Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Ghadir S. Sasa"'
Publikováno v:
Frontiers in Pediatrics, Vol 6 (2019)
Fanconi anemia (FA) is an inherited bone marrow failure and cancer predisposition disorder due to mutations in DNA repair pathways proteins (FANC). The dysfunctional proteins are unable to repair DNA breaks and cause genomic instability. Mutations in
Externí odkaz:
https://doaj.org/article/8b0d991028f6485ebb00f95453481202
Autor:
Qing Zhou, Hye Sun Kuehn, Ivan K. Chinn, Bo Yuan, Sarah K. Nicholas, Chung Wah Wu, Sergio D. Rosenzweig, Gina Cahill, Ghadir S. Sasa, Tiphanie P. Vogel, Amanda Salih
Publikováno v:
Journal of Clinical Immunology. 41:1420-1423
Autor:
Elif Dokmeci, Keith Wilson, Selket Delafontaine, Federica Barzaghi, Simone Cesaro, Jennifer A. Kanakry, Despina Moshous, Sophie Hambleton, Robbert G. M. Bredius, Dimana Dimitrova, Mervi Taskinen, Florian Babor, İkbal Ok Bozkaya, Hasan Hashem, Robert A. Krance, Michael S. Hershfield, Nurten A. Akarsu, Seza Ozen, Polina Stepensky, David Boutboul, Ghadir S. Sasa, Joel P Brooks, Sandra Steinmann, Jignesh Dalal, Isabelle Meyts, Amy P. Hsu, Caroline Schnider, Dennis D. Hickstein, Yener Koc, Guillaume Le Guenno, Minna Koskenvuo, Chip Chambers, Tayfun Güngör, Maria Pia Cicalese, Fabio Candotti, Valentina Baretta, Steven M. Holland, Ingo Müller, Jasmeen Dara, Neven Benedicte, Giorgia Bucciol, Amanda K. Ombrello, Janna Saarela, Stephen Jolles, Ashish R Kumar, Sule Unal, Carrie L. Lucas, Leen Moens, Joris M. van Montfrans, Monica Abreu de Sousa, Ansgar Schulz
Publikováno v:
Journal of Clinical Immunology, 41(7), 1633-1647. SPRINGER/PLENUM PUBLISHERS
Journal of clinical immunology, vol. 41, no. 7, pp. 1633-1647
Journal of Clinical Immunology
Journal of clinical immunology, vol. 41, no. 7, pp. 1633-1647
Journal of Clinical Immunology
Purpose Deficiency of adenosine deaminase 2 (DADA2) is an inherited inborn error of immunity, characterized by autoinflammation (recurrent fever), vasculopathy (livedo racemosa, polyarteritis nodosa, lacunar ischemic strokes, and intracranial hemorrh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ace541f0425652c858e94ad95ce9362
https://link.springer.com/content/pdf/10.1007/s10875-021-01098-0.pdf
https://link.springer.com/content/pdf/10.1007/s10875-021-01098-0.pdf
Autor:
Kristen Campbell, Marcin W. Wlodarski, Kathryn E. Dickerson, Taizo A. Nakano, Yigal Dror, Akiko Shimamura, Michaela Cada, Inga Hofmann, Rabbi Hanna, Timothy S. Olson, Hilda Ding, Tarek M. Elghetany, Ghadir S. Sasa, Jessica A. Pollard, Steven William Allen, Bonnie W Lau
Publikováno v:
Pediatric bloodcancerREFERENCES. 67(10)
Background Myelodysplastic syndromes (MDS) represent a group of clonal hematopoietic stem cell disorders that commonly progress to acute myeloid leukemia (AML). The diagnostics, prognostics, and treatment of adult MDS are established but do not direc
Autor:
Alison A. Bertuch, Christopher G. Tomlinson, Geraldine Aubert, Maria M. Gramatges, Tracy M. Bryan, Bailey Angeline Martin-Giacalone, Sharon E. Plon, Ghadir S. Sasa
Publikováno v:
Leukemia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18271d460c1a541538c85f47734b2ab4
https://europepmc.org/articles/PMC7575615/
https://europepmc.org/articles/PMC7575615/
Publikováno v:
Journal of pediatric hematology/oncology. 43(5)
A transient pancytopenic phase has been described in pediatric leukemia. The characteristic complete recovery of peripheral counts can obscure a clinician's suspicion for malignancy and may impact subsequent follow-up care. The authors describe 4 ped
Autor:
Olive S. Eckstein, Swati Naik, Caridad Martinez, Carl E. Allen, Ghadir S. Sasa, Helen E. Heslop, Robert A. Krance
Publikováno v:
British journal of haematologyReferences. 188(6)
Autor:
Ghadir S. Sasa, Adrianna Vlachos
Publikováno v:
Hematology in the Adolescent Female ISBN: 9783030484453
Bone marrow failure is a collective term used to describe a group of disorders which impair normal hematopoiesis, resulting in single or multiple blood cytopenias. Bone marrow failure varies in the degree and extent of its severity. There is a wide d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d9d164bf18350b14d6da161f4712862
https://doi.org/10.1007/978-3-030-48446-0_26
https://doi.org/10.1007/978-3-030-48446-0_26
Autor:
Robbert G. M. Bredius, Mervi Taskinen, Ingo Müller, Robert A. Krance, Barbara Bosch, Florian Babor, Ashish R Kumar, Minna Koskenvuo, Keith Wilson, Amy P. Hsu, Hasan Hashem, Isabelle Meyts, Ghadir S. Sasa, Janna Saarela, Michael S. Hershfield, Jignesh Dalal, Joris M. van Montfrans, Stephen Jolles, Steven M. Holland, Dennis D. Hickstein, Leen Moens
Publikováno v:
Blood, 130(24), 2682-2688
Blood, 130(24), 2682. American Society of Hematology
Blood, 130(24), 2682. American Society of Hematology
Deficiency of adenosine deaminase 2 (DADA2) is caused by biallelic deleterious mutations in CECR1 DADA2 results in variable autoinflammation and vasculopathy (recurrent fevers, livedo reticularis, polyarteritis nodosa, lacunar ischemic strokes and in
Autor:
Baheyeldin Salem, LaQuisa Hill, Shreeya Patel, Tami John, Caridad Martinez, Brian D. Friend, George Carrum, John Craddock, Robert A. Krance, Premal Lulla, Rammurti T. Kamble, Carlos A. Ramos, Helen E. Heslop, Ghadir S. Sasa, Erin E Doherty, Khaled Yassine, Ibrahim N. Muhsen
Publikováno v:
Transplantation and Cellular Therapy. 27:S406-S407