Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Ignacio, Bergada"'
Autor:
Kevin C J Yuen, Gudmundur Johannsson, Ken K Y Ho, Bradley S Miller, Ignacio Bergada, Alan D Rogol
Publikováno v:
Endocrine Connections, Vol 12, Iss 7, Pp 1-19 (2023)
Growth hormone deficiency (GHD) is a clinical syndrome that can manifest either as isolated or associated with additional pituitary hormone deficie ncies. Although diminished height velocity and short stature are useful and important clin ical marker
Externí odkaz:
https://doaj.org/article/d648e617175949ae9a9510acf8088a7a
Autor:
Kevin C J Yuen, Gudmundur Johannsson, Ken K Y Ho, Bradley S. Miller, Ignacio Bergada, Alan D Rogol
Publikováno v:
Endocrine Connections.
Growth hormone deficiency (GHD) is a clinical syndrome that can manifest either as isolated or associated with additional pituitary hormone deficiencies. Although diminished height velocity and short stature are useful and important clinical markers
Autor:
F Martin, Ferolla, E Walter, Yfran, M Gabriela, Ballerini, Ana, Caratozzolo, Analía, Toledano, Ana C, Giordano, Patricio L, Acosta, Hamilton, Cassinelli, Ignacio, Bergada, M Gabriela, Ropelato, María M, Contrini, Eduardo L, López, Normando, Mascardi
Publikováno v:
The Journal of Infectious Diseases. 226:958-966
Background 25-hydroxyvitamin D (VD) effects on lung function and immune-modulation might affect respiratory syncytial virus (RSV) infection outcomes. We aimed to assess VD levels on admission and their association with life-threatening RSV disease (L
Autor:
Guillermo Alonso, Carolina Arias Cau, Alicia Belgorosky, G Benzrihen, Ignacio Bergada, Debora Braslavsky, Sally Camper, Marta Ciaccio, S D'Amato, Isabel D Palma, Veronica Figueroa, Veronica Forclaz, Ana Keselman, Jacob Kitzman, Susana Mallea Gil, Hospital Militar Central, Buenos Aires Argentina, Roxana Marino, Marcelo Marti, Mirta Miras, Natalia Perez Garrido, Pablo Ramirez, Sebastian Vishnopolska, Maria Andrea Camilletti, Julian Martinez Mayer, Augusto Chaves Murriello, Gonzalo Chirino Felker, Maria Perez-Millan
Publikováno v:
Journal of the Endocrine Society. 6:A462-A463
Hypopituitarism with deficiency of one or more pituitary hormones (combined pituitary hormone deficiency or CPHD) can vary in severity and age at presentation. Additionally, the hormone abnormalities may evolve with time necessitating frequent evalua
Autor:
Claire Rochette, Nicolas Jullien, Alexandru Saveanu, Emmanuelle Caldagues, Ignacio Bergada, Debora Braslavsky, Marija Pfeifer, Rachel Reynaud, Jean-Paul Herman, Anne Barlier, Thierry Brue, Alain Enjalbert, Frederic Castinetti
Publikováno v:
PLoS ONE, Vol 10, Iss 5, p e0126648 (2015)
LHX4 is a LIM homeodomain transcription factor involved in the early steps of pituitary ontogenesis. To date, 8 heterozygous LHX4 mutations have been reported as responsible of combined pituitary hormone deficiency (CPHD) in Humans. We identified 4 n
Externí odkaz:
https://doaj.org/article/cc9aa415b3a5416ca27db31833e7f380
Akademický článek
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Autor:
Romina Grinspon, Patricia Bedecarras, Maria de Fatima Borges, Luciane Bussmann, German Iniguez, Ana Rocha, Elisabete Mantovani Rodrigues Resende, Veronica Figueroa Gacitua, Andrea Forrester, Carlos Milani, Viviana Osta, Maria Jose Rial, Silvia Gottlieb, Ana Chiesa, Ana Keselman, Andrea Arcari, Hamilton Cassinelli, Mirta Gryngarten, Patricia Papendieck, Marina Troiano, Florencia Clement, Maria SoledadRodriguez Prieto, Rosa Enacan, Ignacio Bergada, Maria Gabriela Ropelato, Maria Gabriela Ballerini, Segio Recabarren, Teresa Sir-Petermann, Ethel Codner, Vinicius Brito, Berenice Mendonca, Jean-Yves Picard, Nathalie Josso, Veronique Garzino, Rodolfo Rey
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5641f502133229d1bcbb10f56141f73e
https://doi.org/10.1210/endo-meetings.2011.part4.p13.p3-734
https://doi.org/10.1210/endo-meetings.2011.part4.p13.p3-734
Autor:
Analia Veronica Freire, Maria Eugenia Escobar, Mirta Gryngarten, Andrea Arcari, Maria Gabriela Ballerini, Marisol Morini, Ignacio Bergada, Maria Gabriela Ropelato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4f1c5be308d233799a4cbc19e6ec78d
https://doi.org/10.1210/endo-meetings.2011.part4.p13.p3-714
https://doi.org/10.1210/endo-meetings.2011.part4.p13.p3-714
Autor:
Mercedes Traversa, Martín Rodríguez, Maria Silvia Perez, Félix Puchulu, Sabrina Andrea Foscaldi, Ignacio Bergada, Gustavo Daniel Frechtel, Ariel Pablo Lopez
Publikováno v:
Diabetes research and clinical practice. 91(2)
Introduction There are at least six subtypes of Maturity Onset Diabetes of the Young (MODY) with distinctive genetic causes. MODY 3 is caused by mutations in HNF1A gene, an insulin transcription factor, so mutations in this gene are associated with i
Akademický článek
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