Neudle.com: progressive myoclonic epilepsy

Differential
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abdominal x-ray

adverse drug reaction

Alzheimer's disease, early onset

Alzheimer's disease, familial

ammonia

amyloid angiopathy, cerebral

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

anorexia

anti IgLON5

antibiotics

antibodies to measles

anticonvulsants

anticonvulsants, selection of

antithyroid antibodies

autonomic dysfunction

Babinski sign

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion, bilateral

behavioral disorder

biologic markers

bismuth

Borrelia miyamotoi infection

bradykinesia

brain atrophy

brain biopsy

brain biopsy, false negative

calcification, intracranial

CAT scan, emission, abnormal

CAT scan, false negative

cataracts

central nervous system, infection of

cerebellar atrophy, primary

cerebellar degeneration

cerebellar plaques, amyloid

cerebral cortex

cerebral cortical atrophy

cerebral glucose metabolism

cerebral vasculature

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

cherry red spot-myoclonus syndrome

chromosomal abnormality

chronic progressive external ophthalmoplegia

cigarette smoking

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

cognition

color vision, impaired

congenital infection, CNS

congenital paresis

cortical blindness

cranial nerve palsies

Creutzfeldt-Jakob disease, genetic

crying, pathologic

deep gray nuclei

degenerative diseases of CNS

dementia, differential diagnosis of

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

dementia, treatment of

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental milestones, loss of

differential diagnosis

diplopia

doll's head maneuver

downward deviation of eyes

dyssynergia cerebellaris myoclonica

dystonia

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

electroencephalogram, video monitoring with

electromyogram

electron microscopy

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, autoimmune

encephalopathy

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, progressive

enterovirus

enterovirus infection of CNS

epidemic

episodic disorders

episodic neurologic deficits

episodic unconsciousness

extralimbic encephalitis

eye movement, disorders of

eye movement, painful

eye, pain in

faciobrachial dystonic seizure

fatal familial insomnia

fatigue

fever

fine motor function, impaired

finger nose finger test

flaccid paralysis

floaters

gait disorder

gamma amino butyric acid receptor antibody

genetic neurologic disorders

genetic testing

globus pallidus, lesion of

glutamic acid decarboxylase, antibody

glycine receptor antibodies

granular osmiphilic material

gray matter

growth retardation

hallucination

hallucination, visual

hand-foot-mouth disease

heralding manifestation

hoarseness

hyperammonemic encephalopathy

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

intellectual deterioration

intestinal pseudoobstruction

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral of CNS

introverted

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

juvenile paresis

Kearns-Sayre syndrome

Leber's hereditary optic neuropathy

Leigh's disease

Leigh's disease, adult variety

lethargy

leucine rich glioma inactivated 1 antibodies

leukocyte enzyme abnormality

memory, defect of recent

memory, impairment of

meningitis

meningitis, aseptic

meningitis, neutrophilic

meningitis, treatment of

meningoencephalitis

mental retardation

mental status, abnormal

MERRF syndrome

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

motor neuron disease, misdiagnosis

movement disorder

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, sulcal hyperintensity

MRI, susceptibility weighted

multinucleated giant cell

muscle biopsy

muscle weakness

muscle weakness, proximal

mutism

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelination of nervous system

myelitis

myelitis, longitudinal

myoclonus, stimulus sensitive

myopathy

myopathy, mitochondrial

neurologic complications

neurologic complications of, systemic cancer

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, ataxia, retinitis pigmentosa

next-generation sequencing

ophthalmoplegia, progressive external

opsoclonus

opsoclonus-myoclonus syndrome

optic atrophy

optic atrophy, hereditary

optic neuropathy

oral ulcerations

ornithine transcarbamylase deficiency

paralysis, acute areflexic

paraparesis, spastic

parasomnia

paratonia

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

persistent vegetative state

personality change

phonophobia

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polyneuropathy

pontocerebellar atrophy

potassium channel antibodies

prion disease

prognosis

progressive encephalomyelitis with rigidity syndrome

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 problems in neurologic disorders

psychomotor retardation

psychosis

psychosis, acute

ptosis

pursuit eye movements, abnormal

pyruvate metabolism, abnormality of

quadriparesis

ragged-red fibers

Ramsay Hunt syndrome

rapidly progressing neurologic illness

real-time quaking-induced conversion

REM sleep behavior disorder

remote effect of cancer on the nervous system

reversible neurologic disorder

rubella encephalitis, progressive

rubella syndrome

rubella virus

rubeola virus

saccadic eye movements, abnormal

seizure

seizure, children

seizure, drug resistance

seizure, treatment of

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

short stature

skin, biopsy

sleep pathology and physiology

slow virus infection of CNS

spinal cord, lesion of

spinocerebellar ataxia

spirochete infection

spongy degeneration of brain

status epilepticus, intractable

steroid

steroid therapy, CNS treatment and complications with

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

sudden death

symmetric brain lesions

systemic illness

tandem gait, ataxic

tau protein

temporal lobe, lesion, bilateral

temporalis muscle wasting

teratoma, ovarian

thalamus, lesion of-bilateral

thymoma

thyroiditis

toxins, nervous system

transient neurologic deficit

transplacental virus infections

treatment of neurologic disorder

unconsciousness, episodic

unconsciousness, transient

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

vision, blurred, monocular

visual loss

visuospatial disturbance

vocalizations

walking, difficulty with

weakness

weakness, acute

weakness, focal

weakness, generalized

weight loss

wheelchair

white matter disease

white matter disease, subcortical

wide based gait

word-finding difficulty

Showing articles 200 to 250 of 5415 << Previous Next >>

Genetic Localization of the Familial Adult Myoclonic Epilepsy (FAME) Gene to Chromosome 8q24
Neurol 53:1180-1183, Plaster,N.M.,et al, 1999

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

N-Acetylcysteine Therapy for Unverricht-Lundborg Disease
Neurol 52:426-427, Selwa,L.M., 1999

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

Topiramate in Clinical Practice:First Year's Postlicensing Experience in a Specialist Epilepsy Clinic
JNNP 66:759-763, Kellett,M.W.,et al, 1999

Seizures and Creutzfeldt-Jakob Disease
NCMJ 60:108-109, Cokgor,I.,et al, 1999

Progressive Aphasia with Rapidly Progressive Dementia in a 49 Year Old Woman
JNNP 66:238-243, Greene,J.D.W.,et al,, 1999

Isolated,Chronic,Epilepsia Partialis Continua in an HIV-Infected Patient
Arch Neurol 56:111-114, Bartolomei,F.,et al, 1999

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

Cefuroxime-Induced Encephalopathy
Neurol 50:1873-1875, Herishanu,Y.O.,et al, 1998

Clinicopath Conf
Dementia with Lewy Bodies, Anaplastic Astrocytoma of Right Insular Region, Case 7-1998, NEJM 338:603, 61098., 1998

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

Acute Leukoencephalopathies:Differential Diagnosis and Investigation
The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998

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

CSF Antigliadin Antibodies and the Ramsay Hunt Syndrome
Neurol 49:1131-1133, Chinnery,P.F.,et al, 1997

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Clinicopath Conf
Progressive Supranuclear Palsy, Case 26, 1997, NEJM 337:549-55697., , 1997

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Bilirubin Metabolism and Kernicterus
Adv Pediatr 44:173-229, Gourley,G.R., 1997

Alzheimer Disease and Nonfluent Progressive Aphasia
Arch Neurol 53:1072-1078, Greene,J.D.W.,et al, 1996

A Woman with a Relapsing Psychosis Who Got Better with Prednisone
Lancet 347:1288, Cohen,L.,et al, 1996

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

Treatment of Advanced Parkinson's Disease by Posterior GPi Pallidotomy:1-Year Results of a Pilot Study
Ann Neurol 40:355-366, 3411996., Baron,M.S.,et al, 1996

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

Progressive Ataxia, Focal Seizures, and Malabsorption Syndrome in a 41 Year Old Woman
JNNP 60:225-230, Mumford,C.J.,et al, 1996

Effect of GPi Pallidotomy on Motor Function in Parkinson's Disease
Lancet 346:1383-1387, Lozano,A.M.,et al, 1995

Systemic Sclerosis Sine Scleroderma:An Unusual Presentation in Scleroderma Renal Crisis
J Rheumatol 22:557-560, Molina,J.F.,et al, 1995

Stereotactic Ventral Pallidotomy for Parkinson's Disease
Neurol 45:753-761, Dogali,M.,et al, 1995

Clinicopath Conf
Arteritis, Unclassified, with Giant-Cell Reaction & Multiple Infarcts of the Brain & Neuropathy, Cas, 5-199532:452-459,1995., 1995

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

AIDS-Associated Progressive Multifocal Leukoencephalopathy Revealed by New-Onset Seizures
Am J Med 99:64-68, Moulignier,A.,et al, 1995

Ceftazidime-Related Nonconvulsive Status Epilepticus
Arch Int Med 154:586-589, Klion,A.D.,et al, 1994

Intravascular Lymphomatosis:A Clinicopathological Study of Three Cases
J Cancer Res Clin Oncol 120:164-168, Liszka,U.,et al, 1994

Chromosome 14-Encoded Alzheimer's Disease:Genetic and Clinicopathological Description
Ann Neurol 36:362-367, Haltia,M.,et al, 1994

Ekbom's Syndrome:Lypomas, Ataxia, and Neuropathy with MERRF
Muscle & Nerve 17:943-945994., Calabresi,P.,et al, 1994

Clinicopath Conf
Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) , with Amyloid (KURU) Plaques, Case 17-1993, N, JM 328:66,1993., 1993

Encephalopathy from Abuse of Bismuth Subsalicylate (Popto-Bismol)
Neurol 43:1265, Jungreis,A.C.&Schaumburg,H.H., 1993

Juvenile Myoclonic Epilepsy
Arch Neurol 50:594-598, Grunewald,R.A.&Panayiotopoulos,C.P., 1993

Ifosfamide-Induced Nonconvulsive Status Epilepticus
Arch Neurol 50:1104-1105, Wengs,W.J.,et al, 1993

The Clinical Spectrum of Cerebral Amyloid Angiopathy:Presentations Without Lobar Hemorrhage
Neurol 43:2073-2079, Greengerg,S.M.,et al, 1993

Progr Myoclonus Epilepsy of Unverricht-Lundborg Type:Clin & Molecular Genetic Study from US 4 Affected Sibs
Neurol 43:2284-2286, Lehesjoki,A.E.,et al, 1993

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Fatal Rabies Associated with Extensive Demyelination
Arch Neurol 50:317-323, Nelson,D.A.&Berry,R.G., 1993

Progressive Multifocal Leucoencephalopathy
Brit J Hosp Med 50:187-192, Sweeney,B.J.,et al, 1993

Drug Induced Creutzfeldt-Jakob Like Syndrome
J Psychiatr Neurosci 17:103-105, Finelli,P.F., 1992

The Role of Hypotension in Septic Encephalopathy Following Surgical Procedures
& Stevens, M. , Arch Neurol 49:653-656., Wijdicks,E.F.M., 1992

Juvenile Myoclonic Epilepsy, Underdiagnosed and Treatment May Have to be Life Long
BMJ 305:4-5, Timmings,P.L.&Richens,A., 1992

Leksell's Posteroventral Pallidotomy in the Treatment of Parkinson's Disease
J Neurosurg 76:53-61, Laitinen,L.V.,et al, 1992

Recurrent Encephalopathy and Seizures in a US Native with HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis
Neurol 42:658-661, Smith,C.R.,et al, 1992

Showing articles 200 to 250 of 5415 << Previous Next >>