Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ifeyinwa Emmanuela Obiorah"'
Publikováno v:
Case Reports in Rheumatology, Vol 2018 (2018)
Intravascular lymphoma is a rare type of lymphoma, characterized by growth of lymphoma cells within the microvasculature. The majority of the cases are of B-cell lineage, although rare examples of T or NK lineage have also been reported. The lymphoma
Externí odkaz:
https://doaj.org/article/5c919c33df8a47c4bdcd3870a1350666
Autor:
Fernanda Gutierrez-Rodrigues, Daniel L. Kastner, David B. Beck, Patrycja Hoffmann, Marcela A. Ferrada, Bhavisha A Patel, Nisha Patel, Megan Trick, Neal S. Young, Peter C. Grayson, Zhijie Wu, Ifeyinwa Emmanuela Obiorah, Daniela Ospina Cardona, Alina Dulau-Florea, Lorena Wilson, Emma M. Groarke, Weixin Wang, Katherine R. Calvo, Jennifer Lotter, Amanda K. Ombrello
Publikováno v:
Blood Adv
Somatic mutations in UBA1 involving hematopoietic stem and myeloid cells have been reported in patients with the newly defined VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome. Here, we report clinical hematologic manifestati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2df64cab59785aaf70a43d21a8a103f2
https://doi.org/10.1182/bloodadvances.2021004976
https://doi.org/10.1182/bloodadvances.2021004976
Autor:
Weixin Wang, Katherine R. Calvo, Hao-Wei Wang, Inhye E. Ahn, Ivo M.B. Francischetti, Adrian Wiestner, Robert J. Kreitman, Ifeyinwa Emmanuela Obiorah, Mark Raffeld
Publikováno v:
Leuk Lymphoma
Simultaneous occurrence of hairy cell leukemia (HCL) and chronic lymphocytic leukemia/small lymphocytic lymphoma (termed CLL) is very rare. Clinical characteristics, pathology and management of these cases have not been well described. We present six
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bbde5849cd845cbd8d4223b35ca616c
https://pubmed.ncbi.nlm.nih.gov/32755330
https://pubmed.ncbi.nlm.nih.gov/32755330
Autor:
Daniel L. Kastner, Achim Werner, Megan Trick, Emma M. Groarke, David B. Beck, Zhijie Wu, Amanda K. Ombrello, Ifeyinwa Emmanuela Obiorah, Ivona Aksentijevich, Marcela A. Ferrada, Neal S. Young, Shawn M. Burgess, Keith A. Sikora, Peter C. Grayson, Weixin Wang, Katherine R. Calvo, Alina Dulau-Florea, Bhavisha A Patel
Publikováno v:
Blood. 136:20-21
Somatic mutations in UBA1 in hematopoietic stem cells and myeloid cells have recently been described and are associated with adult-onset severe autoinflammatory diseases including relapsing polychondritis, Sweet syndrome, polyarteritis nodosa, and gi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2511da18c7e6fccbb1a4aeba8341c9a
https://doi.org/10.1182/blood-2020-140480
https://doi.org/10.1182/blood-2020-140480