Zobrazeno 1 - 10
of 80
pro vyhledávání: '"Luisa Bay"'
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 9 (2021)
Abstract Glycogen storage disease type I is an autosomal recessive disorder of carbohydrate metabolism that manifests mainly by hepatomegaly and hypoglycemia with short fasts. Despite strict therapy, patients present long-term renal and liver complic
Externí odkaz:
https://doaj.org/article/1d73ed9acea64deaaac3451021869be2
Autor:
Luisa Bay
Publikováno v:
Revista Paraguaya de Reumatología, Vol 3, Pp 1-1 (2017)
Externí odkaz:
https://doaj.org/article/a5c9f130f06d4a60928e452c9dcd190e
Autor:
Ariana Díaz, Luciano D’Attilio, Federico Penas, Bettina Bongiovanni, Estefanía Massa, Agata Cevey, Natalia Santucci, Oscar Bottasso, Nora Goren, María Luisa Bay
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 13 (2023)
IntroductionTuberculosis (TB) is a major health problem characterized by an immuno-endocrine imbalance: elevated plasma levels of cortisol and pro- and anti-inflammatory mediators, as well as reduced levels of dehydroepiandrosterone. The etiological
Externí odkaz:
https://doaj.org/article/0ad8ec77ccf44e64ae55619ac745042c
Autor:
Bettina Bongiovanni, Ariana Díaz, Natalia Santucci, Luciano David D’Attilio, Oscar Bottasso, Rogelio Hernández Pando, María Luisa Bay
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Dehydroepiandrosterone (DHEA) is an androgen synthesized by the adrenal cortex, which is an intermediary in the biosynthesis of sex hormones, such as testosterone and estradiol. DHEA mostly circulates as a conjugated ester, in the form of sulfate (DH
Externí odkaz:
https://doaj.org/article/030a50de3ba44223a2ba8036a1b6dc7f
Autor:
Ariana Díaz, Magdalena Diab, Dulce Mata-Espinosa, Estela Bini, Luciano D'Attilio, Oscar Bottasso, Rogelio Hernández-Pando, María Luisa Bay, Bettina Bongiovanni
Publikováno v:
Cytokine. 168:156229
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71841525d76e5d14e12b63f00d837403
https://doi.org/10.1016/j.cyto.2023.156229
https://doi.org/10.1016/j.cyto.2023.156229
Autor:
Lynda E. Polgreen, Luisa Bay, Lorne A. Clarke, Nathalie Guffon, Simon A. Jones, Joseph Muenzer, Ana Lorena Flores, Kathryn Wilson, David Viskochil
Publikováno v:
American journal of medical genetics. Part A. 188(10)
Mucopolysaccharidosis Type I (MPS I) is caused by deficiency of α-L-iduronidase. Short stature and growth deceleration are common in individuals with the attenuated MPS I phenotype. Study objectives were to assess growth in individuals with attenuat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9738a2cf2231978ff083bda228c63d88
https://pubmed.ncbi.nlm.nih.gov/35869927
https://pubmed.ncbi.nlm.nih.gov/35869927
Autor:
Walter Gardeñez, Mauricio Rassetto, Natalia Santucci, Oscar Bottasso, Bettina Bongiovanni, María Luisa Bay, Diego Bértola, Luciano D’Attilio, Georgina Florencia Gallucci, Ariana Díaz
Publikováno v:
PLoS ONE
PLoS ONE, Vol 16, Iss 9, p e0257214 (2021)
PLoS ONE, Vol 16, Iss 9, p e0257214 (2021)
Our earlier studies in tuberculosis (TB) patients indicate that in those where the process evolves to a larger pulmonary involvement, the immune endocrine response may promote an unfavorable environment. Chronic infectious diseases, and their persist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11746c816e36f3cc3452ba87bc0d5c45
https://pubmed.ncbi.nlm.nih.gov/34506568
https://pubmed.ncbi.nlm.nih.gov/34506568
Autor:
Graciela Zuccaro, Hernán Eiroa, Hernan Amartino, Mariana Cazalas, Claudia Arberas, Adriana Berretta, Claudio A S Parisi, Guillermo Drelichman, Marcela Pereyra, Carmen De Cunto, Luisa Bay, Adriana Copiz, Alberto Maffey, Hugo Botto, Alejandro Fainboim, Virginia Fano, Graciela Espada, Andrea Schenone, Norberto Guelber, Alejandra Antacle, Rodrigo Remondino, Raquel Staciuk, Norma Spécola
Publikováno v:
Archivos Argentinos de Pediatria. 119
Here we describe the current challenges of mucopolysaccharidosis type I: the need for an adequate classification, establishing its relationship to therapeutic indications; an early diagnosis, from neonatal screening, its advantages and barriers, to c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27199487412c5fa7d22223a634696872
https://doi.org/10.5546/aap.2021.e193
https://doi.org/10.5546/aap.2021.e193
Autor:
Georgina, Gallucci, Ariana, Díaz, Rocío Del Valle, Fernandez, Bettina, Bongiovanni, Matilde, Imhoff, Estefanía, Massa, Natalia, Santucci, Diego, Bértola, Susana, Lioi, María Luisa, Bay, Oscar, Bottasso, Luciano, D'Attilio
Publikováno v:
Life Sciences. 301:120614
Previous studies in TB patients showed an immuno-endocrine imbalance characterized by a disease-severity associated increase in plasma levels of proinflammatory cytokines and glucocorticoids (GCs). To analyze the potential immunomodulatory effect of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94af48c0de02bada683537377622b6e4
https://doi.org/10.1016/j.lfs.2022.120614
https://doi.org/10.1016/j.lfs.2022.120614
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 9 (2021)
Journal of Inborn Errors of Metabolism and Screening v.9 2021
Journal of Inborn Errors of Metabolism and Screening
Instituto Genética para Todos (IGPT)
instacron:IGPT
Journal of Inborn Errors of Metabolism and Screening v.9 2021
Journal of Inborn Errors of Metabolism and Screening
Instituto Genética para Todos (IGPT)
instacron:IGPT
Glycogen storage disease type I is an autosomal recessive disorder of carbohydrate metabolism that manifests mainly by hepatomegaly and hypoglycemia with short fasts. Despite strict therapy, patients present long-term renal and liver complications. D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c56d6a9df990cfd6f8b8981cc8d9e1b
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942021000100307&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942021000100307&tlng=en