Neudle.com: "polyneuropathy critically ill children"

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abortion, spontaneous

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, infants and children

acute ataxia of childhood

acute disseminated encephalomyelitis

acute disseminated encephalomyelitis, relapsing

adolescent medicine

advances in neurology

adverse drug reaction

albendazole

algorithm

alternating hemiplegia

alternating hemiplegia of childhood

AMPA receptor antibodies

anemia

angiitis, isolated of CNS

angiitis, isolated of CNS, tumefactive

angiography, cerebral, beaded vessels

angiography, cerebral

angiotensin-converting enzyme

animal exposure

anti GQ1b IgG antibody

antibiotics

antibodies to measles

anticardiolipin antibodies

anticoagulant, treatment

antiphospholipid antibodies

antiphospholipid antibody syndrome

aspartate aminotransferase

attention deficit disorder with hyperactivity

atypical lymphocytes

auditory evoked brainstem potentials

autism

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

bacterial infection

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

baylisascariasis

behavioral disorder

behavioral disorder, acute

botulinum toxin

botulism

botulism antitoxin

botulism immune globulin

calcification, intracranial

calf hypertrophy

carcinoma

cardiomyopathy

cardiopulmonary bypass

carpal tunnel syndrome

cauda equina, enhancement

caudate nucleus, atrophy

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

cerebellitis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral infarction, hemorrhagic

cerebral infarction, subcortical

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebral venous thrombosis, etiology

cerebral venous thrombosis, recurrent

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, bilateral

cerebrovascular accident, multiple

cerebrovascular accident, prevention of

cerebrovascular accident, three territory involvement

cerebrovascular accident, thrombolytic agents in treatment

cerebrovascular accident, topographic pattern

cerebrovascular accident, young adult

cerebrovascular disease

chest x-ray, abnormal

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

cognition

collagen vascular disease

collapsin response mediator protein 5 IgG

coma

complications

confusion

congenital birth defects

congenital infection, CNS

congenital infection, viral

controversies in neurology

conversion reaction

conversion reaction, children

cortical blindness

cortical infarction

cortical infarction, small

coryza

cough

coumarin

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniectomy, decompressive

crawl regression

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, weak

crying

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, childhood

dementia, rapidly progressive

dermatitis herpetiformis

dermatographism

developmental disability

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diarrhea

differential diagnosis

difficulty climbing stairs

disability rating scale, neurological

disability, neurological

disorientation

DPPX, antibodies, encephalitis

dural sinus thrombosis

dyskinesia

dyskinesia, drug induced

dyskinesia, facial

dysphagia

dystonia

dystonia, drug induced

dystrophin

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, etiology

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, metabolic

encephalopathy, progressive

endocarditis, marantic

endovascular therapy

enterovirus

eosinophilia

epidemiology of neurology

Epstein-Barr virus

evidence-based research

evoked potentials

exercise intolerance

eye movement, disorders of

facial nerve palsy

faciobrachial dystonic seizure

fibrinolytic agents, intra-venous local infusion

fine motor function, impaired

frontal lobe, pathologic signs of

fundus, abnormality of

fungal infection, CNS

gadolinium

gait disorder

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, supranuclear

gaze palsy, vertical

gender

gene mutation

genetic neurologic disorders

genetic screening

genetic testing

geographic location

Gilles de la Tourette syndrome

glaucoma

glutamic acid decarboxylase, antibody

granulomatous disease

gray matter

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, variant forms of

helminthic infection of CNS

heparin

heparin, low-molecular-weight

heralding manifestation

herpes simplex encephalitis

human immunodeficiency virus type 1

human immunodeficiency virus type 1, acute infection

Huntington's chorea

Huntington's disease, children

hypertension, children and adolescents

hypothalamus, disturbance of

hypotonia

hypotonia, infants

hypoxia

immunization, neurologic complications with

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion body myositis

infant, evaluation of

infection

infectious mononucleosis

infectious mononucleosis, neurologic findings with

influenza

influenza A virus

influenza immunization

insomnia

intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral

irritability

irritable baby

jaundice

Kearns-Sayre syndrome

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

Leigh's disease

lethargy

leucine rich glioma inactivated 1 antibodies

leukocytosis

leukoencephalopathy

level of consciousness, decreased

limbic encephalitis

livedo reticularis

liver disease

liver function enzymes

lupus anticoagulant

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, paraaortic

lymphoma

lymphomatoid granulomatosis

malabsorption

malaise

malformation, vascular

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningismus

meningitis

meningitis, aseptic

meningitis, carcinomatous

meningitis, eosinophilic

meningoencephalitis

mental status, abnormal

MERRF syndrome

mesial temporal lobe

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

microangiopathy, brain

microcephaly

migraine

migraine, seizures in

misdiagnosis

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitral valve lesion

molecular genetics

monoclonal antibodies

mortality

movement disorder

movement disorder, drug induced

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, angiography

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR

MRI, negative

MRI, punctate pattern

multiple organ failure

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle wasting, diffuse

muscle weakness

muscular dystrophy

muscular dystrophy, central nervous system abnormality

muscular dystrophy, Duchenne

mutism

mycoplasma

mycoplasma pneumoniae

myelitis

myelitis, transverse

myelitis, transverse, recurrent

myelopathy

myocardial infarction

myoclonus

myoglobinuria

myopathy

myopathy, critically ill

myopathy, mitochondrial

myositis

myotonia dystrophica

neonatal infection, viral

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

neurexin-3 alpha antibodies

neurocutaneous disease

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination, focal

neurologic signs

neurologic symptoms

neurological intensive care

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal cell surface antigen

neuropathy

neuropathy, acute

neuropathy, peripheral

neuropathy, vasculitic, systemic

obsessive-compulsive disorder

obstetric complications

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, progressive external

opisthotonus

opportunistic infection

opportunistic infection, CNS

paralysis, acute areflexic

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

partial thromboplastin time, prolonged

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

peripheral blood smear

persistent vegetative state

personality change

petechiae

pigmentary retinopathy

pitfalls

plasmapheresis

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pneumonia

POLG1 gene

poliomyelitis-like illness

polycythemia, primary

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polyneuritis

polyneuropathy

polyneuropathy, critically ill

polyneuropathy, critically ill, children

port wine nevus

postpartum

posttransplant lymphoproliferation disorder

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prethrombotic state

prevention of neurologic disorders

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

protein C deficiency

protein S deficiency

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary infiltrates

quadriparesis

raccoon

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

renal vein thrombosis

respirator

respiratory failure

respiratory tract infection

scleroderma, neurologic involvement with

screening

sedimentation rate, elevated

seizure

seizure, children

seizure, differential diagnosis of

seizure, hysterical

seizure, neonatal

seizure, nonepileptic

sensorineural hearing loss

septicemia

seroconversion

serologic testing

serologic testing, false negative

seronegative

serositis

serum alanine aminotransferase

short stature

skin, lesions in neurologic disorders

sleep pathology and physiology

slow virus infection of CNS

small for dates infant, problems in

sore throat

spasticity

speech disorder

speech disorder, childhood

speech, delayed development of

spinal cord

spinal cord, lesion of

splenomegaly

spontaneous remission

status epilepticus

steroid

steroid therapy, CNS treatment and complications with

stiff joints

streptococcal infection

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

Sturge-Weber syndrome

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

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

suck, poor

sural nerve

systemic illness

systemic juvenile idiopathic arthritis

systemic lupus erythematosus

tachycardia

temporal lobe, lesion

temporal lobe, lesion, bilateral

thrombotic microangiopathy

thymoma

tic

tissue plasminogen activator, intravenous

titubation

toxins, nervous system

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

tremor

tremulousness

trigeminal nerve

trigeminal neuropathy

trinucleotide repeats

tripping

ultrasonography, head

urinary retention

vaccination, neurologic complications with

vaccine

valvulopathy

vasculopathy

venous thrombosis, non-cerebral

viral infection

viral infection, CNS

virus, slow

visual acuity, decreased

weakness, generalized

weakness, infant

weakness, progressive

web sites

weight loss

white matter disease

white matter disease, subcortical

workup

Showing articles 0 to 50 of 6632 Next >>

Clinicopathologic Conference, Infant Botulism, Case 3-2024
NEJM 390:358-366, Case 3-2024, 2024

Unpacking the CNS Manifestations of Epstein-Barr Virus:An Imaging Perspective
AJNR 44:1002-1008, Soni,N.,et al, 2023

Infectious Mononucleosis: Rapid Evidence Review
Am Fam Physician 107:71-78, Sylventer,J.E.,et al, 2023

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

An 8-Year-Old with Acute Onset Ataxia
Neurol 99:305-310, McLaren, J.R.,et al, 2022

Updates on Sturge-Weber Syndrome
Stroke 53:3769-3779, Yeom,S.E.&Comi,A.M., 2022

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

Clinicopathologic Conference, Systemic Juvenile Idiopathic Arthritis
NEJM 385:1220-1229, Case 29-2021, 2021

Acute Flaccid Myelitis: Cause, Diagnosis, and Management
Lancet 394:334-397, Murphy, O.C.,et al, 2021

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

Diagnosis and Management of the Antiphospholipid Syndrome
NEJM 378:2010-2021, Garcia, D. & Erkan, D., 2018

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

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

A 15-month-old boy with Progressive Lethargy and Spasticity
Neurol 89:e135-e139, Zhang, R.,et al, 2017

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

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

Development of a Suspicion Index to Aid Diagnosis of Niemann-Pick Disease Type C
Neurol 78:1560-1567,1546, Wijburg, F.A.,et al, 2012

The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
Stroke 43:2871-2876, Pescini, F.,et al, 2012

Neurologic Complications of Influenza A (H1N1)pdm09
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Diagnosis and Management of Cerebral Venous Thrombosis: A Statement for Healthcare Professionals From the American Heart Association/American Stroke Association
Stroke 42:1158-1192, Saposnik,G.,et al, 2011

Late onset autism and anti-NMDA-receptor encephalitis
Lancet 378:98;378, Creten, C.,et al, 2011

Diagnosis and Management of the Antiphospholipid Syndrome
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Pediatric Encephalitis: What Is the Role of Mycoplasma Pneumoniae
Pediatrics 120:305-313, Christie,L.J., et al, 2007

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

Acute Disseminated Encephalomyelitis
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The Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal Infection (PANDAS) Subgroup: Separating Fact From Fiction
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The Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal Infection (PANDAS) Etiology for Tics and Obsessive-Compulsive Symptoms: Hypothesis or Entity? Practical Considerations for the Clinician
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Diagnostic Delay in Psychogenic Nonepileptic Seizures
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Subacute Sclerosing Panencephalitis
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Dystonia and Chorea in Acquired Systemic Disorders
JNNP 65:436-445, Janavs,J.L.&Aminoff,M.J., 1998

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

The Polymerase Chain Reaction:Application to Nervous System Disease
Ann Neurol 34:513-523, Darnell,R.B., 1993

Neurologic Manifestations of Progressive Systemic Sclerosis
Arch Neurol 49:1292-1295, Averbuch-Heller,L.,et al, 1992

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

Neurologic Manifestations of Infection with Human Immunodeficiency Virus, Clinical Features & Pathogenesis
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Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
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Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
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Unveiling the Clinical and Imaging Signatures of Intravascular Lymphoma of the Central Nervous System:A Multicentric Cohort Study
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A 56-Year-Old Woman with New-Onset Hoarsement and Dysphagia
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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A 68-YEar-Old Man with Progressive Numbness, Vertigo, and Cognitive Decline
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Slowly Expanding Lesions Differentiate Pediatric Multiple Sclerosis from Myelin Oligodendrocyte Glycoprotein Antibody Disease
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Diagnosis and Management of ANCA-Associated Vasculitis
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Diagnosis and Management of Cerebral Venous Thrombosis:A Scientific Statement From the American Heart Association
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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Showing articles 0 to 50 of 6632 Next >>