Neudle.com: neurodegeneration with brain iron accumulation

Differential
(Click to cross reference)

aceruloplasminemia

adrenoleukodystrophy

adverse drug reaction

akathisia

algorithm

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, guamian type of

anemia

anemia, iron deficiency

anticonvulsants

aspartate aminotransferase

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

bone marrow infarction

bone marrow necrosis

bradykinesia

Brueghel's syndrome

calcification, intracranial

Canavan's disease

carbamazepine

carbon monoxide poisoning

carotid angiogram

carotid artery disease

carotid artery occlusion, neck

carotid artery thrombus

carotid artery, intraluminal clot

CAT scan

CAT scan, abdomen

CAT scan, abnormal

CAT scan, false negative

cataracts

caudate nucleus

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

centrum semiovale

cerebellar degeneration

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral infarction, hemorrhagic

cerebral ischemia

cerebral venous thrombosis, deep

cerebro hepato renal syndrome

cerebrovascular accident

chromosomal abnormality

chromosome 20

cirrhosis

Clinical Pathologic Conference(C.P.C.)

copper metabolism, abnormal

cornea, opacification in infancy-causes of

corpus callosum, lesion of

degenerative diseases of CNS

dementia

dementia, childhood

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

developmental milestones, loss of

developmental retardation

diabetes mellitus

dialysis

differential diagnosis

disability rating scale, neurological

disability, neurological

disorientation

disseminated intravascular coagulation(DIC)

drug abuse, inhalation

drug induced neurologic disorders

dystonia musculorum deformens

dystonia, cervical

dystonia, symptomatic

dystonia, treatment of

electrical fields, alternating

electronystagmography

encephalopathy, delayed

encephalopathy, post anoxic

fundus, abnormality of

general paresis of the insane

genetic linkage

genetic neurologic disorders

genetic testing

gliosis

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

globus pallidus, stimulation

globus pallidus, swelling

GLUT1 deficiency syndrome

glutaric acidemia

gray matter

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

handwriting

headache

hemochromatosis

hemoglobin abnormality, neurologic complications of

hemophagocytic lymphohistiocytosis

hemophagocytosis

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

heralding manifestation

herpes virus infection

human immunodeficiency virus type 1

hypoxic encephalopathy

intellectual deterioration

intracerebral hemorrhage

iron, brain

iron, serum

iron, serum, elevated

iron, serum, low

Jakob-Creutzfeldt disease

Kearns-Sayre syndrome

lactic dehydrogenase(LDH)

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

lead poisoning

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leukodystrophy

leukoencephalopathy

level of consciousness, decreased

liver biopsy

liver disease

liver function enzymes

macular degeneration

magnetic susceptibility

maple syrup urine disease

McDonald criteria for MS

MELAS syndrome

memory, impairment of

mental retardation

mental status, abnormal

metachromatic leukodystrophy

methanol intoxication

methyl benzene

metronidazole

microhemorrhage, intracerebral

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, complications with

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion weighted

MRI, eye of tiger sign

MRI, field strength

MRI, field strength, high

MRI, gradient-echo

MRI, high signal intensity of basal ganglia

MRI, hypointense signal foci on

MRI, paramagnetic effect

MRI, starfield pattern

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRI, volumetry

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, diagnosis of

multiple sclerosis, early onset

multiple sclerosis, monosymptomatic

multiple sclerosis, plaque

multiple sclerosis, presenting manifestations

myoclonus

myoclonus, epilepsy

myopathy, mitochondrial

myopia

neoplastic angioendotheliosis

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neurodegeneration with brain iron accumulation

neurofibrillary degeneration

neurofibromatosis 1

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic signs

neuronal cell death

neuronal ceroid-lipofuscinosis

neuronal degeneration

neurons

neuropathology

neuropathology, brain

neuropathy

neuropathy, hereditary peripheral

paramagnetic rim lesion, MR

paranoia

parenteral alimentation

paresthesias

Parkinson disease

Parkinson disease, differential diagnosis of

Parkinson disease, familial

Parkinson disease, pathogenesis of

Parkinson disease, postencephalitic

Parkinsonism syndrome

pergolide

peroxisomal disease

pigmentary retinopathy

postural abnormality

practice guidelines

pramipexole

pregnancy, neurologic complications in

prognosis

progressive neurologic disorder

psychiatric disorder

psychiatric problems in neurologic disorders

pulvinar

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

refractive errors

Refsum's disease

respiratory failure

restless leg syndrome

sensorineural hearing loss

sickle cell crisis

sickle cell disease

skin, biopsy

skin, lesions in neurologic disorders

sleep

soluble interlukin 2 receptor

spastic diplegia

spasticity

speech disorder

speech disorder, childhood

spinocerebellar degeneration

splenomegaly

static encephalopaty of childhood with neurodegeneration in adulthood

Still's disease

stimulation, deep brain

striatal encephalitis

striatonigral degeneration

striatum, lesion of

striatum, lesion of, bilateral

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

subcortical U fibers

subependymal nodules

substantia nigra

symmetric brain lesions

syphilis, neurologic complications with

systemic illness

tapetoretinal degeneration

thalamus

thalamus, atrophy of

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

thrombocytosis

treatment of neurologic disorder

uremic encephalopathy

visual acuity, decreased

visual evoked response

visual field defect

visual impairment

visual loss

walking, difficulty with

weakness

white matter disease

white matter disease, periventricular

workup

Showing articles 50 to 100 of 16256 << Previous Next >>

Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
Ann Neurol 24:692-694, Sethi,K.D.,et al, 1988

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
Neurol 38:154-155, Tennison,M.B.,et al, 1988

MR Imaging in a Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 11:1057-1058, Tanfani,G.,et al, 1987

Magnetic Resonance Imaging in Multiple Sclerosis:Decreased Signal in Thalamus & Putamen
Ann Neurol 22:546-550, Drayer,B.P.,et al, 1987

Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism
Neurol 35:227-234, Jankovic,J.,et al, 1985

MR Imaging of Hallervorden-Spatz Disease
J Comput Assist Tomogr 9:491-493, Littrup,P.J.,et al, 1985

Hallervorden-Spatz Disease:Cysteine Accumulation & Cysteine Dioxygenase Deficiency in the Globus Palladus
Ann Neurol 18:482-489, Perry,T.L.,et al, 1985

Computed tomography in Hallervorden-Spatz disease
Neurol 30:1128-1130, Dooling,E.C.,et al, 1980

Alzheimer Neurofibrillary Tangles in Diseases Other Than Senile & Presenile Dementia
Ann Neurol 5:288-294, Wisniewski,K.,et al, 1979

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

Neuro CPC of MGH
Metachromatic Leukodystrophy, NEJM 267:1198-12041962., , 1962

Multiple Giant Perivascular Spaces in Hypomelanosis of Ito
Ann Neurol 99:825-826, Chammas,D.E.,et al, 2026

Creutzfeldt-Jakob-Like Presentation in Anti-AMPAR Encephalitis
Ann Neurol 99:1466-1467, Durbano,K.et al, 2026

Safety and Outcomes of Dibigatran Reversal with Idarucizumab Before IV Thrombolysis in Patients with Acute Ischemic Stroke
Neurol 106:e218012, Saflund,M.,et al, 2026

Cerebral Syphilitic Vasculitis Presenting with Recurrent Stroke
Stroke 57:e197-e198, Yilmaz,E.,et al, 2026

Unilateral Primary Angiitis of the Central Nervous System: A Rare and Under-Recognized Entity
AJNR 47:589-595, Rai,P.,et al, 2026

Brain CT for Diagnosis of Intracranial Disease in Ambulatory Patients with Cancer:Assessment of the Diagnostic Value of Scanning without Contrast Prior to With Contrast
AJNR 47:694-698, Wang,E.,et al, 2026

Zorevunersen in Children and Adolescents with Dravet Syndrome
NEJM 394:969-982, Laux,L.,et al, 2026

Niemann-Pick Type C Disease
www.UpToDate.com, Nov, Schiffmann, R., 2026

Association of Changes in Activity Patterns with Brain Atrophy and Disability Progression in People with Multiple Sclerosis
Neurol 106:e214678, e214742, Fitzgerald,K.C.,et al, 2026

Using Susceptibility-Based Imaging in Highly Active Late-Onset Multiple Sclerosis
Neurol 106:e214794, Sosa,S.M.,et al, 2026

A 49-Year-Old Man with Meningoencephalitis and Persistent Altered Mental Status
Neurol 106:e214777, Hariswar,P.T.,et al, 2026

Multiple Giant Perivascular Spaces in Hypomelanosis of Ito
Ann Neurol 99:825-826, Chammas,D.E.,etal, 2026

Iatrogenic Cerebral Amyloid Angiopathy after Cardiac Surgery, Two Case Reports
Neurol 106:e214819, Brunet de Courssou,J-B.,et al, 2026

Clinical Manifestations of Primary CNS T-Cell Lymphoma, Retrospective Study of Histopathologic, Molecular, and Neuroimaging Fetures
Neurol 106:e24744, Muller,K.J.,et al, 2026

A 52-Year Old Man with Acute-Onset Blindness
Neurol 106:e214827, Brown,A.M.,et al, 2026

Frequency of AQP4 and MOG Antibodies in Patients with Optic Neuritis Fulfilling Minimal New Multiple Sclerosis MRI Criteria
Neurol 106:e214753, Deschamps,R.,et al, 2026

Patterns and Factors Associated with Cerebral Infarction on MRi in Tuberculous Meningitis: Secondary Anlysis of the ACT-TBM Trial
Stroke 57:856-864, Chandu,M.,et al, 2026

Syphilis as an Important Modern-Day Risk Factor for Intracranial Vasculopathy and Ischemic Stroke:A Teaching Case
Stroke 57:e108-e111, Higham-Kessler,C.,et al, 2026

Ribbon-Like Sign in Convexity Subarachnoid Hemorrhage
Ann Neurol 99:881-882, Liu,S-X.,et al, 2026

Minimally Invasive Surgery Versus Open Craniotomy with Clot Evacuation after Intracerebral Hemorrhage
Ann Neurol 99:871-880, Murthy, S.B.,et al, 2026

Case Fatality of Subarachnoid hemorrhge by Aneurysm Location
Neurol 106:e214918, Asikinen,.,et al, 2026

Using Susceptibility-Based Imaging in highly ctive Late-Onset Multiple Sclerosis
Neurol 106:e214794, Sosa,S.M.,et al, 2026

Asundexian for Secondary Stroke Prevention
NEJM 394:1467-1479, 1540, Sharm,M.,et al, 2026

Bilateral Posterior Limb Internal Capsule T2 Hyperintensity and Severe Cerebellar Atrophy in 2 Lifelong Friends
Neurol 106:e218014, Inoue,H.,et al, 2026

Deep Venous Dural Arteriovenous Fistula Mimicking Progressive Dementia
Stroke 57:e180-181, Langlois-Therien,T.,et al, 2026

Dental Flossing May Lower the Risk for Incident Ischemic Stroke, Cardioembolic Stroke Subtype, and Atrial Fibrillation
Stroke 57:1275-1282, Sen,S.,et al, 2026

Status Epilepticus After Carotid Endarterectomy:An Illustrative Case of Cerebral Hyperfusion Syndrome
Stroke 57:e188-191, Reuter,P.,et al, 2026

Syphilitic Aortitis Presenting as Aortic Arch Thrombus and Acute Ischemic Stroke
Neurol 106:e214868, Ferro,J.,et al, 2026

Cerebral Amyloid Angiopathy
NEJM 394:1836-1845, Greenberg,S.M., 2026

Endovascular Therapy for Medium-Vessel Occlusion Stroke - Narrowing the Target Population
NEJM 394:1955-1957,1894, Ospel,J.M. & Hill, M.D., 2026

A 28-Year-Old Man with Seizures and Thalamic Lesions
Neurol 106:e218065, Santos-Rojo,A.B.,et al, 2026

A 35-Year-Old Patient with Rapidly Progressive Ascending Weakness Leading to Loss of Brainstem Reflexes
Neurol 106:e218059, Lyons,H.J.,et al, 2026

A Woman with Parkinson Disease, Dyskinesia, Rhadomyolysis, Subcutaneous Emphysema, and Pneumomediastinum
Neurol 106:e218064, Iqbal,M.M.,et al, 2026

Autoimmune Encephalitis as Treatment-Responsive Cause of Rapidly Progressive Dementia
Neurol 106:e214933, van Steenhoven,R.W.,et al, 2026

A 32-Year-Old Woman with Progressive Vision Loss and Confusion
Neurol 106:e214988, Kumar,A.B.,et al, 2026

Congenital Zika Syndrome
NEJM 394:e2, Bacin,F. & Montenegro,M.A., 2026

Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
Stroke 57:148-156, Mania-Paris,L.,et al, 2026

Showing articles 50 to 100 of 16256 << Previous Next >>