Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Fréderic Gottrand"'
Autor:
Ivie Maneschy, Luis A. Moreno, Azahara I. Ruperez, Andrea Jimeno, María L. Miguel-Berges, Kurt Widhalm, Anthony Kafatos, Cristina Molina-Hidalgo, Dénes Molnar, Fréderic Gottrand, Cinzia Le Donne, Yannis Manios, Evangelia Grammatikaki, Marcela González-Gross, Mathilde Kersting, Jean Dallongeville, Sonia Gómez-Martinez, Stefaan De Henauw, Alba M. Santaliestra-Pasías, on behalf of the HELENA Study Group
Publikováno v:
Nutrients, Vol 14, Iss 15, p 3033 (2022)
Adolescence is recognized as a time of rapid physiological and behavioral change. In this transition, eating behavior is still being formed and remains an integral part of a person’s lifestyle throughout his or her life. This study aims to assess e
Externí odkaz:
https://doaj.org/article/b096208b842b42318b3c42935e8fd5b5
Autor:
Marion Almes, Anne Spraul, Mathias Ruiz, Muriel Girard, Bertrand Roquelaure, Nolwenn Laborde, Fréderic Gottrand, Anne Turquet, Thierry Lamireau, Alain Dabadie, Marjorie Bonneton, Alice Thebaut, Babara Rohmer, Florence Lacaille, Pierre Broué, Alexandre Fabre, Karine Mention-Mulliez, Jérôme Bouligand, Emmanuel Jacquemin, Emmanuel Gonzales
Publikováno v:
Diagnostics, Vol 12, Iss 5, p 1169 (2022)
Background: Cholestasis is a frequent and severe condition during childhood. Genetic cholestatic diseases represent up to 25% of pediatric cholestasis. Molecular analysis by targeted-capture next generation sequencing (NGS) has recently emerged as an
Externí odkaz:
https://doaj.org/article/71ba909fe65b4bb7be1a22d10e514f3b
Navigating global collaboration: challenges faced by the international network on esophageal atresia
Autor:
Frédéric Gottrand, Usha Krishnan, Anke Widenmann, Michaela Dellenmark Blom, Luigi Dall’Oglio, Rene Wijnen, Michiel van Wijk, JoAnne Fruithof, Daniel von Allmen, Tom Kovesi, Christophe Faure
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-3 (2024)
Abstract The International Network on Esophageal Atresia (INoEA) stands as a beacon of collaboration in addressing the complexities of this congenital condition on a global scale. The eleven board members, from various countries (USA, Canada, France,
Externí odkaz:
https://doaj.org/article/0bfa3699d3a84146b303578a77c181f1
Akademický článek
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Autor:
Lamisse Mansour-Hendili, Cyril Gitiaux, Madeleine Harion, Céline Latouche, Bénédicte Heron, Tanya Stojkovic, Mélanie Rama, Thomas Smol, Anne Sophie Jourdain, Karine Mention, Yann Nadjar, Manuel Schiff, Julie Lemale, Jamal Ghoumid, Frédéric Gottrand, Cécile Talbotec, Agnès Rötig, Benoît Funalot, Isabelle Desguerre
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Sodium dependent multivitamin transporter (SMVT) deficiency is a very rare autosomal recessive disorder characterized by multisystemic clinical manifestations due to combined biotin, panthotenic acid and lipoic acid deficiency. About 10 families have
Externí odkaz:
https://doaj.org/article/996c5f2b1d304ade96264a8eba265cad
Autor:
Matthieu Groh, Julien Rohmer, Nicolas Etienne, Wadih Abou Chahla, Antoine Baudet, Aurélie Chan Hew Wai, Cécile Chenivesse, Irena Clisson Rusek, Vincent Cottin, Matthieu Decamp, Pascal De Groote, Fanny Delahousse, Nicolas Duployez, Stanislas Faguer, Frédéric Gottrand, Florent Huang, Thierry Leblanc, Antoine Magnan, Thierry Martin, Geoffrey Mortuaire, Antoine Néel, Luc Paris, Arnaud Petit, Julien Rossignol, Nicolas Schleinitz, Juliette Soret-Dulphy, Delphine Staumont-Salle, Benjamin Terrier, Louis Terriou, Jean-François Viallard, Guillaume Lefèvre, Jean-Emmanuel Kahn
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-35 (2023)
Abstract Eosinophilic-related clinical manifestations are protean and the underlying conditions underpinning eosinophilia are highly diverse. The etiological workup of unexplained eosinophilia/hypereosinophilia can be challenging, and can lead someti
Externí odkaz:
https://doaj.org/article/1286a876df1e46fea03f30a2bd0da951
Autor:
The International EA-QOL Group, Michaela Dellenmark Blom, Stefanie Witt, Benjamin Zendejas, Ivana Sabolić, Juan Domingo Porras-Hernandez, Natalie Durkin, Simon Eaton, Kjersti Birketvedt, Alba Sánchez Galán, Katalin Eszter Müller, Anna Rozensztrauch, Tutku Soyer, Siqi Li, Anastasia Fourtaka, Corne de Vos, Graham Slater, Ana Špoljarić, John Bennett, Ragnhild Emblem, Zita Andrásdi, Robert Smigiel, Dariusz Patkowski, Çiğdem Ulukaya Durakbaşa, Marina Stilinović, Frederic Gottrand, Dora Škrljak Šoša, Tomislav Luetić, Sylwester Gerus, Shen Yang, Yong Zhao, Yichao Gu, Shuangshuang Li, Diego Rodriguez-Alvirde, Orsolya Kadenczki, Miram Pasini, Vuokko Wallace, Anke Widenmann, Feliciana Milagres Sikwete, Jinshi Huang, Leopoldo Martínez Martínez, Kate Abrahamsson, Shawn Izadi, Benno M Ure, Daniel Sidler, Julia H Quitmann, Jens Dingemann
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundEsophageal atresia (EA) is a rare congenital anomaly characterized by a discontinuity of the esophagus. Following surgical repair, survival rates have improved dramatically the past decenniums and today exceed 90%, but the children commonly
Externí odkaz:
https://doaj.org/article/4829ecacbcbb4ffebab6b964fbec1314
Autor:
Lucie Marousez, Farid Ichou, Philippe Lesnik, Léa Chantal Tran, Marie De Lamballerie, Frédéric Gottrand, Delphine Ley, Jean Lesage
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Sterilized donor milk (DM) is frequently used for feeding preterm infants. To date, the effect of different modes of DM sterilization on short-chain fatty acids (SCFAs) remains unknown. We aimed to quantify SCFAs in DM samples after two types of milk
Externí odkaz:
https://doaj.org/article/c779de264b8e4f27822d255ffeb898db
Autor:
Dominique Turck, Frédéric Gottrand
La gastroentérologie pédiatrique a bénéficié du progrès des connaissances physiopathologiques, des avancées technologiques (notamment endoscopiques) et des innovations thérapeutiques pour devenir une spécialité pédiatrique majeure. Son cha
Autor:
Gloria Pérez-Gimeno, Miguel Seral-Cortes, Sergio Sabroso-Lasa, Luis Mariano Esteban, Empar Lurbe, Laurent Béghin, Frederic Gottrand, Aline Meirhaeghe, Manon Muntaner, Anthony Kafatos, Dénes Molnár, Catherine Leclercq, Kurt Widhalm, Mathilde Kersting, Esther Nova, Diego F. Salazar-Tortosa, Marcela Gonzalez-Gross, Christina Breidenassel, Kathrin Sinningen, Thaïs De Ruyter, Idoia Labayen, Azahara I. Rupérez, Gloria Bueno-Lozano, Luis A. Moreno
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
IntroductionFrom genome wide association study (GWAS) a large number of single nucleotide polymorphisms (SNPs) have previously been associated with blood pressure (BP) levels. A combination of SNPs, forming a genetic risk score (GRS) could be conside
Externí odkaz:
https://doaj.org/article/01412b0f74104bf292612ed01c030cee