Neudle.com: myoclonic ataxia

Differential
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abdominal distention

abdominal x-ray

adverse drug reaction

altered states of consciousness

alternating rapid movement

aluminum

AMPA receptor antibodies

antibiotics, neurologic complications with

antibodies to measles

anticonvulsants

anticonvulsants, effectiveness

anticonvulsants, selection of

antidepressant

antioxidant

antithyroid antibodies

ataxia, truncal, associated with ocular oscillations

autonomic dysfunction

axonal spheroid

Babinski sign

bacterial infection

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

bovine spongiform encephalopathy

carbon monoxide poisoning

CAT scan, emission, abnormal

cataracts

celiac disease, adult

central nervous system, infection of

cephalosporins

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellum

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral glucose metabolism

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, young adult

cherry red spot

cherry red spot-myoclonus syndrome

chromosomal abnormality

chromosome 12

chromosome 2

chromosome 21

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clonazepam

clonus

coenzyme Q10 deficiency

cognition

cogwheel rigidty

cold intolerance

color vision, impaired

congenital infection, CNS

congenital paresis

conjugate gaze, forced

contactin associated protein like 2 antibodies

cortical-basal ganglionic degeneration

cranial nerve palsies

Creutzfeldt-Jakob disease, genetic

crying

deafness

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delirium

dementia

dementia, differential diagnosis of

dementia, rapidly progressive

dementia, reversible

dementia, transmissible

dementia, treatment of

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

diplopia

disability, neurological

dizziness

doll's head maneuver

downward gaze, paralysis of

Dravet syndrome

drooling

drug induced neurologic disorders

dyssynergia cerebellaris myoclonica

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

electromyogram

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, diagnosis of

encephalitis, etiology

encephalitis, paraneoplastic

encephalitis, viral

encephalitis, viral-causes of

encephalomyelitis

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, parainfectious

enterovirus

enterovirus infection of CNS

enzyme, defect

epidemic

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

exome sequencing

eye movement, disorders of

facial movement disorder

faciobrachial dystonic seizure

falling

familial

fasciculation

fatal familial insomnia

fatigue

fever

fine motor function, impaired

finger nose finger test

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

gliadin antibodies

globus pallidus, lesion of

GluD2

glutamic acid decarboxylase, antibody

granular osmiphilic material

grasp reflex

gray matter

gyrus, abnormal

Hallervorden Spatz disease

hallucination

hand-foot-mouth disease

heavy metal intoxication

heralding manifestation

hoarseness

human immunodeficiency virus type 1

hydrocephalus

hyperhidrosis

hyperpigmentation of skin

hypothalamus, disturbance of

hypothyroidism

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

idiopathic

imbalance

imbalance, postural

immune reconstitution inflammatory syndrome

immunohistochemistry

immunosuppressive agents

immunotherapy

impotence

inattention

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

intellectual deterioration

intestinal biopsy

intestinal pseudoobstruction

intrauterine infection

intrauterine infection, viral of CNS

introverted

irritability

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

juvenile paresis

Kearns-Sayre syndrome

Leber's hereditary optic neuropathy

Leigh's disease

Leigh's disease, adult variety

leucine rich glioma inactivated 1 antibodies

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

limbic encephalitis

linear lesion

lipid storage disorder of CNS

lithium

liver function enzymes

lymphadenopathy

lysosomal storage disease

macular degeneration

maculopathy

malabsorption

malabsorption syndrome

malaise

masked facies

MELAS syndrome

memory, defect of recent

memory, impairment of

mental status, abnormal

mitochondrial disease

mitochondrial encephalomyopathy

motor neuron disease, misdiagnosis

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, diffusion weighted

MRI, false negative

MRI, FLAIR

MRI, high signal intensity of basal ganglia

MRI, negative

MRI, pelvis

MRI, spinal cord

MRI, susceptibility weighted

mutism

myelitis

myelitis, longitudinal

myoclonus, orthostatic

myoclonus, segmental

myoclonus, stimulus sensitive

myoclonus, treatment of

myoclonus-ataxia syndrome

myopathy

myopathy, mitochondrial

neuraminidase deficiency

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroaxonal leukodystrophy

neuroblastoma

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic signs

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, ataxia, retinitis pigmentosa

neurosyphilis

neurotoxic

neurotoxin

next-generation sequencing

ocular motility, disorders of

oculomasticatory myorhythmia

old age, neurology of

olivary degeneration, hypertrophic

ophthalmoplegia

ophthalmoplegia, progressive external

opsoclonus

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic atrophy

optic atrophy, hereditary

optic neuropathy

oral ulcerations

organ transplantation

orthostatic hypotension

paralysis, acute areflexic

paraparesis, spastic

parasomnia

Parkinson disease

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleurisy

pneumonia

polymerase chain reaction

polyneuropathy

pons, lesion of

pontocerebellar atrophy

potassium channel antibodies

pregnancy, neurologic complications in

prevention of neurologic disorders

prion disease

prognosis

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

protein 14-3-3, cerebrospinal fluid

protein 14-3-3, cerebrospinal fluid, false negative

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

Purkinje cell surface antibody

pursuit eye movements, abnormal

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

ragged-red fibers

Ramsay Hunt syndrome

rapidly progressing neurologic illness

rash

rash, hand

real-time quaking-induced conversion

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal failure

respiratory failure

respiratory tract infection

rubella encephalitis, progressive

rubella syndrome

rubella virus

rubeola virus

saccadic eye movements, abnormal

salivation, excessive

SCN1A gene

sedimentation rate, elevated

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, tonic-clonic

seizure, treatment of

senile plaques

sensorineural hearing loss

sensory loss, cortical

seroconversion

serologic testing

serologic testing of cerebrospinal fluid

short stature

sleep apnea, obstructive

sleep pathology and physiology

slow virus infection of CNS

slurred speech

snout reflex

sodium channel dysfunction

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 16

spinocerebellar ataxia type 7

splenium of corpus callosum

spongy degeneration of brain

stem cell transplantation

steroid

steroid therapy, CNS treatment and complications with

stiff man syndrome

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

stuporous

stuttering

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

suck, poor

suicide

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, neurologic complications with

temporal lobe, lesion, bilateral

teratoma, ovarian

term infant

thalamus, lesion of

thalamus, lesion of-bilateral

toxins, nervous system

transplacental virus infections

treatment of neurologic disorder

tremor

tremor, intention

tremor, postural

triangle of Guillain and Mollaret

trinucleotide repeats

ultrasonography

unconsciousness

unconsciousness, episodic

unconsciousness, transient

Unverricht-Lundborg disease

visual acuity, decreased

visual impairment

visual loss

visuospatial disturbance

vitreous opacities

vocalizations

walking, difficulty with

whole genome sequencing

wide based gait

Wolfram syndrome

writing

Showing articles 950 to 1000 of 1474 << Previous Next >>

Clinicopath Conf
Cerebral Amyloid Angiopathy, Case 27-1991, NEJM 325:42-54991., , 1991

Microangiopathy of the Brain, Retina, and Ear:Improvement without Immunosuppressive Therapy
Stroke 22:933-937, Gordon,D.L.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Presynaptic Parkinsonism in Olivopontocerebellar Atrophy:Clinical, pathological, and Neurochemical Evidence
Ann Neurol 30:425-428, Pascual,J.,et al, 1991

Infarction in the Anterior Rostral Cerebellum (the Territory of the Lateral Branch of the Superior Cerebellar Artery)
Neurol 41:253-258, Amarenco,P.,et al, 1991

Central Nervous System Involvement in Von Hippel-Lindau Disease
Neurol 41:41-46, Filling-Katz,M.R.,et al, 1991

Lateral Medullary Infarction:Prognosis in an Unselected Series
Neurol 41:244-248, Norrving,B.&Cronqvist,S., 1991

Myoclonus in Adult Huntington's Disease
Ann Neurol 29:213-215, Vogel,C.M.,et al, 1991

Multistate Outbreak of Poisonings Associated with Illicit Use of Gamma Hydroxy Butyrate
JAMA 265:447-448, , 1991

Hashimoto's Encephalopathy:A Steroid-Responsive Disorder Associated with High Anti-Thyroid Antibody Titers-Report of 5 Cases
Neurol 41:228-233, Shaw,P.J.,et al, 1991

Localization of Idiopathic Generalized Epilepsy on Chromosome 6p in Families of Juvenile Myoclonic epilepsy patients
Neurol 41:1651-1655, Durner,M.,et al, 1991

Truncal Asterixis Associated with Ceftazidine, A Third-Generation Cephalosporin
Neurol 41:2008, Hillsley,R.E.&Massey,E.W., 1991

Clinicopath Conf
Case 50-1991, Renal Cell Carcinoma & Inflammatory Polyneuropathy (? paraneoplastic) , NEJM 325:1723-, 735, 199, 1991

Does Ageing Aggravate Parkinsonisn Disability?
JNNP 54:780-782, Blin,J.,et al, 1991

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Reversal of a Neurologic Paraneoplastic Syndrome with Octreotide (Sandostatin) in a Pt with Glucagonoma
Am J Med 91:434-436, Holmes,A.,et al, 1991

Acute Cerebellar Ataxia in a Child with Transient Pontine Lesions Demonstrated by MRI
Neuropediatrics 22:225-227, Groen,R.J.M.,et al, 1991

Cumulative Risks of Developing Extrapyramidal Signs, Psychosis, or Myoclonus in the Course of Alzheimer's Disease
Arch Neurol 48:1141-1143, Chen,J.,et al, 1991

Idiopathic Myelopathies with White Matter Vacuolation in Non-AIDS Patients
Human Pathol 22:816-824, Kamin,S.S.&Petito,C.K., 1991

Creutzfeldt-Jakob Disease and Other Transmissible Spongiform Encephalopathies
Ed, F. O. Bastian, Mosby Year Book, St. Louis 9:153, Maertens,P.&Quindlen,E.A., 1991

Neurological Sequelae of Cerebral Malaria in Children
Lancet 336:1039-1043, Brewster,D.R.,et al, 1990

Coincidence of Myoclonus and Multiple Sclerosis:Dramatic Response to Clonazepam
Neurol 40:1633-1634, Smith,C.R.&Scheinberg,L., 1990

Cerebral Glucose Hypermetabolism in Friedreich's Ataxia Detected with Positron Emission Tomography
Ann Neurol 28:750-757, Gilman,S.,et al, 1990

Sensory Ataxic Hemiparesis in Thalamic Hemorrhage
Stroke 21:1749-1753, Dobato,J.L.,et al, 1990

Capsular Hypesthetic Ataxic Hemiparesis
Stroke 21:24-33, Helgason,C.M.&Wilbur,A.C., 1990

Relative Increase of T Cells Expressing Gamma/Delta Rather than Alpha/Beta Receptor in Ataxia-Telangietasia
NEJM 322:73-76, 1241990., Carbonari,M.,et al, 1990

Epileptic Seizures and Syndromes
Lancet 336:161-163, Gram,L., 1990

Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy
Ann Neurol 27:103-106, Goutieres,F.,et al, 1990

Olivopontocerebellar Atrophy:MR Diagnosis and Relationahip to Multisystem Atrophy
Radiology 174:693-696, Savoiardo,M.,et al, 1990

Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
JNNP 53:297-305, Klockgether,T.,et al, 1990

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

Neuropsychological Changes in Olivopontocerebellar Atrophy
Arch Neurol 47:997-1001, Berent,S.,et al, 1990

Cortical-Basal Ganglionic Degeneration
Neurol 40:1203-1212, Riley,D.E.,et al, 1990

Geriatrics:Gait Disorders in the Elderly
NEJM 322:1441-1446, Sudarsky,L., 1990

'Rubral'Gait Ataxia
Neurol 40:1004-1005, Felice,K.J.,et al, 1990

Acceleration-Induced Loss of Consciousness, A Review of 500 Episodes
Arch Neurol 47:764-776, Whinnery,J.E.&Whinnery,A.M., 1990

Migraine Assoc with Focal Cerebral Edema, CSF Pleocytosis, & Prog Cerebellar Ataxia:MRI Documentation
Neurol 40:1284-1287, Goldstein,J.M.,et al, 1990

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 1990

Miller Fisher Syndrome Associated with Q Fever
JNNP 53:615-616, Diaz Ortuno,A.,et al, 1990

Neurological Deterioration in Young Adults with Phenylketonuria
Lancet 336:602-605, Thompson,A.J.,et al, 1990

Acute Triphenyltin Intoxication:A Case Report
JNNP 53:356-357, Wu,RM.,et al, 1990

Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
Ann Neurol 27:448-449, Katafuchi,Y.,et al, 1990

A Quantitative Evaluation of Pontine Volume by Computed Tomography in Patients with Cerebral Degeneration
Neurol 40:1241-1245, Chida,K.,et al, 1990

Antemortem Diagnosis of Diffuse Lewy Body Disease
Neurol 40:1523-1528, Crystal,H.A.,et al, 1990

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

Chronic Acetazolamide Monotherapy in the Treatment of Juvenile Myoclonic Epilepsy
Neurol 40:1677-1681, Resor,S.R.&Resor,L.D., 1990

Myoclonic Status Epilepticus:A Clinical and Electroencephalographic Study
Neurol 40:1199-1202, Jumao-as,A.&Brenner,R.P., 1990

Movement Disorders in Alcoholism:A Review
Neurol 40:741-746, Neiman,J.,et al, 1990

Ataxic Sensory Neuropathy and Dorsal Root Ganglionitis Associated with Sjogren's Syndrome
Ann Neurol 27:304-315, Griffin,J.W.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Showing articles 950 to 1000 of 1474 << Previous Next >>