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Differential
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Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adverse drug reaction
affect, inappropriate
akinetic mute
Alexanders disease
amniocentesis
asymptomatic
ataxia
attention deficit disorder with hyperactivity
auditory evoked brainstem potentials
Balint's syndrome
Bassen-Kornzweig syndrome
behavioral disorder
Binswanger disease
blindness
bone marrow transplantation
brain biopsy
brain scan, abnormal
calcification, intracranial
Canavan's disease
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, demyelinating disease
cataracts
cerebellar lesion
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
children
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
color vision
color vision, impaired
complications
conjunctival biopsy
corpus callosum, lesion of
cortical blindness
crying, pathologic
cultured skin fibroblasts
deafness
decerebrate posture
dementia
dementia, childhood
dementia, presenile
dementia, rapidly progressive
demyelinating disease
diet
DNA probes
drug induced neurologic disorders
dysarthria
dysarthria-clumsy hand syndrome
dysmorphic
dysphagia
dysphasia
dyspraxia
electroencephalogram, abnormalities of
electron microscopy
electronystagmography
electroretinograph
encephalopathy
enzyme, defect
epidemiology of neurology
erucic acid therapy
evoked potentials
familial
fatty acid, elevated plasma content
frontal lobe, pathologic signs of
fundus, abnormality of
gait disorder
gangliosidosis GM1
gangliosidosis, generalized
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
grasp reflex
Hallervorden Spatz disease
hearing loss
hearing problems in children
hepatomegaly
HMGcoA reductase inhibitors
hormone replacement
hyperpigmentation of skin
hyperreflexia
hypogonadism
hypotonia
impotence
inattention
inborn errors of metabolism
inclusion bodies
inclusion bodies, intracytopasmic
intellectual deterioration
Kearns-Sayre syndrome
Kluver-Bucy syndrome
Krabbe's disease
Laurence-Moon-Bardet-Biedl syndrome
leukemia
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
lipid storage disorder of CNS
Lorenzo's oil
lovastatin
macular degeneration
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
misdiagnosis
mitochondrial disease
mortality
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, demyelinating disease
MRI, spinal cord
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
muscular dystrophy
myelodysplasia
myelomalacia
myopathy, mitochondrial
myopia
nerve biopsy
nerve conduction studies
neuroaxonal dystrophy
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
Niemann-Pick disease
night blindness
oleic acid therapy
ophthalmoplegia, plus syndrome
optic atrophy
optic nerve
optic neuropathy
paraparesis
paraparesis, familial spastic
paraparesis, spastic
PAS positive
PAS positive material in the brain
Pelizaeus Merzbacher
peroxisomal disease
peroxisomes
personality change
pigmentary retinopathy
polyneuropathy
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
quadriparesis
refractive errors
Refsum's disease
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
seizure
seizure, neonatal
sensorineural hearing loss
skin, biopsy
skin, darkening of
somatosensory evoked potentials
spinal cord, lesion of
spinal cord, pathologic exam of
spinocerebellar degeneration
spongy degeneration of brain
steroid therapy, CNS treatment and complications with
symmetric brain lesions
tapetoretinal degeneration
temporal lobe, lesion
temporal lobe, lesion, bilateral
testicular atrophy
testicular biopsy
treatment of neurologic disorder
ultrasonography
urinary incontinence
Usher's syndrome
very long chain fatty acids
visual evoked response
visual field defect
visual loss
visual loss, slow
weight loss
white matter disease
white matter disease, unilateral
x-linked hydrocephalus
x-linked mental retardation
Showing articles 100 to 150 of 577 << Previous Next >>

Rosai-Dorfman Disease: Rare Presentation as Isolated Mediastinal and Hilar Lymphadenopathy
Cureus DOI 10.7759/cureus, Lateef, N.,et al, 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

An Older Man with Memory Impairment and Convulsions
BMJ 358:J2824, Zhao, X.,et al, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

CNS Cryptococcosis in HIV
eMedicine.com Nov 2017, Gliksman, F.J. & Singh, N.N., 2017

A 37-Year-Old Man with Multiple Cranial Neuropathies
Neurol 86:e66-e70, OLoghlen, S.,et al, 2016

Hydrocephalus in Children
Lancet 387:788-799, Kahle, K.T.,et al, 2016

Discriminating Long Myelitis of Neuromyelitis Optica from Sarcoidosis
Ann Neurol 79:437-447, Flanagan, E.P.,et al, 2016

Longitudinally Extensive Spinal Cord Lesions Disclosing Occult Systemic Sarcoidosis
JAMA Neurol 73:600-601, Sechi, E.,et al, 2016

Clinicopathologic Conference, Somnolence due to the Cerebral Fat Embolism Syndrome
NEJM 375:370-378, Case 23-2016, 2016

Central Nervous System Vasculitis in Rheumatoid Arthritis:A Case Report
JSM Arthritis 1:1005, Lagrutta,M.,et al, 2016

Corpus Callosum Splenium Hyperintensity in Fragile X-Associated Tremor Ataxia Syndrome
Neurol 84:e194, Renard, D.,et al, 2015

Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
JNNP 86:774-781, Van Egmond, M.E.,et al, 2015

Will Neuroimaging Reveal a Severe Intracranial Injury in this Adult with Minor Head Trauma?
JAMA 314:2672-2681,2629, Easter, J.S.,et al, 2015

Fat Embolism Syndrome: Case Report of a Clinical Conundrum
J Anaesthesiol Clin Pharmacol 30:412-414, Nandi, R.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Legionella
Adams & Victors Principles of Neurology, Chp 32, pg 709, Ropper, A.H.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Brain Abscess
Adams & Victors Principles of Neurology, Chp 32, pg 714, Ropper, A.H.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Sarcoidosis
Adams & Victors Principles of Neurology, Chp 32, pg 721, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Treatment of Langerhans Cell Histiocytosis
UptoDate Oct. 2014, McClain, K.L., 2014

Clinical Manifestations, Pathologic Features, and Diagnosis of Langerhans Cell Histiocytosis
UptoDate Oct. 2014, McClain, K.L., 2014

Nocardiosis of the Central Nervous System
Medicine 93:19-32, Anagnostou, T.,et al, 2014

Neurological Acro-Osteolysis
BMJ 348:g473, Mitchell, L.,et al, 2014

Unconscious Patient after Elective Bilateral Total Knee Arthroplasty
Stroke 45:e38-e39, Mustanoja, S.,et al, 2014

Newborn Screening for Fragile X Syndrome
JAMA Neurol 71:355-359, Tassone, F., 2014

Brain Mass with Hilar Adenopathy
Neurol 82:e161-e162, Jordan, J.T.,et al, 2014

Brugada Syndrome in Spinal and Bulbar Muscular Atrophy
Neurol 82:1813-1821, Araki, A.,et al, 2014

Mycoplasma Pneumoniae Infection: Neurologic Complications
www.MedLink.com, Oct, Greenlee, J.E., 2013

CNS-Immune Reconstitution Inflammatory Syndrome in the Setting of HIV Infection, Part 1: Overview and Discussion of Progressive Multifocal Leukoencephalopathy-Immune Reconstitution Inflammatory Syndrome and Cryptococcal-Immune Reconstitution Inflammatory Syndrome
AJNR 34:1297-1307, Post, M.J.D.,et al, 2013

Granulomatous Meningitis due to Rheumatoid Arthritis
Acta Neurol Belg 112:193-197, Duray, M.C.,et al, 2012

Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

Mystery Case: Hypoglossal Nerve Palsy in Occipito-Temporal Pneumatization
Neurol 79:e109-e110, Renard, D.,et al, 2012

Central Nervous System Aspergillosis
Medicine 91:328-336, Kourkoumpetis, T.,et al, 2012

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

Dopa-Responsive Dystonia Revisited
Arch Neurol 69:1558-1562, Tadic, V.,et al, 2012

Clinicopathologic Conference,Brain Abscess due to Toxoplasma and Advanced HIV Infection
NEJM 366:745-755, Case 6-2012, 2012

Clinicopathologic Conference, Rocky Mountain Spotted Fever
NEJM 366:1434-1443, Case 11-2011, 2012

Clinicopathologic Conference, Ileocolonic Intussusception Associated with Syncope (Neurologic Intussusception)
NEJM 366:1522-1536, Case 12-2012, 2012

Guillain-Barre syndrome associated with pulmonary tuberculosis
BMJ Case Reports DOI:10.1136/bcr-01-2012-5484, Taha, A.A. & Tee, K.H.A., 2012

When A Brain Lesion Necessitates Chest CT
Conn Med 75:143-146, Finelli,P.F., 2011

Blind, Breathless, and Paralysed from Benign Malaria
Lancet 377:438, Flower,B.,et al, 2011

An unusual cause of stroke and hypoxia
BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011

In-flight Seizures and Fatal Air Embolism
Arch Neurol 68:661-664, Arnaiz, J.,et al, 2011

Unexplained Hyponatremia: Seek and You Will Find
Nephron Physiol 118:66-71, Hoorn, E.J.,et al, 2011

Multiple Ring-Enhancing Lesions of the Brain
J Postgrad Med 56:307-316, Garg, R.K. & Sinha, M.K., 2010

Spinal Cord Sarcoidosis: Clinical and Laboratory Profile and Outcome of 31 Patients in a Case-Control Study
Medicine 89:133-140, Cohen-Aubart,F.,et al, 2010

Diagnostic Role of Target Lesion on Diffusion-WEighted Imaging, A Case of Cerebral Aspergillosis and Review of the Literature
Neurologist 16:364-367, Finelli,P.F.,et al, 2010

Pulmonary AVMs, including hereditary hemorrhagic telangiectasia: Diagnosis and Treatment
UpTo Date, August, Gossage, J.R., 2010

Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
NEJM 362:929-940, Case 7-2010, 2010

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009



Showing articles 100 to 150 of 577 << Previous Next >>