Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Kenneth C. Swanson"'
Autor:
Michelle E. Savedra, James D. Hoyer, Jennifer L. Oliveira, Phuong L. Nguyen, Jessica Szuberski, Camila Dergam-Larson, Aruna Rangan, Tavanna R. Porter, Min Shi, Kenneth C. Swanson, Ronald S. Go, Sarah E. Brunker
Publikováno v:
International journal of laboratory hematologyREFERENCES. 43(4)
Introduction Methemoglobin (MetHb) and sulfhemoglobin (SHb) measurements are useful in the evaluation of cyanosis. When one or both values are elevated, additional analysis is important to establish the etiology of the disorder. Methemoglobinemia occ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7e6a37552c8df6df97d6f00b41afd1b
https://pubmed.ncbi.nlm.nih.gov/34092029
https://pubmed.ncbi.nlm.nih.gov/34092029
Autor:
Mrinal M. Patnaik, Kenneth C. Swanson, Ayalew Tefferi, James D. Hoyer, Jennifer L. Oliveira, Stefan K.G. Grebe, Molly S. Hein, Michelle E. Savedra, Animesh Pardanani, Tavanna R. Porter, David S. Viswanatha, Lori Frederick, Lea M. Coon
Publikováno v:
American journal of hematology.
Hereditary erythrocytosis is associated with high oxygen affinity hemoglobin variants (HOAs), 2,3-bisphosphoglycerate deficiency and abnormalities in EPOR and the oxygen-sensing pathway proteins PHD, HIF2α, and VHL. Our laboratory has 40 years of ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9e3becdd42296dd4f5bd64f505830ed
https://pubmed.ncbi.nlm.nih.gov/29790589
https://pubmed.ncbi.nlm.nih.gov/29790589
Autor:
Tyler J. Winkler, Rachel LaCount, D. Brian Dawson, Michael W. Kent, Xiayuan Liang, Jennifer L. Oliveira, Kenneth C. Swanson, James D. Hoyer, Christopher C. Silliman, Michelle L. Kluge, Charles W. Breaux
Publikováno v:
Hemoglobin. 38:8-12
Hyperunstable hemoglobinopathy (HUH) [dominantly inherited β-thalassemia (β-thal)] is a relatively rare form of congenital hemolytic anemia in which mutations occur in the genes encoding for α and β chains, or both chains of the hemoglobin (Hb) m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ba755a992433f157f78413f42162a05
https://doi.org/10.3109/03630269.2013.853672
https://doi.org/10.3109/03630269.2013.853672
Autor:
Lauren Lubrano, D. Brian Dawson, Jennifer L. Oliveira, Kenneth C. Swanson, Gerald Sandler, Michael J. Donnelly, James D. Hoyer
Publikováno v:
Hemoglobin. 38:137-141
Hb Memphis [α23(B4)Glu→Gln; HBA2: c.70G C (or HBA1)] is a stable hemoglobin (Hb) variant caused by a substitution of glutamine for glutamic acid at residue 23 of the α2- or α1-globin chain. Heterozygous Hb Memphis has no known clinical or hemato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac914910130b7db543b122f611ad6b33
https://doi.org/10.3109/03630269.2013.867866
https://doi.org/10.3109/03630269.2013.867866
Autor:
Lea M. Coon, Anderson B. Collier, Philip M. Monteleone, Jennifer L. Oliveira, Samuel Umaru, Kenneth C. Swanson, James D. Hoyer
Publikováno v:
Hemoglobin. 40(2)
Hemoglobin (Hb) variants may be associated with low oxygen saturation and exacerbated episodes of anemia from common stressors such as viral infections. These attributes frequently cause increased clinical concern and unnecessary and expensive testin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::740642e12481780d1bad2a1d91c06ec6
https://pubmed.ncbi.nlm.nih.gov/26681102
https://pubmed.ncbi.nlm.nih.gov/26681102
Publikováno v:
Hemoglobin. 38(4)
A novel β(0)-thalassemia (β-thal) frameshift mutation, HBB: c.209delG; p.Gly70Valfs*20, is described in a 21-year-old African American female with β-thalassemia major (β-TM) due to compound heterozygosity for the β(0)-thal mutation HBB: c.92+2T>
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b5fb8676681d3ae5c93ebcc406bffd1
https://pubmed.ncbi.nlm.nih.gov/24986053
https://pubmed.ncbi.nlm.nih.gov/24986053
Publikováno v:
Journal of Pediatric Hematology/Oncology. 27:618-620
Summary: Hemoglobin Abruzzo is a stable hemoglobin variant with increased oxygen affinity, clinically causing compensatory erythrocytosis in affected patients. Heterozygosity of this variant with or without β-thalassemia has been previously describe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76734a6ee8fa65edf94e23845686025a
https://doi.org/10.1097/01.mph.0000188114.50200.b3
https://doi.org/10.1097/01.mph.0000188114.50200.b3
Autor:
Rendell W. Ashton, Rachel M. Taliercio, Kenneth C. Swanson, James D. Hoyer, Patricia Wendt, Leonard J. Horwitz, Jennifer L. Oliveira
Publikováno v:
Hemoglobin. 37(4)
A previously unreported β chain hemoglobin (Hb) variant, Hb Grove City [β38(C4)Thr→Ser, ACC>AGC; HBB: c.116C>G], was discovered in a woman who presented with hypoxia and mild anemia. Her young daughter also tested positive for the variant and dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee6a94c82497f82dbc78338fe9aee6ee
https://pubmed.ncbi.nlm.nih.gov/23651408
https://pubmed.ncbi.nlm.nih.gov/23651408
Autor:
Linda Nelson, Courtney Judd, James D. Hoyer, Jennifer L. Oliveira, Mudra Kumar, Kenneth C. Swanson
Publikováno v:
Hemoglobin. 38:211-212
The increasing availability of DNA sequencing of globin genes has improved our ability to detect conditions that were presumed to be extremely rare. These conditions may remain undiagnosed due to unfamiliarity with clinical presentation, relative una
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8acafc5b9ec4a60993ff389fcf0b378
https://doi.org/10.3109/03630269.2014.895378
https://doi.org/10.3109/03630269.2014.895378
Publikováno v:
Hemoglobin. 34(6)
A new β hemoglobin (Hb) variant, Hb Cambridge-MA [β144(HC1)β146(HC3)Lys-Tyr-His→0 (AAG>TAG) (HGVS: HBB c.433 A>T] is described. The variant was characterized by high performance liquid chromatography (HPLC), alkaline, acid, globin chain and capi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73f23052f44cef54ca027861a96016aa
https://pubmed.ncbi.nlm.nih.gov/21077764
https://pubmed.ncbi.nlm.nih.gov/21077764