Neudle.com: ataxia periodic

Neurology Specific Literature Search

Differential
(Click to cross reference)

abdominal distention

abducens nerve paralysis

acute cerebellar ataxia

Addison's disease

adverse drug reaction

Alexanders disease

Alexanders disease, adult onset

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

amaurosis fugax

aminoacidopathies

amyloid angiopathy, cerebral

aneurysm, vertebral basilar system

angiitis, granulomatous of CNS

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, negative

angiography, posterior fossa

angiography, vertebral artery

anti MAG antibodies

antibodies to measles

antibodies to voltage-gated calcium channels

arteritis, temporal

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, truncal

autoimmune disease

autoimmune GFAP astrocytopathy

autonomic dysfunction

bacterial infection

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavior modification

behavior, combative

behavioral disorder

Behcet's syndrome

benign positional vertigo

bitemporal visual field defect

bladder dysfunction

brain biopsy, stereotaxic

brainstem, glioma

brainstem, infarction of

brainstem, lesion of

brucellosis, nervous system involvement with

calcification, intracranial

calcium antagonist

calcium channel dysfunction

carpo-pedal spasm

CAT scan, abnormal

CAT scan, angiography

CAT scan, metrizamide

celiac disease, adult

central core disease

central nervous system, infection of

central retinal artery occlusion

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellar peduncle

cerebellar vermis

cerebral cortex

cerebral cortical atrophy

cerebral infarction

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chloride channel dysfunction

choreoathetosis

chorioretinitis

chromosomal abnormality

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

collagen vascular disease

concentration, impaired

conversion reaction

cornea, abnormal

cranial nerve palsies

craniopharyngioma

cryopyrin-associated periodic syndrome

Cushing's syndrome

deafness, sudden

deafness, unilateral

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dentate nuclei, lesion of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

differential diagnosis

digital subtraction angiography

disability, neurological

diurnal variation

down-beat nystagmus

down-beat nystagmus, primary position of gaze

downward gaze, paralysis of

drug induced neurologic disorders

dystonia, psychogenic

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, viral

encephalopathy, acute

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

Epstein-Barr virus

exercise intolerance

exome sequencing

eye movement, disorders of

face, numbness of

facial movement disorder

facial nerve palsy

facial weakness

faciobrachial dystonic seizure

failure to thrive

familial hemiplegic migraine

familial periodic ataxia

fever, recurrent

fine motor function, impaired

fingerprint bodies

Fisher's syndrome

fistula, perilymphatic

Friedreich's ataxia

frontal bossing

frontal lobe, pathologic signs of

fundus, abnormality of

gaze palsy, supranuclear

gaze palsy, vertical

genetic neurologic disorders

genetic testing

gliadin antibodies

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

gluten sensitivity

gluten-free diet

gram positive rod

granular osmiphilic material

Guillain Barre syndrome

hallucination, auditory

hallucination, visual

Hand-Schuller-Christian disease

head circumference

head turning, neurologic complications with

headache, bifrontal

headache, elderly

headache, episodic

headache, occipital

headache, recurrent

headache, severe

hemianopia, homonymous

hemimyoclonic jerks

hemosiderosis of CNS, superficial

hepatosplenomegaly

hyperadrenalism

hyperinsulinism

hyperparathyroidism

hyperpigmentation of skin

hyperthyroidism

hypertrophic intracranial pachymeningitis

hypoglycorrhachia

hypokalemic periodic paralysis

hypoparathyroidism

hypothalamus, disturbance of

iatrogenic neurologic disorders

imbalance, postural

immunomodulation

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

intestinal biopsy

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intrinsic hand muscles, wasting of

islet cell tumor

Jakob-Creutzfeldt disease

jaw claudication

lactic acidemia

leg weakness, bilateral

leucine rich glioma inactivated 1 antibodies

leukoencephalopathy

level of consciousness, decreased

limbic encephalitis

lymphadenopathy

lysosomal storage disease

malignant hyperpyrexia

maple syrup urine disease

medulla oblongata, neoplasm of

memory, defect of recent

memory, impairment of

Meniere's disease

meningeal enhancement

meningitis, aseptic

meningitis, bacterial

meningitis, carcinomatous

meningitis, elderly

meningitis, fungal

meningitis, Mollaret's

meningitis, recurrent

meningoencephalitis

meningoencephalomyelitis

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

microhemorrhage, intracerebral

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, hemiplegic

molecular genetics

mononeuropathy multiplex

motor dysfunction

motor neuron disease

motor neuron disease, misdiagnosis

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, psychogenic

MRI, angiography

MRI, contrast enhanced

MRI, curvilinear peppering enhancement

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, nodular enhancement

multimodal neuroimaging

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, pain in

multiple sclerosis, paroxysmal symptoms in

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

myasthenia gravis

myasthenic syndrome

myoclonic jerks

myoclonus, epilepsy

myotonia congenita

myxedema, neurologic manifestations of

nasal septum, perforation of

nausea and vomiting

neoplasm, pituitary

neoplasm, primary of CNS

neoplasm, primary of CNS-metastasizing to subarachnoid space

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination, focal

neurologic signs

neurologic symptoms

neurologic symptoms, unexplained

neurologic testing

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, recurrent

neuropathy, sensory

neuropathy, vasculitic, systemic

neurotoxicity, acute

nystagmus, gaze-paretic

nystagmus, hereditary

nystagmus, intermittent

nystagmus, monocular

nystagmus, periodic

nystagmus, periodic alternating

nystagmus, primary position of gaze

nystagmus, vertical

ocular motility, disorders of

oculomasticatory myorhythmia

old age, neurology of

ophthalmoplegia

ophthalmoplegia, recurrent

ophthalmoplegia, total

optic atrophy, bilateral

optic neuropathy, ischemic

otitis, neurologic complications with

pain, abdominal

pain, testicular

palatal myoclonus

paralysis, acute areflexic

paramyotonia congenita

parathyroid adenoma

Parkinson disease

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

paroxysmal tonic upgaze

PAS positive material in the brain

pathologic reflex

patient information and support

periarteritis nodosa

periodic paralysis

periodic paralysis, thyrotoxic

perivascular enhancement

perivascular inflammation

peroxisomal disease

Persistent postural-perceptual dizziness

personality change

personality disorder

pheochromocytoma

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polyneuropathy, chronic relapsing

pons, lesion of

posterior leukoencephalopathy syndrome

potassium channel antibodies

potassium channel dysfunction

precipitating factors

pregnancy, neurologic complications in

primary aldosteronism

primary episodic ataxia

progressive neurologic disorder

psychiatric disorder

psychiatric problems in neurologic disorders

psychosis, acute

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriplegia, transient

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

REM sleep behavior disorder

remote effect of cancer on the nervous system

respiratory tract infection

retinal artery occlusion

retinal detachment

reversible cerebral vasoconstrictive syndromes

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

saccadic eye movements, abnormal

sedimentation rate, elevated

seizure, differential diagnosis of

selective serotonin reuptake inhibitors

sensorineural hearing loss

serologic testing

serotonin norepinephrine reuptake inhibitors

skin, lesions in neurologic disorders

skull bone, thickening

sleep pathology and physiology

slow virus infection of CNS

sodium channel dysfunction

spinocerebellar ataxia

spinocerebellar ataxia type 6

spinocerebellar degeneration

spongy degeneration of brain

startle myoclonus

startle reaction

status epilepticus

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

storage disease of CNS

stress, emotional

strokelike episodes

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

subarachnoid hemorrhage, cerebral convexity

subcortical U fibers

superior cerebellar peduncle

supratentorial lymphocytic inflam parenchy perivasc enhanc responsive to steroids

symmetric brain lesions

systemic illness

tandem gait, ataxic

temporal lobe, lesion

temporal lobe, lesion, bilateral

testicular biopsy

thalamus, lesion of

third nerve palsy

toxic encephalopathy

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

tremor, intention

tremor, postural

tremor, psychogenic

trigeminal neuralgia

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

Trousseau's sign

unconsciousness

unconsciousness, episodic

unconsciousness, transient

upgaze, paralysis of

upgaze, sustained

urea-cycle enzymopathies

urinary frequency

urinary incontinence

vaccination, neurologic complications with

valsalva maneuver

vasospasm, cerebral

vertebral artery

vertebral artery disease

vertebral artery occlusion

vertebral artery stenosis

vertebral-basilar insufficiency

vertigo, episodic

vertigo, treatment of

violent behavior

viral infection

viral infection, CNS

Virchow-Robin spaces, dilated

vision, blurred

visual field defect

visuospatial disturbance

vitamin E deficiency

vitreous opacities

Vogt-Koyanagi-Harada syndrome

walking, difficulty with

weakness, acute

weakness, episodic

weakness, generalized

Whipple's disease

white matter disease

wide based gait

Showing articles 950 to 1000 of 1935 << Previous Next >>

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

Drug Points, Transient Hemiparesis with Topiramate
BMJ 318:845, Stephen,L.J.,et al, 1999

Familial Paroxysmal Dystonic Choreoathetosis,Clinical Findings in a Large Japanese Family and Genetic Linkage to 2q
Arch Neurol 56:721-726, Matsuo,H.,et al, 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Topiramate-Treated Cluster Headache
Neurol 53:234-236, Wheeler,S.D.&Carrazana,E.J., 1999

Multiple Sclerosis in Children Under 6 Years of Age
Neurol 53:478-484, Ruggieri,M.,et al, 1999

Clinicopath Conf,Multifocal Inflammatory Leukoencephalopathy Related to Combination Chemo with Fluorouracil/levamisole
NEJM 341:512-519, Case 24-1999, 1999

Dancing Eyes-Dancing Feet
Lancet 354:390, Imtiaz,K.E.&Vora,J.P., 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Neurologic Complications in Children with Enterovirus 71 Infection
NEJM 341:936-942, Huang,C-C.,et al, 1999

A Man with Progressive Weakness in His Legs
Lancet 354:830, van der Meulen,M.F.G.,et al, 1999

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

Cerebellar Ataxia Associated with Subclinical Celiac Disease Responding to Gluten-Free Diet
Neurol 53:1606-1608, Pellecchia,M.T.,et al, 1999

Creutzfeldt-Jakob Disease Presenting as Complex Partial Status Epilepticus: A Report of Two Cases
JNNP 66:406-407, Rees,J.H.,et al, 1999

Leukoencephalopathy and Raised Brain Lactate from Heroin Vapor Inhalation ("Chasing the Dragon")
Neurol 53:589-1048, Kriegstein,A.R., et al, 1999

Opsoclonus as a Dominant Sign in Primary Sjogrens Syndrome
Neuro-Opthlhal 22:135-138, Lubec,D.,et al, 1999

Pseudochoreoathetosis in Four Patients with Hypesthetic Ataxic Hemiparesis in a Thalamic Lesion
J Neurol 246:1075-1079, Kim, J.W., et al, 1999

Herpes Simplex Encephalitis (HSE) and the Immunocompromised: A Clinical and Autopsy Study of HSE in the Settings of Cancer and Human Immunodeficiency Virus-Type 1 Infection
Hum Pathol 29:215-222, Schiff,D. &Rosenblum,M.K., 1998

Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
AJR 171:1131-1137, Antunez, E.,et al, 1998

Hypophosphatemia-Induced Neuropathy: Clinical and Electrophysiologic Findings
Muscle Nerve 21:650-652, Siddiqui,M.F. &Bertorini,T.E., 1998

Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
, Ghika,J. &Bogousslavsky, J., 1998

Hypothalamic Activation in Cluster Headache Attacks
Lancet 352:275-278, 2531998., May,A.,et al, 1998

Occult Giant Cell Arteritis:Ocular Manifestations
Am J Ophthalmol 125:521-526, Hayreh,S.S.,et al, 1998

Transient Monocular Blindness and Antiphospholipid Antibodies in Systematic Lupus Erythematosus
Neurol 51:535-540, Donders,R.C.J.M.,et al, 1998

Role of Anticardiolipin Antibodies in Young Persons with Migraine & Trans Focal Neuro Events, Prospect Study
Neurol 50:1433-1440, Tietjen,G.E.,et al, 1998

Disequilibrium in Patients with Atherosclerosis; Relevance of Pontine Ischemic Rarefaction
Neurol 51:570-573, Kwa,V.I.H.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

An Open-Label Trial of Gabapentin Treatment of Paroxysmal Symptoms in Multiple Sclerosis Patients
Neurol 51:609-611, Solaro,C.,et al, 1998

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

Endozepine Stupor. Recurring Stupor Linked to Endozepine-4 Accumulation
Brain 121:127-133, Lugaresi,E.,et al, 1998

Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998

Clinicopath Conf,Sarcoidosis,with Involvement of Spinal Cord,Brain,Mediastinal Lymph Nodes and ? Lung,Case 35-1998
NEJM 339:1534-1541, , 1998

Adult Brainstem Gliomas
Neurol 51:1136-1139, Landolfi,J.C.,et al, 1998

Ophthalmoplegic Migraine:Reversible Enhancement and Thickening of the Cisternal Segment of the Oculomotor Nerve on Contrast-Enhanced MR Images
AJNR 19:1887-1891, Mark,A.S.,et al, 1998

Lateral Medullary Infarction
Stroke, Pathophysiology, Diagnosis and management, Churchhill Livingstone, NY 3rd Ed, Ch 22, p. 534, Amarenco,P.,et al, 1998

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

Diffusion-Weighted MRI in Trans Global Amnesia:Elev Signal Intensity in Mesial Temporal Lobe
Ann Neurol 43:164-170, 1511998., Strupp,M.,et al, 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Susac Syndrome
Medicine 77:3-11, Papo,T.,et al, 1998

Characteristic Magnetic Resonance Imaging Findings in Machado-Joseph Disease
Arch Neurol 55:33-37, Murata,Y.,et al, 1998

Presentation of Narcolepsy After 40
Neurol 50:459-465, Rye,D.B.,et al, 1998

Chronic Progressive Leukoencephalopathy in Adult Celiac Disease
Neurol 50:820-822, Beyenburg,S.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998

A 35-Year-Old Bricklayer with Hemimyoclonic Jerks
Lancet 351:1926, Grunewald,T.,et al, 1998

Atypical Herpes Simplex Virus Encephalitis Diagnosed by PCR Amplification of Viral DNA from CSF
Neurol 51:554-559, Fodork,P.A.,et al, 1998

Diagnostic Utility of the Polymerase Chain Reaction in 2 Cases of Suspected Whipple Disease
Arch Int Med 158:801-803, Tasken,K.,et al, 1998

Ischemic Optic Neuropathy Associated with Internal Carotid Artery Dissection
Arch Neurol 55:715-719, Biousse,V.,et al, 1998

Paroxysmal Tonic Upgaze:a Reappraisal of Outcome
Ann Neurol 43:514-520, Hayman,M.,et al, 1998

Showing articles 950 to 1000 of 1935 << Previous Next >>