Neudle.com: familial episodic ataxia

Differential
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abducens nerve paralysis

acanthocytosis

acetazolamide

acoustic nerve

acromicria

acyl CoA dehydrogenase deficiency

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

antibodies to voltage-gated calcium channels

anticonvulsants

anticonvulsants, effectiveness

anticonvulsants, selection of

antimetabolite

aphasia

apnea

apnea, primary central

autonomic dysfunction

Babinski sign

basal ganglia

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

biotin deficiency

biotinidase deficiency

bladder dysfunction

blindness

blood dyscrasias, neurologic findings with

calcification, intracranial

calcium channel dysfunction

caudate nucleus, atrophy

central core disease

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortical atrophy

cerebral edema

cerebral infarction, subcortical

cerebral palsy

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure low

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

channelopathy

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot-myoclonus syndrome

children

chloride channel dysfunction

chorea

chorea, familial

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

clonus

cobalamin C deficiency

Cockayne's syndrome

cognition

cogwheel rigidty

color vision, impaired

corpus callosum, lesion of

cortical blindness

cranial nerve palsies

cranial neuropathy, multiple

cry, abnormal

cry, weak

cryopyrin-associated periodic syndrome

cultured skin fibroblasts

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

differential diagnosis

difficulty climbing stairs

diplopia

disease modifying agents

down-beat nystagmus

down-beat nystagmus, primary position of gaze

Dravet syndrome

drooling

dropped head syndrome

dyssynergia cerebellaris myoclonica

electroencephalogram, abnormalities of

electromyogram

encephalopathy

encephalopathy, progressive

enzyme, defect

epicanthal folds

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

exercise

exercise intolerance

exome sequencing

eye movement, disorders of

Fabry's disease

facial appearance, abnormal

facial expression abnormality

facial nerve palsy, bilateral

familial hemiplegic migraine

familial periodic ataxia

fine motor function, impaired

fingerprint bodies

fish

fluorescene in situ hybridization

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

gout

granular osmiphilic material

growth hormone deficiency

Hallervorden Spatz disease

hemophagocytic lymphohistiocytosis, cerebromeningeal

Huntington's disease, children

hypertrophic intracranial pachymeningitis

hypofibrinogenemia

hypogonadism

hypokalemia

hypokalemic periodic paralysis

hypomyelination

hyponatremia

hypopigmentation of skin

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inappropriate behavior

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

incoordination

intellectual deficit

intellectual deterioration

intracerebral hemorrhage

intracranial pressure, increased

Kearns-Sayre syndrome

keratoconus

Korsakoff's psychosis

Laurence-Moon-Bardet-Biedl syndrome

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

lipid storage disorder of CNS

liver disease

lymphadenopathy

lysosomal storage disease

macrognathia

macular degeneration

malformation, CNS, congenital

malignant hyperpyrexia

maple syrup urine disease

MELAS syndrome

memory, impairment of

meningismus

meningitis, aseptic

meningitis, carcinomatous

meningitis, CSF cell count-normal

meningoencephalopathy

mental retardation

MERRF syndrome

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methotrexate

methylhydrazine derivatives

methylmalonic acidemia

Mexican

microcephaly

microdontia

microhemorrhage, intracerebral

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

molecular genetics

monoamine oxidase inhibitors

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR

MRI, muscle

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle biopsy

muscle pain

muscle weakness

muscle weakness, proximal

myopathy, mitochondrial

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic testing

neuromuscular disease, electrodiagnosis of

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, hereditary peripheral

neuropathy, peripheral

neurotoxin

neutropenia

next-generation sequencing

nystagmus, gaze-paretic

nystagmus, hereditary

oculodentodigital dysplasia

ophthalmoplegia

ophthalmoplegia, progressive external

opisthotonus

optic atrophy

optic atrophy, bilateral

optic atrophy, hereditary

optokinetic nystagmus, abnormal

orthostatic hypotension

paramyotonia congenita

paraparesis

paraparesis, familial spastic

paraparesis, spastic

paresthesias

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

patient information and support

periodic paralysis

peroxisomal disease

personality change

pleocytosis of cerebrospinal fluid

poison, mercury

poison, neurologic problems with

POLG1 gene

polydactyly

polymerase chain reaction

pons, atrophy

pons, lesion of

pontocerebellar atrophy

postural abnormality

potassium channel antibodies

potassium channel dysfunction

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

pretectal syndrome

primary episodic ataxia

procarbazine

prognathism

prognosis

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

proteinuria

pseudobulbar palsy

pseudoretinitis pigmentosa

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

respiratory tract infection

salivation, excessive

seizure, photosensitive

seizure, psychomotor-temporal lobe

seizure, tonic-clonic

seizure, treatment of

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

short stature

skin, biopsy

skin, lesions in neurologic disorders

skull bone, thickening

slurred speech

small vessel disease

small vessel disease, cerebral

smiling

sodium channel dysfunction

spastic diplegia

spasticity

speech disorder

speech disorder, childhood

speech, delayed development of

speech, loss of

Spielmeyer Vogt syndrome

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 6

spinocerebellar degeneration

steroid therapy, CNS treatment and complications with

storage disease of CNS

strabismus

stress, emotional

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

stuttering

subarachnoid hemorrhage

subcortical U fibers

substantia nigra

suck, poor

symmetric brain lesions

temporal lobe, lesion

tongue, protrusion of

topiramate

toxins, nervous system

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

treatment of neurologic disorder

tremor

tremor, intention

tremulousness

trinucleotide repeats

tubulopathy

undiagnosed

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

urinary frequency

urinary incontinence

urine test for metabolic disorders

Usher's syndrome

vasculopathy

venous thrombosis, non-cerebral

vertigo

vertigo, episodic

vertigo, treatment of

vinblastine

vincristine neurotoxicity

violent behavior

visual evoked response

visual field defect

visual fields, constricted

vitamin E deficiency

vocal cord paralysis

walking, difficulty with

weakness

weakness, progressive

white matter disease, subcortical

wide based gait

Wolfram syndrome

wrist drop

Showing articles 500 to 550 of 5796 << Previous Next >>

Neurologic Complications of Primary Sjogren's Syndrome
Medicine 61:247-257, Alexander,E.L.,et al, 1982

Nevoid Basal Cell Carcinoma Syndrome & Epilepsy
Ann Neurol 11:372-376, Murphy,M.J.,et al, 1982

Fragile X Chromosome & X-Linked Mental Retardation
CMA Journal 127:123-126, Larbrisseau,A.,et al, 1982

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981

Neurologic Complications of Hyperthyroidism
Arch Neurol 38:669-670, Bulens,C., 1981

Meningeal Carcinomatosis
Arch Neurol 38:696-699, Theodore,W.H.,et al, 1981

Encephalopathy in Infants & Children With Chronic Renal Disease
Arch Neurol 38:656-658, Foley,C.M.,et al, 1981

Biochemical Genetics Of Neurologic Disease
NEJM 305:1181-1193, Rosenberg,R.N., 1981

Von Recklinghausen Neurofibromatosis
NEJM 305:1617-1627, Riccardi,V.M., 1981

Computed Tomography in Cerebrotendinous Xanthomatosis
Neurol 31:1463-1465, Berginer,V.M.,et al, 1981

Double-blind, Triple-crossover Trial of Low Doses of Oral Physostigmine in Inherited Ataxias
Neurol 31:288-292, Kark,R.A.P.,et al, 1981

Neurologic Complications of Lymphomatoid Granulomatosis
Neurol 31:619-620, Hogan,P.J.,et al, 1981

Ataxia with Aniridia of Gillespie:A Case Report
Neurol 31:95-97, Lechtenberg,R.,et al, 1981

Cerebellar Atrophy Demonstrated by Computed Tomography
Neurol 31:405-412, Koller,W.C.,et al, 1981

Abetalipoproteinemia, Report of Two Cases & Review of Therapy
Arch Neurol 37:659-662, Illingworth,D.R.,et al, 1980

Central Nervous System Toxicity Associated With Metronidazole Therapy
Ann Int Med 93:59-60, Kusumi,R.K.,et al, 1980

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

Benign Familial Neonatal Seizures
E. , Arch Neurol 37:47-48980., Pettit,R., 1980

Use of Adrenal Biopsy in Diagnosing Adreno-leukomyeloneuropathy
Arch Neurol 37:634-636, Weiss,G.M.,et al, 1980

Lafora Disease:Diagnosis by Liver Biopsy
Ann Neurol 8:409-415, Nishimura,R.N.,et al, 1980

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

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980

Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
Neurol 30:319-322, Lima,L.,et al, 1980

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Familial Tapetorentinal Degeneration & Epilepsy
Arch Neurol 36:544-546, Cohan,S.L.,et al, 1979

Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Neurol 29:880-881, Kuritzky,A.,et al, 1979

Familial Psychosis & Diverse Neurologic Abnormalities in Adult-Onset Gaucher's Disease
Arch Neurol 36:95-99, Neil,J.F.,et al, 1979

Clinical & Biochemical Aspects of Trichopoliodystrophy
Ann Neurol 5:65-71, Grover,W.D.,et al, 1979

CT Scans in Menkes Disease
Neurol 29:304-312, Seay,A.R.,et al, 1979

Familial Inverted Choreoathetosis
Neurol 29:1627-1631, Fisher,M.,et al, 1979

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Clinical Pathological Conference, Reticulum Cell Sarcoma of Brain
NEJM 299:1349-1359, Case Record 49-1978,Mass.Gen.Hosp., 1978

The Lissencephaly, (Agyria) Syndrome in Siblings
Arch Neurol 35:608-611, Garcia,C.A.,et al, 1978

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Familial Vascular Malformation or Chance Occurrence
Neurol 28:98, Barre,R.G.,et al, 1978

Blue Rubber Bleb Nevus Syndrome with CNS Involvement & Thrombosis of a Vein of Galen Malformation
Ann Neurol 3:464, Waybright,E.A.,et al, 1978

Extreme Insulin Resistance in Ataxia Telangiectasia
NEJM 298:1164, Bar,R.S.,et al, 1978

Dominant Spinopontine Atrophy
Arch Neurol 35:156, Pogacar,S.,et al, 1978

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Ataxia Telangiectasia
Arch Neurol 35:553-554, Teplitz,R.L., 1978

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

The Cherry-red Spot-Myoclonus Syndrome
Ann Neurol 3:234, Rapin,I.,et al, 1978

Familial Cavernous Angiomas
Arch Neurol 35:746-749, Bicknell,J.M.,et al, 1978

Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978

Progressive Dialysis Encephalopathy
Ann Neurol 4:199-204, Lederman,R.J.,et al, 1978

CNS Lesions in Cystinuria
Arch Neurol 34:638, Blackburn,C.R.B.,et al, 1977

Reversible Corticospinal Tract Disease Due to Hyperthyrodisim
Arch Neurol 34:647, Garcia,C.A.,et al, 1977

The Central Nervous System in a Case of Neurolathyrism
Neurol 27:1176, Striefler,M.,et al, 1977

CT Scanning & Diagnosis of Adrenoleukodystrophy
Neurol 27:884, Greenberg,H.S.,et al, 1977

Showing articles 500 to 550 of 5796 << Previous Next >>