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 250 to 300 of 2208 << Previous Next >>

Cerebral Venous Sinus Thrombosis in Homocystinuria: Dietary Intervention in Conjunction with Anticoagulation
Sage Open Med Case Reports 5:1-4, Yap, S.,et al, 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
JAMA Neurol 74:114-118, , 2017

Clinical Decision-Making in Functional and Hyperkinetic Movement Disorders
Neurol 88:118-123,114, van der Salm, S.M.A.,et al, 2017

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 2017

Successful Management of Super-Refractory Status Epilepticus with Thalamic Deep Brain Stimulation
Ann Neurol 81:142-146, Lehtimaki, K.,et al, 2017

A 35-year-old Woman with Hyperstartling Stiffness, and Accidental Falls
Neurol 88:e38-e41, Russo, S.P.,et al, 2017

Characteristics in Limbic Encephalitis with Anti-Adenylate Kinase 5 Autoantibodies
Neurol 88:514-524,508, Do, L. & Chanson, E., 2017

Investigations in GABA? Receptor Antibody-Associated Encephalitis
Neurol 88:1012-1020,1010, Spatola, M.,et al, 2017

A 45-year-old Woman with Right Limb Weakness
Neurol 88:e103-e107, Li, S.,et al, 2017

Neurological Autoantibody Prevalence in Epilepsy on Unknown Etiology
JAMA Neurol 74:397-402,384, Dubey, D.,et al, 2017

ED Misdiagnosis of Cerebrovascular Events in the Era of Modern Neuroimaging
Neurol 88:1468-1477, Tarnutzer, A.A.,et al, 2017

A Young Woman with Progressive Headache and Pancytopenia
Neurol 88:e132-e136, Conrad, E.C.,et al, 2017

Primary Angiitis of the Central Nervous System
Stroke 48:1248-1255, Boulouis, G.,et al, 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Arteriovenous Malformations of the Brain
NEJM 376:1859-1866, Solomon, R.A. & Connolly, E.S., 2017

Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017

Autoimmune Encephalitis: Pathophysiology and Imaging Review of an Overlooked Diagnosis
AJNR 38:1070-1078, Kelley, B.P.,et al, 2017

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

A Demure Teenager and Her Dystonic Foot
Neurol 89:e71-e75, Cullinane, P.W.,et al, 2017

A Case of Altered Mental Status, Not Otherwise Specified
Neurol 89:e154-e158, Swor, D.E.,et al, 2017

Sarcoidosis Limbic Encephalitis
Iran J Neurol 16:156-158, Toudou-Daouda, M.,et al, 2017

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
Neurol 89:e182-e187, Tabuas-Pereira, M.,et al, 2017

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
NEJM 377:1648-1656, Blumcke, I.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Clinical Pathologic Conference, West Nile Virus Encephalitis
NEJM 377:1878-1886, Case 34-2017, 2017

Adult-Onset Niemann-Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult
Front Neurol doi.10.3398/jneur.2017.00108, Piroth,T.,et al, 2017

Autoimmune Limbic Encephalitis Associated with Type 1 Diabetes Mellitus
J Clin Res Pediatr Endocrinol 9:387-388, Akin,O.,et al, 2017

Autoimmune Encephalitis: Pathophysiology and Imaging Review of an Overlooked Diagnosis
AJNR 38:1070-1078, Kelley, B.P.,et al, 2017

Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
Front Neurol soi.10.3389/fneur.2017.00376,Aug, Zhou,C.,et al, 2017

Differential Diagnosis
Thoracic Key, Southerland,A.W.,et al, 2016

Chronic Herpes Simplex Type-1 Encephalitis with Intractable Epilepsy in an Immunosuppressed Patient
Infection 44:121-125, Laohathai, C.,et al, 2016

Pseudoradial Nerve Palsy Caused by Acute Ischemic Stroke
J Invest Med Case Report doi:10.1177/2324709616658310, Tahir, H.,et al, 2016

Subarachnoid Hemorrhage
Medscape Aug, Becske, T. & Lutsep, H.L., 2016

Rapidly Progressive Quadriplegia and Encephalopathy
JAMA Neurol 73:1363-1366, Wynn, D.,et al, 2016

Autoantibodies to Glutamic Acid Decarboxylase in Patients with Epilepsy and Their Relationship with Type 1 Diabetes: A Pilot Study
JNNP 87:676-677, Moloney T.C.,et al, 2016

Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
JAMA Neurol 73:888-890, Kawarai, T.,et al, 2016

An 11-year-old Boy with Language Disorder and Epilepsy
Neurol 86:e48-e53, Dong, L. & Zhou, X., 2016

Leukodystrophy and Progressive Myoclonic Epilepsy Disclosing DRPLA
Neurol 86:e58-e59, Sgobbi de Souza, P.V.,et al, 2016

Validation of Clinicoradiological Criteria for the Diagnosis of Cerebral Amyloid Angiopathy-Related Inflammation
JAMA Neurol 73:197-202, Auriel, E.,et al, 2016

Antibiotic-Associated Encephalopathy
Neurol 86:963-971, Bhattacharyya, S.,et al, 2016

Pneumorrhahcis
Neurol 86:e134-e135, Thakur, S.,et al, 2016

Orthostatic Myoclonus Associated with CASPR2 Antibodies
Neurol 86:1353-1355, Govert, F.,et al, 2016

Proptosis, Headache, and Fever in a Healthy Young Woman
Neurol 86:e168-e172, Orquera, J.,et al, 2016

A Clinical Approach to Diagnosis of Autoimmune Encephalitis
Lancet Neurol 15:391-404, Graus, F.,et al, 2016

Rituximab Treatment for Autoimmune Limbic Encephalitis in an Institutional Cohort
Neurol 86:1683-1691,1655, Lee, W.J.,et al, 2016

Practice Guideline Update Summary: Botulinum Neurotoxin for the Treatment of Blepharospasm, Cervical Dystonia, Adult Spasticity, and Headache
Neurol 86:1818-1826, Simpson, D.M.,et al, 2016

Distinguishing Neuroimaging Features in Patients Presenting with Visual Hallucinations
AJNR 37:774-781, Winton-Brown, T.T.,et al, 2016

Showing articles 250 to 300 of 2208 << Previous Next >>