Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Maria Caimari"'
Autor:
Chrysanthi Kouri, Grit Sommer, Idoia Martinez de Lapiscina, Rawda Naamneh Elzenaty, Lloyd J.W. Tack, Martine Cools, S. Faisal Ahmed, Christa E. Flück, Saygin Abali, Zehra Yavas Abali, Leyla Akin, Maricruz Almaraz, Laura Audí, Murat Aydin, Antonio Balsamo, Federico Baronio, Jillian Bryce, Kanetee Busiah, Maria Caimari, Núria Camats-Tarruella, Ariadna Campos-Martorell, Luis Castaño, Anna Casteràs, Semra Çetinkaya, Yee-Ming Chan, Hedi L. Claahsen-van der Grinten, Ines Costa, Fatma Feyza Darendeliler, Justin H. Davies, Isabel Esteva, Helena Fabbri-Scallet, Courtney A. Finlayson, Emilio Garcia, Beatriz Garcia Cuartero, Alina German, Evgenia Globa, Gil Guerra-Junior, Julio Guerrero, Tulay Guran, Sabine E. Hannema, Olaf Hiort, Josephine Hirsch, Leuan Hughes, Marco Janner, Zofia Kolesinska, Katherine Lachlan, Anna Lauber-Biason, Jana Krenek Malikova, Dagmar l'Allemand, Nina Lenhnerr-Taube, Angela Lucas-Herald, Jamala Mammadova, Kenneth MсElreavey, Veronica Mericq, Isabel Mönig, Francisca Moreno, Julia Mührer, Marek Niedziela, Anna Nordenstrom, Burçe Orman, Sukran Poyrazoglu, Jose M. Rial, Meilan M. Rutter, Amaia Rodríguez, Tara Schafer-Kalkhoff, Kay-Sara Sauter, Sumudu Nimali Seneviratne, Maria Sredkova-Ruskova, Rieko Tadokoro-Cuccaro, Ajay Thankamony, Mónica Tomé, Amaia Vela, Malgorzata Wasniewska, David Zangen, Nataliya Zelinska
Publikováno v:
EBioMedicine, Vol 99, Iss , Pp 104941- (2024)
Summary: Background: Steroidogenic factor 1 (SF-1/NR5A1) is essential for human sex development. Heterozygous NR5A1/SF-1 variants manifest with a broad range of phenotypes of differences of sex development (DSD), which remain unexplained. Methods: We
Externí odkaz:
https://doaj.org/article/85fc4633ac7a47e48fff5e498c208fd3
Autor:
Jose Antonio Delgado, Juan Robles Bauza, Maria Caimari Jaume, Josep Miquel Bauça, Gerardo Pérez Esteban
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 512
Background-aim Different protocols exist for newborn screening of congenital hypothyroidism (CH) worldwide, with different thyrotropin cut-off values for repetition and confirmation tests. This study aimed to assess local protocol in terms of specifi
Autor:
Antoni Aguiló, Aina Yañez, Maria Caimari, Antoni Burguera, Bartolome Burguera, Elena Cabeza, Juan Tur, Antoni Colom, Marga Frontera, Estefanía Piñero, Marta E. Couce, Esther Cardo
Publikováno v:
Obesity Facts. 4:400-406
AIMS: To test the feasibility of a school-based intervention, which combines an incentive-driven physical activity program with lifestyle lectures, and its potential beneficial outcome on children’s metabolic parameters. METHODS: We conducted a 6-m
Akademický článek
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Autor:
Cristina Armero-Bujaldón, Estefanía Moratalla Jareño, Diego de Sotto-Esteban, María Caimari Jaume
Publikováno v:
Anales de Pediatría, Vol 96, Iss 4, Pp 376-377 (2022)
Externí odkaz:
https://doaj.org/article/083d919597ff4384a95e0f89f0c6850c
Autor:
Lila Maria Caimari
Publikováno v:
Histoire, économie & société. :41
A partir de un vasto corpus de textos producidos por la Policía de la Capital y la Policía Federal Argentina a lo largo del siglo XX, este artículo analiza la paradójica celebración de elementos provenientes de la misma cultura popular que la po
Autor:
Susana Ares Segura, Carmen Temboury Molina, María Jesús Chueca Guindulain, Gema Grau Bolado, María Jesus Alija Merillas, María Caimari Jaume, Paula Casano Sancho, José Carlos Moreno Navarro, José Manuel Rial Rodríguez, Amparo Rodríguez Sánchez
Publikováno v:
Anales de Pediatría, Vol 89, Iss 4, Pp 254.e1-254.e7 (2018)
Resumen: El objetivo de este documento es revisar las recomendaciones actuales en el manejo del hijo de madre con patología autoinmune tiroidea. En este 2017 se ha publicado la guía de la Asociación Americana de Tiroides para el diagnóstico y man
Externí odkaz:
https://doaj.org/article/dddde39fa38c4351b82b3602c8a073dc
Autor:
Susana Ares Segura, Carmen Temboury Molina, María Jesús Chueca Guindulain, Gema Grau Bolado, María Jesus Alija Merillas, María Caimari Jaume, Paula Casano Sancho, José Carlos Moreno Navarro, José Manuel Rial Rodríguez, Amparo Rodríguez Sánchez
Publikováno v:
Anales de Pediatría (English Edition), Vol 89, Iss 4, Pp 254.e1-254.e7 (2018)
The objective of this document is to review the current recommendations in the management of the foetus and the newborn child born to mothers with autoimmune thyroid disease. In 2017, the American Thyroid Association published guidelines for the diag
Externí odkaz:
https://doaj.org/article/9bb3ed1295ee4d23819a7a1bb545b975
Autor:
Jana Malikova, Núria Camats, Mónica Fernández-Cancio, Karen Heath, Isabel González, María Caimarí, Miguel del Campo, Marian Albisu, Stanislava Kolouskova, Laura Audí, Christa E Flück
Publikováno v:
PLoS ONE, Vol 9, Iss 8, p e104838 (2014)
Human NR5A1/SF-1 mutations cause 46,XY disorder of sex development (DSD) with broad phenotypic variability, and rarely cause adrenal insufficiency although SF-1 is an important transcription factor for many genes involved in steroidogenesis. In addit
Externí odkaz:
https://doaj.org/article/ed8db0b77dc64bc6ba506d50bb9995e1