Neudle.com: white matter tracts

Differential
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abducens nerve paralysis

acrocyanosis

acute disseminated encephalomyelitis

acute disseminated encephalomyelitis, multiphasic

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

aggression

Aicardi-Goutieres syndrome

albendazole

Alexanders disease

Alexanders disease, adult onset

ANA

anatomy of

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

animal exposure

anterior tibial muscle weakness

aspartate aminotransferase

ataxia

ataxia, cerebellar

ataxia, sensory

atherosclerosis, generalized

attention deficit disorder with hyperactivity

atypical

auditory evoked brainstem potentials

autonomic dysfunction

bacterial infection, CNS

Bannayan-Riley-Ruvalcaba syndrome

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

baylisascariasis

bedridden

behavioral disorder

Bickerstaff's brainstem encephalitis

bladder dysfunction

bone marrow transplantation

Brown Sequard syndrome

brucellosis

brucellosis, nervous system involvement with

bulbar palsy

calcification, intracranial

calcifications, intracranial, punctate

carphology

CAT scan

CAT scan, abnormal

CAT scan, myelogram with

CAT scan, serial

CAT scan, spinal cord

CAT scan, spine

central nervous system, infection of

cerebellar lesion

cerebral cortex

cerebral cortical atrophy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count, normal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, pressure increased

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

Charcot-Marie-Tooth

chest x-ray, abnormal

chilbran skin lesions

children

Clinical Pathologic Conference(C.P.C.)

cognition

coma

confusion

congenital malformation

consanguinity

coronavirus

corpus callosum

corpus callosum, lesion of

corpus callosum, thinning

cough

COVID-19

cry, abnormal

cultured skin fibroblasts

degenerative diseases of CNS

dementia

dementia, childhood

dementia, subcortical

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

developmental disability

developmental milestones, loss of

developmental retardation

diagnostic criteria

diet

differential diagnosis

difficulty going down stairs

diplopia

distal muscle atrophy

distal muscle weakness

drooling

dropped head syndrome

electroencephalogram, abnormalities of

electromyogram

ELISA

encephalitis

encephalitis, bornavirus

encephalitis, brainstem

encephalitis, viral

encephalopathy

encephalopathy, progressive

endemic area

enzyme, defect

enzyme, muscle disease

eosinophilia

epicanthal folds

epidemiology of neurology

episodic neurologic deficits

evoked potentials

exome sequencing

face, numbness of

facial appearance, abnormal

falling

false negative

familial

fatty acid, elevated plasma content

feeding disorder

fever

flu-like illness

fundus, abnormality of

genetic diagnosis, prenatal

genetic neurologic disorders

glycogen storage disease

gram negative rod

Guillain Barre syndrome

hearing problems in children

helminthic infection of CNS

hemangioma

hemiparesis

hemiplegia

hemiplegia, progressive

hepatic failure

hepatic failure, acute

hepatitis

hepatolenticular degeneration(Wilson's disease)

hexosaminidase-A

high arched feet

homocystinuria

hot, red, angry babies

human immunodeficiency virus type 1

human parechovirus

human T-lymphotropic virus type I(HTLV-I)

hyperhomocysteinemia

hyperpyrexia, CNS disorder causing

hypotension, systemic

hypotonia

hypoxia

hypoxic encephalopathy

hypoxic-ischemic leukoencephalopathy

imbalance

immunosuppression

immunosuppressive agents

impulsivity

in situ hybridization

inclusion bodies

infection

inferior occipitofrontal fasciculus

intellectual deficit

intellectual deterioration

interferon alpha

internal capsule

intrauterine

intrinsic hand muscles, wasting of

irritability

Jakob-Creutzfeldt disease

Jewish

Krabbe's disease

lactate

lactic dehydrogenase(LDH)

laughing

laughing, pathologic

leg weakness, bilateral

lethargy

leuko-araiosis

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukoencephalitis, acute necrotizing hemorrhagic

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

lipid storage disorder of CNS

lipomatosis

liver function enzymes

Lorenzo's oil

lysosomal storage disease

macrocephaly

magnetic transfer imaging

meconium staining

memory, defect of recent

memory, impairment of

meningeal enhancement

meningismus

meningitis, aseptic

meningitis, brucellosis

meningitis, eosinophilic

meningitis, noninfectious

meningoencephalitis

mental status, abnormal

metachromatic leukodystrophy

metachromatic leukodystrophy, late-infantile

Meyer's loop

microaneurysm, retinal

microcephaly

microdontia

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, FLAIR

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, hypointense signal foci on

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, T1 weighted high signal foci

MRI, volumetry

MRS

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle spasm

mutism

mycoplasma

mycoplasma pneumoniae

myelitis

myelitis, longitudinal

myelomalacia

myeloneuropathy

myelopathy

myelopathy, ascending

myelopathy, chronic progressive

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

nerve root enhancement

neuroaxonal leukodystrophy

neurogenic bladder

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neurological intensive care

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

oculodentodigital dysplasia

opisthotonus

optic ataxia

optic chiasm, enlarged

optic nerve, enlarged

paraparesis, familial spastic

paraparesis, spastic

paraparesis, spastic, tropical

parechovirus encephalitis

Parkinson disease

Parkinson disease, arteriosclerotic

PAS positive material in the brain

pediatric neurology

Pelizaeus Merzbacher

penis, pigmented macules

pleocytosis of cerebrospinal fluid

pneumonia

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyps, gastrointestinal tract

pons, lesion of

posterior column disease

prenatal

prenatal diagnosis by amniocentesis

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pulmonary infiltrates

pyramidal

pyramidal tract

pyramidal tract dysfunction

raccoon

radiculopathy

rapidly fatal neurologic illness

rapidly progressing neurologic illness

respiratory tract infection

retrovirus

reversible neurologic disorder

sedimentation rate, elevated

severe acute respiratory syndrome

skin, darkening of

skin, lesions in neurologic disorders

somatosensory evoked potentials

somnolence

spasticity

speech disorder, childhood

speech, loss of

spinal cord, herniation

spinal cord, lesion of

spinal cord, pathologic exam of

spontaneous remission

startle reaction

steroid therapy, CNS treatment and complications with

subcortical U fibers

suck, poor

symmetric brain lesions

syndactyly

systemic lupus erythematosus

temporal lobe, lesion

temporal lobe, lesion, bilateral

term infant

testicular atrophy

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

toe walking

tone, muscle, increased

tractography

transient neurologic deficit

trauma

treatment of neurologic disorder

vaccination, neurologic complications with

vasculitides

vasogenic edema

vibratory sensation, abnormal

viral infection

viral infection, CNS

Virchow-Robin spaces, dilated

visual loss

walking, delayed

walking, difficulty with

Wallerian degeneration

weakness

weakness, generalized

weakness, progressive

wheelchair

white matter disease

white matter disease, periventricular

white matter tracts

wide based gait

Showing articles 50 to 100 of 2347 << Previous Next >>

Lentiviral Gene Therapy for Cerebral adrenoleukodystrophy
NEJM 391:1302-1312,1358, Eichler,F.,et al, 2024

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

Partially Reversible FLAIR Hyperintensity Along the Brainstem Surface in Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
Neurol 102:e208064, Wu, J.,et al, 2024

Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
Ann Neurol 95:407-409, Tsibonakis,A.,et al, 2024

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
Neurol 102:e209258, Lail,G.,et al, 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

Uncommon Causes of Nontraumatic Intracerebral Hemorrhage
Stroke 55:1416-1427, Tartarin,H.,et al, 2024

Brainstem Chipmunk Sign: A Diagnostic Imaging Clue Across All Subtypes of Alexander Disease
AJNR 45:769-776, Armangue,T.,et al, 2024

Clinicopathologic Conference, Legionella Infection Complicated by Rhabdomyolysis
NEJM 391:1039-1048, Case 29-2024, 2024

Diagnosis of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease:International MOGAD Panel Proposed Criteria
Lancet Neurol doi.org110.1016/51474-4422(22)00431-8, Banwell,B.,et al, 2023

Severe Amyloid-Related Imaging Abnormalities After Anti-B-Amyloid Monoclonal Antibody Treatment
Neurol 101:1079-1080, Bonami,S.,et al, 2023

Tuberous Sclerosis Complex:Clinical Features
www.UptoDate.com, Dec, Randle,S., et al, 2023

A 40-Year-Old Woman Presenting with Encepatholopathy and Paraparesis
Neurol 101:e94-e98, AlSabah,A.,et al, 2023

Intracerebral Haemorrhage Caused by Iatrogenic Cerebral Amyloid Angiopathy in a Patient with a History of Neurosurgery 35 Years Earlier
Lancet 402:11, Fandler-Hofler,et al, 2023

Shrimp Sign in Ataxic Cerebellar Progressive Multifocal Leukoencephalopathy
Neurol 101:918-919, Varela,F.J.,et al, 2023

Rapidly Progressive Dementia in a Man With HIV Infection and Undetectable Plasma Viral Load
Neurol 100:344-348, Chishimba,L.C.,et al, 2023

Clinical,Neuroimaging,and Genetic Markers in Cerebral Amyloid Angiopatny-Related Inflammation:A Systematic Review and Meta-Analusis
Stroke 54:178-188, Theodorou,A.,et al, 2023

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

Monkeypox-Associated Central Nervous System Disease:A Case Series and Review
Ann Neurol 93:893-905, Money,K.M.,et al, 2023

Posterior Reversible Encephalopathy Syndrome
NEJM 388:2171-2178, Geocadin,R.G., 2023

Progressive Hemiparesis and White Matter Abnormalities in an HIV-Negative Patient
Neurol 100:1156-1163, Jabbari,E.,et al, 2023

Characteristics of Progressive Multifocal Leukoencephalopathy Associated with Sarcoidosis without Therapeutic Immune Suppression
JAMA Neurol 80:624-633, McEntire,C.R.S.,et al, 2023

Opioid-Associated Amnestic Syndrome Progressing to Diffuse Leukoencephalopathy
Neurohospitalist 13:109-110, Meng,D., & Randhawa,J., 2023

Amyloid-Related Imaging Abnormalities:An Update
AJR 220:562-575, Roytman,M.,et al, 2023

Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies
AJNR 43:2-10, Benjamin, P.,et al, 2022

A 55-Year-Old Woman with Recurrent Episodes of Aphasia and Vision Changes
Neurol 98:330-335, Jeanneret, V.,et al, 2022

Lenvatinib Therapy for Advanced Thyroid Cancer: Real-Life Data on Safety, Efficacy, and Some Rare Side Effects
JENDSO 6:1-7, Hamidi, S.,et al, 2022

Unilateral Leukoencephalopathy Revealing Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Ann Neurol 91:889-890, Gollion, C.,et al, 2022

Neuromyelitis Optica Spectrum Disorder
NEJM 387:631-639, Wingerchuk, D.M. & Lucchinetti, C.F., 2022

Neuroimaging Findings in Parechovirus Encephalitis: A Case Series of Pediatric Patients
Pediatr Neurol 130:41-45, Tierradentro-Garcia, L.O.,et al, 2022

Clinical and Structural Findings in Patients with Lesion-Induced Dystonia
Neurol 99:e1957-e1967, Corp, D.T.,et al, 2022

Atypical Presentation of Primary Angiitis of Central Nervous System Responsive to Rituximab
Stroke 53:e490-e494, Kesav, P.,et al, 2022

New Onset Focal Tremor in Patient with Human Immunodeficienccy Virus
Clin Infect Dis 75:1861-1863, Finelli,P.F., 2022

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

The Boston Criteria Version 2.0 for Cerebral Amylois Angiopathy:A Multicentre, Retrospective, MRI-Neuropathology Diagnostic Accuracy Study
Lancet Neurol 21:714-725, Charidimou,A.,et al, 2022

Drug-Related Demyelinating Syndromes: Understanding Risk Factors, Pathophysiological Mechanisms and Magnetic Resonance Imaging Findings
Mult Scler Rel Dis 55:103146, Rimkus, C.M.,et al, 2021

A Middle-Aged Man with Progressive Gait Abnormalities
Neurol 97:e2423-e2428, Lin, J.,et al, 2021

Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
Neurol 97:875-878, Dinov, D.,et al, 2021

A Middle-Aged Man with a History of Muscle Pain Presenting with Progressive Leukoencephalopathy and Subsequent Coma
Neurol 97:910-915, Jakobsson, A.S.,et al, 2021

Unilateral PRimary Angiitis of the Central Nervous System
Ann Neurol 90:999-1000, Santyr,B.,et al, 2021

A 65-Year-Old Woman with Tremor
Neurol 97:e1257-e1261, Ye, J.,et al, 2021

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

A 71-Year-Old Man with Horizontal Gaze Palsy, Anarthria, and Quadriparesis
Neurol 96:1146-1150, Cheema, I.,et al, 2021

Clinicopathologic Conference, Delayed Postthypoxic Leukoencephalopathy
NEJM 384:2438-2445, Case 19-2021, 2021

Bilateral Temporal Pole Involvement in Adult-Onset X-Linked Adrenoleukodystrophy
JAMA Neurol 78:367-368, Liu, M.,et al, 2021

A Triad of Tremor, Ataxia, and Cognitive Impairment
Neurol 96:e1802-e1803, Au, L.W.C.,et al, 2021

Progressive Multifocal Leukoencephalopathy in a Patient with Progressive Multiple Sclerosis Treated With Ocrelizumab Monotherapy
JAMA Neurol 78:736-740, Patel,A.,et al, 2021

Clinical and Neuroimaging Findings in MOGAD-MRI and OCT
Clin Exp Immunol 206:266-281, Bartels,F.,et al, 2021

Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral Sclerosis
J Clin Med 9:1-12, Rizzo, G.,et al, 2020

Showing articles 50 to 100 of 2347 << Previous Next >>