Neudle.com: idiopathic generalized dystonia

Differential
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abscess, intracerebral

abscess, intracranial

abscess, sphenoid sinus

advances in neurology

adverse drug reaction

algorithm

alpha-fetoprotein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

AMPA receptor antibodies

amyloidosis

amyotrophic lateral sclerosis

anemia

ankle edema

anti GQ1b IgG antibody

anticholinergic drugs

apraxia of eye movements

areflexia

artane

arthralgia

arthrogryposis multiplex

ascites

ataxia

ataxia telangiectasia

ataxia, cerebellar

ataxia, truncal

ataxic-dystonia syndromes

athetosis

athetosis, causes of

atlanto-axial subluxation

ATP1A3 gene

attention deficit disorder with hyperactivity

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

autonomic neuropathy

Babinski sign

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

benign essential tremor

calcification, intracranial

camptocormia

carbamazepine

carcinoembryonic antigen

carcinoma

carotid artery disease

carotid artery occlusion, neck

carotid artery stenosis

CAT scan

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, isodense lesion with acute hemorrhage

cataracts

catecholamine

cavernous sinus, syndrome

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellum

cerebral cortical atrophy

cerebral hypoperfusion

cerebral ischemia

cerebral palsy

cerebral palsy, associated problems with

cerebral vasculature, calcification

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, infancy and childhood

choreoathetosis, paroxysmal

chromosomal abnormality

chromosome 11

chromosome 14

chromosome 9

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

deferiprone

degenerative diseases of CNS

delay in diagnosis

dementia

dental procedure, neurologic complications with

depression

dermatomyositis

developmental milestones, loss of

developmental retardation

differential diagnosis

dopa responsive dystonia

dopamine

drooling

drop attacks

drug induced neurologic disorders

dural sinus thrombosis

dysarthria

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dyskinesia

dyskinesia, causes of

dyskinesia, drug induced

dystonia musculorum deformens

dystonia musculorum deformens, carrier

dystonia, axial

dystonia, cervical

dystonia, children

dystonia, classification

dystonia, etiology of

dystonia, evaluation of

dystonia, symptomatic

dystonia, treatment of

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, focal

encephalitis, paraneoplastic

encephalopathy

encephalopathy, progressive

endarterectomy, carotid

enzyme, defect

episodic neurologic deficits

equinovarus

esophageal varices

exome sequencing

eye movement, disorders of

facial expression abnormality

facial movement disorder

fine motor function, impaired

foot deformity

frontal lobe, pathologic signs of

fungal infection, CNS

gait disorder

galactorrhea

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

genetic neurologic disorders

genetic testing

gests antagoniste

Gilles de la Tourette syndrome

globus pallidus

globus pallidus, stimulation

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

granuloma, pulmonary

grasp reflex

growth retardation

Guillain Barre syndrome

heparin, subcutaneous

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hydrocephalus, normal pressure

hypoparathyroidism, idiopathic

hyporeflexia

hyposmia

hypotonia

iatrogenic neurologic disorders

inborn errors of metabolism

inclusion bodies, intranuclear

intellectual deficit

intellectual deterioration

intracranial hypertension, benign

intracranial pressure, increased

iron, brain

jugular foramen syndrome

Kayser-Fleischer ring

klippel feil syndrome

L-dopa

leg spasms

leg spasms, painful

leg weakness, bilateral

leucine rich glioma inactivated 1 antibodies

liver function enzymes

lymphoma

masked facies

mastoiditis

memory, impairment of

meningismus

meningitis

meningitis, carcinomatous

meningitis, fungal

meningitis, syphilitic

meningitis, TB

mental retardation

mental status, abnormal

monoclonal antibodies

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, paroxysmal

movement disorder, treatment of

MRI

MRI pattern

MRI, abnormal

MRI, eye of tiger sign

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

multiple sclerosis

multiple system atrophy

Munchausen syndrome

muscle diseases, characteristics of

muscle pain

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myelitis, transverse, idiopathic

myelitis, transverse, prognosis

myelopathy

myelopathy, chronic progressive

myopathy, carcinomatous

myopathy, thyroid disease causing

neurocutaneous disease

neuroendocrinology

neurologic complications of, surgery

neurologic disease, diagnoses of

neurologic signs

neuronal intranuclear inclusion disease

next-generation sequencing

NMDA antagonists

norepinephrine

numb clumsy hands syndrome

nystagmus

nystagmus, monocular

obsessive-compulsive disorder

ocular motility, disorders of

otitis, neurologic complications with

Parkinson disease, differential diagnosis of

Parkinson disease, dystonia with

Parkinson disease, juvenile

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal hemiplegia

paroxysmal neurologic deficits

parsidol

pathology

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

penicillamine

personality change

phenylketonuria

pigmentary retinopathy

plasmapheresis

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, neurologic problems with

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

primary familial brain calcification

PRKN gene

progeria

prognosis

progressive neurologic disorder

prolactin, elevated

pseudohypoparathyroidism

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing, neurologic problems

psychosis

pupil, abnormality in neurologic disorders

pupil, tonic

quadriparesis

quality of life

radiation hypersensitivity

radiculopathy

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reversible neurologic disorder

sedimentation rate, elevated

seizure

sensorineural hearing loss

sensory level

sensory tricks

serologic testing

serologic testing, false negative

seronegative

sexual dysfunction in neurologic disease

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

spastic dysphonia

speech disorder

speech disorder, childhood

speech disorder, non aphasic

spinal cord

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 28

spinocerebellar degeneration

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulation, deep brain

stimulation, deep brain, bilateral

striatal encephalitis

striopallidodentate calcifications, familial idiopathic

substantia nigra

symmetric brain lesions

thalamus, lesion of-bilateral

thrombocytopenia

thrombophlebitis

thrombophlebitis, prophylaxis

transient ischemic attack

transient ischemic attack, limb shaking

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor

tremor, postural

trientine dihydrochloride

trigeminal neuralgia

tripping

tyrosine hydroxylase deficiency

unconsciousness

unconsciousness, transient

walking, difficulty with

Werdnig-Hoffman disease

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Clinical and Vascular Outcome in Internal Carotid Artery Versus Middle Cerebral Artery Occlusions After Intravenous Tissue Plasminogen Activator
Stroke 33:2066-2071, Linfante, I.,et al, 2002

Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10
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Giant-cell Arteritis
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Reversible Chorea and Focal Dystonia in Vitamin B12 Deficiency
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Polymyalgia Rheumatica and Giant-Cell Arteritis
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Response of Intra-Arterial and Combined Intravenous and Intra-Arterial Thrombolytic Therapy in Patients with Distal Internal Carotid Artery Occlusion
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Out of Africa, Trypanosomiasis
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CADASIL Mimicking Primary Angiitis of the Central Nervous System
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Prediction of Early Neurological Deterioration Using Diffusion- and Perfusion-Weighted Imaging in Hyperacute Middle Cerebral Artery Ischemic Stroke
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AAC/AHA/NHLBI Clinical Advisory on the Use and Safety of Statins
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Arterial Reocclusion in Stroke Patients Treated with Intravenous Tissue Plasminogen Activator
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Guillain-Barre Syndrome Following Acute Falciparum Malaria
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Complete Recovery After Early Intraarterial Recombinant Tissue Plasminogen Activator Thrombolysis of Carotid T Occlusion
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Risk Factors for Traumatic and Bloody Lumbar Puncture in Children with Acute Lymphoblastic Leukemia
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Poliomyelitis Due to West Nile Virus
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West Nile Virus Encephalitis
NEJM 347:1225-1226, Peterson,L.R.,et al, 2002

A Poliomyelitis-like Syndrome from West Nile Virus Infection
NEJM 347:1279-1280, Leis,A.A., et al, 2002

A Tourist With Dengue Fever and Visual Loss
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Tick Paralysis in Children
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Hemolytic Anemia Presenting as Idiopathic Intracranial Hypertension
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Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
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Disease-Modifying Therapy in Multiple Sclerosis: Strategies for Optimizing Management
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Blepharospasm
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Ptosis as a Remote Effect of Therapeutic Botulinum Toxin B Injection
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Headache Diagnosis in Patients with Treated Idiopathic Intracranial Hypertension
Neurol 58:1551-1553, Friedman,D.I. &Rausch,E.A., 2002

Thrombocytosis in Patients with Biopsy-Proven Giant Cell Arteritis
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Diagnostic Criteria for Idiopathic Intracranial Hypertension
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Legionella Infection
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Fat embolism syndrome and elective knee arthroplasty
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Temporal Arteritis and Guillain-Barr� Syndrome
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Post-Streptococcal Autoimmune Dystonia With Isolated Bilateral Striatal Necrosis
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Mycoplasma Pneumoniae Encephalitis in Childhood
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Drug-Induced Pisa Syndrome (Pleurothotomus)
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Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
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HIV-Related Movement Disorders, Epidemiology, Pathogenesis and Management
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The Differential Diagnosis of Multiple Sclerosis
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Ataxia Associated with Hashimotos Disease: Progressive Non-Familial Adult Onset Cerebellar Degeneration with Autoimmune Thyroiditis
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Brainstem Gliomas in Adults: Prognostic Factors and Classification
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Clinical Spectrum of Posterior Ischemic Optic Neuropathy
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Postpartum Blindness
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Imaging of the Internal Carotid Artery: The Dilemma of Total Versus Near Total Occlusion
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Collateral Ability of the Circle of Willis in Patients With Unilateral Internal Carotid Artery Occlusion
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Deterioration Following Improvement with tPA Therapy: Carotid Thrombosis and Reocclusion
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Wartenberg's Migrant Sensory Neuritis
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Showing articles 850 to 900 of 2630 << Previous Next >>