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Differential
(Click to cross reference)
Albright disease
arachnoid granulation
arachnoid granulation, giant
asymptomatic
basal ganglia, calcification of
basal ganglia, lesion of
Bence Jones protein
bitemporal visual field defect
bone marrow biopsy
bone survey
brain atrophy
brain scan, abnormal
brainstem, lesion of
calcification, intracranial
carcinoma
carcinoma of breast
CAT scan
CAT scan, abnormal
CAT scan, base of skull
CAT scan, skull bone changes
cataracts
central retinal vein occlusion
cerebellar lesion
children
choroid plexus, abnormality of
Clinical Pathologic Conference(C.P.C.)
clivus
Cockayne's syndrome
cornea, opacity of
cranial neuropathy, multiple
deafness
dentate nuclei, lesion of
developmental retardation
diabetes insipidus
diabetes mellitus, neurologic manifestations of
dural venous sinus
dwarfism
dysmorphic
dysphagia
ear, abnormal
ear, pain in
epistaxis
epistaxis, recurrent
facial nerve palsy
facial nerve palsy, recurrent
fatigue
fibrous dysplasia
fibrous dysplasia of orbit
fundus, abnormality of
gene
genetic neurologic disorders
Hand-Schuller-Christian disease
headache
headache, severe
hearing loss
heralding manifestation
hyperpigmentation of skin
hyperviscosity
hyperviscosity syndrome
hypothalamus, lesion of
intellectual deficit
jugular foramen syndrome
lymphangiomatosis
lymphoma
malignant external otitis
mastoid opacification
meningeal enhancement
meningeal gliomatosis
meninges
meningioma
meningioma, intraosseous
meningitis
meningitis, bacterial
meningitis, pseudomonas
meningitis, recurrent
mental retardation
metastasis to bone
microcephaly
misdiagnosis
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, FLAIR
MRI, incidental finding
MRI, mass effect on
MRI, skull bone changes
multiple myeloma
neoplasm, intracranial with metastasis extracranially
neoplasm, metastatic to CNS
neoplasm, pituitary
neoplasm, primary intracerebral
neoplasm, primary of CNS
neurofibromatosis 1
neuropathology, brain
oligodendroglioma
optic atrophy
osteoblastic lesions, causes of
osteolytic lesion, causes of
otitis, neurologic complications with
otorrhea, cerebrospinal fluid
photosensitivity, skin
pineal
pituitary stalk
pituitary, adenoma
pituitary, enlargement
pituitary, lesion of
plasmacytoma
pleocytosis of cerebrospinal fluid
pons, lesion of
precocious puberty
primary leptomeningeal gliomatosis
prolactinoma
pseudarthrosis
pseudomonas aeruginosa
pupil, abnormality in neurologic disorders
radiation therapy, CNS treatment and complications with
review article
sarcoidosis
sarcoidosis, CNS
scoliosis
scotoma, central
sedimentation rate, elevated
seizure
sella turcica, enlargement of
sinus, neoplasm of
sinuses, diseases of
skull bone, erosion
skull x-ray
skull x-ray, abnormal
skull x-ray, bony defect on
skull, metastatic carcinoma to
symmetric brain lesions
temporal bone, metastasis to
treatment of neurologic disorder
Virchow-Robin spaces, dilated
visual acuity, decreased, monocular
visual loss
visual loss, slow
visual loss, slow-unilateral
Showing articles 1700 to 1750 of 3637 << Previous Next >>

Syncope
NEJM 343:1856-1862, Kapoor,W.N., 2000

Adverse Cardiovascular and Central Nervous System Events Associated with Dietary Supplements Containing Ephedra Alkaloids
NEJM 343:1833-1838,1886, Haller,C.A. & Benowitz,N.L., 2000

Gray Matter Heterotopia
Neurol 55:1603-1608, Barkovich,A.J. & Kuzniecky,R.I., 2000

The Value of Informant Versus Individual's Complaints of Memory Impairment in Early Dementia
Neurol 55:1724-1726, Carr,D.B.,et al, 2000

Conjugal Multiple Sclerosis: Population-Based Prevalence and Recurrence Risks in Offspring
Ann Neurol 48:927-931, Evers,G.C.,et al, 2000

Prevention of Ischaemic Stroke
BMJ 321:1455-1459, Gubitz,G. & Sandercock,P., 2000

De Novo Mutation in the Notch3 Gene Causing CADASIL
Ann Neurol 47:388-391, Joutel,A.,et al, 2000

Familial Form of Intracranial Cavernous Angioma:MR Imaging Findings in 51 Families
Radiology 214:209-216, Brunereau,L.,et al, 2000

Association Between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene
NEJM 342:1560-1567, Lucking,C.B.,et al, 2000

Occupational Exposure to Methyl Isobutyl Ketone Causes Lasting Impairment in Working Memory
Neurol 54:1853-1855, Grober,E.&Schaumburg,H.H., 2000

National Institutes of Health Consensus Conference: Tuberous Sclerosis Complex
Arch Neurol 57:662-665, Hyman,M.H.&Whittemore,V.H., 2000

Angiographic and Clinical Characteristics of Patients with Cerebral Arteriovenous Malformations Associated with Hereditary Hemorrhagic Telangiectasia
AJNR 21:1016-1020, Matsubara,S.,et al, 2000

Anticoagulation for Chronic Atrial Fibrillation
JAMA 283:2901-2903, Stern,S.,et al, 2000

Amnesia Due to Fornix Infarction
Stroke 31:1418-1419, Moudgil,S.S.,et al, 2000

A Locus for Paroxysmal Kinesigenic Dyskinesia Maps to Human Chromosome 16
Neurol 54:125-130, Bennett,L.B.,et al, 2000

Amnesic Syndrome with Bilateal Mesial Temporal Lobe Involvement in Hashimoto's Encephalopathy
Neurol 54:737-739, McCabe,D.J.H.,et al, 2000

The Brain Code in Health and Disease
Arch Neurol 57:50-51, Rosenberg,R.N., 2000

Autosomal Dominant Diffuse Leukoencephalopathy with Neuroaxonal Spheroids
Neurol 54:463-468, van der Knaap,M.S.,et al, 2000

Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
Ann Neurol 47:152-161, 143, Flanigan,K.M.,et al, 2000

Amyotrophic lateral Sclerosis Mimic Syndromes, A Population-Based Study
Arch Neurol 57:109-113, Traynor,B.J.,et al, 2000

Risk of Subarachnoid Haemorrhage in First Degree Relatives of Patients with Subarachnoid Haemorrhage: Follow Up Study Based on National Registries in Denmark
BMJ 320:141-145, Gaist,D.,et al, 2000

An 80-Year-Old Man With Memory Loss
JAMA 283:1046-1053, Larson,E.B., 2000

Desmin Myopathy, a Skeletal Myopathy with Cardiomyopathy Caused by Mutations in the Desmin Gene
NEJM 342:770-780, Dalakas,M.C.,et al, 2000

Decision Analysis and Guidelines for Anticoagulant Therapy to Prevent Stroke in Patients with Atrial Fibrillation
Lancet 355:956-962, Thomson,R.,et al, 2000

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000

Cytomegalovirus Ventriculoencephalitis Presenting as a Wernicke's Encephalopathy-like Sydrome
Neurol 55:1910-1913, Torgovnick,J.,et al, 2000

Distribution of Cranial MRI Abnormalities in Patients with Symptomatic and Subclinical CADASIL
BJR 73:256-265, Coulthard, A.,et al, 2000

Familial Neuromyelitis Optica (Devics Syndrome) with Late Onset in Japan
Neurol 55:318-320, Yamakawa,K.,et al, 2000

Bicuspid Aortic Valve - A Silent Danger: Analysis of 50 Cases of Infective Endocarditis
Clin Inf Dis 30:336-341, Lamas, C.C. & Eykyn, S.J., 2000

Seizures and Creutzfeldt-Jakob Disease
NCMJ 60:108-109, Cokgor,I.,et al, 1999

Distal Myopathies:Clinical and Molecular Diagnosis and Classification
JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999

Visual Field Defects Associated with Vigabatrin Therapy
JNNP 67:716-722, Lawden,M.C.,et al, 1999

MR Angiography as a Screening Tool for Intracranial Aneurysms:Feasibility, Test Characteristics, and Interobserver Agreement
AJR 173:1469-1475, Raaymakers,T.W.M.,et al, 1999

Diagnosis and Treatment of Wilson's Disease
Semin Neurol 19:261-270, Brewer,G.J.,et al, 1999

Ion Channel Diseases:Episodic Disorders of the Nervous System
Semin Neurol 19:363-369, Ptacek,L.J., 1999

Musculoskeletal and Neurologic Outcomes in Patients with Previously Treated Lyme Disease
Ann Int Med 131:919-926, Shadick,N.A.,et al, 1999

Fetal Surgery for Myelomeningocele, Promise, Progress, and Problems
JAMA 282:1873-1874,1819,1826, Simpson,J.L., 1999

Neural-Tube Defects
NEJM 341:1509-1519,1485, Botto,L.D.,et al, 1999

Antiepileptic Drug Regimens and Major Congenital Abnormalities in the Offspring
Ann Neurol 46:739-746, Samren,E.B.,et al, 1999

A Locus for Febrile Seizures (FEB3) Maps to Chromosome 2q23-24
Ann Neurol 46:671-678, Peiffer,A.,et al, 1999

Localization of a Gene for Myoclonus-Dystonia to Chromosome 7q21-q31
Ann Neurol 46:794-798, Nygaard,T.G.,et al, 1999

Genetic Localization of the Familial Adult Myoclonic Epilepsy (FAME) Gene to Chromosome 8q24
Neurol 53:1180-1183, Plaster,N.M.,et al, 1999

Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999

Autosomal Dominant Myofibrillar Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy Linked to Chromosome 10q
Ann Neurol 46:684-692,681, Melberg,A.,et al, 1999

The Roussy-Levy Family:From the Original Description to the Gene
Ann Neurol 46:770-773, Plante-Bordeneuve,V.,et al, 1999

Coma in a Park
Lancet 354:1090, Pilz,B.,et al, 1999

Recurrent Orbital Myositis,Report of a Familial Incidence
Arch Neurol 56:1407-1409, Maurer,I.&Zierz,S., 1999

Factors Associated with Ischemic Stroke During Aspirin Therapy in Atrial Fibrillation, Analysis of 2012 Participants in the SPAF-I-III Clinical Trials
Stroke 30:1223-1229, Hart,R.G.,et al, 1999

Risk Assessment and Anticoagulation for Primary Stroke Prevention in Atrial Fibrillation
Stroke 30:1218-1222, Kalra,L.,et al, 1999

Familial Paroxysmal Dystonic Choreoathetosis,Clinical Findings in a Large Japanese Family and Genetic Linkage to 2q
Arch Neurol 56:721-726, Matsuo,H.,et al, 1999



Showing articles 1700 to 1750 of 3637 << Previous Next >>