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Differential
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aceruloplasminemia
adrenoleukodystrophy
adverse drug reaction
akathisia
algorithm
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, guamian type of
anemia
anemia, iron deficiency
anticonvulsants
aspartate aminotransferase
ataxia
ataxia, cerebellar
axonal spheroid
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
behavioral disorder
biologic markers
blood transfusion
bone marrow biopsy
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
ceruloplasmin, serum
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 20
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clonazepam
Cockayne's syndrome
cognition
coma
compression fracture
confusion
consanguinity
copper deficiency
copper metabolism, abnormal
cornea, opacification in infancy-causes of
corpus callosum, lesion of
cortical blindness
cyanide poison
deafness
deep gray nuclei
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)
diurnal variation
DNA probes
dopamine agonist
dopaminergic neurons
drug abuse
drug abuse, inhalation
drug induced neurologic disorders
dysarthria
dysphagia
dyspnea
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, symptomatic
dystonia, treatment of
electrical fields, alternating
electronystagmography
electroretinograph
embolism, fat
encephalitis
encephalopathy
encephalopathy, delayed
encephalopathy, post anoxic
enzyme, defect
equinovarus
Fahr disease
familial
ferritin, elevated
ferritinemia
fever
fundus, abnormality of
gabapentin
gadolinium
gait disorder
gene
gene mutation
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)
herpes virus infection
human immunodeficiency virus type 1
hydrocephalus
hyperactivity
hyperreflexia
hypoxia
hypoxic encephalopathy
imbalance
infection
insomnia
intellectual deficit
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
MELAS syndrome
memory, impairment of
mental retardation
mental status, abnormal
metachromatic leukodystrophy
methanol intoxication
methyl benzene
metronidazole
microhemorrhage, intracerebral
midbrain
midbrain, lesion of
mineralization
mongolism
mortality
Motor Band Sign
motor neuron disease
movement disorder
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, plaque
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
neurosyphilis
neurotoxic
neurotoxin
night blindness
normal
opiate
optic atrophy
optic nerve
optic neuropathy
osteoporosis
pain
pain, leg
palilalia
PANK2 mutation
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
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
rigidity
rituximab
ropinirole
Schilder's disease
sea-blue histiocytes
seizure
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
tremor
tuberous sclerosis
unconsciousness
undiagnosed
uremic encephalopathy
urinary incontinence
Usher's syndrome
viral infection
viral infection, CNS
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 0 to 50 of 15713 Next >>

Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
Ann Neurol 87:10-11, Van Samkar, A.,et al, 2020

Clinicopathologic Conference,Aceruloplasminemia, Hereditary
NEJM 383:1974-1983, Case 35-2020, 2020

Fat Embolism Syndrome in Sickle Cell Disease
J Clin Med 9:1-12, Tsitsikas, D.A.,et al, 2020

"Motor Band Sign" in Susceptibility-Weighted Imaging in Motor Neuron Disease
Ann India Acad Neurol 23:821-822, Prabhu,A.N., 2020

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

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

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
AJNR 38:1467-1474, Bond, K.M.,et al, 2017

Intracranial Lesions with Low Signal Intensity on T2-Weighted MR Images - Review of Pathologies
Pol J Radiol 80:40-50, Zimny, A.,et al, 2015

An Unusual Case of Adult-Onset Stills Disease with Hemophagocytic Syndrome, Necrotic Leukoencephalopathy and Disseminated Intravascular Coagulation
Case Reports Rheum Article ID 128623, Namas, R.,et al, 2014

The Thalamus and Multiple Sclerosis
Neurol 80:210-219, Minagar, A.,et al, 2013

Assessing Abnormal Iron Content in the Deep Gray Matter of Patients with Multiple Sclerosis verus Healthy Controls
AJNR 33:252258, Habib,C.A.,et al, 2012

Random skin biopsy and bone marrow biopsy for diagnosis of intravascular large B cell lymphoma
Ann Hematol 90:417-421, Matsue, K.,et al, 2011

Mineralization of the Deep Gray Matter with Age: A Retrospective Review with Susceptibility-Weighted MR Imaging
AJNR 29:176-183, Harder,S.L.,et al, 2008

T2* and FSE MRI Distinguishes Four Subtypes of Neurodegeneration With Brain Iron Accumulation
Neurol 70:1614-1619, McNeill,A.,et al, 2008

Gray Matter Involvement in Multiple Sclerosis
Neurol 68:634-642, Pirko,I.,et al, 2007

Individual Dopaminergic Neurons Show Raised Iron Levels in Parkinson Disease
Neurol 68:1820-1825, Oakley,A.E.,et al, 2007

Quantitative Assessment of Iron Accumulation in the Deep Gray Matter of Multiple Sclerosis by Magnetic Field Correlation Imaging
AJNR 28:1639-1644, Ge,Y.,et al, 2007

The "Eye-of-the-Tiger" Sign is Not Pathognomonic of the PANK2 Mutation
Arch Neurol 63:292-293, Kumar,N.,et al, 2006

Restless Legs Syndrome: Is Treatable But Under-Recognised
BMJ 333:457-458, Medcalf,P. &Bhatia,K.P., 2006

Pallidal Stimulation Improves Pantothenate Kinase-Associated Neurodegeneration
Ann Neurol 57:738-741,613, Castelnau,P.,et al, 2005

MRI T2 Hypointensity of the Dentate Nucleus is Related to Ambulatory Impairment in Multiple Sclerosis
J Neurol Sci 234:17-24, Tjoa,C.W.,et al, 2005

Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003

Restless Legs Syndrome
NEJM 348:2103-2109, Earley,C.J., 2003

Diagnostic Approach in Patients with Symmetric Imaging Lesions of the Deep Gray Nuclei
The Neurologist 9:250-261, Finelli,P.F.&DiMario,Jr,F.J., 2003

T2 Hypointensity in the Deep Gray Matter of Patients With Multiple Sclerosis
Arch Neurol 59:62-68, Bakshi,R.,et al, 2002

Reduced Signal Intensity of T2 Weighted MR Imaging of Thalamus and Putamen in Multiple Sclerosis in Japan
Rinsho Shinkeigaku 40:677-682, Nishii,T.,et al, 2000

Hyperintense Basal Ganglia on T1-Weighted MR Imaging
AJR 172:1109-1115, Lai,P.H.,et al, 1999

Atypical MRI Features of Wilson's Disease:High Signal in Globus Pallidus on T1-Weighted Images
Neuroradiology 39:171-174, Mochizuki,H.,et al, 1997

Clinicopath Conf
Genetic Hemochromatosis, Micronodular Cirrhosis of Liver, Case 10-1997, NEJM 336:939-94797., , 1997

MRI In Patients with General Paresis
Neuroradiology 38:120-123, Zifko,U.,et al, 1996

Carotid Artery Thrombus Associated with Severe Iron-Deficiency Anemia and Thrombocytosis
Stroke 27:1002-1005, Akins,P.T.,et al, 1996

MRI of the Brain in Wilson Disease:T2 Signal Loss Under Therapy
J Comput Assist Tomogr 19:635-638, Engelbrecht,V.,et al, 1995

Magnetic Resonance Imaging of Brain Iron in Health and Disease
J Neurol Sci 134:19-26,1, Vymazal,J.,et al, 1995

Iron-Related Damage in Acute Ischemic Stroke
Stroke 25:1543-1546, Davalos,A.,et al, 1994

T2 Relaxation Time in Patients with Parkinson's Disease
Neurol 43:697-700, Antonini,A.,et al, 1993

Amyotrophic Lateral Sclerosis:T2 Shortening in Motor Cortex at MR Imaging
Radiology 189:843-846, Oba,H.,et al, 1993

Toluene Abuse Causing Reduced MR Signal Intensity in the Brain
AJR 161:1259-1261, Caldemeyer,K.S.,et al, 1993

Hallervorden-Spatz Disease with Bilat Invol of Globus Pallidus & Substantia Nigra:MR Demonstra
J Comput Assist Tomogr 17:961-963, Porter-Grenn,L.,et al, 1993

Atypical MR Presentation of Wilson Disease:A Possible Consequence of Paramagnetic Effect of Copper
Neuroradiology 34:222-224, Brugieres,P.,et al, 1992

Delayed Encephalopathy after Acute Carbon Monoxide Intoxication:MR Imaging Features & Cerebral White Matter Lesions
Radiology 184:117-122, Chang,K.H.,et al, 1992

Biological Significance of Iron-Related Magnetic Resonance Imaging Changes in the Brain
Arch Neurol 49:711-717, Pujol,J.,et al, 1992

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Follow-up MR STudies in Hallervorden-Spatz Disease
J Comput Assist Tomogr 14:118-120, Gallucci,M.,et al, 1990

Striatonigral Degeneration:Clinical, MRI, & Pathologic Correlation
Neurol 40:710-711, O'Brien,C.,et al, 1990

MR Findings in Meige Syndrome
J Comput Assist Tomogr 13:116-118, Piazza,P.,et al, 1989

Magnetic Resonance Imaging in Pathologically Proven Hallervorden-Spatz Disease
Neurol 39:440-442, Schaffert,D.A.,et al, 1989

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



Showing articles 0 to 50 of 15713 Next >>