Zobrazeno 1 - 10
of 140
pro vyhledávání: '"Gabriel A. Martos-Moreno"'
Autor:
Ana Zamora Auñón, Blanca Guijo Alonso, Eva María De Andrés Esteban, Jesús Argente, Gabriel Á. Martos-Moreno
Publikováno v:
Anales de Pediatría, Vol 100, Iss 6, Pp 428-437 (2024)
Resumen: Introducción: El tratamiento de la obesidad infanto-juvenil, basado en modificaciones higiénico-dietéticas, ofrece habitualmente un éxito limitado y presenta una alta tasa de abandono del seguimiento por parte de los pacientes. La invest
Externí odkaz:
https://doaj.org/article/9a43de9eb4a24b148c74514b91bbe434
Publikováno v:
Global Pediatrics, Vol 7, Iss , Pp 100126- (2024)
Childhood obesity continues to be a major health problem worldwide with the consequent associated comorbidities becoming apparent at very early ages and increasing throughout life. Although the prevention of obesity is essential, it is no less true t
Externí odkaz:
https://doaj.org/article/a76095d7c4914e94939a98b477379865
Autor:
David Chamoso-Sanchez, Francisco Rabadán Pérez, Jesús Argente, Coral Barbas, Gabriel A. Martos-Moreno, Francisco J. Rupérez
Publikováno v:
Frontiers in Molecular Biosciences, Vol 10 (2023)
Introduction: Obesity results from an interplay between genetic predisposition and environmental factors such as diet, physical activity, culture, and socioeconomic status. Personalized treatments for obesity would be optimal, thus necessitating the
Externí odkaz:
https://doaj.org/article/500fd7c1938542f99857297e2f0ff3c0
Autor:
Elizabeth Forsythe, Robert M. Haws, Jesús Argente, Philip Beales, Gabriel Á. Martos-Moreno, Hélène Dollfus, Costel Chirila, Ari Gnanasakthy, Brieana C. Buckley, Usha G. Mallya, Karine Clément, Andrea M. Haqq
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Background Bardet–Biedl syndrome is a rare genetic disease associated with hyperphagia and early-onset, severe obesity. There is limited evidence on how hyperphagia and obesity affect health-related quality of life in patients with Bardet
Externí odkaz:
https://doaj.org/article/95baf4bee81746aaaf9b8a040bb3a09a
Autor:
Laura J. Grange, John J. Reynolds, Farid Ullah, Bertrand Isidor, Robert F. Shearer, Xenia Latypova, Ryan M. Baxley, Antony W. Oliver, Anil Ganesh, Sophie L. Cooke, Satpal S. Jhujh, Gavin S. McNee, Robert Hollingworth, Martin R. Higgs, Toyoaki Natsume, Tahir Khan, Gabriel Á. Martos-Moreno, Sharon Chupp, Christopher G. Mathew, David Parry, Michael A. Simpson, Nahid Nahavandi, Zafer Yüksel, Mojgan Drasdo, Anja Kron, Petra Vogt, Annemarie Jonasson, Saad Ahmed Seth, Claudia Gonzaga-Jauregui, Karlla W. Brigatti, Alexander P. A. Stegmann, Masato Kanemaki, Dragana Josifova, Yuri Uchiyama, Yukiko Oh, Akira Morimoto, Hitoshi Osaka, Zineb Ammous, Jesús Argente, Naomichi Matsumoto, Constance T.R.M. Stumpel, Alexander M. R. Taylor, Andrew P. Jackson, Anja-Katrin Bielinsky, Niels Mailand, Cedric Le Caignec, Erica E. Davis, Grant S. Stewart
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-22 (2022)
The SMC5/6 complex is critical for genome stability. Here, the authors identify mutations in SLF2 and SMC5 as cause of Atelís Syndrome characterized by microcephaly, short stature, anemia, segmented chromosomes and mosaic variegated hyperploidy.
Externí odkaz:
https://doaj.org/article/bfe3845b80824c5996d10d21e1575e9d
Autor:
Gabriel Á. Martos-Moreno, Julián Martínez-Villanueva, Rocío González-Leal, Vicente Barrios, Sara Sirvent, Federico Hawkins, Julie A. Chowen, Jesús Argente
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Background: Body fat content and distribution in childhood is influenced by sex and puberty, but interethnic differences in the percentage and distribution of body fat also exist. The abdominal visceral/subcutaneous fat ratio has been the main featur
Externí odkaz:
https://doaj.org/article/34dd5489a6224eeabf7a9b36b2ce0cd4
Publikováno v:
Anales de Pediatría, Vol 88, Iss 6, Pp 356.e1-356.e11 (2018)
Resumen: La hipofosfatasia es una enfermedad ultra-rara del metabolismo mineral óseo causada por un déficit de actividad de la fosfatasa alcalina, debido a la existencia de mutaciones en el gen ALPL. Clínicamente, se caracteriza por el desarrollo
Externí odkaz:
https://doaj.org/article/f220322769304a2bbb956e23f3b65516
Autor:
Gabriel Á. Martos-Moreno, Mercedes Gil-Campos, Gloria Bueno, Pilar Bahillo, Susana Bernal, Albert Feliu, Alfonso M. Lechuga-Sancho, Enrique Palomo, Rafael Ruiz, Amaia Vela
Publikováno v:
Nutrición Hospitalaria, Vol 30, Iss 4, Pp 787-793
Los objetivos de este estudio son, realizar una descripción de las características demográficas, antropométricas y de las alteraciones metabólicas de niños atendidos por obesidad resaltando las características aquellos casos de obesidad de ini
Externí odkaz:
https://doaj.org/article/37629274446a40f2b570646e43417035
Autor:
Andrea M, Haqq, Wendy K, Chung, Hélène, Dollfus, Robert M, Haws, Gabriel Á, Martos-Moreno, Christine, Poitou, Jack A, Yanovski, Robert S, Mittleman, Guojun, Yuan, Elizabeth, Forsythe, Karine, Clément, Jesús, Argente
Publikováno v:
The Lancet Diabetes & Endocrinology. 10:859-868
Impaired cilial signalling in the melanocortin-4 receptor (MC4R) pathway might contribute to obesity in patients with Bardet-Biedl syndrome and Alström syndrome, rare genetic diseases associated with hyperphagia and early-onset severe obesity. We ai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2962797ee5aa807f76cc357fb3df073
https://doi.org/10.1016/s2213-8587(22)00277-7
https://doi.org/10.1016/s2213-8587(22)00277-7
Autor:
Janire, Escudero García, Álvaro, Martín Rivada, Amalia, Uribe Posada, Verónica, Sanz Santiago, Jesús, Argente, Gabriel Ángel, Martos-Moreno
Publikováno v:
Endocrinología, Diabetes y Nutrición (English ed.). 69:576-583
Development of cystic fibrosis-related diabetes (CFRD) is associated with worsening of nutritional status and lung function, as well as increased mortality. The relevance of diagnosing the «pre-diabetic» status in these patients has not been addres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4910979aa1d4df02c82edbe8806261b
https://doi.org/10.1016/j.endien.2021.08.009
https://doi.org/10.1016/j.endien.2021.08.009