Neudle.com: startle epilepsy

Differential
(Click to cross reference)

abdominal distention

abdominal x-ray

acquired immunodeficiency syndrome

Addison's disease

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

algorithm

alien hand syndrome

alkylating agents

altered states of consciousness

alternating hemiplegia

alternating rapid movement

aluminum

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

amenorrhea

ammonia

AMPA receptor antibodies

amyloid angiopathy, cerebral

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiokeratoma

anorexia

anterior horn cell disease

anti IgLON5

anti Ri antibody

antibiotics

antibiotics, neurologic complications with

antibodies to measles

anticonvulsants

anticonvulsants, discontinuation in seizure-free epileptics

anticonvulsants, effectiveness

anticonvulsants, untoward effects of

antioxidant

antiphospholipid antibodies

antithyroid antibodies

apraxia of eye movements

aqueduct of Sylvius, stenosis

ataxia, truncal, associated with ocular oscillations

ataxic gait

atypical

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

autonomic nervous system

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavior, combative

behavioral disorder

behavioral disorder, acute

bone marrow transplantation

bone pain

boomerang sign

Borrelia miyamotoi infection

bradykinesia

brain atrophy

brain biopsy

brain biopsy, false negative

brain scan

brainstem, atrophy

brainstem, dysfunction

burning feet, differential diagnosis of

busulfan

cachexia

CAG repeats

calcification, intracranial

calcium antagonist

calcium antagonist, side effects of

carbidopa

carcinoma

carcinoma of bladder

carcinoma of pancreas

cardiac arrest

cardiac arrest and resuscitation

CAT scan, false negative

cataracts

catatonia

caudate nucleus, atrophy

ceftazidime

celiac disease, adult

central nervous system, infection of

central pontine myelinolysis

cephaloridine

cephalosporins

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar plaques, amyloid

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, young adult

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

choreoathetosis, paroxysmal

chorioretinitis

chromosomal abnormality

chromosome 12

chromosome 2

chromosome 21

chronic progressive external ophthalmoplegia

cigarette smoking

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

clomipramine

clonazepam

clonus

cobalamin C deficiency

collapsin response mediator protein 5 IgG

corpus callosum, lesion of

cortical blindness

cortical-basal ganglionic degeneration

cranial neuropathy

C-reactive protein, elevated

Creutzfeldt-Jakob disease, genetic

cytomegalic inclusion disease

cytomegalovirus infection

deep gray nuclei

degenerative diseases of CNS

dementia, differential diagnosis of

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, transmissible

dementia, treatment of

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

dilantin

diplopia

disorientation

downward deviation of eyes

downward gaze, paralysis of

DPPX

DPPX, antibodies

DPPX, antibodies, encephalitis

Dravet syndrome

drooling

dropped head syndrome

drowsiness

drug induced neurologic disorders

drug interactions

drug overdose

dysarthria

dysequilibrium syndrome

dyskinesia

dyskinesia, buccal lingual facial

dyssynergia cerebellaris myoclonica

dystonia

dystonia, face

dystonia, focal

dystonia, treatment of

echolalia

eclampsia

eclampsia, postpartum

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electroencephalogram, pediatric patients

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

electroencephalogram, video monitoring with

electromyogram

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, etiology

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, unknown etiology

encephalitis, viral

encephalomyelitis

encephalomyelitis, autoimmune

encephalopathy

encephalopathy, anoxic

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, post anoxic

encephalopathy, progressive

encephalopathy, septic

enteritis

enterovirus

enterovirus infection of CNS

enzyme, defect

ependymal

epidemiology of neurology

epilepsia partialis continua

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

episodic unconsciousness

extralimbic encephalitis

extrapyramidal

eye movement, disorders of

eye movement, painful

eye, pain in

facial appearance, abnormal

facial movement disorder

facial weakness

faciobrachial dystonic seizure

fine motor function, impaired

fingerprint bodies

Fisher C.M.

floaters

frontal lobe, pathologic signs of

fucosidosis

fundus, abnormality of

fungal infection, CNS

gadolinium

gait disorder

gamma amino butyric acid receptor antibody

gamma hydroxybutyric acid

gangliosidosis GM2

gastrointestinal disease, neurologic complications

Gaucher's disease

Gaucher's disease, adult onset

gaze palsy

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

genetic neurologic disorders

globus pallidus, lesion of

glutamic acid decarboxylase, antibody

glycine receptor antibodies

glycoprotein

gout

granular osmiphilic material

Hallervorden Spatz disease

hallucination

hallucination, olfactory

hallucination, visual

headache, sudden onset of

hemianopia, homonymous

hemiballismus

hemimyoclonic jerks

hemiparesis

hemiparesis, transient

hemiplegia

hemolytic-uremic syndrome

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes simplex encephalitis

human immunodeficiency virus type 1

Huntington's chorea

Huntington's disease, children

hydrocephalus

hydrocephalus, normal pressure

hydroxyindole acetic acid 5(5HIAA)

hydroxytryptophan L-5(L-5 HTP)

hyperactivity

hyperammonemic encephalopathy

hyperpigmentation of skin

hyperreflexia

hypersomnia

hypertension

hypertensive encephalopathy

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

hypoxic encephalopathy

iatrogenic neurologic disorders

immune reconstitution inflammatory syndrome

inappropriate behavior

inattention

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incontinence, fecal

incontinentia pigmenti

incoordination

infection

infection, recurrent

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deterioration

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial pressure, increased

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jewish

juvenile myoclonus epilepsy

Kearns-Sayre syndrome

Korsakoff's psychosis

Krabbe's disease

kuru plaques

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

L-dopa, drug interactions with and side effects of

Leber's hereditary optic neuropathy

Leigh's disease

lenticular nucleus, lesion of, bilateral

lethargy

leucine rich glioma inactivated 1 antibodies

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

levitation

Lewy body disease, diffuse

life expectancy

limbic encephalitis

linear lesion

lipid storage disorder of CNS

lithium

liver biopsy

liver disease

liver function enzymes

lymphadenopathy

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lysosomal storage disease

macrocephaly

malabsorption

malabsorption syndrome

malaise

malformation, CNS, congenital

malignancy screen

meconium staining

mediastinum, lymph-node biopsy

mediastinum, mass of

medulla oblongata, lesion of

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningismus

meningitis

meningitis, aseptic

meningitis, CSF cell count-normal

meningitis, fungal

meningitis, neutrophilic

meningitis, syphilitic

meningitis, TB

meningitis, treatment of

meningoencephalitis

mental retardation

mental status, abnormal

methylmalonic acidemia

metronidazole

microangiopathic hemolytic anemia

microangiopathy, brain

mitochondrial disease

mitochondrial encephalomyopathy

monoclonal antibodies

motor neuron disease, misdiagnosis

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, paroxysmal

movement disorder, treatment of

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, FLAIR

MRI, hypointense signal foci on

MRI, linear enhancement

MRI, negative

MRI, nodular enhancement

MRI, pelvis

MRI, ring sign

MRI, spinal cord

MRI, sulcal hyperintensity

MRI, susceptibility weighted

MRS

multinucleated giant cell

muscle weakness, proximal

mutism

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelination of nervous system

myelitis

myelitis, longitudinal

myelitis, transverse

myelitis, transverse, recurrent

myoclonus, differential diagnosis of

myoclonus, epilepsy

myoclonus, face

myoclonus, post anoxic

myoclonus, segmental

myoclonus, sleep

myoclonus, stimulus sensitive

myoglobinuria

myopathy

myopathy, mitochondrial

neonatal abstinence syndrome

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve conduction studies

neuraminidase deficiency

neurexin-3 alpha antibodies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroendocrinology

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, multifocal

neurologic examination

neurologic signs

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

ocular motility, disorders of

oculocephalic reflex

oculomasticatory myorhythmia

opsoclonus-myoclonus syndrome

optic atrophy

optic chiasm, enlarged

optic nerve

optic nerve, enlarged

optic nerve, lesion of

optic neuropathy

organ transplantation

ornithine transcarbamylase deficiency

paraneoplastic brainstem encephalitis

paranoia

paraparesis

paraparesis, familial spastic

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal kinesigenic dyskinesia

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

pediatric neurology

penicillin

pericarditis

persistent vegetative state

personality change

phonophobia

pigmentary retinopathy

pituitary stalk

pituitary stalk, lesion of

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pleurisy

pneumoencephalogram(PEG)

pneumonia

polymerase chain reaction

polyneuropathy

polyneuropathy, uremic

pontocerebellar atrophy

post transplant lymphoproliferative disease

posterior leukoencephalopathy syndrome

postpartum

potassium channel antibodies

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prion disease

prognosis

progressive encephalomyelitis with rigidity syndrome

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

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, dilated, bilateral

pupil, dilated, episodic

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

rabies, nervous system involvement with

ragged-red fibers

Ramsay Hunt syndrome

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

recurrent

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal failure

renal transplantation

respiratory depression

respiratory failure

restless leg syndrome

reticulum cell sarcoma

reversible neurologic disorder

scoliosis, neurologic association with

screening

sea-blue histiocytes

sedimentation rate, elevated

seizure, classification of

seizure, diagnosis of

seizure, drug resistance

seizure, drug-induced

seizure, EEG normal during

seizure, EEG pattern in

seizure, noise induced

seizure, paradoxical

seizure, photosensitive

seizure, precipitating factors

seizure, prognosis in adults

seizure, stimulus sensitive

seizure, teenager

seizure, tonic-clonic

seizure, treatment of

seizure, withdrawal

selective serotonin reuptake inhibitors

sensorineural hearing loss

sensory loss

sensory loss, cortical

septicemia

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

skin, lesions in neurologic disorders

sleep pathology and physiology

slow virus infection of CNS

slurred speech

snout reflex

sodium channel dysfunction

speech disorder, childhood

speech, loss of

sphingolipodoses

spinal cord

spinal cord, lesion of

spinal cord, pathologic exam of

spinocerebellar ataxia

spirochete infection

splenium of corpus callosum

splenomegaly

spongy degeneration of brain

staphylococcal protein A column therapy

status epilepticus, intractable

status epilepticus, nonconvulsive

steatorrhea

stem cell transplantation

stereotypy

steroid

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulant drugs

storage disease of CNS

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

stuporous

stuttering

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

subacute sclerosing panencephalitis, adult onset

subarachnoid hemorrhage

symmetric brain lesions

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

thalamus, lesion of-bilateral

thrombocytopenia

thrombophlebitis

thrombotic microangiopathy

thymoma

thyroid stimulating immunoglobulins

tone, muscle, increased

tongue, biting

tonic cerebellar fits

topiramate

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

transient neurologic deficit

treatment of neurologic disorder

tricyclic antidepressant

trigeminal neuralgia

trinucleotide repeats

unconsciousness, episodic

unconsciousness, transient

Unverricht-Lundborg disease

upgaze

upgaze, paralysis of

urea-cycle enzymopathies

uremia

uremic encephalopathy

venous thrombosis, non-cerebral

vision, blurred, monocular

visual acuity, decreased

visual evoked response

visual field defect

visual impairment

visual loss

visuospatial disturbance

vitreous opacities

vocalizations

walking, difficulty with

weakness

weakness, acute

weakness, focal

weakness, generalized

weight loss

Wernicke's encephalopathy

wheelchair

Whipple's disease

white matter disease

white matter disease, periventricular

white matter disease, subcortical

wide based gait

word-finding difficulty

wrist drop

Showing articles 100 to 150 of 3618 << Previous Next >>

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

Busulphan and Phenytoin
Ann Int Med 111:1049-1050, Grigg,A.P.,et al, 1989

Neonatal Seizures:Current Concepts and Revised Classification
Pediatrics 84:422-428, Volpe,J.J., 1989

Nifedipine and Myoclonic Disorders
Nephron 51:281, Pedro-Botet,M.L.,et al, 1989

Rapidly Progressive Dementia Caused by Spongiform Encephalopathy
West J Med 148:313-319, Enos,B.E.&Vinters,H.V., 1988

Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988

A Creutzfeldt-Jakob Like Syndrome Due to Lithium Toxicity
JNNP 51:120-123, Smith,S.J.M.&Kocen,R.S., 1988

Myoclonus During Combined Tricyclic Antidepressant and Lithium Treatment
J Clin Psychopharmacol 8:446-447, Devanand,D.P.,et al, 1988

Outcome from Coma After Cardiopulmonary Resuscitation:Relation to Seizures & Myoclonus
Neurol 38:401-405, Krumholz,A.,et al, 1988

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Seizures & Myoclonus in Patients with Alzheimer's Disease
Neurol 36:1226-1230, Hauser,W.A.,et al, 1986

Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986

Creutzfeldt-Jakob Disease of Long Duration:Clinicopathological Characteristics
Ann Neurol 16:295-304, Brown,P.,et al, 1984

Startle Epilepsy:A Clinical Study
Ann Neurol 16:78-81, Saenz-Lope,E.,et al, 1984

Meperidine-Associated Myoclonus & Seizures in Long-Term Hemodialysis Patients
Ann Neurol 14:593, Hochman,M.S., 1983

Clinicopathological Conference
Case 49-1983, Creutzfeldt-Jakob, NEJM 309:1440-1449983., , 1983

Dialysis Encephalopathy, Clinical, Electroencephalographic & Interventional Aspects
Medicine 62:129-141, O'Hare,J.A., 1983

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

Cephaloridine Encephalopathy
BMJ 283:409-410, Taylor,R.,et al, 1981

Startle Epilepsy Complicating Down Syndrome During Adulthood
Ann Neurol 7:78-80, Gimenez-Roldan,S.,et al, 1980

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

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

The Late Postpatrum Eclampsia Controversy
Obstet Gynecol 55:74-78, Sibai,B.M.,et al, 1980

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

Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease)
Brain 101:333-344, Masters,C.L.,et al, 1978

Familial Chorea & Myoclonus Epilepsy
Neurol 28:913-919, Takahata,N.,et al, 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

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

Familial Paroxysmal Dystonic Choreoathetosis & its Differentiation From Related Syndromes
Ann Neurol 2:285, Lance,J.W., 1977

Clonazepam & Branchial Myoclonus
Ann Neurol 1:306, Gledhill,R.F., 1977

Serotonin & Myoclonic Seizures
NEJM 296:101, Munsat,T.L., 1977

Long-term Therapy of Myoclonus & Other Neurologic Disorders with L-5-Hydroxytryptophan & Carbidopa
NEJM 296:70, VanWoert,M.H.,et al, 1977

Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients
Medicine 55:467, Knox,D.L.,et al, 1976

Neurologic Disorders in Renal Failure (1st of Two Parts)
NEJM 294:143, Raskin,N.H.,et al, 1976

Levodopa-Induced Myoclonus
Arch Neurol 32:331-334, Klawans,H.L., 1975

Case Records of MGH
NEJM 29l:l4l, 1974; 29l:263, 1974 Subscute Sclerosing Panencephalitis., , 1974

Case Records of MGH-NEJM 285:621
1971., , 1971

Studies in Myoclonus Epilepsy (Lafora Body Form)
Neurol 20:160, Sakai,M.,et al, 1970

Neurologic Disorders Seen In the Uremic Patient
Arch Int Med 126:781, Tyler,H.R., 1970

Encephalitis with Myoclonus in Whipple's Disease
JNNP 32:338, Stoupel,N.,et al, 1969

Whipple's Disease & Papilledema
Arch Int Med 123:74, Switz,D.M.,et al, 1969

Neurological Examination of the Comatose Patient
Acta Neurol Scan Suppl. 38, Vol45969., Fisher,C.M., 1969

Studies in Myoclonus Epilepsy (Lafora Body Form)
Arch Neurol 19:15, Yokoi,S.,et al, 1968

Neurologic Disorders in Renal Failure
Am J Med 44:734, Tyler,H.R., 1968

Myoclonic Jerks & Falls:Aetiology, Classification & Treatment
Med Journ of Aust 1:114, Lance,J., 1968

Sensory Precipitated Seizures:A Review
J Nerv Ment Dis 141:524-539, Daube,J.R., 1966

Clinical Picture in Creutzfeldt-Jakob Disease
Trans of Amer Neuro Assn 5:l47, Fisher,C.M., 1960

Spectrum of Intracranial Hemorrhages in Cerebral Venous Thrombosis, A Pictorial Case Series and Review of Pathophysiology and Management
Neurologist 30:45-51, Jha,S.,et al, 2025

Showing articles 100 to 150 of 3618 << Previous Next >>