Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Berline Francis"'
Autor:
Deepali K. Bhat, Purevdorj B. Olkhanud, Arunakumar Gangaplara, Fayaz Seifuddin, Mehdi Pirooznia, Angélique Biancotto, Giovanna Fantoni, Corinne Pittman, Berline Francis, Pradeep K. Dagur, Ankit Saxena, J. Philip McCoy, Ruth M. Pfeiffer, Courtney D. Fitzhugh
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Haploidentical hematopoietic stem cell transplantation (haplo-HSCT) is a widely available curative option for patients with sickle cell disease (SCD). Our original non-myeloablative haplo-HSCT trial employing post-transplant (PT) cyclophosphamide had
Externí odkaz:
https://doaj.org/article/24e70ed7cf154c4e8c2147f41d584da8
Autor:
Ruth M. Pfeiffer, Courtney D. Fitzhugh, Deepali K Bhat, Mehdi Pirooznia, Angelique Biancotto, Corinne A. Pittman, Ankit Saxena, J. Philip McCoy, Arunakumar Gangaplara, Pradeep K. Dagur, Giovanna Fantoni, Fayaz Seifuddin, Purevdorj B. Olkhanud, Berline Francis
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Vol 12 (2021)
Frontiers in Immunology, Vol 12 (2021)
Haploidentical hematopoietic stem cell transplantation (haplo-HSCT) is a widely available curative option for patients with sickle cell disease (SCD). Our original non-myeloablative haplo-HSCT trial employing post-transplant (PT) cyclophosphamide had
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4774b77ea9a58381a22fe036dbef0413
http://europepmc.org/articles/PMC8669726
http://europepmc.org/articles/PMC8669726
Autor:
Pranava Sinha, Siva Rajamarthandan, Matthew A. Brown, Berline Francis, Meghan K. O'Leary‐Kelly
Publikováno v:
Journal of cardiac surgeryREFERENCES. 35(1)
Background Congenital heart disease (CHD) continues to be among the most common birth defects, affecting an estimated 40 000 births annually in the United States. The most common complication of CHD is heart failure. With improved medical management
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1df66f48031edb8e673039b4f5d066f2
https://pubmed.ncbi.nlm.nih.gov/31705822
https://pubmed.ncbi.nlm.nih.gov/31705822
Autor:
Arunakumar Gangaplara, J. Philip McCoy, Courtney D. Fitzhugh, Deepali K Bhat, Berline Francis
Publikováno v:
Blood. 134:803-803
Sickle cell disease (SCD) is an inherited blood disorder in which red blood cells are sickle-shaped as a result of an amino acid alteration from glutamate to valine at the sixth position of the β-globin chain. Hematopoietic stem cell transplant (HSC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b13bc3230289190076d4ac330d7435a
https://doi.org/10.1182/blood-2019-130711
https://doi.org/10.1182/blood-2019-130711