Neudle.com: movement disorder delayed onset

Differential
(Click to cross reference)

abdominal distention

abdominal muscle paralysis

abducens nerve paralysis, bilateral

acanthocytosis

accommodation

acid maltase deficiency

acid maltase deficiency, adult

acute ataxia of childhood

acute cerebellar ataxia

acyl CoA dehydrogenase deficiency

addiction, heroin

addiction, heroin-neurologic complications with

adolescent medicine

adoption

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

Alexanders disease, adult onset

algorithm

alkalosis

alkalosis, respiratory

alpha-synuclein

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement, impaired

Alzheimer's disease

amblyopia, toxic

AMPA receptor antibodies

amphiphysin antibodies

amyloid plaques

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

aneurysm

angiography, cerebral

angiography, posterior fossa

ankle clonous

anosmia

anterior cerebral artery

anterior cerebral artery territory infarction

anterior horn cell disease

anti GQ1b IgG antibody

anti IgLON5

antibodies to measles

antibodies to voltage-gated calcium channels

anticholinergic drugs

anticoagulant, treatment in CVD

anticonvulsants

anticonvulsants, untoward effects of

antidepressant

antiphospholipid antibody syndrome

antistreptolysin titer

arterial dissection, carotid

arterial dissection, multiple

arterial dissection, vertebral

attention deficit disorder with hyperactivity

atypical

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

automatic behavior

automobile accidents

autonomic dysfunction

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

brachial neuritis, acute

brachial plexus neuropathy

campylobacter infection

canned food

carbon monoxide poisoning

carcinoma

carcinoma of lung

cardiac arrest

cardiac arrest and resuscitation

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, muscle

catalepsy

cauda equina, enhancement

caudate nucleus, atrophy

caudate nucleus, lesion of, bilateral

CD4 counts

central nervous system, infection of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar cognitive affective syndrome

cerebellar degeneration

cerebral cortical atrophy

cerebral edema

cerebral infarction

cerebral palsy

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular disease

cerebrovascular disease, risk factors in

cervical spine injury

cervical spine manipulation

chemosis

cherry red spot

cherry red spot-myoclonus syndrome

chewing, impaired

children

chiropractic manipulation

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

congenital heart disease

conjunctival injection

consanguinity

constipation

controversies in neurology

convergence

conversion reaction

corneal reflex, abnormal

corpus callosum, lesion of

cortical ribbon sign

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, childhood

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, treatment of

denervation of muscle

denervation potentials

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diagnostic criteria

diaphragmatic paralysis

diarrhea

diarrhea, bloody

diet

differential diagnosis

difficulty climbing stairs

diplopia

disease modifying agents

disorientation

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dopamine depleting agents

DPPX

DPPX, antibodies

DPPX, antibodies, encephalitis

dropped head syndrome

drowsiness

drug abuse, neurologic complications of

drug addiction

drug induced neurologic disorders

dyskinesia, buccal lingual facial

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, classification

dystonia, delayed onset

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, face

dystonia, focal

dystonia, treatment of

dystonia, truncal

dystonic reaction, acute

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electromyogram

electromyogram, decremental response

electromyogram, incremental response

electron microscopy

emergencies, neurologic

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, post anoxic

enteritis

enterovirus

enterovirus infection of CNS

enzyme, defect

epidemiology of neurology

exercise-related muscle strength increase

exome sequencing

extraocular muscle lesion

eye movement, disorders of

eye, pain in

facial nerve palsy

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

frontal lobe, atrophy

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

gag reflex, depressed

gait disorder

gait speed

gait, waddling

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

gaze palsy

gaze palsy, supranuclear

gene

gene mutation

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

geniculate body, lateral

genu of corpus callosum

gests antagoniste

GFAP gene

Gilles de la Tourette syndrome

glaucoma

glaucoma, acute

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

glycine receptor antibodies

GM1 ganglioside antibodies

grasping

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

gynecomastia

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination

hallucination, visual

head injury, delayed deterioration following

head nodding

headache

headache, severe

headache, sudden onset of

hearing loss

hemianopia

hemianopia, homonymous

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes virus

highly active antiretroviral therapy

human immunodeficiency virus type 1

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's chorea, late onset

Huntington's chorea, misdiagnosis of

Huntington's chorea, presymptomatic detection of

Huntington's chorea, sporadic form

Huntington's disease, children

hypocalcemia, causes of

hypocretin

hypoglycorrhachia

hypokalemia

hypokalemic paralysis

hypoxic encephalopathy

iatrogenic neurologic disorders

inclusion bodies, intranuclear

incoordination

infantile hemiplegia

infection

infectious mononucleosis

infectious mononucleosis, neurologic findings with

injection neuropathy

insomnia

intellectual deficit

intellectual deterioration

internal cerebral vein

intestinal pseudoobstruction

intracranial pressure, increased

intrinsic hand muscles, wasting of

iron, brain

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, young adult

laryngismus stridulus

laughing, pathologic

L-dopa

L-dopa, delayed treatment in Parkinsonism

L-dopa, drug interactions with and side effects of

left handedness

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

level of consciousness, decreased

Lewy body

Lewy body disease, diffuse

lid closure, weakness of

limbic encephalitis

lipid storage disorder of CNS

liver function enzymes

lymphoma involving CNS

lysosomal storage disease

macrocephaly

manganese intoxication

masked facies

masseter muscle wasting

McLeod syndrome

Melkersson's syndrome

mellaril

memory

memory, impairment of

meningeal enhancement

meningismus

meningitis

meningitis, aseptic

meningitis, carcinomatous

meningitis, recurrent

meningoencephalitis

mental retardation

mental status, abnormal

metabolic disorder, primary

metabolic disorder, primary-screening tests

metoclopramide

microcephaly

middle cerebellar peduncle, lesion

mild cognitive impairment

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

modafinil

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, hyperkinetic

movement disorder, treatment of

MRI

MRI, abnormal

MRI, brachial plexus

MRI, contrast enhanced

MRI, diffusion weighted

MRI, eye of tiger sign

MRI, muscle

MRI, negative

MRI, paramagnetic effect

MRI, spinal cord

multiple sclerosis

multiple sleep latency test

muscle atrophy, progressive

muscle strength, testing

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenic syndrome

mycotoxin

myelinolysis, extrapontine

myelitis

myelitis, transverse

myelopathy

myelopathy, chronic progressive

myopia, sudden onset of

near reflex, spasm of

neck pain

neck weakness

nemaline rod myopathy

nemaline rod myopathy, adult onset

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve root biopsy

nerve root enhancement

neuritis

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neurofibrillary degeneration

neuroleptic

neuroleptic, atypical

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic signs

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuropathology, brain

neuropathy

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

next-generation sequencing

Niemann-Pick disease

nitroproprionic acid

NMDA antagonists

numbness, generalized

nusinersen

nutritional deficiency

nystagmus

nystagmus, monocular

obsessive-compulsive disorder

ocular motility, disorders of

oculogyric crisis

oculopharyngeal muscular dystrophy

old age, neurology of

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, total

oral contraceptives, cerbrovascular disease and

orthopnea

osmotic demyelination syndrome

otitis, neurologic complications with

paralysis, acute areflexic

paraparesis

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

paresthesias

paresthesias, hands

Parkinson disease

Parkinson disease, dementia with

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, hemiparesis in

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, nonmotor problems of

Parkinson disease, on-off phenomena in

Parkinson disease, presymptomatic detection

Parkinson disease, treatment of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

pathologic reflex

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

peptides, brain

perioral numbness

peripheral blood smear

perseveration

personality change

phenothiazine

phenothiazine, dyskinesia associated with

Pick's disease

pigmentary retinopathy

Pisa syndrome

PLEDs

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polysomnogram

pons, lesion of

positive sharp waves

post infectious cerebellar ataxia

posterior choroidal artery

postinfectious

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

preclinical

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

prion disease

PRKN gene

prognosis

progressive neurologic disorder

progressive spinal muscular atrophy

protein 14-3-3, cerebrospinal fluid

protozoan infection

proximal muscle atrophy

pseudoabducens palsy

pseudomyotonia

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, light reflex, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadrantanopsia, homonymous

quadriparesis

quadriparesis, acute

quadriparesis, progressive

quadriplegia

quality of life

quinine

rabies, nervous system involvement with

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

REM sleep behavior disorder

remote effect of cancer on the nervous system

repetitive nerve stimulation

reserpine treatment in movement disorder

respiratory failure

respiratory tract infection

salivation, excessive

sarcoidosis

saxitoxin

scoliosis

scoliosis, neurologic association with

screening

sedimentation rate, elevated

seizure, unknown origin

senile plaques

sensorineural hearing loss

sensory tricks

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

seronegative

shell fish poisoning

sinemet

single photon emission computed tomography

skin, biopsy

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, classification

steroid therapy, CNS treatment and complications with

stimulant drugs

stimulation, deep brain

stool culture

stooped posture

streptococcal infection

streptococcus pyogens

striatal encephalitis

striatum, lesion of

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

subacute sclerosing panencephalitis, adult onset

subarachnoid hemorrhage

sugarcane, mildewed

swallow evaluation

symmetric brain lesions

tardive dyskinesia, treatment of

tardive dystonia

tardive pain syndrome

temporal lobe, atrophy

temporal lobe, lesion

temporalis muscle wasting

tetany

tetany, latent

tetany, normocalcemic

tetrabenazine

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

tic

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

toxins, nervous system

transient ischemic attack

trauma

treatment of neurologic disorder

tricyclic antidepressant

trinucleotide repeats

ventricular enlargement

visual acuity, decreased

visual field defect

visual fields, constricted

visual loss

visual loss, sudden

visuospatial disturbance

vital capacity

vitamin deficiency

von Bonsdorff's sign

Waldenstrom's macroglobulinemia

walking, difficulty with

weakness

weakness, acute

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

Showing articles 450 to 500 of 17977 << Previous Next >>

Human Neurexin-3a Antibodies Associate with Encephalitis and Alter Synapse Development
Neurol 86:2235-2242,2222, Gresa-Arribas, N.,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

And Why Not Thrombolysis in the Ambulance (At Least for Some)?
Neurol 87:214-219, Rosenberg, G. & Steiner, I., 2016

Complete Lingual Palsy from Bilateral Dejerine Syndrome (Bilateral Medial Medullary Stroke)
Neurol 87:550, Tsetsou, S.,et al, 2016

Ocular Manifestations in Systemic Lupus Erythematosus
Br J Ophthalmol 100:135-144, Silpa-Archa,S.,et al, 2016

Wilson Disease
Yamada Textbook of Gastroenterology Chp 102, Metabolic Diseases of Liver, 6th Ed, Sunderam, S.S., & Sokol, R.J., 2016

NMDA-Receptor Encephalitis
DynaMed Plus Sept 2016, Rae-Grant, A.,et al, 2016

Bilateral Hypertrophy of Masseteric and Temporalis Muscles, our Fifteen Patients and Review of Literature
Eur Rev Med Pharmacol Sci 20:7-11, Graziano, P.,et al, 2016

Extraintestinal Manifestations of Coeliac Disease
Nat Rev Gastroenterol Hepatol 12:561-571, Leffler, D.A.,et al, 2015

Bells Palsy: Aetiology, Clinical Features and Multidisciplinary Care
JNNP 86:1356-1361, Eviston, T.J.,et al, 2015

Molybdenum Cofactor Deficiency
Neurol 85:e175-e178, Nagappa, M.,et al, 2015

Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015

Isolated Lingual Dyskinesia in Multiple Sclerosis
JAMA Neurol 72:1196-1197, Park, J.E.,et al, 2015

Paroxysmal Kinesigenic Dyskinesia
Neurol 85:1546-1553, Huang, X.J.,et al, 2015

Paroxysmal Dystonia as a Manifestation of Multiple Sclerosis
Neurologist 19:132-134, Machado, C.,et al, 2015

Stent-Retriever Thrombectomy after Intravenous t-PA vs. t-PA Alone in Stroke
NEJM 372:2285-2295,2347, Saver, J.L.,et al, 2015

Thrombectomy within 8 hours after Symptom Onset in Ischemic Stroke
NEJM 372:2296-2306,2347, Jovin, T.G.,et al, 2015

Screening with MRI for Accurate and Rapid Stroke Treatment
Neurol 84:2438-2444, 2394, Shah, S.,et al, 2015

Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
JNNP 86:774-781, Van Egmond, M.E.,et al, 2015

A 44-year-old Woman with Rapidly Progressive Weakness and Ophthalmoplegia
Neurol 85:e22-e27, Schreck, K.C.,et al, 2015

Treatment Concepts for Wake-Up Stroke and Stroke with Unknown Time of Symptom Onset
Stroke 46:2707-2713, Thomalla, G. & Gerloff, C., 2015

A 27-Year Old Man with Rapidly Progressive Coma
Neurol 85:e74-e78, Wong,J.M.,et al, 2015

Seizing the Clinical Presentation in Adult Onset Stills Disease
Autoimmun Rev 14:472-477, Narula, N.,et al, 2015

Anti-DPPX Encephalitis,Pathogenic Effects of Antibodies on Gut and Brain Neurons
Neurol 85:890-897, Piepgras,J.,et al, 2015

Demyelinating Encephalopathy in Adult Onset Stills Disease: Case Report and Review of the Literatures
Clin Neurol Neurosurg 115:2213-2216, Jie, W., et al, 2015

Acute Headache Diagnosis in Pregnant Women
Neurol 85:1024-1030, Robbins, M.S.,et al, 2015

Plasma Levels of Apolipoprotein E and Risk of Dementia in the General Population
Ann Neurol 77:301-311, Rasmussen, K.L.,et al, 2015

"Noncognitive" Symptoms of Early Alzheimer Disease
Neurol 84:617-622, Masters, M.C.,et al, 2015

Implementing a Mobile Stroke Unit Program in the United States
JAMA Neurol 72:229-234, Rajan, S.,et al, 2015

Clinical Laboratory and Findings of 21 Patients with Radiation-Induced Myopathy
JNNP 86:152-158, Ghosh, P.S. & Milone M., 2015

Clinicopathologic Conference, Botulism
NEJM 372:364-372, Case 3-2015, 2015

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

Effects of Golden Hour Thrombolysis
JAMA Neurol 72:25-30,9, Ebinger, M.,et al, 2015

MRI in X-Linked Adrenoleukodystrophy
Neurol 84:211, Siddiqui, S.,et al, 2015

When it is Safe to Return to Driving Following First-Ever Seizure?
JNNP 86:60-64, Brown, J.W.L.,et al, 2015

Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
NEJM 372:1151-1162, Miller, B.L.,et al, 2015

Rates of Ischemic Stroke During Warfarin Treatment for Atrial Fibrillation
Stroke 46:1120-1122, Tung, J.M.,et al, 2015

Clinicopathologic Conference, Invasive Neisseria Meningitidis Infection and Primary C8 Deficiency
NEJM 372:1454-1462, Case 11-2015, 2015

Premature Ventricular Complexes on Screening Electrocardiogram and Risk of Ischemic Stroke
Stroke 46:1365-1367, Agarwal, S.K.,et al, 2015

Tonic Eye Deviation in Stiff-Person Syndrome
Neurol 84:e124-e127, Chakravarthi, S.,et al, 2015

Evidence-Based Guideline: Management of an Unprovoked First Seizure in Adults
Neurol 84:1705-1713, Krumholz, A.,et al, 2015

Stent-Retriever Thrombectomy after Intravenous t-PA vs. t-PA Alone in Stroke
NEJM 372:DOI:10.1056/NEJMoa1415061, DOI:10.1056 NEJM e1503217, Saver, J.L.,et al, 2015

Thrombectomy within 8 Hours after Symptom Onset in Ischemic Stroke
NEJM 372:DOI:10.1056 NEJMoa1503780, DOI:1056NEJM e1503217, Jovin, T.G.,et al, 2015

Ocular Motor Abnormalities in Bilateral Paramedian Thalamic Stroke
Neurol 84:e155-e158, Gooneratne, I.K.,et al, 2015

Clinicopathologic Conference, CAT Scratch Disease (Encephalopathy Associated with Bartonella Henselae)
NEJM 372:2050-2058, Case 16-2015, 2015

Rotavirus-Associated Mild Encephalopathy with a Reversible Splenial Lesion (MERS)
BMC Infect Dis 15:446, Karampatsas, K.,et al, 2015

Sturge-Weber Syndrome
UptoDate , Nov, Bodensteiner, J.B., 2014

Acute Myopia and Angle Closure Glaucoma from Topiramate in a Seven-Year-Old: A Case Report and Review of the Literature
BMC Pediatrics 14:96, Rapoport, Y.,et al, 2014

Distinctive Pattern of White Matter Injury in Neonates with Rotavirus Infection
Neurol 84:21-27,13, Yeom, J.S.,et al, 2014

A Case of Early-Onset Rapidly Progressive Dementia
JAMA Neurol 71:1445-1449, Cachia, D.,et al, 2014

Showing articles 450 to 500 of 17977 << Previous Next >>