Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Barbara Gruner"'
Autor:
Kane M. Laks, Cara Hirner, Barbara Gruner, Jared Coberly, Katsiaryna Laziuk, Bindu Kanathezhath Sathi
Publikováno v:
Case Reports in Hematology, Vol 2020 (2020)
EF Bart’s disease is a rare form of nontransfusion-dependant thalassemia (NTDT) due to the coinheritance of homozygous hemoglobin E (βE/βE) genotype with hemoglobin H disease. These individuals are routinely found to have thalassemia intermedia w
Externí odkaz:
https://doaj.org/article/ddd2193f791e4190b19acf05361c44e0
Autor:
Jason E. Farrar, Anupama Narla, Kelly Walkovich, Helge Hartung, Grzegorz Nalepa, Adrianna Vlachos, Evangelia Atsidaftos, Jeffrey M. Lipton, Mohammad Lutfi Lababidi, Jonathan Bernstein, Ellen Muir, Zora R. Rogers, Thomas W. Loew, Waseem Alhushki, Colin A. Sieff, Bertil Glader, Barbara Gruner, Christine M. Knoll, Arun R Panigrahi
Publikováno v:
Pediatr Blood Cancer
Background Diamond-Blackfan anemia (DBA) is an inherited bone marrow failure syndrome characterized by anemia, short stature, congenital anomalies, and cancer predisposition. Most cases are due to mutations in genes encoding ribosomal proteins (RP) l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f35da0422ca685604b2d6c0cfaafb63
https://europepmc.org/articles/PMC8273758/
https://europepmc.org/articles/PMC8273758/
Publikováno v:
Blood. 136:7-8
Introduction Red blood Cell (RBC) transfusion therapy is an important disease modifying treatment in sickle cell disease (SCD). RBC alloimmunization is one of the more serious complications associated with transfusion therapy and limits its wider cli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fc5c7115f2231edf0bda7c70f8b1ebe
https://doi.org/10.1182/blood-2020-140168
https://doi.org/10.1182/blood-2020-140168
Publikováno v:
Indian Journal of Medical and Paediatric Oncology. 39:530-532
Prognosis for refractory/recurrent metastatic osteosarcoma (OS) remains dismal with 3-year survival rates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef797355326c10fc6cbe3ab6737b3433
https://doi.org/10.4103/ijmpo.ijmpo_83_17
https://doi.org/10.4103/ijmpo.ijmpo_83_17
Publikováno v:
American Journal of Clinical Pathology. 152:S151-S152
Objectives Fetal/neonatal alloimmune thrombocytopenia (FNAIT) occurs when maternal IgG alloantibodies against paternal human platelet antigens (HPA) cross the placenta and cause the destruction of fetal platelets. The vast majority (up to 95%) of FNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73ed7220395be18df97b556dd7c9bae5
https://doi.org/10.1093/ajcp/aqz131.002
https://doi.org/10.1093/ajcp/aqz131.002
Publikováno v:
Clinical Pediatrics. 56:90-92
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a18320393a1ff9722c8b6f1696cc905
https://doi.org/10.1177/0009922816678978
https://doi.org/10.1177/0009922816678978
Autor:
Talissa A. Altes, Cara Hirner, Yoshida Yilin, Lila Wahidi Nolan, Michael Raymond Weaver, Carlos Leiva Salinas, Bindu Kanathezhath Sathi, Vinod Balasa, Barbara Gruner
Publikováno v:
Blood. 134:2276-2276
Introduction Children and adults with sickle cell disease (SCD) suffer from overt stroke, the prevalence of which has been reported to be 11% < 20 years. More commonly, they suffer from silent cerebral Infarction (SCI) that has a reported prevalence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36c7224fa8ae537311c1b74ddce222ae
https://doi.org/10.1182/blood-2019-122975
https://doi.org/10.1182/blood-2019-122975
Autor:
Barbara Gruner, Kelly Walkovich, Christine M. Knoll, Mohammad Lufti Lababidi, Jason E. Farrar, Anupama Narla, Helge Hartung, Zora R. Rogers, Waseem Alhushki, Evangelia Atsidaftos, Ellen Muir, Bertil Glader, Arun R Panigrahi, Colin A. Sieff, Jeffrey M. Lipton, Adrianna Vlachos, Grzegorz Nalepa
Publikováno v:
Blood. 132:755-755
Diamond Blackfan anemia (DBA) is a rare, inherited bone marrow failure syndrome characterized by anemia, congenital anomalies and a predisposition to cancer. The patients usually present during infancy or early childhood, but can also present in adul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b29c4e5bf0f45033599eb182f40142b5
https://doi.org/10.1182/blood-2018-99-113570
https://doi.org/10.1182/blood-2018-99-113570
Autor:
Huidong Shi, Charles W. Caldwell, Kristen H. Taylor, Michael X. Wang, Barbara Gruner, Deiter J. Duff
Publikováno v:
Blood. 106:4524-4524
Background: Increasing evidence indicates that the minimal residual disease in childhood precursor B lymphoblastic leukemia (B-ALL) can predict the clinical outcome of the patients. With the combination of multicolor flow cytometry and B-cell recepto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddd6b1eb4580a2409c28c4fa4f5c3d3f
https://doi.org/10.1182/blood.v106.11.4524.4524
https://doi.org/10.1182/blood.v106.11.4524.4524