Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Robert, Molokie"'
Autor:
Desiree R. Azizoddin, Matthew Allsop, Subrina Farah, Farah Salim, Joshua Hauser, Ashton R. Baltazar, Robert Molokie, Jane Weber, Christine Weldon, Lawrence Feldman, Joanna L. Martin
Publikováno v:
Cancer Medicine, Vol 12, Iss 7, Pp 8629-8638 (2023)
Abstract Background We evaluated whether patients' initial screening symptoms were related to subsequent utilization of supportive care services and hospitalizations, and whether patient‐level demographics, symptoms, hospitalizations, and supportiv
Externí odkaz:
https://doaj.org/article/d09e256838c74fd6afd04540b4803a42
Publikováno v:
IEEE Journal of Translational Engineering in Health and Medicine, Vol 8, Pp 1-8 (2020)
Acute chest syndrome (ACS) is the leading cause of death among people with sickle cell disease. ACS is clinically defined and diagnosed by the presence of a new pulmonary infiltrate on chest imaging with accompanying fever and respiratory symptoms li
Externí odkaz:
https://doaj.org/article/24d8927ee043479b98809c75317cb27f
Publikováno v:
Haematologica, Vol 104, Iss 12 (2019)
Externí odkaz:
https://doaj.org/article/48108971c8074c79a223f4c5d34ce3fd
Autor:
Vinzon Ibanez, Kestis Vaitkus, Xu Zhang, Jagadeesh Ramasamy, Angela E Rivers, Yogen Saunthararajah, Robert Molokie, Donald Lavelle
Publikováno v:
Blood Advances.
Increased Fetal Hemoglobin (HbF) levels reduce the symptoms of SCD and increase the lifespan of patients. Because the curative strategies of bone marrow transplantation and gene therapy technologies remain unavailable to large numbers of patients, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b6f19d42dd12a9df360fb0e8c52d3b8
https://doi.org/10.1182/bloodadvances.2022009558
https://doi.org/10.1182/bloodadvances.2022009558
Autor:
Desiree R. Azizoddin, Matthew Allsop, Subrina Farah, Farah Salim, Joshua Hauser, Ashton R. Baltazar, Robert Molokie, Jane Weber, Christine Weldon, Lawrence Feldman, Joanna L. Martin
Publikováno v:
Cancer medicineREFERENCES.
We evaluated whether patients' initial screening symptoms were related to subsequent utilization of supportive care services and hospitalizations, and whether patient-level demographics, symptoms, hospitalizations, and supportive care service utiliza
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1209dadf4468dcddca5a5c176e074137
https://pubmed.ncbi.nlm.nih.gov/36573460
https://pubmed.ncbi.nlm.nih.gov/36573460
Autor:
Robert Molokie, Donald Lavelle, Michel Gowhari, Michael Pacini, Lani Krauz, Johara Hassan, Vinzon Ibanez, Maria A Ruiz, Kwok Peng Ng, Philip Woost, Tomas Radivoyevitch, Daisy Pacelli, Sherry Fada, Matthew Rump, Matthew Hsieh, John F Tisdale, James Jacobberger, Mitch Phelps, James Douglas Engel, Santhosh Saraf, Lewis L Hsu, Victor Gordeuk, Joseph DeSimone, Yogen Saunthararajah
Publikováno v:
PLoS Medicine, Vol 14, Iss 9, p e1002382 (2017)
BACKGROUND:Sickle cell disease (SCD), a congenital hemolytic anemia that exacts terrible global morbidity and mortality, is driven by polymerization of mutated sickle hemoglobin (HbS) in red blood cells (RBCs). Fetal hemoglobin (HbF) interferes with
Externí odkaz:
https://doaj.org/article/c7733c856c0b41248e7cccfad4c6af2d
Autor:
Verlin Joseph, Jinhai Huo, Robert Cook, Roger B. Fillingim, Yingwei Yao, Gebre Egziabher-Kiros, Enrique Velazquez Villarreal, Xinguang Chen, Robert Molokie, Diana J. Wilkie
Publikováno v:
Pain management nursing : official journal of the American Society of Pain Management Nurses. 23(4)
Patients with cancer have pain due to their cancer, the cancer treatment and other causes, and the pain intensity varies considerably between individuals. Additional research is needed to understand the factors associated with worst pain intensity. O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6853c2beda918c969a1982e1022d1aae
https://pubmed.ncbi.nlm.nih.gov/35227646
https://pubmed.ncbi.nlm.nih.gov/35227646
Autor:
Chaher H, Alhandalous, Jin, Han, Lewis, Hsu, Michel, Gowhari, Johara, Hassan, Robert, Molokie, Taimur A, Abbasi, Victor R, Gordeuk
Publikováno v:
American journal of hematology. 90(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6a6943b2ccb93c4727788b78f94d36b1
https://pubmed.ncbi.nlm.nih.gov/26453077
https://pubmed.ncbi.nlm.nih.gov/26453077
Autor:
Santosh, Saraf, Mohammed, Farooqui, Giovanni, Infusino, Bharvi, Oza, Seema, Sidhwani, Michel, Gowhari, Stephen, Vara, Weihua, Gao, Lani, Krauz, Donald, Lavelle, Joseph, DeSimone, Robert, Molokie, Yogen, Saunthararajah
Publikováno v:
British journal of haematology. 153(3)
In sickle cell disease (SCD), vigorous reticulocytosis is required to partially compensate for chronic hemolytic anaemia. Consequently, early renal damage, insufficient to cause azotemia but sufficient to cause erythropoietin deficiency and chronic r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5f9cfc8f6d8b905c1225e3083a18782e
https://pubmed.ncbi.nlm.nih.gov/21418176
https://pubmed.ncbi.nlm.nih.gov/21418176
Autor:
Robert Molokie, Sucha Nand
Publikováno v:
Journal of Clinical Apheresis. 5:206-212
Plasmapheresis is being used with considerable frequency in the management of malignant and non-malignant disorders. More recently, staphylococcal Protein A immunoadsorption has been employed in similar clinical situations. In patients with malignanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51a7dd90f171e38b68e46edc53c8b8c6
https://doi.org/10.1002/jca.2920050408
https://doi.org/10.1002/jca.2920050408