Neudle.com: myoclonus focal

Differential
(Click to cross reference)

abdominal contractions

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome-related complex

acute disseminated encephalomyelitis

Addison's disease

advances in neurology

adverse drug reaction

altered states of consciousness

alternating hemiplegia

alternating rapid movement

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

ammonia

AMPA receptor antibodies

amphiphysin antibodies

amyloid angiopathy, cerebral

angiitis, granulomatous of CNS

angiitis, isolated of CNS

antibiotics, neurologic complications with

antibodies to measles

anticholinergic drugs

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, cognitive function with

anticonvulsants, effectiveness

anticonvulsants, mechanism of action of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

apraxia of eye movements

apraxia, constructional

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder, acute

brain biopsy, false negative

brainstem, infarction of

brainstem, lesion of

Brueghel's syndrome

burning feet

burning feet, differential diagnosis of

calcification, intracranial

CAR syndrome

carbon monoxide poisoning

cardiac arrest and resuscitation

CAT scan, complication with

CAT scan, contrast enhanced

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, pelvis

catatonia

ceftazidime

central nervous system, infection of

central pontine myelinolysis

cephalosporins

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar plaques, amyloid

cerebellitis

cerebellum

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral venous thrombosis

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

cervical spondylosis

chemotherapy, CNS treatment and complications with

children

chorea

choreoathetosis

chromosomal abnormality

chromosome 2

chronic progressive external ophthalmoplegia

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

contactin associated protein like 2 antibodies

cortical blindness

cortical ribbon sign

cortical-basal ganglionic degeneration

Creutzfeldt-Jakob disease, genetic

crying, pathologic

cytomegalic inclusion disease

cytomegalovirus infection

deep gray nuclei

degenerative diseases of CNS

dementia, rapidly progressive

demyelinating disease

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

diplopia

disorientation

distal muscle atrophy

distal muscle weakness

DPPX, antibodies, encephalitis

dysequilibrium syndrome

dyskinesia

dyskinesia, buccal lingual facial

dystonia, delayed onset

dystonia, focal

dystonic reaction, acute

echolalia

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electromyogram

emergencies, neurologic

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, etiology

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalitis, unknown etiology

encephalitis, viral

encephalomyelitis

encephalopathy

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, post anoxic

encephalopathy, progressive

enteritis

epidemiology of neurology

epilepsia partialis continua

escherichia coli

extralimbic encephalitis

eye movement, disorders of

faciobrachial dystonic seizure

frontal lobe, pathologic signs of

fungal infection, CNS

gait disorder

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

gliomatosis cerebri

glutamic acid decarboxylase, antibody

glycine

granular osmiphilic material

hallucination, visual

handedness

head injury

headache

headache, sudden onset of

hemiparesis, transient

hemolytic-uremic syndrome

hepatitis

hepatomegaly

herpes simplex encephalitis

herpes virus

herpes zoster

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

human immunodeficiency virus type 1

hydrocephalus

hydrocephalus, normal pressure

hyperammonemic encephalopathy

hypertensive encephalopathy

hypoglycorrhachia

hyponatremia

hypoxia, newborn

hypoxic encephalopathy

immunology and the nervous system

immunosuppression

immunotherapy

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

infantile spasm

insomnia

intellectual deficit

intellectual deterioration

intracranial pressure, increased

intrinsic hand muscles, wasting of

irritability

Jakob-Creutzfeldt disease

juvenile distal and segmental muscular atrophy

juvenile myoclonus epilepsy

lactic acidemia

laminectomy, cervical

language disorder in adults

leucine rich glioma inactivated 1 antibodies

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

levitation

life support, withdrawal of

lymphoma involving CNS

lymphoma, primary of CNS

memory, defect of recent

memory, impairment of

meningismus

meningitis

meningitis, fungal

meningitis, syphilitic

meningitis, TB

mental retardation

mesial temporal lobe

microangiopathic hemolytic anemia

microinfarcts

migraine

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoclonal antibodies

movement disorder, delayed onset

movement disorder, extrapyramidal

movement disorder, treatment of

MRI

MRI, abnormal

MRI, diffusion weighted

MRI, FLAIR

MRI, negative

MRI, pelvis

MRI, susceptibility weighted

multinucleated giant cell

multiple sclerosis

multiple system atrophy

muscle biopsy

muscle cramp

muscle weakness

muscle weakness, proximal

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myasthenia gravis, paraneoplastic

myasthenic syndrome

myelitis

myelitis, transverse, recurrent

myoclonus, post anoxic

myoclonus, segmental

myoclonus, stimulus sensitive

myoclonus, treatment of

neoplasm, primary of CNS

nerve conduction studies

neurexin-3 alpha antibodies

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, multifocal

neurologic signs

neurologic symptoms

neuromuscular junction

neuromuscular junction, abnormality of

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, paraneoplastic

occupational neurologic disorders

olivary degeneration, hypertrophic

onconeural antibodies

ophthalmoplegia

opsoclonus

opsoclonus-myoclonus syndrome

optic atrophy

ornithine transcarbamylase deficiency

paraneoplastic cerebellar degeneration

paratonia

Parkinson disease

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

penicillin

peripheral nerve, lesion of

persistent vegetative state

personality change

phenylketonuria

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pneumoencephalogram(PEG)

POEMS syndrome

polymerase chain reaction

polyneuropathy

polyneuropathy, uremic

posterior inferior cerebellar artery syndrome

posterior leukoencephalopathy syndrome

potassium channel antibodies

precipitating factors

prion disease

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

recurrent

Red flags

remote effect of cancer on the nervous system

renal failure

renal transplantation

respiratory failure

restless leg syndrome

reticulum cell sarcoma

salivation, excessive

seizure, clicking sound with

seizure, drug resistance

seizure, drug-induced

seizure, precipitating factors

seizure, spinal

seizure, stimulus sensitive

seizure, tonic-clonic

seizure, treatment of

sensory loss

sensory loss, cortical

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

Shiga toxin

short stature

sleep apnea, obstructive

sleep pathology and physiology

slow virus infection of CNS

slurred speech

snout reflex

sodium channel dysfunction

sodium valproate

sodium valproate, intravenous

sodium valproate, toxicity

spinal cord, injury of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, vascular malformation of

staphylococcal protein A column therapy

status epilepticus, intractable

status epilepticus, myoclonic

status epilepticus, nonconvulsive

steroid therapy, CNS treatment and complications with

stiff man syndrome

storage disease of CNS

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

stuttering

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

subacute sclerosing panencephalitis, adult onset

subdural hematoma

symmetric brain lesions

tandem gait, ataxic

tauopathy

temporal lobe, lesion

temporal lobe, lesion, bilateral

thrombotic microangiopathy

toxoplasmosis, acquired

toxoplasmosis, CNS

treatment of neurologic disorder

triangle of Guillain and Mollaret

Trousseau's sign

upgaze, paralysis of

urea-cycle enzymopathies

uremia

uremic encephalopathy

visuospatial disturbance

walking, difficulty with

Wernicke's encephalopathy

wheelchair

Whipple's disease

white matter disease

white matter disease, periventricular

white matter disease, subcortical

Showing articles 900 to 950 of 2208 << Previous Next >>

Pseudoulnar Palsy From a Small Infarct of the Precentral Knob
Neurol 54:2185, Phan,T.G.,et al, 2000

Status Epilepticus Associated with Cefepime
Neurol 54:2153-2155, Dixit,S.,et al, 2000

Status Epilepticus In Stroke, Report on a Hospital-Based Stroke Cohort
Neurol 54:350-354, Rumbach,L.,et al, 2000

Prevalence of Nonconvulsive Status Epilepticus in Comatose Patients
Neurol 54:340-345, Towne,A.R.,et al, 2000

The Value of Pelvic Thrusting in the Diagnosis of Seizures and Pseudoseizures
Neurol 54:227-229, Geyer,J.D.,et al, 2000

Glatiramer Acetate (Copaxone) Treatment in Relapsing-Remitting MS
Neurol 54:813-817, Ge,Y.,et al, 2000

Uses of Botulinum Toxin Injection in Medicine Today
BMJ 320:161-165, Munchau,A. & Bhatia,K.P., 2000

Language Disturbances in Corticobasal Degeneration
Neurol 54:990-992, Frattali,C.M.,et al, 2000

Using Serial Registered Brain Magnetic Resonance Imaging to Measure Disease Progression in Alzheimer Disease
ArchNeurol 57:339-344, Fox,N.C.,et al, 2000

Progressive Cerebral Atrophy in MS
Neurol 54:807-812,782, Fox,N.C.,et al, 2000

Psychogenic Status Epilepticus in Children: Psychiatric and Other Risk Factors
Neurol 54:969-970, Pakalnis,A.,et al, 2000

Myoclonus Secondary to Albuterol (Salbutamol) instillation
Neurol 54:2022-2023, Micheli,F.,et al, 2000

Clinicopath Conf., Pick's Disease, Case 11-2000
NEJM 342:1110-1117, , 2000

Early Diffusion-Weighted MR Imaging Abnormalities in Sustained Seizure Activity
AJR 174:1304-1306, Kassem-Moussa,H.K.,et al, 2000

Motor Strokes Sparing the Leg
Arch Neurol 57:513-518, de Freitas,G.R.,et al, 2000

Managing Status Epilepticus
BMJ 320:953-954, Heafield,M.T.E., 2000

Clinicopath Conf, Neurocysticercosis, Left Temporal Lobe, End-Stage with Calicification, Epilepsy
NEJM 343:420-427, Case 24-2000, 2000

Life-Threatening Tinnitus
Lancet 356:308, Javaheri,S. et al, 2000

Levetiracetam for Partial Seizures: Results of A Double-Blind, Randomized Clinical Trial
Neurol 55:236-242, Cereghino,J.J. et al, 2000

C1/C2 Rotary Subluxation Due to Spasmodic Torticollis
JNNP 69:135-136, Dalvie,S. et al, 2000

Serotonin Sydrome
Medicine 79:201-209, Mason,P.J. et al, 2000

Intrathecal Baclofen for the Treatment of Dystonia in Patients with Reflex Sympathetic Dystrophy
NEJM 343:625-630,654, van Hilten,B.J. et al, 2000

Intravenous Valproate is Well Tolerated in Unstable Patients with Status Epilepticus
Neurol 55:722-724, Sinha,S. & Naritoku,D.K., 2000

The Split Hand in ALS has a Cortical Basis
J Neurol Sci 180:66-70, Weber,M.,et al, 2000

Alien Hand Sign in Creutzfeldt-Jakob Disease
JNNP 68:103-104, Inzelberg,R.,et al, 2000

Hypertrophic Olivary Degeneration: Metaanalysis of the Temporal Evolution of MR Findings
AJNR 21:1073-1077, Goyal, M.,et al, 2000

Delayed Movement Disorders After Carbon Monoxide Poisoning
Eur Neurol 42:141-144, Choi,I.S. &Cheon,H.Y., 1999

Suprascapular Neuropathy
J Am Acad Orthop Surg 7:358-367, Romeo, A.A.,et al, 1999

Oxcarbazepine: Double-blind, Randomized, Placebo-control, Monotherapy Trial for Partial Seizures
Neurol 52:732-737, Schachter,S.C. et al, 1999

Creutzfeldt-Jakob Disease Presenting as Complex Partial Status Epilepticus: A Report of Two Cases
JNNP 66:406-407, Rees,J.H.,et al, 1999

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

Treatment of Absence Status with Intravenous Valproate
Neurol 52:889-890, Alehan,F.K.,et al, 1999

Medical Management of Epilepsy in Adults
Neurol 51:S15-S20, Mattson,R.H., 1999

MRI Abnormalities Associated with Partial Status Epilepticus
Neurol 52:1021-1027, Lansberg,M.G.,et al, 1999

Cardiac Asystole and Bradycardia as a Manifestation of Left Temporal Lobe Complex Partial Seizure
Ann Int Med 130:581-583, Locatelli,E.R.,et al, 1999

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

MRI Abnormalities Associated with Partial Status Epilepticus
Neurol 52:1021-1027, Lansberg, M.G.,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

Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
JNNP 66:172-176, Seipelt,M.,et al, 1999

Diagnosis of Viral Infections of the Central Nervous System
NEJM 340:483-484, Huang,C.,et al, 1999

Improvement in Adult-Onset Rasmussen's Encephalitis with Long-Term Immunomodulatory Therapy
Neurol 52:738-742, Leach,J.P.,et al, 1999

Adult-Onset MELAS Presenting as Herpes Encephalitis
Arch Neurol 56:241-243, Sharfstein,S.R.,et al, 1999

Distal Myasthenic Gravis
Neurol 52:632-634, Nations,S.P.,et al, 1999

Neuro-Ophthalmologic Manifestations of a paraneoplastic Syndrome and Testicular Carcinoma
Neurol 52:864-867, Bennett,J.L.,et al, 1999

Epilepsia Partialis Continua:A New Manifestation of Anti-Hu-Associated Paraneoplastic Encephalomyelitis
Ann Neurol 45:255-258, Shavit,Y.B.,et al, 1999

"Toilet Seat" Sciatic Neuropathy
Arch Neurol 56:116, Holland,N.R.,et al, 1999

Primary and Transitional Progressive MS,A Clinical and MRI Cross-Sectional Study
Neurol 52:839-845, Stevenson,V.L.,et al, 1999

Postictal Nose-Rubbing in the Diagnosis,Lateralization,and Localization of Seizures
Neurol 52:743-745, Geyer,J.D.,et al, 1999

Serial Magnetic Resonance Imaging of Cerebral Atrophy in Preclinical Alzheimer's Disease
Lancet 353:2125, Fox,N.C.,et al, 1999

Computed Tomography and Magnetic Resonance Imaging in Mild to Moderate Head Injury:Early and late Imaging Related to Outcome
Ann Neurol 46:70-78, van der Naalt,J.,et al, 1999

Showing articles 900 to 950 of 2208 << Previous Next >>