dc.contributor.author | Winkelmann, Juliane | |
dc.contributor.author | Levy-Lahad, Ephrat | |
dc.contributor.author | King, Mary-Claire | |
dc.contributor.author | Anikster, Yair | |
dc.contributor.author | Sener, Elif F. | |
dc.contributor.author | Schormair, Barbara | |
dc.contributor.author | Zeligson, Sharon | |
dc.contributor.author | Marek-Yagel, Dina | |
dc.contributor.author | Strom, Tim M. | |
dc.contributor.author | Shohat, Mordechai | |
dc.contributor.author | Singer, Amihood | |
dc.contributor.author | Rubinow, Alan | |
dc.contributor.author | Pras, Elon | |
dc.contributor.author | Tekin, Mustafa | |
dc.contributor.author | Padeh, Shai | |
dc.contributor.author | Zlotogorski, Abraham | |
dc.contributor.author | Berkun, Yackov | |
dc.contributor.author | Press, Joseph J. | |
dc.contributor.author | Mukamel, Masha | |
dc.contributor.author | Voth, Isabel | |
dc.contributor.author | Hashkes, Philip J. | |
dc.contributor.author | Harel, Liora | |
dc.contributor.author | Hoffer, Vered | |
dc.contributor.author | Ling, Eduard | |
dc.contributor.author | Pierce, Sarah B. | |
dc.contributor.author | Segel, Reeval | |
dc.contributor.author | Walsh, Tom | |
dc.contributor.author | Barash, Judith | |
dc.contributor.author | Yalcinkaya, Fatos | |
dc.contributor.author | Lee, Ming K. | |
dc.contributor.author | Klevit, Rachel E. | |
dc.contributor.author | Renbaum, Paul | |
dc.contributor.author | Weinberg-Shukron, Ariella | |
dc.contributor.author | Elkan, Paulina Navon | |
dc.contributor.author | Kasapcopur, Ozgur | |
dc.date.accessioned | 2021-03-02T23:16:10Z | |
dc.date.available | 2021-03-02T23:16:10Z | |
dc.date.issued | 2014 | |
dc.identifier.citation | Elkan P. N. , Pierce S. B. , Segel R., Walsh T., Barash J., Padeh S., Zlotogorski A., Berkun Y., Press J. J. , Mukamel M., et al., "Mutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy", NEW ENGLAND JOURNAL OF MEDICINE, cilt.370, sa.10, ss.921-931, 2014 | |
dc.identifier.issn | 0028-4793 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_11675ae9-3287-45d8-838a-a83382bb0452 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/17190 | |
dc.identifier.uri | https://doi.org/10.1056/nejmoa1307362 | |
dc.description.abstract | BackgroundPolyarteritis nodosa is a systemic necrotizing vasculitis with a pathogenesis that is poorly understood. We identified six families with multiple cases of systemic and cutaneous polyarteritis nodosa, consistent with autosomal recessive inheritance. In most cases, onset of the disease occurred during childhood. | |
dc.language.iso | eng | |
dc.subject | Klinik Tıp | |
dc.subject | TIP, GENEL & İÇECEK | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Tıp | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Temel Tıp Bilimleri | |
dc.title | Mutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy | |
dc.type | Makale | |
dc.relation.journal | NEW ENGLAND JOURNAL OF MEDICINE | |
dc.contributor.department | Edmond & Lily Safra Childrens Hosp , , | |
dc.identifier.volume | 370 | |
dc.identifier.issue | 10 | |
dc.identifier.startpage | 921 | |
dc.identifier.endpage | 931 | |
dc.contributor.firstauthorID | 42187 | |