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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 1200 to 1250 of 3637 << Previous Next >>

Dabigatran Challenges Warfarins Superiority for Stroke Prevention in Atrial Fibrillation
Stroke 41:1307-1309, Schwartz,N.E. &Albers,G.W., 2010

Optimal Screening Strategy for Familial Intracranial Aneurysms: A Cost-Effectiveness Analysis
Neurol 74:1671-1679, Bor,A.S.E., et al, 2010

Detection of Paroxysmal Atrial Fibrillation with Transtelephonic EKG in TIA or Stroke Patients
Neurol 74:1666-1670, 1662, e94, Gaillard,N., et al, 2010

Clincopath Conf, Pheochromocytoma
NEJM 362:1815-1823, Case 14-2010, 2010

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

Screening for Intracranial Aneurysms in Patients with Bicuspid Aortic Valve
Neurol 74:1430-1433, Schievink,W.I., et al, 2010

Diagnostic Accuracy of Confrontation Visual Field Tests
Neurol 74:1184-1190, Kerr,N.M., et al, 2010

Clinical Reasoning: Seizures in a Child With Sensorineural Deafness and Agitation
Neurol 74:e61-e63, Auvin,S., et al, 2010

Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
NEJM 362:1181-1191, Lupski,J.R., et al, 2010

Prolactinomas
NEJM 362:1219-1226, Klibanski,A., 2010

Clinical Spectrum of CADASIL and the Effect of Cardiovascular Risk Factors on Phenotype: Study in 200 Consecutively Recruited Individuals
Stroke 41:630-634, Adib-Samii,P., et al, 2010

Absence Epilepsies With Widely Variable Onset are a Key Feature of Familial GLUT1 Deficiency
Neurol 75:432-440, Mullen,S.A., et al, 2010

Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., et al, 2010

Familial Neuromyelitis Optica
Neurol 75:310-315, Matiello,M., et al, 2010

A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
Neurol 75:259-264, Herv�,D., et al, 2010

The Use of Neuroimaging in the Diagnosis of Mitochondrial Disease
Dev Disabil Res Rev 16:129-135, Friedman, S.D.,et al, 2010

Recent Insights into Cerebral Cavernous Malformations: The Molecular Genetics of CCM
FEBS J 277:1070-1075, Riant, F.,et al, 2010

The Floppy Infant: Evaluation of Hypotonia
Pediatrics in Review 30:e66-e76, Peredo, D. & Hannibal M., 2009

The Expanding Phenotype of GLUT1-Deficiency Syndrome
Brain & Dev 31:545-552, Brockmann,K., 2009

Acute Limbic Encephalitis and Glutamic Acid Decarboxylase Antibodies:A Reality?
J Neurosci 287:69-71, Blanc,F.,et al, 2009

Voltage-gated Potassium Channel-associated Limbic Encepahlitis in the West of Scotland:Case Reports and Literature Review
Scott Med J 54:27-31, Reid,J.M.,et al, 2009

Dabigatran Versus Warfarin in Patients with Atrial Fibrillation
NEJM 361:1139-1151, 1200, Connolly,S.,et al, 2009

Association of Parental Dementia With Cognitive and Brain MRI Measures in Middle-Aged Adults
Neurol 73:2071-2078, 2054, Debette,S.,et al, 2009

Enzyme Replacement Therapy With Agalsidase Alfa in Patients With Fabrys Disease: An Analysis of Registry Data
Lancet 374:1986-1996, 1950, Mehta,A.,et al, 2009

Limbic Encephalitis Associated With Antibodies to the NMDA Receptor in Hodgkin Lymphoma
Neurol 73:2039-2040, Zanid,M.S.,et al, 2009

Clinical and Mutational Spectrum of Neurofibromatosis Type 1-Like Syndrome
JAMA 302:2111-2118, 2150, 2170, Messian,L.,et al, 2009

Autism
Lancet 374:1627-1638, Levy,S.,et al, 2009

Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
AJNR 30:1971-1976, Uggetti,C.,et al, 2009

Autoimmune Targets of Heart and Skeletal Muscles in Myasthenia Gravis
Arch Neurol 66:1334-1338, 1322, Suzuki,S.,et al, 2009

Leukodystrophies: Classification, Diagnosis, and Treatment
Neurologist 15:319-328, Costello,D.,et al, 2009

Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
NEJM 360:1656-1665, Case 12-2009, 2009

Practice Parameter: Evaluation of the Child with Microcephaly (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
Neurol 73:887-897, Ashwal,S.,et al, 2009

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Cardiac Workup of Ischemic Stroke: Can We Improve Our Diagnostic Yield?
Stroke 40:2893-2898, Morris,J.G.,et al, 2009

Clinicopath Conf., Atypical Hemolytic-Uremic Syndrome
NEJM 361:389-400, Case 23-2009, 2009

Disclosure of APOE Genotype for Risk of Alzheimers Disease
NEJM 361:245-254,298, Green,R.C.,et al, 2009

Neurological Consequences of Atrioesophageal Fistula After Radiofrequency Ablation in Atrial Fibrillation
Arch Neurol 66:884-887, St�llberger,C.,et al, 2009

A Large-Scale International Meta-Analysis of Paraoxonase Gene Polymorphisms in Sporadic ALS
Neurol 73:16-24,11, Wills,A.-M.,et al, 2009

Current Status of Stroke Risk Stratification in Patients with Atrial Fibrillation
Stroke 40:2607-2610, Hart,R.G. &Pearce,L.A., 2009

Parkinsons Disease
Lancet 373:2055-2066, Lees,A.J.,et al, 2009

A Multidisciplinary Study of Patients with Early-Onset PD with and Without Parkin Mutations
Neurol 72:110-116,106, Lohmann,E.,et al, 2009

Genetic Aspects of Alzheimer Disease
The Neurologist 15:80-86, Williamson,J.,et al, 2009

A Multicenter, Prospective Pilot Study of Gamma Knife Radiosurgery for Mesial Temporal Lobe Epilepsy: Seizure Response, Adverse Events, and Verbal Memory
Ann Neurol 65:167-175, Barbaro,N.M.,et al, 2009

Diagnosis and New Treatment in Muscle Channelopathies
JNNP 80:360-365, Meola,G.,et al, 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and KCNJ10 Mutations
NEJM 360:1960-1970, Bockenhauer,D.,et al, 2009

Hippocampal Lesion Patterns in Acute Posterior Cerebral Artery Stroke: Clinical and MRI Findings
Stroke 40:2042-2045, Szabo,K.,et al, 2009

A 49-Year-Old Man with Contractures, Weakness, and Cardiac Arrhythmia
Neurol 72:2036-2043, Kissel,J.T.,et al, 2009

Neurofibromatosis Type 2
Lancet 373:1974-1986, Astagiri,A.R.,et al, 2009

Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
Neurol 73:430-437, Verhagen,M.M.M.,et al, 2009



Showing articles 1200 to 1250 of 3637 << Previous Next >>