Zobrazeno 1 - 10
of 81
pro vyhledávání: '"Roberta M Kato"'
Autor:
Patjanaporn Chalacheva, Maha Khaleel, John Sunwoo, Payal Shah, Jon A Detterich, Roberta M Kato, Wanwara Thuptimdang, Herbert J Meiselman, Richard Sposto, Jennie Tsao, John C Wood, Lonnie Zeltzer, Thomas D Coates, Michael C K Khoo
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0178353 (2017)
Painful vaso-occlusive crisis (VOC), a complication of sickle cell disease (SCD), occurs when sickled red blood cells obstruct flow in the microvasculature. We postulated that exaggerated sympathetically mediated vasoconstriction, endothelial dysfunc
Externí odkaz:
https://doaj.org/article/941a13a049fb46ba981b2a6e8e8f8f00
Autor:
Wanwara Thuptimdang, Payal Shah, Maha Khaleel, John Sunwoo, Saranya Veluswamy, Roberta M. Kato, Thomas D. Coates, Michael C. K. Khoo
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Recent studies have shown that individuals with sickle cell disease (SCD) exhibit greater vasoconstriction responses to physical autonomic stressors, such as heat pain and cold pain than normal individuals, but this is not the case for mental stress
Externí odkaz:
https://doaj.org/article/8a1f6d398282464c97055a0c2d43c456
Autor:
Payal Shah, Maha Khaleel, Wanwara Thuptimdang, John Sunwoo, Saranya Veluswamy, Patjanaporn Chalacheva, Roberta M. Kato, Jon Detterich, John C. Wood, Lonnie Zeltzer, Richard Sposto, Michael C.K. Khoo, Thomas D. Coates
Publikováno v:
Haematologica, Vol 105, Iss 1 (2020)
Vaso-occlusive crisis (VOC) is a hallmark of sickle cell disease (SCD) and occurs when deoxygenated sickled red blood cells occlude the microvasculature. Any stimulus, such as mental stress, which decreases microvascular blood flow will increase the
Externí odkaz:
https://doaj.org/article/4f6db0419d794251ba9eaefb868499e4
Autor:
Arash Sabati, Jon A Detterich, Roberta M. Kato, Imran R. Masood, Daniel Cerrone, K. Lewinter, Payal Shah
Publikováno v:
Pediatric Cardiology. 43:54-61
Low forced vital capacity (FVC) is associated with decreased exercise capacity in CHD. Multiple prior cardiac surgeries have been associated with low FVC. We seek to understand the relationship between low FVC, number of cardiac surgeries and cardiop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6831cb48e8126bd40aa5549864dea66
https://doi.org/10.1007/s00246-021-02692-0
https://doi.org/10.1007/s00246-021-02692-0
Autor:
Jon A Detterich, John C. Wood, Roberta M. Kato, Richard Sposto, John B. Sunwoo, Maha Khaleel, Saranya Veluswamy, Wanwara Thuptimdang, Lonnie K. Zeltzer, Michael C.K. Khoo, Payal Shah, Patjanaporn Chalacheva, Thomas D. Coates
Publikováno v:
Haematologica
Vaso-occlusive crisis (VOC) is a hallmark of sickle cell disease (SCD) and occurs when deoxygenated sickled red blood cells occlude the microvasculature. Any stimulus, such as mental stress, which decreases microvascular blood flow will increase the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2896802351efb9e675efe53761e3d5a1
http://europepmc.org/articles/PMC6939522
http://europepmc.org/articles/PMC6939522
Autor:
Roberta M. Kato, Payal Shah, John B. Sunwoo, Wanwara Thuptimdang, Michael C.K. Khoo, Saranya Veluswamy, Maha Khaleel, Thomas D. Coates
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Frontiers in Physiology
Frontiers in Physiology
Recent studies have shown that individuals with sickle cell disease (SCD) exhibit greater vasoconstriction responses to physical autonomic stressors, such as heat pain and cold pain than normal individuals, but this is not the case for mental stress.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b46f22522ad24efb1212ef9b3dc99a9b
https://doi.org/10.3389/fphys.2021.698209
https://doi.org/10.3389/fphys.2021.698209
Autor:
Jon A Detterich, John C. Wood, Roberta M. Kato, Joo-Yeun Oh, Payal Shah, Honglei Liu, Michael C.K. Khoo, Thomas D. Coates, Patjanaporn Chalacheva, Bruke Tedla, Silvie Suriany, Rakesh P. Patel, Henry Jay Forman, Ginger L. Milne
Publikováno v:
Free Radic Biol Med
Sickle cell disease (SCD) is a monogenetic disease that results in the formation of hemoglobin S. Due to more rapid oxidation of hemoglobin S due to intracellular heme and adventitious iron in SCD, it has been thought that an inherent property of SCD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8fd5eb8c3fcf051f036402b8e64b741
https://doi.org/10.1016/j.freeradbiomed.2019.07.004
https://doi.org/10.1016/j.freeradbiomed.2019.07.004
Autor:
Patjanaporn Chalacheva, Saranya Veluswamy, John B. Sunwoo, Jon A Detterich, Silvie Suriany, John C. Wood, Roberta M. Kato, Wanwara Thuptimdang, Thomas D. Coates, Christopher C Denton, Michael C.K. Khoo, Payal Shah, Honglei Liu
Publikováno v:
American journal of hematologyREFERENCES. 96(3)
Alpha thalassemia is a hemoglobinopathy due to decreased production of the α-globin protein from loss of up to four α-globin genes, with one or two missing in the trait phenotype. Individuals with sickle cell disease who co-inherit the loss of one
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7d2cce7926526e51475ed1339804f20
https://pubmed.ncbi.nlm.nih.gov/33247606
https://pubmed.ncbi.nlm.nih.gov/33247606
Autor:
Rory Kamerman-Kretzmer, Roberta M. Kato, Katy Peck, Thomas G. Keens, Eugene Y. Sohn, Sally L. Davidson Ward
Publikováno v:
Pediatric pulmonology.
Background Two modes of ventilation commonly used in children requiring chronic home mechanical ventilation (HMV) via tracheostomy are Assist Control (AC) and Synchronized Intermittent Mandatory Ventilation with Pressure Support (SIMV+PS). There has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fff59aba0f64935f22f593c93651971
https://pubmed.ncbi.nlm.nih.gov/33006249
https://pubmed.ncbi.nlm.nih.gov/33006249
Autor:
Jon A Detterich, John C. Wood, Roberta M. Kato, Michael C.K. Khoo, Silvie Suriany, Maha Khaleel, Patjanaporn Chalacheva, Christopher C Denton, Kelly Russell, Thomas D. Coates, Richard Sposto, Henry Jay Forman, Saranya Veluswamy, Adam Bush, Payal Shah
Publikováno v:
Am J Hematol
Sickle cell disease (SCD) is a monogenic hemoglobinopathy associated with significant morbidity and mortality. Cardiopulmonary, vascular and sudden death are the reasons for the majority of young adult mortality in SCD. To better understand the clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0f02b1a057b15b93379faf204f5e3fa
https://pubmed.ncbi.nlm.nih.gov/33108017
https://pubmed.ncbi.nlm.nih.gov/33108017