HHT diagnosis by Mid-infrared spectroscopy and artificial neural network analysis

BACKGROUND: The vascular disorder Hereditary Hemorrhagic Telangiectasia (HHT) is in general an inherited disease caused by mutations in the TGF-β/BMP receptors endoglin or ALK1 or in rare cases by mutations of the TGF-β signal transducer protein Smad4 leading to the combined syndrome of juvenile pol...

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Detalles Bibliográficos
Autores principales: Lux, Andreas, Müller, Ralf, Tulk, Mark, Olivieri, Carla, Zarrabeita, Roberto, Salonikios, Theresia, Wirnitzer, Bernhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3698163/
https://www.ncbi.nlm.nih.gov/pubmed/23805858
http://dx.doi.org/10.1186/1750-1172-8-94

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3698163/
https://www.ncbi.nlm.nih.gov/pubmed/23805858
http://dx.doi.org/10.1186/1750-1172-8-94

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