Raquel Corripio
Overview
Explore the profile of Raquel Corripio including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
37
Citations
285
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0
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Recent Articles
1.
Escartin R, de Peray B, Couto Y, Martinez-Mejias A, Corripio R
J Clin Med
. 2025 Jan;
14(1.
PMID: 39797309
The goal of childhood obesity treatment is to benefit the physical and mental health of children who suffer from it and to prevent complications, improving their quality of life and...
2.
Corripio R, Soriano-Guillen L, Herrero F, Castro-Feijoo L, Escribano A, Sol-Ventura P, et al.
Front Endocrinol (Lausanne)
. 2024 Dec;
15:1498726.
PMID: 39703867
Objective: Idiopathic central precocious puberty (CPP) precipitates epiphyseal fusion of growth plates in long bones, leading to reduced adult stature. Gonadotropin-releasing hormone analogues (GnRHa) are the treatment of choice for...
3.
Ramos-Rodriguez M, Subirana-Granes M, Norris R, Sordi V, Fernandez A, Fuentes-Paez G, et al.
Cell Genom
. 2024 Jul;
4(8):100604.
PMID: 38959898
Insulinomas are rare neuroendocrine tumors arising from pancreatic β cells, characterized by aberrant proliferation and altered insulin secretion, leading to glucose homeostasis failure. With the aim of uncovering the role...
4.
Gomez-Munoz L, Perna-Barrull D, Caroz-Armayones J, Murillo M, Rodriguez-Fernandez S, Valls A, et al.
Front Immunol
. 2024 Jun;
15:1439643.
PMID: 38919614
[This corrects the article DOI: 10.3389/fimmu.2022.825426.].
5.
Gomez-Munoz L, Perna-Barrull D, Villalba A, Rodriguez-Fernandez S, Ampudia R, Teniente-Serra A, et al.
Front Immunol
. 2024 Jun;
15:1439246.
PMID: 38898887
[This corrects the article DOI: 10.3389/fimmu.2020.611522.].
6.
Baena N, Monk D, Aguilera C, Fraga M, Fernandez A, Gabau E, et al.
Clin Epigenetics
. 2024 May;
16(1):62.
PMID: 38715103
Background: Temple syndrome (TS14) is a rare imprinting disorder caused by maternal UPD14, imprinting defects or paternal microdeletions which lead to an increase in the maternal expressed genes and a...
7.
Couto-Rosende Y, Garcia-Tirado D, Palacio-Marco M, Caixas A, Corripio R
J Clin Med
. 2023 Jun;
12(12).
PMID: 37373659
Prader-Willi Syndrome (PWS) is the most frequent cause of genetic obesity. Early reports indicate that children with PWS require 20-40% fewer calories than healthy children to maintain adequate growth. Growth...
8.
Pellikaan K, Nguyen N, Rosenberg A, Coupaye M, Goldstone A, Hoybye C, et al.
J Clin Endocrinol Metab
. 2023 Jun;
108(12):e1720-e1730.
PMID: 37267430
Context: Prader-Willi syndrome (PWS) is a complex disorder combining hypothalamic dysfunction, neurodevelopmental delay, hypotonia, and hyperphagia with risk of obesity and its complications. PWS is caused by the loss of...
9.
Gomez-Munoz L, Perna-Barrull D, Murillo M, Armengol M, Alcalde M, Catala M, et al.
Noncoding RNA
. 2023 Mar;
9(2).
PMID: 36960962
The partial remission (PR) phase of type 1 diabetes (T1D) is an underexplored period characterized by endogenous insulin production and downmodulated autoimmunity. To comprehend the mechanisms behind this transitory phase...
10.
Gamez S, Cobo J, Fernandez-Lafitte M, Coronas R, Parra I, Oliva J, et al.
J Clin Med
. 2023 Feb;
12(3).
PMID: 36769803
Prader-Willi syndrome (PWS) is a genetic disorder produced by a lack of expression of paternally derived genes in the 15q11-13 region. Research has generally focused on its genetic and behavioral...