Sequential decisions on FAS sequencing guided by biomarkers in patients with lymphoproliferation and autoimmune cytopenia

Clinical and genetic heterogeneity renders confirmation or exclusion of autoimmune lymphoproliferative syndrome difficult. To re-evaluate and improve the currently suggested diagnostic approach to patients with suspected FAS mutation, the most frequent cause of autoimmune lymphoproliferative syndrom...

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Hlavní autoři: Rensing-Ehl, Anne, Janda, Ales, Lorenz, Myriam R., Gladstone, Beryl P., Fuchs, Ilka, Abinun, Mario, Albert, Michael, Butler, Karina, Cant, Andrew, Cseh, Anna-Maria, Ebinger, Martin, Goldacker, Sigune, Hambleton, Sophie, Hebart, Holger, Houet, Leonora, Kentouche, Karim, Kühnle, Ingrid, Lehmberg, Kai, Mejstrikova, Ester, Niemeyer, Charlotte, Minkov, Milen, Neth, Olaf, Dückers, Gregor, Owens, Stephan, Rösler, Joachim, Schilling, Freimut H., Schuster, Volker, Seidel, Markus G., Smisek, Petr, Sukova, Martina, Svec, Peter, Wiesel, Thomas, Gathmann, Benjamin, Schwarz, Klaus, Vach, Werner, Ehl, Stephan, Speckmann, Carsten
Médium: Artigo
Jazyk:Inglês
Vydáno: Ferrata Storti Foundation 2013
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3856970/
https://ncbi.nlm.nih.gov/pubmed/23850805
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2012.081901
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