Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Alecia C. Nero"'
Autor:
Caterina P Minniti, Henny H. Billett, Daniel McMahon, Modupe Idowu, Nirmish Shah, Richard A. Drachtman, Archana Sharma, Alexander Glaros, Maureen Okam Okam Achebe, Alecia C Nero, Susanna Curtis, Biree Andemariam
Publikováno v:
Blood. 140:8276-8277
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d9863a6d11e103429f50f0909be8959
https://doi.org/10.1182/blood-2022-169334
https://doi.org/10.1182/blood-2022-169334
Autor:
Deva Sharma, Russell E. Ware, Michael J. Paidas, Lydia H. Pecker, Alecia C. Nero, Andra H. James, Kim Smith-Whitley
Publikováno v:
Br J Haematol
There is an immediate need to address long-standing questions about the reproductive health of girls and women with sickle cell disease (SCD). There are many SCD-related reproductive risks and uncertainties across girls' and women's reproductive life
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e53a360449a749446b8375163cc81d6
https://europepmc.org/articles/PMC8448913/
https://europepmc.org/articles/PMC8448913/
Autor:
Raffaella Colombatti, Alecia C. Nero, Erfan Nur, Cassandra Trimnell, John R. James, Olivera Rajkovic-Hooley, Tom Bailey, Jean-Benoît Arlet, Mariane de Montalembert, Ifeyinwa Osunkwo, Caterina P. Minniti, Suman Jain, Miguel R. Abboud, Fuad El Rassi, Beverley Francis-Gibson, Wasil Jastaniah, Biree Andemariam, Nicholas Ramscar, Marimilia Pita, Baba Inusa
Publikováno v:
Blood. 136:8-10
Background: SWAY was a cross-sectional survey that assessed the global impact and treatment of sickle cell disease (SCD) (James et al. ASH 2019). SCD puts patients at risk of multiple complications driven by vaso-occlusion and hemolytic anemia. Vaso-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74b4c4b0a2213b89defe37bb12ccb0db
https://doi.org/10.1182/blood-2020-137103
https://doi.org/10.1182/blood-2020-137103
Autor:
Tom Bailey, Jean-Benoît Arlet, Beverley Francis-Gibson, Baba Inusa, Caterina P. Minniti, John R. James, Alecia C. Nero, Olivera Rajkovic-Hooley, Raffaella Colombatti, Biree Andemariam, Cassandra Trimnell, Fuad El Rassi, Erfan Nur, Miguel R. Abboud, Nicholas Ramscar, Mariane de Montalembert, Marimilia Pita, Wasil Jastaniah, Ifeyinwa Osunkwo, Suman Jain
Publikováno v:
Blood. 136:3-5
Background: Sickle cell disease (SCD) is associated with many clinical complications, with vaso-occlusive crises (VOCs) being a hallmark of the disease. SCD-related complications are largely driven by vaso-occlusion and hemolytic anemia, and can lead
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2bfd823ce6a2378e59a7753b21a693bd
https://doi.org/10.1182/blood-2020-136073
https://doi.org/10.1182/blood-2020-136073
Autor:
Olivera Rajkovic-Hooley, Suman Jain, Mariane de Montalembert, Biree Andemariam, Ifeyinwa Osunkwo, Fuad El Rassi, Laurie DeBonnett, Nicholas Ramscar, Alecia C. Nero, Tom Bailey, Baba Inusa, Jean Benoit Arlet, Caterina P. Minniti, Miguel R. Abboud, John R. James, Raffaella Colombatti, Marimilia Pita, Wasil Jastaniah, Erfan Nur, Beverley Francis-Gibson, Cassandra Trimnell
Publikováno v:
American journal of hematology, 96(4), 404-417. Wiley-Liss Inc.
American Journal of Hematology
American Journal of Hematology
Sickle cell disease (SCD) is a genetic disorder, characterized by hemolytic anemia and vaso‐occlusive crises (VOCs). Data on the global SCD impact on quality of life (QoL) from the patient viewpoint are limited. The international Sickle Cell World
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66b76675bc2ae4e1ba064e55d1b77bcf
https://pubmed.ncbi.nlm.nih.gov/33393092
https://pubmed.ncbi.nlm.nih.gov/33393092
Autor:
Alecia C. Nero, John R. James, Jean-Benoît Arlet, Biree Andemariam, Caterina P. Minniti, Cassandra Trimnell, Ifeyinwa Osunkwo, Wasil Jastaniah, Fuad El Rassi, Raffaella Colombatti, Laurie DeBonnett, Miguel R. Abboud, Beverley Francis-Gibson, Marimilia Pita, Tom Bailey, Olivera Rajkovic-Hooley, Baba Inusa, Erfan Nur, Mariane de Montalembert, Suman Jain
Publikováno v:
Blood. 138:3026-3026
Background: SCD is an inherited blood disorder that for many patients (pts) has a high clinical burden, results in poor quality of life (QoL), and reduces life expectancy. Gaining a deeper understanding of pt and HCP experiences of SCD is important t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf711241c9bd9816d3f4dbefc2d41a51
https://doi.org/10.1182/blood-2021-145409
https://doi.org/10.1182/blood-2021-145409
Autor:
Richard A. Drachtman, Ifeyinwa Osunkwo, Modupe Idowu, Sharada Sarnaik, Caterina P. Minniti, Alecia C. Nero, E. Leila Jerome Clay, Biree Andemariam, Nirmish Shah, Archana Sharma, Susanna A Curtis, Maureen Achebe
Publikováno v:
Blood. 138:3100-3100
Background: Sickle cell disease (SCD) is an inherited systemic disorder in which sickle hemoglobin (HbS) polymerization triggers red blood cell sickling, chronic hemolytic anemia, and recurrent episodes of vaso-occlusion. SCD-related complications le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d2dd221aa491537f68925a2e84a9945
https://doi.org/10.1182/blood-2021-153459
https://doi.org/10.1182/blood-2021-153459
Autor:
Caterina P. Minniti, Baba Inusa, Raffaella Colombatti, Biree Andemariam, Wasil Jastaniah, Tom Bailey, Ifeyinwa Osunkwo, Jean-Benoît Arlet, F. El Rassi, Olivera Rajkovic-Hooley, Erfan Nur, Alecia C. Nero, Suman Jain, Laurie DeBonnett, John R. James
Publikováno v:
Value in Health. 23:S343
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f02fcafa774802cc888a71b71c52aec
https://doi.org/10.1016/j.jval.2020.04.1303
https://doi.org/10.1016/j.jval.2020.04.1303
Autor:
Caterina P. Minniti, Jean-Benoit Arlet, Alecia C. Nero, Erfan Nur, Ifeyinwa Osunkwo, Miguel R. Abboud, Raffaella Colombatti, Suman Jain, Laurie DeBonnett, F. El Rassi, Biree Andemariam, J. Waller, John James, M. de Montalembert, Baba Inusa, W. J. Jastaniah, Beverly Francis-Gibson
Publikováno v:
HemaSphere. 3:1026-1027
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b486cf2c18d33e8cb5ea582131a490a8
https://doi.org/10.1097/01.hs9.0000567668.61996.c4
https://doi.org/10.1097/01.hs9.0000567668.61996.c4
Publikováno v:
Advances in experimental medicine and biology. 1013
Sickle cell disease (SCD) and β-thalassemia are among the most common inherited diseases, affecting millions of persons globally. It is estimated that 5-7% of the world's population is a carrier of a significant hemoglobin variant. Without early dia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7893dff013c395f1e48198447ed7eea6
https://pubmed.ncbi.nlm.nih.gov/29127675
https://pubmed.ncbi.nlm.nih.gov/29127675