Neudle.com: extrapyramidal movement disorder progressive

Differential
(Click to cross reference)

acquired immunodeficiency syndrome

adolescent medicine

adverse drug reaction

akathisia

akinesia of eyelid function

alcohol, neurologic complications with

alternating hemiplegia

alternating hemiplegia of childhood

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, Parkinson-dementia-complex

anticardiolipin antibodies

anticonvulsants, untoward effects of

antiphospholipid antibody syndrome

aphasia

aphasia, progressive, primary

apraxia

apraxia of eye movements

apraxia of eyelid opening

arbovirus

areflexia

ataxia

ataxia telangiectasia

autoimmune basal ganglia encephalitis

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

benign essential tremor

bent spine syndrome

bilirubin encephalopathy

biologic markers

biotin

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

blepharospasm

blinking

blinking, reduced

bone marrow transplantation

botulinum toxin

botulinum toxin, complications of

brainstem, infarction of

carcinoembryonic antigen

carcinoma

carcinoma of breast

cardiomyopathy

carotid artery disease

carotid artery occlusion, neck

carotid artery stenosis

caudate nucleus, atrophy

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellitis, autoimmune

cerebellum, disease of

cerebral cortex

cerebral hypoperfusion

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, three territory involvement

choreoathetosis, paroxysmal

chromosomal abnormality

chromosome 11

chromosome 20

chronic progressive external ophthalmoplegia

cirrhosis

Clinical Pathologic Conference(C.P.C.)

cognition

cogwheel rigidty

collagen vascular disease

concussion

confabulation

confusion

congenital infection, CNS

consanguinity

contractures, joint

controversies in neurology

conversion reaction

corpus callosum, thinning

cortical-basal ganglionic degeneration

cost

cost effectiveness

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

Cuba

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, treatment of

Dengue fever

developmental milestones, loss of

developmental retardation

differential diagnosis

diplopia

disorientation

distal muscle atrophy

dopa responsive dystonia

DPPX

DPPX, antibodies, encephalitis

driving

drooling

drug abuse

drug abuse, neurologic complications of

dysarthria

dysdiadochokinesia

dyskinesia

dyskinesia, buccal lingual facial

dystonia, drug induced

dystonia, face

dystonia, focal

dystonia, painful

dystonia, treatment of

electroencephalogram, abnormalities of

electromyogram

encephalitis

encephalitis, autoimmune

encephalitis, episodic

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalopathy

encephalopathy, neonatal

encephalopathy, progressive

endarterectomy, carotid

endemic area

enolase

enzyme, defect

epidemiology of neurology

episodic neurologic deficits

evidence-based research

exercise intolerance

exome sequencing

extralimbic encephalitis

extrapyramidal movement disorder, progressive

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial movement disorder

fatal familial insomnia

fever

fluctuate

fluorescent treponema antibody absorption/false positive

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

frontal behavioral spatial syndrome

frontal lobe, anatomy and physiology

gait disorder

galactorrhea

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

glabellar sign

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

granulomatous disease

growth retardation

Guillain Barre syndrome

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination

hallucination, visual

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

hepatosplenomegaly

heralding manifestation

hippocampus

hippocampus, hyperintense

Horner's syndrome

human immunodeficiency virus type 1

Huntington's chorea

Huntington's disease, children

hydrocephalus

hyperammonemic encephalopathy

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hypothalamus, disturbance of

hypothyroidism

hypotonia

hypoxia

hypoxic encephalopathy

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

intellectual deterioration

internal capsule

intracranial hypertension, benign

intravenous

iron, brain

Isaacs syndrome

Jakob-Creutzfeldt disease

lenticular nucleus, lesion of, bilateral

leukemia

leukoencephalopathy

Lewy body

Lewy body disease, diffuse

lymphadenopathy, hilar

lymphoma

maculopathy

manganese intoxication

marche a petits pas

masked facies

mediastinum, mass of

memory, defect of recent

memory, impairment of

meningitis

meningitis, aseptic

meningitis, carcinomatous

mental retardation

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

methcathinone

methylmalonic acidemia

microcephaly

midbrain, atrophy

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

mimics

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

mitochondrial disease, pathogenesis

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, paroxysmal

MRI

MRI, abnormal

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, false negative

MRI, gradient-echo

MRI, high signal intensity of basal ganglia

MRI, negative

MRI, paramagnetic effect

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRS

multiple sclerosis

multiple system atrophy

neurocutaneous disease

neurodegeneration with brain iron accumulation

neuroendocrinology

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, tempo

neurologic signs

neuron specific enolase

neuronal intranuclear inclusion disease

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral

neurotoxic

neurotoxin

next-generation sequencing

NOTCH2NLC

nutritional deficiency

nystagmus

nystagmus, gaze-evoked

nystagmus, monocular

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculomasticatory myorhythmia

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy

optic neuritis

orthostatic hypotension

paraspinal muscle weakness

parenteral alimentation

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, atypical

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

pathology

pericarditis

peripheral nerve, lesion of

personality change

pigmentary retinopathy

pituitary, lesion of

pleocytosis of cerebrospinal fluid

POLG1 gene

polymerase chain reaction

polyneuropathy

portal caval shunt

posterior inferior cerebellar artery syndrome

postural abnormality

precipitating factors

preclinical

premature infant

prevention of neurologic disorders

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive supranuclear palsy

prolactin, elevated

protein 14-3-3, cerebrospinal fluid

protein 14-3-3, cerebrospinal fluid, false negative

proteinopathy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

ptosis

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

radiation hypersensitivity

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading disorder, acquired

reading problem, causes of

recurrent

remote effect of cancer on the nervous system

rubella encephalitis, progressive

rubella syndrome

rubella virus

Russia

saccadic eye movements

saccadic eye movements, abnormal

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

shaking

sinemet

skin, biopsy

skin, lesions in neurologic disorders

skull x-ray

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

spastic dysphonia

spasticity

speech disorder

speech disorder, childhood

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 2

splenomegaly

spongy degeneration of brain

status epilepticus, intractable

steroid therapy, CNS treatment and complications with

striatum, lesion of, bilateral

stridor

strokelike episodes

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

substantia nigra

subthalamic nucleus

symmetric brain lesions

synucleinopathy

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

temporal lobe, lesion

temporal lobe, lesion, bilateral

term infant

thalamus, lesion of

thalamus, lesion of-bilateral

transient ischemic attack

transient ischemic attack, limb shaking

transient neurologic deficit

travel history

treatment of neurologic disorder

trigeminal neuropathy

trinucleotide repeats

tyrosine hydroxylase deficiency

unconsciousness

unconsciousness, transient

visual evoked response

visual impairment

vitamin deficiency

walking frame

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

Showing articles 100 to 150 of 17967 << Previous Next >>

Involuntary Hand-Shaking: Transient Ischemic Attack, Seizure, or Psychogenic?
Ann Neurol 88:12-13, Sharma, V.K. & Sinha, A.K., 2020

Acute Rheumatic Fever: Clinical Manifestations and Diagnosis
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Sydenham Chorea
www.UptoDate.com, Oct, Gilbert, D.L., 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Orofacial Dyskinesia in a Young Man
JAMA Neurol 76:1517-1518, Tian, X.,et al, 2019

Recurrent Involuntary Contractions of the Face, Arm, and Leg in an Elderly Man
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Diagnostic Tools for Immune Causes of Encephalitis
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Bobblehead-Doll Syndrome
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A 65-year-old Woman with Subacute Hemiballism
Neurol 92:345-349, Cacic, K.,et al, 2019

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

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

Delayed-Onset MRI Findings in Acute Chorea Related to Anoxic Brain Injury
Clin Imaging 48:22-25, Ghasemi, M.,et al, 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Subacute Paresis in a 28-year-old man with HIV
Neurol 90:432-435, Harada, Y.,et al, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

A 75-year-old man with parkinsonism, mood depression, and weight loss
Neurol 90:572-575, Frattini, E.,et al, 2018

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

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

Clinicopathologic Conference, Digitalis Toxicity
NEJM 378:1931-1938, Case 15-2018, 2018

An unusual neuropsychiatric manifestation of systemic lupus erythematosus
Neurol 90:e1929-e1932, Dongkyung, D.,et al, 2018

Encephalitis with mGluR5 antibodies
Neurol 90:e1964-e1972, Spatola, M.,et al, 2018

IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
Neurol 90:1113-1115, Morales-Briceno, H.,et al, 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

Clinicopathological Conference, Insulinoma
NEJM 379:376-384, Case 23-2018, 2018

Isolated Gait Dysfunction Due to Intracranial Hypotension
Neurol 91:271-272, Sasikumar,S.,et al, 2018

Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
Neurol 91:e714-e723, Berridge, G.,et al, 2018

Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
NEJM 379:870-878, CASE 27-2018, 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Chorea Due to Chronic Subdural Hematoma
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Wilson Disease
NIDDK Oct2018, , 2018

Paraneoplastic and Autoimmune Encephalitis
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Abdominal Tremor in Thyrotoxicosis
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Thalamic Deep Brain Stimulation for Tremor in Parkinson Disease, Essential Tremor, and Dystonia
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Zolpidem for the Treatment of Neurologic Disorders
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A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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Precipitous Deterioration of Motor Function, Cognition, and Behavior
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Randomized Controlled Trial of Deutetrabenazine for Tardive Dyskinesia
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Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma Consistent with Neurolymphomatosis
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Efficient Trial Design - FDA Approval of Valbenazine for Tardive Dyskinesia
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A 58-year-old man with Progressive Ptosis and Walking Difficulty
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Diagnosis and Management of Dementia with Lewy Bodies
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Investigations in GABA? Receptor Antibody-Associated Encephalitis
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Reversible Gait Ataxia
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A 13-year-old boy with Chronic Ataxia and Developmental Delay
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Clinical Manifestations of the anti-IgLON5 Disease
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Clinical Decision-Making in Functional and Hyperkinetic Movement Disorders
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Clinicopathologic Conference, Granulomatous Amebic Encephalitis and Sarcoidosis (Inactive)
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Showing articles 100 to 150 of 17967 << Previous Next >>