, enlargement

areflexia

arm swing, reduced

Arnold Chiari malformation

aspartate aminotransferase

ataxia telangiectasia

ataxic-dystonia syndromes

attention deficit disorder with hyperactivity

atypical

autism

autoantibodies

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autoimmune GFAP astrocytopathy

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

basal ganglia, calcification of

basal ganglia, lesion of

behavioral disorder

Benedikt's syndrome

benign essential tremor

benign essential tremor, refractory

benzodiazepine

beta adrenergic blocker

biologic markers

bismuth

blindness

blood dyscrasias, neurologic findings with

Borrelia burgdorferi infection

brainstem, dysfunction

brainstem, dysfunction, eye movement disorders with

brainstem, infarction of

calcification, intracranial

carbamazepine

carbamazepine, toxicity

carbon monoxide poisoning

carbon monoxide poisoning, chronic

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, pelvis

celiac disease, adult

central hypoventilation

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebellitis

cerebellitis, autoimmune

cerebellum, disease of

cerebral blood flow

cerebral cortical atrophy

cerebral edema

cerebral infarction

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, red cells in

cerebrovascular accident

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

children

chills

chorea

chromosomal abnormality

chylomicron retention disease

ciguatera poisoning

cirrhosis

Claude's syndrome

Clinical Pathologic Conference(C.P.C.)

contactin associated protein like 1 antibodies

conversion reaction

copper metabolism, abnormal

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cough

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

dementia, rapidly progressive

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

depression

dermatitis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty going down stairs

dilantin

diplopia

disability, neurological

distal muscle atrophy

distal muscle weakness

down-beat nystagmus, primary position of gaze

DPPX

DPPX, antibodies, encephalitis

drooling

drowsiness

drug abuse

drug induced neurologic disorders

dyskinesia, buccal lingual facial

dystonia, etiology of

dystonia, focal

dystonia, focal lesion causing

dystonia, psychogenic

dystonia, symptomatic

dystonic tremor

electroencephalogram, abnormalities of

electroencephalogram, focal delta activity

electromyogram

electrophoretic pattern, CSF

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, viral

encephalomyelitis

encephalopathy

encephalopathy, Hashimoto's

endemic area

enterovirus

enterovirus infection of CNS

eye movement, disorders of

facial appearance, abnormal

facial weakness

facial weakness, bilateral

failed medical management

fine motor function, impaired

finger nose finger test

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

gait disorder

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

gasoline sniffing

gastrointestinal perforation

genetic neurologic disorders

glucose tolerance test, abnormal

glutamic acid decarboxylase, antibody

granular osmiphilic material

Guillain Barre syndrome, differential diagnosis of

hallucination

hallucination, visual

hammertoes

hand flapping

hand-foot-mouth disease

handwriting

head injury

head injury, brain stem lesion after

head injury, delayed deterioration following

heavy metal intoxication

hemochromatosis, primary

hemorrhage, thalamic

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes zoster

high altitude sickness

high arched feet

HLA

hoarseness

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

hypotension, systemic

hypotonia

hypotonia, infants

hypoxia

hypoxic encephalopathy

IgG4-related disease

imbalance

immunosuppressive agents

immunotherapy

impulsivity

inappropriate antidiuretic(A.D.H.)hormone

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inattention

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

incoordination

infection

inferior olivary nucleus

infertility

insomnia

intellectual deficit

intellectual deterioration

intelligence quotient

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

internuclear ophthalmoplegia, unilateral

intestinal biopsy

introverted

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

jaundice

joint hypermobility

Kayser-Fleischer ring

lactic dehydrogenase(LDH)

lateropulsion

laughing, pathologic

lead poisoning

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

lethargy

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

leukoencephalopathy, toxic

leukopenia

level of consciousness, decreased

limbic encephalitis

lip biopsy

lipid storage disorder of CNS

lithium

liver disease

liver function enzymes

liver transplantation

lorazepam

low back pain

Lyme disease

lysosomal storage disease

macrocephaly

malabsorption syndrome

mannitol

Marcus Gunn pupil

Marinesco-Sjogren syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningismus

meningitis

meningitis, aseptic

meningitis, carcinomatous

meningoencephalitis

meningoencephalomyelitis

mental retardation

mental status, abnormal

mesial temporal lobe

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

metallic taste

midbrain

midbrain, atrophy

midbrain, infarction of

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, psychogenic

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, cranial nerves

MRI, diffusion weighted

MRI, high signal foci on

MRI, lumbosacral plexus

MRI, negative

multiple sclerosis

multiple sclerosis, misdiagnosis

multiple sclerosis, treatment of

multiple system atrophy

muscle weakness, proximal

myelinolysis, extrapontine

neoplastic angioendotheliosis

nephrotic syndrome

nerve biopsy

nerve conduction studies

nerve root enhancement

nerve root hypertrophy

neuroaxonal leukodystrophy

neurologic complications

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic signs

neurologic symptoms

neurologic symptoms, unexplained

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, autoimmune

neuropathy, demyelinating

neuropathy, peripheral

nodopathy, autoimmune

nutritional deficiency

nystagmus

nystagmus, monocular

nystagmus, pendular

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

occupational neurologic disorders

octreotide

ocular dysmetria

ocular motility, disorders of

oculogyric crisis

old age, neurology of

olivary degeneration, hypertrophic

ophthalmoplegia

opsoclonus

opsoclonus, differential diagnosis of

optic atrophy

optic neuropathy

optic neuropathy, bilateral

oral ulcerations

orthostatic hypotension

oscillopsia

osmotic demyelination syndrome

ovarian insufficiency

paralysis, acute areflexic

paraneoplastic cerebellar degeneration

Parkinson disease, benign tremulous

Parkinson disease, drug induced

Parkinson disease, L-dopa nonresponsive

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

peripheral blood smear

perivascular enhancement

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, neurologic problems with

POLR3B

polymerase chain reaction

polymerase chain reaction, false negative

polymyositis

polyneuropathy

pons, lesion of

Poretti-Boltshauser syndrome

positional head-hanging test

posterior inferior cerebellar artery syndrome

prevention of neurologic disorders

prognosis

progressive ataxia and palatal tremor

progressive myoclonic epilepsy

progressive neurologic disorder

propofol

propranolol

prothrombin time, prolonged

psychiatric problems in neurologic disorders

psychological testing, neurologic problems

psychomotor retardation

pursuit eye movements, abnormal

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

reading disorder, acquired

rectal biopsy

recurrent

rehabilitation for neurologic disorders

remote effect of cancer on the nervous system

renal failure

respirations in CNS disease

rheumatoid arthritis factor(R.A.factor)

rubella encephalitis, progressive

rubella virus

Sabin-Feldman dye test

saccadic eye movements, abnormal

salivation, excessive

Schirmer test

sciatica

screening

sedimentation rate, elevated

seizure

seizure, children

seizure, drug-induced

seizure, withdrawal

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

serum alanine aminotransferase

serum glutamic oxaloacetic transaminase

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

sleep apnea, obstructive

sleep pathology and physiology

slurred speech

sodium channel dysfunction

spasticity

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

spinal cord, injury of

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 12

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spinopontine atrophy, dominant

splenium of corpus callosum

stem cell transplantation

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulation, deep brain

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

stuporous

stuttering

suicide

superior cerebellar artery infarction

sweating, abnormality of

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

systemic lupus erythematosus, skin changes in

teeth, number of in infants

temporal lobe

temporal lobe, lesion

temporal lobe, lesion, bilateral

terfenadine

testicular enlargement

tetany

thalamic ataxia syndrome

thalamic dystonia

thalamotomy

thalamus, focused ultrasound ablation

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

third nerve palsy

third nerve palsy, bilateral

thrombocytopenia

thrombotic thrombocytopenia purpura

toxins, nervous system

toxoplasma complement fixation test

toxoplasmosis, acquired

toxoplasmosis, CNS

transient neurologic deficit

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, classification

tremor, differential diagnosis of

tremor, post traumatic

tremor, surgical treatment of

tremor, thalamic

tremor, thalamic stimulation for suppression of

tremor, treatment of

tremor, voice

tremor, writing

triangle of Guillain and Mollaret

trimethoprim-sulfamethoxazole

trinucleotide repeats

vagus nerve stimulation

valium

varicella zoster virus

Venereal Disease Research Laboratory test

vibratory sensation, abnormal

voice, abnormality of

Von Hippel Lindau

walking frame

walking, delayed

walking, difficulty with

weakness

weakness, progressive

weight loss

Wernekinck commissure syndrome

West Nile fever

Western immunoblot test

x-linked intellectual deficit

x-linked mental retardation

zoster sine herpete

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The Spectrum of Fragile X Disorders
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A 58-Year-Old Man With Resting tremor, Bradykinesia, and Distal Numbness
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A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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Neurologic Complications of Babesiosis, United States, 2011-2021
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Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
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Clinical and Structural Findings in Patients with Lesion-Induced Dystonia
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A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
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Autoimmune Nodopathies, An Emerging Dignostic Category
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Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
Neurol 97:875-878, Dinov, D.,et al, 2021

A 65-Year-Old Woman with Tremor
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A Triad of Tremor, Ataxia, and Cognitive Impairment
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Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
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Progressive Ataxia and Palatal Tremor
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Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

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

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

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

Essential Tremor
NEJM 378:1802-1810, Haubenberger, D.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
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Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
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Clinical Manifestations of the anti-IgLON5 Disease
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Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
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A 27-year-old man with Acute-Onset Ataxia
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Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
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A 57-year-old Man with Subacute Gait Difficulty and Hand Tremor
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Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
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Holmes Tremor
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Deep Brain Stimulation of the Dentate Nucleus Improves Cerebellar Ataxia After Cerebellar Stroke
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Degenerative Diseases of the Nervous System, Cerebellar Degeneration
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Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
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The Acquired Metabolic Disorders of the Nervous System, Hashimoto Encephalopathy (Steroid Responsive Encephalopathy Syndrome)
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Recognition and Management of Withdrawal Delirium
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The Acquired Metabolic Disorders of the Nervous System, High-Altitude (mountain) sickness
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Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Lithium
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Enterovirus Vaccines for an Emerging Cause of Brain-Stem Encephalitis
NEJM 370:792-794, McMinn, P.C., 2014

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
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Limbic Encephalitis as the Presenting Feature of Sj�gren Syndrome
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Brainstem Abnormalities and Vestibular Nerve Enhancement in Acute Neuroborreliosis
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The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Clinicopath Conf, Intravascular Large-B-Cell Lympoma
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A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009

Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
Arch Neurol 65:19-25, Amiri,K.,et al, 2008

Reversible Parkinsonism and Ataxia Associated With High-Dose Octreotide
Neurol 70:2345-2346, Espay,A.J., 2008

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

Showing articles 0 to 50 of 2174 Next >>