Insulin Resistance in Obese Children: What Can Metabolomics and Adipokine Modelling Contribute?

por Rupérez, Francisco J., Martos-Moreno, Gabriel Á., Chamoso-Sánchez, David, Barbas, Coral, Argente, Jesús
Publicado 2020

ODP605 Body Mass Index and Weight Reductions in Patients With SRC1 Genetic Variant Obesity After 1 Year of Setmelanotide

por Martos-Moreno, Gabriel Á, Argente, Jesús, Scimia, Cecilia, Ohayan, Olga, Yuan, Guojun, Farooqi, Sadaf
Publicado 2022

OR22-05 Rare Biallelic Variants in Obesity-Related Genes in the Madrid Pediatric Obesity Cohort

por Martos-Moreno, Gabriel Á, Moeller, Ida Hatoum, Martín-Rivada, Álvaro, Pérez-Jurado, Luis A, Argente, Jesús
Publicado 2020

Conservative Treatment for Childhood and Adolescent Obesity: Real World Follow-Up Profiling and Clinical Evolution in 1300 Patients

por Martos-Moreno, Gabriel Á., Martínez-Villanueva Fernández, Julián, Frías-Herrero, Alicia, Martín-Rivada, Álvaro, Argente, Jesús
Publicado 2021

A proteomic approach to obesity and type 2 diabetes

por López-Villar, Elena, Martos-Moreno, Gabriel Á, Chowen, Julie A, Okada, Shigeru, Kopchick, John J, Argente, Jesús
Publicado 2015

Unveiling Metabolic Phenotype Alterations in Anorexia Nervosa through Metabolomics

por Mayo-Martínez, Laura, Rupérez, Francisco J., Martos-Moreno, Gabriel Á., Graell, Montserrat, Barbas, Coral, Argente, Jesús, García, Antonia
Publicado 2021

A Novel Melanocortin-4 Receptor Mutation MC4R-P272L Associated with Severe Obesity Has Increased Propensity To Be Ubiquitinated in the ER in the Face of Correct Folding

por Granell, Susana, Serra-Juhé, Clara, Martos-Moreno, Gabriel Á., Díaz, Francisca, Pérez-Jurado, Luis A., Baldini, Giulia, Argente, Jesús
Publicado 2012

Proteomic analysis allows for early detection of potential markers of metabolic impairment in very young obese children

por Martos-Moreno, Gabriel Á, Sackmann-Sala, Lucila, Barrios, Vicente, Berrymann, Darlene E, Okada, Shigeru, Argente, Jesús, Kopchick, John J
Publicado 2014

Ethnicity Strongly Influences Body Fat Distribution Determining Serum Adipokine Profile and Metabolic Derangement in Childhood Obesity

por Martos-Moreno, Gabriel Á., Martínez-Villanueva, Julián, González-Leal, Rocío, Barrios, Vicente, Sirvent, Sara, Hawkins, Federico, Chowen, Julie A., Argente, Jesús
Publicado 2020

Heterozygous rare genetic variants in non-syndromic early-onset obesity

por Serra-Juhé, Clara, Martos-Moreno, Gabriel Á., Bou de Pieri, Francesc, Flores, Raquel, Chowen, Julie A., Pérez-Jurado, Luis A., Argente, Jesús
Publicado 2019

Bone Mineral Density, Body Composition, and Metabolic Health of Very Low Birth Weight Infants Fed in Hospital Following Current Macronutrient Recommendations during the First 3 Yea...

por Mihatsch, Walter, Dorronsoro Martín, Izaskun, Barrios-Sabador, Vicente, Couce, María L., Martos-Moreno, Gabriel Á., Argente, Jesús, Quero, José, Saenz de Pipaon, Miguel
Publicado 2021

Novel genes involved in severe early-onset obesity revealed by rare copy number and sequence variants

por Serra-Juhé, Clara, Martos-Moreno, Gabriel Á., Bou de Pieri, Francesc, Flores, Raquel, González, Juan R., Rodríguez-Santiago, Benjamín, Argente, Jesús, Pérez-Jurado, Luis A.
Publicado 2017

Defective minor spliceosome mRNA processing results in isolated familial growth hormone deficiency

por Argente, Jesús, Flores, Raquel, Gutiérrez-Arumí, Armand, Verma, Bhupendra, Martos-Moreno, Gabriel Á, Cuscó, Ivon, Oghabian, Ali, Chowen, Julie A, Frilander, Mikko J, Pérez-Jurado, Luis A
Publicado 2014

Efficacy and Safety of Asfotase Alfa in Infants and Young Children With Hypophosphatasia: A Phase 2 Open-Label Study

por Hofmann, Christine E, Harmatz, Paul, Vockley, Jerry, Högler, Wolfgang, Nakayama, Hideki, Bishop, Nick, Martos-Moreno, Gabriel Á, Moseley, Scott, Fujita, Kenji P, Liese, Johannes, Rockman-Greenberg, Cheryl
Publicado 2019

Large exonic deletions in POLR3B gene cause POLR3-related leukodystrophy

por Gutierrez, Mariana, Thiffault, Isabelle, Guerrero, Kether, Martos-Moreno, Gabriel Á., Tran, Luan T., Benko, William, van der Knaap, Marjo S., van Spaendonk, Rosalina M. L., Wolf, Nicole I., Bernard, Geneviève
Publicado 2015

Response to growth hormone in patients with RNPC3 mutations

por Martos‐Moreno, Gabriel Á, Travieso‐Suárez, Lourdes, Pozo‐Román, Jesús, Muñoz‐Calvo, María T, Chowen, Julie A, Frilander, Mikko J, Pérez‐Jurado, Luis A, Hawkins, Federico G, Argente, Jesús
Publicado 2018

Quality of life improvements following one year of setmelanotide in children and adult patients with Bardet–Biedl syndrome: phase 3 trial results

por Forsythe, Elizabeth, Haws, Robert M., Argente, Jesús, Beales, Philip, Martos-Moreno, Gabriel Á., Dollfus, Hélène, Chirila, Costel, Gnanasakthy, Ari, Buckley, Brieana C., Mallya, Usha G., Clément, Karine, Haqq, Andrea M.
Publicado 2023

Mutations in pregnancy‐associated plasma protein A2 cause short stature due to low IGF‐I availability

por Dauber, Andrew, Muñoz‐Calvo, María T, Barrios, Vicente, Domené, Horacio M, Kloverpris, Soren, Serra‐Juhé, Clara, Desikan, Vardhini, Pozo, Jesús, Muzumdar, Radhika, Martos‐Moreno, Gabriel Á, Hawkins, Federico, Jasper, Héctor G, Conover, Cheryl A, Frystyk, Jan, Yakar, Shoshana, Hwa, Vivian, Chowen, Julie A, Oxvig, Claus, Rosenfeld, Ron G, Pérez‐Jurado, Luis A, Argente, Jesús
Publicado 2016

Pathogenic Variants in RNPC3 are Associated with Hypopituitarism and Primary Ovarian Insufficiency

por Akin, Leyla, Rizzoti, Karine, Gregory, Louise C, Corredor, Beatriz, Le Quesne Stabej, Polona, Williams, Hywel, Buonocore, Federica, Mouilleron, Stephane, Capra, Valeria, McGlacken-Byrne, Sinead M, Martos-Moreno, Gabriel Á, Azmanov, Dimitar N., Kendirci, Mustafa, Kurtoglu, Selim, Suntharalingham, Jenifer P., Galichet, Christophe, Gustincich, Stefano, Tasic, Velibor, Achermann, John C., Accogli, Andrea, Filipovska, Aleksandra, Tuilpakov, Anatoly, Maghnie, Mohamad, Gucev, Zoran, Gonen, Z. Burcin, Pérez-Jurado, Luis A, Robinson, Iain, Badge, Robin Lovell, Argente, Jesús, Dattani, Mehul T
Publicado 2022

Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy

por Grange, Laura J., Reynolds, John J., Ullah, Farid, Isidor, Bertrand, Shearer, Robert F., Latypova, Xenia, Baxley, Ryan M., Oliver, Antony W., Ganesh, Anil, Cooke, Sophie L., Jhujh, Satpal S., McNee, Gavin S., Hollingworth, Robert, Higgs, Martin R., Natsume, Toyoaki, Khan, Tahir, Martos-Moreno, Gabriel Á., Chupp, Sharon, Mathew, Christopher G., Parry, David, Simpson, Michael A., Nahavandi, Nahid, Yüksel, Zafer, Drasdo, Mojgan, Kron, Anja, Vogt, Petra, Jonasson, Annemarie, Seth, Saad Ahmed, Gonzaga-Jauregui, Claudia, Brigatti, Karlla W., Stegmann, Alexander P. A., Kanemaki, Masato, Josifova, Dragana, Uchiyama, Yuri, Oh, Yukiko, Morimoto, Akira, Osaka, Hitoshi, Ammous, Zineb, Argente, Jesús, Matsumoto, Naomichi, Stumpel, Constance T.R.M., Taylor, Alexander M. R., Jackson, Andrew P., Bielinsky, Anja-Katrin, Mailand, Niels, Le Caignec, Cedric, Davis, Erica E., Stewart, Grant S.
Publicado 2022