Zobrazeno 1 - 9
of 9
pro vyhledávání: '"S, Cambiazzo"'
Autor:
Claudia Pengue, Gonzalo Cesar, María Gabriela Alvarez, Graciela Bertocchi, Bruno Lococo, Rodolfo Viotti, María Ailén Natale, Melisa D Castro Eiro, Silvia S Cambiazzo, Nancy Perroni, Myriam Nuñez, María Cecilia Albareda, Susana A Laucella
Publikováno v:
PLoS ONE, Vol 14, Iss 6, p e0218260 (2019)
Chronic inflammation, as a consequence of the persistent infection with Trypanosoma cruzi, leads to continuous activation of the immune system in patients with chronic Chagas disease. We have previously shown that increased sera levels of soluble P-s
Externí odkaz:
https://doaj.org/article/119c5d54b9ea49fca77448b54c8579b9
Autor:
Rodolfo Viotti, Claudia Pengue, Gonzalo Leandro Cesar, Bruno Lococo, Susana A. Laucella, María Ailén Natale, Melisa D. Castro Eiro, Graciela Bertocchi, Silvia S. Cambiazzo, María Gabriela Alvarez, Nancy Perroni, Myriam Nuñez, María Cecilia Albareda
Publikováno v:
PLoS ONE
PLoS ONE, Vol 14, Iss 6, p e0218260 (2019)
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
PLoS ONE, Vol 14, Iss 6, p e0218260 (2019)
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Chronic inflammation, as a consequence of the persistent infection with Trypanosoma cruzi, leads to continuous activation of the immune system in patients with chronic Chagas disease. We have previously shown that increased sera levels of soluble P-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0999e36a64ac3bff6d5a95900e89dff5
https://doi.org/10.1371/journal.pone.0218260
https://doi.org/10.1371/journal.pone.0218260
Publikováno v:
Blood. 80:1582-1585
delta beta-Thalassemia and hereditary persistence of fetal hemoglobin (HPFH) are inherited disorders characterized by the persistent synthesis of fetal hemoglobin (HbF) during adult life. The Spanish type of delta beta-thalassemia is a mild thalassem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a934e4af6e59f4526436728d43793a68
https://doi.org/10.1182/blood.v80.6.1582.1582
https://doi.org/10.1182/blood.v80.6.1582.1582
Autor:
M. T. Dibarrart, Pujades Ma, M. A. Calvo, Mariano Linares, A. Miguel-Garcia, A. Miguel-Sosa, S. Cambiazzo, J. L. Vives Corrons
Publikováno v:
European journal of haematology. 55(5)
Oxidative damage to erythrocytes in thalassaemia has been related to generation of free radicals by an excess of denaturated alpha- or beta-globin chains, intracellular iron overload and low concentration of normal haemoglobin (HGB). Two good indicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4572d95b4ee58821c0cbdbf3556be4f6
https://pubmed.ncbi.nlm.nih.gov/7493680
https://pubmed.ncbi.nlm.nih.gov/7493680
Publikováno v:
Blood. 80(6)
delta beta-Thalassemia and hereditary persistence of fetal hemoglobin (HPFH) are inherited disorders characterized by the persistent synthesis of fetal hemoglobin (HbF) during adult life. The Spanish type of delta beta-thalassemia is a mild thalassem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ffd9a6f89117c1ada365707acfe7d5ca
https://pubmed.ncbi.nlm.nih.gov/1520881
https://pubmed.ncbi.nlm.nih.gov/1520881
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Vives Corrons JL; Haematology Laboratory Department, Hospital Clínic i Provincial, University of Barcelona, Spain., Miguel-García A, Pujades MA, Miguel-Sosa A, Cambiazzo S, Linares M, Dibarrart MT, Calvo MA
Publikováno v:
European journal of haematology [Eur J Haematol] 1995 Nov; Vol. 55 (5), pp. 327-31.
Autor:
Vives-Corrons JL; Haematology Laboratory Department, Hospital Clinic i Provincial, University of Barcelona, Spain., Pujades MA, Miguel-García A, Miguel-Sosa A, Cambiazzo S
Publikováno v:
Blood [Blood] 1992 Sep 15; Vol. 80 (6), pp. 1582-5.