Neudle.com: corpus callosum atrophy of

Differential
(Click to cross reference)

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acromicria

adenovirus infection

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

agenesis of corpus callosum

airway obstruction

alcohol, neurologic complications with

alcoholism

alien hand syndrome

Alzheimer's disease

amygdalohippocampectomy

angiography, cerebral, false negative

angiography, cerebral, negative

ankle reflex, absent

anterior tibial muscle weakness

antiviral agents

apnea

aqueduct of Sylvius, stenosis

arm weakness

arteriovenous malformation

arteriovenous malformation, cerebral

attention deficit disorder with hyperactivity

audiogram

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basement membrane

basement membrane thickening

behavioral disorder

Behcet's syndrome

bladder dysfunction

bone marrow transplantation

calcification, intracranial

calcifications, intracranial, punctate

carbon monoxide poisoning

cardiomyopathy

carotid artery disease

carotid artery occlusion, neck

carotid artery stenosis

carotid artery stenosis, intracranial

carotid siphon

carotid-siphon occlusion

CAT scan

CAT scan, abnormal

CAT scan, contrast enhanced

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, mass effect on

cataracts

central nervous system, infection of

centrum semiovale

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar hypoplasia

cerebral cortical atrophy

cerebral dominance

cerebral infarction

cerebral ischemia

cerebral venous thrombosis

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, women

Charcot-Marie-Tooth

children

choroid plexus, enhancement

chromosomal abnormality

chromosome 28

cirrhosis

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

clinodactyly

clubfoot as related to neurologic disease

Cockayne's syndrome

cognition

cold hands sign

commissurotomy, cerebral

confusion

congenital malformation

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, infarction of

corpus callosum, lesion of

corpus callosum, neoplasm of

corpus callosum, thinning

cortical blindness

cortical resection

cortical-basal ganglionic degeneration

counselling

cryptococcal meningitis

cryptococcoma, cerebral

cyanosis

cytomegalovirus infection

deafness

deafness, bilateral

deafness, sudden

degenerative diseases of CNS

dementia

dementia, clinical diagnosis

dementia, differential diagnosis of

dementia, frontotemporal

dementia, presenile

demyelinating disease

dentate nuclei, lesion of

dermatoglyphics

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones, loss of

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

dichotic hearing

differential diagnosis

difficulty going down stairs

diffuse axonal injury

digits, abnormal

diplopia

diplopia, transient

disability, neurological

disconnection syndrome

disorientation

distal muscle weakness

dural sinus thrombosis

ears of the Lynx MR sign

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, video monitoring with

electromyogram

electron microscopy

encephalitis

encephalitis, human immunodeficiency virus type 1

encephalitis, viral

encephalomalacia

encephalopathy

encephalopathy, delayed

encephalopathy, post anoxic

ependymitis

episodic neurologic deficits

erectile dysfunction

exome sequencing

facial weakness

facial weakness, bilateral

finger nose finger test

finger tapping

fluorescein angiography

foot deformity

fornix

fornix, lesion of

fourth ventricle, floor

Fragile-X associated tremor/ataxia-syndrome

frontal lobe, behavior with disease of

frontal lobe, infarction

frontal lobe, lesion of

frontotemporal brain sagging syndrome

fundus, abnormality of

funduscopic exam

fungal infection, CNS

genetic neurologic disorders

genetic testing

genital ulcerations

genu of corpus callosum

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

headache, intermittent

headache, severe

hearing loss

hearing loss, bilateral

hearing loss, sudden, bilateral

hemifacial atrophy

hemiparesis

hemiparesis, transient

hemispherectomy

hepatic failure

hepatolenticular degeneration, non-Wilsonian

herpes simplex encephalitis

heterotopia

high arched feet

hippocampus, hyperintense

human immunodeficiency virus type 1

hydrocephalus

hydrocephalus, exvacuo

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hyperammonemic encephalopathy

iatrogenic neurologic disorders

imbalance

immunosuppression

immunosuppressive agents

impulsivity

inborn errors of metabolism

incoordination

infantile hemiplegia

intellectual deficit

intellectual deterioration

interpeduncular cistern, compressed

intracerebral hemorrhage

leg weakness, bilateral

lens, dislocation of

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

lethargy

leukodystrophy

leukoencephalitis, acute necrotizing hemorrhagic

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

level of consciousness, decreased

life support, withdrawal of

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

malformation, CNS, congenital

malformation, vascular, cerebral

mania

Marchiafava-Bignami disease

memory, defect of recent

memory, impairment of

memory, recent

meningeal enhancement

meninges

meningismus

meningitis

meningitis, lymphomatous

meningitis, neutrophilic

meningoencephalitis

mental retardation

mental status, abnormal

MERS

mesial temporal sclerosis

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

microangiopathy, brain

microangiopathy, retina

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, cerebrovascular disease

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, fetal

MRI, flow void, CSF

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, spinal cord, increased intramedullary cord signal

MRI, T1 weighted high signal foci

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, misdiagnosis

multiple sclerosis, relapsing

multiple subpial transection

myelopathy, chronic progressive

myelopathy, hepatic

myopathy

myopathy, necrotizing

myotonia congenita

myotonia dystrophica

nausea and vomiting

neoplasm, primary of CNS

nerve conduction studies

neuroaxonal leukodystrophy

neurolipidosis IV

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic signs

neuromuscular disease, electrodiagnosis of

neuronal migration disorder

neuropathology

neuropathy

neuropathy, demyelinating

neuroradiology

nutritional deficiency

nystagmus

obesity

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic nerve, hypoplasia of

optic neuropathy

optic neuropathy, nutritional

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

Parkinson disease

Parkinsonism syndrome

paroxysmal nonkinesigenic dyskinesia

photosensitivity, skin

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

POLR3B

polymerase chain reaction

polyneuropathy

polyradiculoneuropathy

posterior column disease

postural abnormality

premature infant

premature infant, problems in

prenatal

prepontine cistern, effaced

primary intracranial hypotension

prognosis

progressive hemifacial atrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

quadriparesis

quadriplegia, transient

quality of life

rapidly fatal neurologic illness

rapidly progressing neurologic illness

recurrent

respiratory failure

retinal artery occlusion

retinal branch artery occlusion

reversible neurologic disorder

reversible splenial lesion syndrome

scoliosis, neurologic association with

scotomata, scintillating

seizure

seizure, children

seizure, intractable

seizure, intractable, treatment of

seizure, neonatal

seizure, surgical treatment of

seizure, treatment of

sensorineural hearing loss

short stature

shunt procedure, ventricular

shunt procedure, ventricular-complications of

skin, biopsy

skin, lesions in neurologic disorders

small vessel disease

somnolence

spastic ataxia

spastic paraplegia, type 11

spastic paraplegia, type 15

spasticity

spinal cord, cervical

spinal cord, compression of

spinal cord, lesion of

splenium of corpus callosum

splenium of corpus callosum, displaced

spontaneous remission

stereotyped behavior

steroid therapy, CNS treatment and complications with

stiff legs

strokelike episodes

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

subdural hematoma

sulfite oxidase deficiency

superior cerebellar peduncle

superior sagittal sinus thrombosis

Susac's syndrome

symmetric brain lesions

sympathetic nervous system

syndactyly

systemic illness

systemic lupus erythematosus

tachycardia

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

temporal lobectomy

temporalis muscle wasting

term infant

thalamus, lesion of

thalamus, lesion of-bilateral

third ventricle, enlargement of

tinnitus

toe walking

tongue, ulcer

tonsillar herniation of cerebellum

toxoplasmosis, CNS

transependymal CSF migration

transient neurologic deficit

treatment of neurologic disorder

tremor

tremor, intention

trinucleotide repeats

ultrasonography, head

ultrasonography, head, fetus-neonate

ventricular enlargement

vision, failure of in childhood

visual acuity, decreased

walking, difficulty with

weakness

weakness, generalized

weight loss

wheelchair

white matter disease

white matter disease, periventricular

wide based gait

Wingspan study

word-finding difficulty

writing

x-linked mental retardation

Showing articles 350 to 400 of 2383 << Previous Next >>

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy
NEJM 381:164-172, Case 21-2019, 2019

A 17-year-old Baseball Player with Right Hand Weakness
Neurol 92:e76-e80, Vachon, C. & Libdeh, A.A., 2019

Subacute Progressive Sensorimotor Symptoms
BMJ 365:doi:10.1136/bmj.l1923, Francis, A.,et al, 2019

Intrathecal Administration of Autologous Mesenchymal Stem Cells in Multiple System Atrophy
Neurol 93:e77-e87, Singer, W.,et al, 2019

A 26-Year Old Man with Right Hand and Arm Weakness
Neurol 93:e927-e933, Elliott,E.J.&Smith,J.D., 2019

Bilateral Alopecia as Clue to Diagnosis of Gomez-Lopez-Hernandez Syndrome in a 38-Year-Old Man
Neurol 93:408-410, Kronlage,C.&Healy,D.G., 2019

Characteristic Head Jerks in Congenital Oculomotor Apraxia due to Joubert Syndrome
Neurol 93:e1125-e1126, Borngraber, F.,et al, 2019

Stridor in Multiple System Atrophy
Neurol 93:630-639, Cortelli, P.,et al, 2019

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

Limbic-Predominant Age-Related TDP-43 Encephalopathy (LATE): Consensus Working Group Report
Brain DOI: 10.1093/brain/awz099, Nelson, P.T.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

The Dangers of PRES
Neurol 92:e282-e285, Chaterine, C.,et al, 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

Bobblehead-Doll Syndrome
NEJM 380:e5, Sacks, C.A., 2019

A 40-Year-Old Woman Presenting with Distal Leg Weakness
Neurol 92:242-247, Fam, D.,et al, 2019

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

Acute Toxic Limbic Encephalopathy Following Glyphosate Intoxication
Neurol 92:534-536, Planche, V.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,et al, 2018

An 18-year-old man with progressive headache and visual loss
Neurol 90:1076-1081, Jiang, N.,et al, 2018

Multiple Sclerosis
NEJM 378:169-180, Reich, D.S.,et al, 2018

Deep Brain Nuclei T1 Shortening after Gadobenate Dimeglumine in Children: Influence of Radiation and Chemotherapy
AJNR 39:24-30, Kinner, S.,et al, 2018

A 60-year-old man with arm weakness and numbness
Neurol 90:190-196, Foster, L.A.,et al, 2018

Nusinersen Versus Sham Control in Later-Onset Spinal Muscular Atrophy
NEJM 378:625-635, Mercuri, E.,et al, 2018

Clinical Reasoning: A Teenager with Left Arm Weakness
Neurol 90:e907-e910, Al-Ghamdi, F.,et al, 2018

Fulminant Encephalopathy with Unusual Brain Imaging in Disulfiram Toxicity
Neurol 90:518-519, Peddawad, D.,et al, 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

Palatal tremor as a presenting symptom of amyotrophic lateral sclerosis
Neurol 90:801-802, Maghzi, A.,et al, 2018

A 30-year-old man with headache and sleep disturbance
Neurol 90:e1535-e1540, English, S.W.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Review of the Neurological Implications of von Hippel-Lindau Disease
JAMA Neurol 75:620-627, Dornbos, D.,et al, 2018

Transient swelling in the globus pallidus and substantia nigra in childhood suggests SENDA/BPAN
Neurol 90:974-976, Ishiyama, A.,et al, 2018

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 379:2452-2461, Case 39-2018, 2018

Hearing and Vision Loss in an Older Man
JAMA Neurol 75:1439-1440, Ho, V.M.,et al, 2018

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Postoperative Visual Loss After Anesthesia for Nonocular Surgery
UptoDate May, Lee, L.A. & Newman, N.J., 2018

A Fatal Case of Undiagnosed Candida Meningitis-Role of Computer-assisted Diagnosis
Neurologist 23:138-140, Finelli, P.F., 2018

Alexander Disease with Features of Both Frontal and Bulbospinal Involvement
Neurol 91:e396-e397, Nam,T-S.,et al, 2018

Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
www.UptoDate.com, May, Koralnik, I.J., 2018

IGG4-Related Hypertrophic Pachymeningitis Coexpressing Antineutrophil Cytoplasmic Antibodies
Neurol 4:e341-e343, Massey, J., 2017

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017

Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
NEJM 377:1723-1732,1786, Finkel, R.S.,et al, 2017

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

Cerebral White Matter Abnormalities in Patients with Charcot-Marie-Tooth Disease
Ann Neurol 81:147-151, Lee, M.,et al, 2017

Showing articles 350 to 400 of 2383 << Previous Next >>