Neudle.com: "periodic ataxia"

Differential
(Click to cross reference)

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

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, 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

degenerative diseases of CNS

delay in diagnosis

delirium

dementia

dementia, rapidly progressive

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

dysarthria

dysphagia

dystonia

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

fasciculation

fatigue

fever

fine motor function, impaired

fingerprint bodies

Fisher's syndrome

fistula, perilymphatic

Friedreich's ataxia

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 injury

head turning

head turning, neurologic complications with

hemianopia, homonymous

hemimyoclonic jerks

hemiparesis

hemiplegia

hemosiderosis of CNS, superficial

hyperpigmentation of skin

hypokalemic periodic paralysis

hypothalamus, disturbance of

iatrogenic neurologic disorders

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic 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 disorder, primary

methotrexate

microhemorrhage, intracerebral

mononeuropathy multiplex

motor neuron disease, misdiagnosis

movement disorder

movement disorder, extrapyramidal

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

neuroophthalmology

neuropathology

neuropathy

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, recurrent

neuropathy, sensory

neuropathy, vasculitic, systemic

nystagmus, gaze-paretic

nystagmus, hereditary

nystagmus, intermittent

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 neuritis

optic neuropathy, ischemic

oscillopsia

otitis, neurologic complications with

paralysis, acute areflexic

paramyotonia congenita

Parkinsonism syndrome

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

quadriplegia, transient

rash

recurrent

REM sleep behavior disorder

remote effect of cancer on the nervous system

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

sinusitis

skin, lesions in neurologic disorders

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

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

uremia

urinary incontinence

uveitis

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 0 to 50 of 1843 Next >>

Recurrent Rhombencephalitis Associatedwith Anti-GAD65 Antibody
Neurol 102:e208040, Alferes,A.R.,et al, 2024

Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
Ann Neurol 95:407-409, Tsibonakis,A.,et al, 2024

A 55-Year-Old Woman with Recurrent Episodes of Aphasia and Vision Changes
Neurol 98:330-335, Jeanneret, V.,et al, 2022

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

When MRI is a Clue in Episodic Ataxia
Neurol 93:e2074-e2075, Dhawan, S.R.,et al, 2019

Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
Pediatr Emer Care 35:e67-e69, Kartal,A., 2019

Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
Pract Neurol 18:5-13, Popkirov, S.,et al, 2018

Recurrent Dysarthria and Ataxia in a Young Girl
JAMA Neurol 75:125-126, Romba, M.,et al, 2018

Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 73:1297-1307, Fang, B.,et al, 2016

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
Adams & Victors Principles of Neurology, Chp 32, pg 710, Ropper, A.H.,et al, 2014

A 72-year-old Man with Rapid Cognitive Decline and Unilateral Muscle Jerks
Neurol 82:e194-e197, Duncan, M.,et al, 2014

Subacute Sclerosing Panencephalitis
www.MedLink.com, February, Auwaeter,P.G.&Johnson,R.T., 2013

Clincopathologic Conference,Graves Disease with Thyrotoxic Periodic Paralysis
NEJM 366:553-560, Case 4-2012, 2012

Multimodal Imaging of Reversible Cerebral Vasoconstriction Syndrome: A Series of 6 Cases
AJNR 33:1403-1410, Marder, C.P.,et al, 2012

Epstein-Barr Virus Infections of the Nervous System
www.medlink.com, Nov, Amlie-Lefond,C., 2011

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
Neurol 77:1287-1294, Prust, M.,et al, 2011

Age and High-Dose Methotrexate are Associated to Clinical Acute Encephalopathy in FRALLE 93 Trial for Acute Lymphoblastic Leukemia in Children
Leukemia 21:238-247, Dufourg, M.N.,et al, 2007

Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
Brain 130:2484-2493, Jen, J.C.,et al, 2007

Clinical Spectrum of Episodic Ataxia Type 2
Neurol 62:17-22, Jen,J.,et al, 2004

Headache and CNS White Matter Abnormalities Associated with Gluten Sensitivity
Neurol 56:385-388, Hadjivassiliou,M.,et al, 2001

Rotational Vertebral Artery Occlusion Syndrome with Vertigo Due to "Labyrinthine Excitation"
Neurol 54:1376-1379, Strupp,M.,et al, 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 1997

Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997

Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p
Ann Neurol 41:8-16, 41997., Baloh,R.W.,et al, 1997

The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996

Diagnostic Guidelines in Central Nervous System Whipple's Disease
Ann Neurol 40:561-568, Louis,E.D.,et al, 1996

Clinicopath Conf
Granulomatous Angiitis of CNS, Case 33-1995, NEJM 333:1135-1143995., , 1995

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Abnormal Eye Movements in Creutzfeldt-Jakob Disease
Ann Neurol 34:192-197, Grant,M.P.,et al, 1993

Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
Neurol 41:429-433, Baloh,R.W.&Winder,A., 1991

Neurologic Manifestations of Giant Cell Arteritis
Am J Med 89:67-72, Reich,K.A.,et al, 1990

Paroxysmal Cerebellar Ataxia
Aust NZ J Med 19:113-117, Feeney,G.F.&Boyle,R.S., 1989

Creutzfeldt-Jakob Disease without Periodic Sharp Wave Complexes:A Clinical, EEG, and Path Study
Neurol 38:1056-1060, Zochodne,D.W.,et al, 1988

Magnetic Resonance Imaging in Familial Paroxysmal Ataxia
Arch Neurol 45:547-549, Vighetto,A.,et al, 1988

Neuro-Ophthalmologic Findings in Vestibulocerebellar Ataxia
Arch Neurol 43:1050-1053, Farris,B.K.,et al, 1986

The Leaking Labyrinth
BMJ 293:220-221, O'Donoghue,G.M.&Colman,B.H., 1986

Relapsing Ophthalmoparesis-Sensory Neuropathy Syndrome
Neurol 35:595-596, Kaplan,J.G.,et al, 1985

Acetazolamide-Responsive Episodic Ataxia Syndrome
Neurol 33:1212-1214, Zasorin,N.L.,et al, 1983

Clin. Path. Conference
Fibrillary Astrocytoma of Medulla, with Invasion of Subarachnoid Space, Case Record 6-1981, NEJM 304, 3430,1981., 1981

Paroxysmal Symptoms as the First Manifestations of Multiple Sclerosis
JNNP 43:296-304, Twomey,J.A.,et al, 1980

Focal Neurologic symptoms in hypercalcemia
Neurol 30:200-201, Longo,D.L.,et al, 1980

Familial Periodic Ataxia
Arch Neurol 36:568-569, Donat,J.R.,et al, 1979

Hereditary Paroxysmal Ataxia:Response to Acetazolamide
Neurol 28:1259-1264, Griggs,R.C.,et al, 1978

Showing articles 0 to 50 of 1843 Next >>