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23 Nov 2009 
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Databases on the web - Neurology
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Database on the web
Description: Contains information on mutations associated with Alzheimer's Disease.
Subject areas: Medical genetics, Neurology

Database on the web
Description: Contains information on diseases and mutations associated with Adenylosuccinate Lyase.
Subject areas: Medical genetics, Neurology

Database on the web
Description: Contains information on mutations associated with Amyotrophic lateral sclerosis (SOD1, ALS and others).
Subject areas: Medical genetics, Neurology

Database on the web
Description: An unbiased and regularly updated collection of genetic association studies performed on Alzheimer disease phenotypes, containing studies published in peer-reviewed journals available in English.

Database on the web
Description: A repository of information about brain structures from different species. Contains to date four interrelated modules: Brain Parts (brain regions, major fiber tracts, and ventricles), Cell Types, Relations (between structures from different neuroanatomical atlases), and Connections.
Subject areas: Neuroscience, Neurology

Database on the web
Description: Database of expression in the developing human brain with 2D and 3D image data along with standard text data.
Content: Images, Expression, Curated

Database on the web
Description: Freely available bioscience images contributed by academics, researchers, Learned Societies, industry and individuals with rights cleared for educational purposes

Database on the web
Description: Contains information on mutations associated with Inherited Peripheral Neuropathies.
Subject areas: Medical genetics, Neurology

Database on the web
Description: Contains information on mutations and disorders associated with the L1CAM gene.
Subject areas: Medical genetics, Neurology

Database on the web
Description: Contains information on mutations assocated with Lowe Syndrome.

Database on the web
Description: A database of neurological microarray data.
Subject areas: Neurology, Neuroscience

Database on the web
Description: Contains information on mutations and disorders associated with the MECP2 gene causing Rett Syndrome.
Subject areas: Medical genetics, Neurology

Database on the web
Description: A human Lafora disease mutation database, including information on mutations in two genes causing Lafora disease: EPM2A on chromosome 6q24 and NHLRC1 (EPM2B) on chromosome 6p22.3.

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