Zobrazeno 1 - 10
of 34
pro vyhledávání: '"sickle cell syndromes"'
Autor:
German F Sáenz-Renauld
Publikováno v:
Acta Médica Costarricense, Vol 47, Iss 4, Pp 173-179 (2005)
Es notorio que en Costa Rica la frecuencia de las variantes más comunes de la hemoglobina (Hb) (S Y C) puede ser trazada desde África. Estas hemoglobinas son dos marcadores genéticos que han mantenido un equilibrado polimorfismo contra la presión
Externí odkaz:
https://doaj.org/article/6c61ed2e6005412c8a5b78934be5a685
Autor:
Maria Concetta Renda, Disma Renda, Angela Piazza, Giuseppina Calvaruso, Emanuela Fecarotta, Antonino Giangreco, Aurelio Maggio
Publikováno v:
Thalassemia Reports, Vol 4, Iss 2 (2014)
In patients with β-thalassemia and sickle cell syndromes there is an important secondary iron overload due to regular blood transfusions and increased duodenal iron absorption. As in genetic hemochromatosis, also the secondary iron storage leads to
Externí odkaz:
https://doaj.org/article/7ba7f3025b264ca09ca6e54430ef1bce
Autor:
M.S. Gonçalves, I.L. Queiroz, S.A. Cardoso, A. Zanetti, A.C. Strapazoni, E. Adorno, A. Albuquerque, A. Sant'Ana, M.G. dos Reis, A. Barral, M. Barral Netto
Publikováno v:
Brazilian Journal of Medical and Biological Research, Vol 34, Iss 10, Pp 1309-1313 (2001)
Sickle cell disease has a worldwide distribution and is a public health problem in Brazil. Although vaso-occlusive crisis (VOC) is one of the most important clinical features of the disease, there are still several steps of its pathogenesis which are
Externí odkaz:
https://doaj.org/article/8f5cd887c7dd46469328cee249945163
Autor:
Khalid Hafiani, Halima Bazoui, My Mustapha Hafid, Youssef El Madhi, Omar Amahmid, Driss Belghyti, Youssef El Guamri, Samira Marhabene, Khadija El Kharrim
Publikováno v:
Asian Pacific Journal of Tropical Disease, Vol 7, Iss 11, Pp 688-690 (2017)
Objective: To highlight the epidemiological characteristics and plot the current mapping of the sickle cell syndromes in children under 15 years old. Methods: A descriptive study was conducted on children with sickle cell disease over a period of 4 y
Publikováno v:
Expert Review of Molecular Diagnostics, 17(3), 281-291
Hemoglobinopathies constitute the most common severe monogenic disorders worldwide, with an increasing global burden each year. The benefit of applying programmes for preconception carrier screening, with the option of prenatal diagnosis, to minimize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7672162a334372ec4dfa605cbd16973f
https://hdl.handle.net/1887/115960
https://hdl.handle.net/1887/115960
Autor:
Emanuela Fecarotta, Antonino Giangreco, Aurelio Maggio, Giuseppina Calvaruso, Angela Piazza, Disma Renda, Maria Concetta Renda
Publikováno v:
Thalassemia Reports, Vol 4, Iss 2 (2014)
Thalassemia Reports; Volume 4; Issue 2; Pages: 2729
Thalassemia Reports; Volume 4; Issue 2; Pages: 2729
In patients with β-thalassemia and sickle cell syndromes there is an important secondary iron overload due to regular blood transfusions and increased duodenal iron absorption. As in genetic hemochromatosis, also the secondary iron storage leads to
Autor:
Maryse Etienne-Julan, Vanessa Tarer, Marie-Dominique Hardy-Dessources, Marie Laure Lalanne-Mistrih, Benoit Tressières, Danièle Mougenel, Philippe Connes, Yann Lamarre, Nathalie Lemonne, Olivier Hue, Xavier Waltz
Publikováno v:
Clinical Hemorheology and Microcirculation
Clinical Hemorheology and Microcirculation, IOS Press, 2015, 59, pp.37-43. ⟨10.3233/CH-131742⟩
Clinical Hemorheology and Microcirculation, IOS Press, 2018, pp.37-43. ⟨10.3233/CH-131742⟩
Clinical Hemorheology and Microcirculation, IOS Press, 2015, 59, pp.37-43. ⟨10.3233/CH-131742⟩
Clinical Hemorheology and Microcirculation, IOS Press, 2018, pp.37-43. ⟨10.3233/CH-131742⟩
International audience; The hematocrit-to-viscosity ratio (HVR) has been widely used has an estimate of red blood cell (RBC) oxygen transport effectiveness into the microvasculature or as an oxygen delivery index. However, no study investigated the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecde62627a8b9438a2bd250a14959eeb
https://hal.univ-antilles.fr/hal-01163460
https://hal.univ-antilles.fr/hal-01163460
Autor:
Sáenz-Renauld, German F
Publikováno v:
Acta Médica Costarricense, Vol 47, Iss 4, Pp 173-179 (2005)
Acta Médica Costarricense, Volume: 47, Issue: 4, Pages: 173-179, Published: OCT 2005
Acta Médica Costarricense, Volume: 47, Issue: 4, Pages: 173-179, Published: OCT 2005
Es notorio que en Costa Rica la frecuencia de las variantes más comunes de la hemoglobina (Hb) (S Y C) puede ser trazada desde África. Estas hemoglobinas son dos marcadores genéticos que han mantenido un equilibrado polimorfismo contra la presión
Autor:
Waltz, Xavier, Hardy-Dessources, Marie-Dominique, Lemonne, Nathalie, Mougenel, Danièle, Lalanne-Mistrih, Marie-Laure, Lamarre, Yann, Tarer, Vanessa, Tressières, Benoit, Etienne-Julan, Maryse, Hue, Olivier, Connes, Philippe
Publikováno v:
Clinical Hemorheology and Microcirculation
Clinical Hemorheology and Microcirculation, IOS Press, 2013, 2013 May 29. [Epub ahead of print]
Clinical Hemorheology and Microcirculation, IOS Press, 2013, 2013 May 29. [Epub ahead of print]
International audience; The hematocrit-to-viscosity ratio (HVR) has been widely used has an estimate of red blood cell (RBC) oxygen transport effectiveness into the microvasculature or as an oxygen delivery index. However, no study investigated the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0ef534a2c4e717ad32393c6eebadc2aa
https://www.hal.inserm.fr/inserm-01081701/document
https://www.hal.inserm.fr/inserm-01081701/document
Autor:
Danièle Mougenel, Nathalie Lemonne, Maryse Etienne-Julan, Yann Lamarre, Marie Laure Lalanne-Mistrih, Olivier Hue, Marie-Dominique Hardy-Dessources, Xavier Waltz, Vanessa Tarer, Philippe Connes, Benoit Tressières, Aurélien Pichon
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e52471 (2012)
PLoS ONE
PLoS ONE, Public Library of Science, 2012, 7 (12), pp.e52471. ⟨10.1371/journal.pone.0052471⟩
PLoS ONE
PLoS ONE, Public Library of Science, 2012, 7 (12), pp.e52471. ⟨10.1371/journal.pone.0052471⟩
Background/aimAlthough it has been hypothesized that muscle metabolism and fatigability could be impaired in sickle cell patients, no study has addressed this issue.MethodsWe compared muscle metabolism and function (muscle microvascular oxygenation,