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Mutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy

dc.contributor.authorWinkelmann, Juliane
dc.contributor.authorLevy-Lahad, Ephrat
dc.contributor.authorKing, Mary-Claire
dc.contributor.authorAnikster, Yair
dc.contributor.authorSener, Elif F.
dc.contributor.authorSchormair, Barbara
dc.contributor.authorZeligson, Sharon
dc.contributor.authorMarek-Yagel, Dina
dc.contributor.authorStrom, Tim M.
dc.contributor.authorShohat, Mordechai
dc.contributor.authorSinger, Amihood
dc.contributor.authorRubinow, Alan
dc.contributor.authorPras, Elon
dc.contributor.authorTekin, Mustafa
dc.contributor.authorPadeh, Shai
dc.contributor.authorZlotogorski, Abraham
dc.contributor.authorBerkun, Yackov
dc.contributor.authorPress, Joseph J.
dc.contributor.authorMukamel, Masha
dc.contributor.authorVoth, Isabel
dc.contributor.authorHashkes, Philip J.
dc.contributor.authorHarel, Liora
dc.contributor.authorHoffer, Vered
dc.contributor.authorLing, Eduard
dc.contributor.authorPierce, Sarah B.
dc.contributor.authorSegel, Reeval
dc.contributor.authorWalsh, Tom
dc.contributor.authorBarash, Judith
dc.contributor.authorYalcinkaya, Fatos
dc.contributor.authorLee, Ming K.
dc.contributor.authorKlevit, Rachel E.
dc.contributor.authorRenbaum, Paul
dc.contributor.authorWeinberg-Shukron, Ariella
dc.contributor.authorElkan, Paulina Navon
dc.contributor.authorKasapcopur, Ozgur
dc.date.accessioned2021-03-02T23:16:10Z
dc.date.available2021-03-02T23:16:10Z
dc.date.issued2014
dc.identifier.citationElkan 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.issn0028-4793
dc.identifier.othervv_1032021
dc.identifier.otherav_11675ae9-3287-45d8-838a-a83382bb0452
dc.identifier.urihttp://hdl.handle.net/20.500.12627/17190
dc.identifier.urihttps://doi.org/10.1056/nejmoa1307362
dc.description.abstractBackgroundPolyarteritis 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.isoeng
dc.subjectKlinik Tıp
dc.subjectTIP, GENEL & İÇECEK
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.titleMutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy
dc.typeMakale
dc.relation.journalNEW ENGLAND JOURNAL OF MEDICINE
dc.contributor.departmentEdmond & Lily Safra Childrens Hosp , ,
dc.identifier.volume370
dc.identifier.issue10
dc.identifier.startpage921
dc.identifier.endpage931
dc.contributor.firstauthorID42187


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