Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jennifer Keates-Baleeiro"'
Publikováno v:
Case Reports in Oncological Medicine, Vol 2015 (2015)
Morbid obesity presents unique challenges in managing additional disease processes. A 16-year-old male with a history of central diabetes insipidus (DI) and hypothyroidism developed destructive lesions in both his right mandible and brain, which were
Externí odkaz:
https://doaj.org/article/e6830732d1a040bca880812c3ea953d0
Publikováno v:
Journal of pediatric hematology/oncology. 42(4)
Phosphoglycerate kinase (PGK) is glycolytic enzyme critical in the creation of adenosine triphosphate. Mutations in the gene for this enzyme, PGK1, are associated with PGK deficiency, which is characterized by neurologic symptoms, nonhereditary spher
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40747142b1b8f39488c8631ed6c00931
https://pubmed.ncbi.nlm.nih.gov/30951021
https://pubmed.ncbi.nlm.nih.gov/30951021
Autor:
Sharada A. Sarnaik, Ofelia A. Alvarez, William Owen, Murtadha Al-Khabori, Ashok Raj, Thomas Moulton, Bruce A. Barton, Charles T. Quinn, Suzie A. Noronha, Beng Fuh, Connie M. Piccone, Mark T. Gladwin, Philip Maes, Jennifer Keates-Baleeiro, Ed Parsley, Emad Salman, Nirmish Shah, Cameron K. Tebbi, Lewis L. Hsu, Abdulkareem Al-Momen, Kamar Godder, Yasser Wali, Jason M. Fixler, Claudia R. Morris, Yurdanur Kilinç, Christophe F. Chantrain, Suvankar Majumdar, Natalie L. Kamberos, Elena Cela de Julián, L. Vandy Black, Meenakshi Goyal-Khemka, Rebecca T. Gorney, Julie Kanter, Courtney D. Thornburg, Alex George, Zeynep Karakas, Betty S. Pace, Clarisse Lopes De Castro Lobo, Debra E. Cohen, Tammuella Singleton, Alexis A. Thompson, Clifford M. Takemoto, Joseph L. Lasky, Miguel R. Abboud, India Sisler, Rachelle Nuss, Shari S. Kronsberg, Claire S. Padgett, Adlette Inati, James F. Casella, Marty Emanuele, Richard A. Drachtman, Gregory J. Kato, Anne Schaefer, Anne M. Marsh
Publikováno v:
JAMA : the journal of the American Medical Association
Key PointsQuestionCan poloxamer 188, an agent that is reported to reduce blood viscosity and cell-cell interactions, effectively reduce the duration of vaso-occlusive episodes (painful crises) in hospitalized patients with sickle cell disease? Findin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e84aea32135688abaf3dfc1b204648c
https://doi.org/10.1001/jama.2021.3414
https://doi.org/10.1001/jama.2021.3414
Publikováno v:
Journal of Blood Disorders & Transfusion.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4676cad06986672aad016defdaebedd2
https://doi.org/10.4172/2155-9864.1000405
https://doi.org/10.4172/2155-9864.1000405
Autor:
Jennifer Keates-Baleeiro, Ian S. Hitchcock, Rose Chen, Norma E. Fox, Amy E. Geddis, Haydar Frangoul
Publikováno v:
Experimental Hematology. 37:495-503
Objective To genetically and functionally characterize mutations of c-Mpl that lead to thrombocytopenia in a child with congenital amegakaryocytic thrombocytopenia. Materials and Methods We identified two c-Mpl mutations in a child with clinical feat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c079a7effb491ac6034fdd3cc864faf0
https://doi.org/10.1016/j.exphem.2009.01.001
https://doi.org/10.1016/j.exphem.2009.01.001
Publikováno v:
Case Reports in Oncological Medicine
Case Reports in Oncological Medicine, Vol 2015 (2015)
Case Reports in Oncological Medicine, Vol 2015 (2015)
Morbid obesity presents unique challenges in managing additional disease processes. A 16-year-old male with a history of central diabetes insipidus (DI) and hypothyroidism developed destructive lesions in both his right mandible and brain, which were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b68e2c33694cbfc25023d5e988b972ec
https://pubmed.ncbi.nlm.nih.gov/26697250
https://pubmed.ncbi.nlm.nih.gov/26697250
Publikováno v:
Bone Marrow Transplantation. 38:285-289
Idiopathic pneumonia syndrome (IPS) is a rare complication following stem cell transplant (SCT) and its incidence among pediatric SCT recipients is not known. To assess the incidence of IPS, we retrospectively reviewed the incidence of IPS at our cen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0a56c578f4e5b37d38b31c66171f795
https://doi.org/10.1038/sj.bmt.1705436
https://doi.org/10.1038/sj.bmt.1705436
Autor:
Haydar, Frangoul, Jennifer, Keates-Baleeiro, Cassie, Calder, Becky, Manes, Christine, Crossno, Victoria L, Castaneda, Jennifer, Domm
Publikováno v:
Pediatric transplantation. 14(4)
CAMT is a very rare cause of thrombocytopenia in infants. Most of the patients will progress to marrow failure. Allogeneic stem cell transplant remains the only curative therapy. We present two patients with CAMT who underwent an unrelated donor bone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::984498a20faa3d20047d2b1a5b3d4441
https://pubmed.ncbi.nlm.nih.gov/19490489
https://pubmed.ncbi.nlm.nih.gov/19490489
Publikováno v:
Blood. 108:1110-1110
Congenital amegakaryocytic thrombocytopenia (CAMT) is an inherited bone marrow syndrome due mutation of the thrombopoietin receptor c-Mpl. Affected children present with thrombocytopenia at birth and absence or severe reduction of megakaryocytes in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc38b5ecd55f88608306fa8a742479a0
https://doi.org/10.1182/blood.v108.11.1110.1110
https://doi.org/10.1182/blood.v108.11.1110.1110