Neudle.com: ataxia periodic

Differential
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abdominal distention

abducens nerve paralysis

acetazolamide

acute cerebellar ataxia

Addison's disease

adverse drug reaction

alcohol

Alexanders disease

Alexanders disease, adult onset

algorithm

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

amaurosis fugax

aminoacidopathies

aminoacidurias

amyloid angiopathy, cerebral

anemia

aneurysm

aneurysm, vertebral basilar system

angiitis

angiitis, granulomatous of CNS

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, negative

angiography, posterior fossa

angiography, vertebral artery

antibodies to measles

antibodies to voltage-gated calcium channels

autoimmune GFAP astrocytopathy

autonomic dysfunction

axonal injury

Babinski sign

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

blindness

brain biopsy

brain biopsy, stereotaxic

brainstem, glioma

brainstem, infarction of

brainstem, lesion of

brucellosis

brucellosis, nervous system involvement with

bulbar palsy

calcification, intracranial

calcium antagonist

calcium channel dysfunction

CAT scan, angiography

CAT scan, metrizamide

cataracts

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

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

channelopathy

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

children

chills

chloride channel dysfunction

chorea

choreoathetosis

chorioretinitis

chromosomal abnormality

chromosome 19

Chvostek sign

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

cognition

cogwheel rigidty

collagen vascular disease

coma

coma, episodic

complications

concentration, impaired

cranial nerve palsies

craniopharyngioma

cryopyrin-associated periodic syndrome

degenerative diseases of CNS

delay in diagnosis

delirium

dementia

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dentate nuclei, lesion of

depression

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diarrhea

diet

differential diagnosis

digital subtraction angiography

diplopia

disability, neurological

down-beat nystagmus, primary position of gaze

downward gaze, paralysis of

drowsiness

drug induced neurologic disorders

dystonia, psychogenic

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

electromyogram

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, viral

encephalopathy

encephalopathy, acute

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

eye movement, disorders of

face, numbness of

facial movement disorder

facial nerve palsy

facial weakness

faciobrachial dystonic seizure

failure to thrive

falling

familial

familial hemiplegic migraine

familial periodic ataxia

fine motor function, impaired

fingerprint bodies

Fisher's syndrome

fistula, perilymphatic

Friedreich's ataxia

frontal bossing

frontal lobe, pathologic signs of

fundus, abnormality of

gait disorder

gaze palsy

gaze palsy, supranuclear

gaze palsy, vertical

gene

gene mutation

genetic neurologic disorders

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

gluten sensitivity

gluten-free diet

gram positive rod

granular osmiphilic material

Guillain Barre syndrome

gynecomastia

hallucination

hallucination, auditory

hallucination, visual

Hand-Schuller-Christian disease

head circumference

head injury

head turning

head turning, neurologic complications with

hemianopia, homonymous

hemimyoclonic jerks

hemiparesis

hemiplegia

hemosiderosis of CNS, superficial

hyperpigmentation of skin

hypertrophic intracranial pachymeningitis

hypoglycorrhachia

hypokalemia

hypokalemic periodic paralysis

hypothalamus, disturbance of

hypotonia

iatrogenic neurologic disorders

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

incoordination

infection

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

iritis

irritability

islet cell tumor

Jakob-Creutzfeldt disease

leg weakness, bilateral

leptospirosis

lethargy

leucine rich glioma inactivated 1 antibodies

level of consciousness, decreased

lightheaded

limbic encephalitis

lymphadenopathy

lysosomal storage disease

macrocephaly

malaise

malignant hyperpyrexia

maple syrup urine disease

mastoiditis

medulla oblongata, neoplasm of

memory, defect of recent

memory, impairment of

Meniere's disease

meningeal enhancement

meningitis

meningitis, aseptic

meningitis, bacterial

meningitis, carcinomatous

meningitis, elderly

meningitis, fungal

meningitis, Mollaret's

meningitis, recurrent

meningitis, TB

meningoencephalitis

meningoencephalomyelitis

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

methotrexate

microcephaly

microhemorrhage, intracerebral

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mononeuropathy multiplex

motor neuron disease, misdiagnosis

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, psychogenic

MRI, contrast enhanced

MRI, curvilinear peppering enhancement

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR

MRI, negative

MRI, nodular enhancement

multimodal neuroimaging

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, pain in

multiple sclerosis, paroxysmal symptoms in

muscle weakness, causes of

muscle weakness, proximal

myxedema, neurologic manifestations of

nasal septum, perforation of

nausea and vomiting

negative

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

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology

neuropathy

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, recurrent

neuropathy, sensory

neuropathy, vasculitic, systemic

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 ataxia

optic atrophy

optic atrophy, bilateral

optic neuritis

optic neuropathy, ischemic

oscillopsia

otitis, neurologic complications with

paralysis, acute areflexic

paramyotonia congenita

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

paroxysmal tonic upgaze

PAS positive

PAS positive material in the brain

pathologic reflex

pathology

patient information and support

periarteritis nodosa

pericarditis

periodic paralysis

periodic paralysis, thyrotoxic

perivascular enhancement

perivascular inflammation

peroxisomal disease

Persistent postural-perceptual dizziness

personality change

personality disorder

pheochromocytoma

pleocytosis of cerebrospinal fluid

pleurisy

pneumonia

polymerase chain reaction

polyneuropathy

polyneuropathy, chronic relapsing

polyuria

pons, lesion of

posterior leukoencephalopathy syndrome

potassium

potassium channel antibodies

potassium channel dysfunction

precipitating factors

pregnancy, neurologic complications in

primary aldosteronism

primary episodic ataxia

prognosis

progressive neurologic disorder

psychiatric disorder

psychiatric problems in neurologic disorders

psychosis

psychosis, acute

ptosis

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, tonic

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriplegia, transient

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

recurrent

red eye

REM sleep behavior disorder

remote effect of cancer on the nervous system

respiratory tract infection

retinal artery occlusion

retinal detachment

retinopathy

reversible cerebral vasoconstrictive syndromes

review article

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rhinorrhea

Romberg's sign

rubeola virus

saccadic eye movements, abnormal

sedimentation rate, elevated

seizure

seizure, differential diagnosis of

seizure, focal

selective serotonin reuptake inhibitors

sensorineural hearing loss

serologic testing

serotonin norepinephrine reuptake inhibitors

short stature

sinusitis

skin, biopsy

skin, lesions in neurologic disorders

skull bone, thickening

sleep pathology and physiology

slow virus infection of CNS

slurred speech

sneeze

sodium channel dysfunction

sore throat

spinocerebellar ataxia

spinocerebellar ataxia type 6

spinocerebellar degeneration

spongy degeneration of brain

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

storage disease of CNS

stress, emotional

strokelike episodes

stuttering

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

swimming

symmetric brain lesions

temporal lobe, lesion

temporal lobe, lesion, bilateral

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

Trousseau's sign

unconsciousness

unconsciousness, episodic

unconsciousness, transient

upgaze

upgaze, paralysis of

upgaze, sustained

urea-cycle enzymopathies

vaccination, neurologic complications with

vertebral artery disease

vertebral artery occlusion

vertebral artery stenosis

vertebral-basilar insufficiency

vertigo

vertigo, episodic

vertigo, treatment of

violent behavior

viral infection

viral infection, CNS

Virchow-Robin spaces, dilated

vision, blurred

visual field defect

visual loss

visuospatial disturbance

vitamin E deficiency

vitreous opacities

vocalizations

Vogt-Koyanagi-Harada syndrome

walking, difficulty with

weakness

weakness, acute

weakness, episodic

weakness, generalized

Showing articles 1000 to 1050 of 1935 << Previous Next >>

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Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Myelopathy Caused by Nitrous Oxide Toxicity
AJNR 19:894-896, 9941998., Pema,P.J.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998

Cerebral Manifestation of Wilson's Disease Successfully Treated with Liver Transplantation
Neurol 51:863-865, Bax,R.T.,et al, 1998

CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
Neurol 51:882-884, Abe,Y.,et al, 1998

Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
Ann Neurol 44:350-356, Delanoe,C.,et al, 1998

Development of Wernicke-Korsakoff Syndrome After Long Intervals Following Gastrectomy
Arch Neurol 55:1242-1245, Shimomura,T.,et al, 1998

Acute Therapy for Cluster Headache with Sumatriptan:Findings of a One-Year Long-Term Study
Neurol 51:980-911, Gobel,H.,et al, 1998

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

Ataxic Hemiparesis,Critical Appraisal of a Lacunar Syndrome
Stroke 29:2549-2555, Gorman,M. J.,et al, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Recurrent Carotid Stenosis Results of the Asymptomatic Carotid Atherosclerosis Study
Stroke 29:2018-2025, Moore,W.S.,et al, 1998

Vertigo
Lancet 352:1841-1846, Baloh,R.W., 1998

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

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

Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
Neurol 49:1598-1604, Brandmann,O.,et al, 1997

Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Efficacy of Sphenopalatine Ganglion Blockade in 66 Pts Suffering from Cluster Headache
J Neurosurg 87:876-880, Sanders,M.&Zuurmond,W.W.A., 1997

Neuroimaging in Presumed Primary Headache Disorders
Semin Neurol 17:373-382, Frishberg,B.M., 1997

Ocular Findings in Ramsay Hunt Syndrome
J Neuro-Ophthalmol 17:199-201, Mansour,A.M.&Bailey,B.J., 1997

Basilar Artery Embolism, Clin Synd & Neuroradiologic Patterns in Pts Without Perm Occl of Basilar Artery
Neurol 49:1346-1352, Schwarz,S.,et al, 1997

Giant Cell Arteritis With Unusual Flow-Related Neuroophthalmologic Manifestations
Neurol 49:1463-1465, Galetta,S.L.,et al, 1997

Diffusion-Weighted MRI in Transient Global Amnesia Precipitated by Cerebral Angiography
Stroke 28:2311-2314, Woolfenden,A.R.,et al, 1997

Ataxia and Slurred Speech after Artesunate Treatment for Falciparum Malaria
NEJM 336:1328, Miller,L.G.&Panosian,C.B., 1997

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

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

Serum Autoantibodies in Childhood Opsoclonus-Myoclonus Syndrome:Analysis of Antigenic Targets in Neural Tissues
J Pediatr 130:878-884, 8851997., Connolly,A.M.,et al, 1997

Postprandial Transient Visual Loss
Ophthalmology 104:397-401, Levin,L.A.&Mootha,V.V., 1997

Severe but Transient Parkinsonism after Tetanus Vaccination
JNNP 63:258, Reijneveld,J.C.,et al, 1997

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

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

Rapid Spongiform Degeneration of the Cerebrum and Cerebellum in Creutzfeldt-Jakob Encephalitis:Serial MR Findings
AJNR 18:583-586, Tzeng,B-C.,et al, 1997

Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,et al, 1997

Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
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CIDP:Clinical Features & Responses to Trtm in 67 Consecutive Pts with/without a Monoclonal Gammopathy
Neurol 48:321-328, Gorson,K.G.,et al, 1997

A 36-Year-Old Woman Recuperating From a Stroke
JAMA 277:1970-1976, Alexander,M., 1997

Alternating Amaurosis Fugax and Temporal Arteritis
Am J Ophthalmol 123:850-851, Finelli,P.F., 1997

Pure or Predominant Sensory Stroke Due to Brain Stem Lesion
Stroke 28:1761-1764, Kim,J.S.&Bae,Y.H., 1997

Clinicopath Conf
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Frataxin Gene of Friedreich's Ataxia is Targeted to Mitochondria
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Showing articles 1000 to 1050 of 1935 << Previous Next >>