Montserrat Amat Bou
Investigador
Research group
Professional network profiles
Last Publications
- Molina-Giraldo PX, Murillo-Garcia S, Meis L, Sans-Capdevila O, Amat-Bou M, Llobet-Garcès M, Jimenez-Chillaron JC, Ramon-Krauel M and Lerin C A time-restricted feeding intervention in children and adolescents with obesity: The TRansForm study protocol Frontiers in Nutrition . 9: 1026694-1026694.
- Ramon-Krauel M, Amat-Bou M, Serrano M, Martinez-Monseny T and Lerin C Targeting the Gut Microbiome in Prader-Willi Syndrome. Journal of Clinical Medicine . 10(22): 5328.
- Ramon-Krauel M, Leal-Witt MJ, Osorio-Conles Ó, Amat-Bou M, Lerin C and Selva DM Relationship between adiponectin, TNFa, and SHBG in prepubertal children with obesity. Molecular and Cellular Pediatrics . 8(1): 3-3.
Projects
- Project name:
- SGR 2022-2024_Malaties metabòliques d'origen pediàtric
- Leader
- Carles Lerin Martinez
- Funding entities:
- Agaur - Agència de Gestió d'Ajuts Universitaris i de Recerca
- Code
- 2021 SGR 00661
- Starting - finishing date:
- 2022 - 2025
- Project name:
- El microbioma intestinal como diana terapéutica en el síndrome de Prader-Willi: efectos metabólicos y en el comportamiento de los pacientes
- Leader
- Marta Ramon Krauel
- Funding entities:
- Instituto de Salud Carlos III (ISCIII)
- Code
- PI20/00301
- Starting - finishing date:
- 2021 - 2025
- Project name:
- Modulación de la dieta durante las primeras etapas de la vida como estrategia de prevención de la obesidad infantil
- Leader
- Carles Lerin Martinez
- Funding entities:
- Ministerio de Economía Y Competitividad (MINECO), Fundació Privada per a la Recerca i la Docència Sant Joan de Déu - FSJD, Lerin Martinez, Carles
- Code
- PDC2021-121816-100
- Starting - finishing date:
- 2021 - 2024
News
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Research into treatments to combat obesity and excessive sleepiness in children with Prader-Willi syndrome
Researchers from Sant Joan de Déu have promoted various research projects in recent years to advance the understanding of Prader-Willi syndrome and study new treatments for children affected by this rare disease.