Zobrazeno 1 - 10
of 13
pro vyhledávání: '"David Araujo Vilar"'
Autor:
Antia Fernandez-Pombo, Everardo Josue Diaz-Lopez, Ana I. Castro, Sofia Sanchez-Iglesias, Silvia Cobelo-Gomez, Teresa Prado-Moraña, David Araujo-Vilar
Publikováno v:
Cells, Vol 12, Iss 5, p 725 (2023)
Type 2 familial partial lipodystrophy (FPLD2) is a laminopathic lipodystrophy due to pathogenic variants in the LMNA gene. Its rarity implies that it is not well-known. The aim of this review was to explore the published data regarding the clinical c
Externí odkaz:
https://doaj.org/article/a73ac91d5f184d9cb7d96d85e0be43a8
Autor:
Christian Costa-Lathan, Nestor Vazquez-Agra, Ana-Teresa Marques-Afonso, Anton Cruces-Sande, Miguel-Angel Martinez-Olmos, David Araujo-Vilar, Alvaro Hermida-Ameijeiras
Publikováno v:
Journal of Investigative Medicine. 71:149-158
We aimed to evaluate the role of plasma phenylalanine (Phe) levels and its fluctuations in some neurocognitive domains and brain magnetic resonance imaging (MRI) findings in adult patients with phenylketonuria (PKU). It was an observational study tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4716fe1c5c503718875e7accdc81059
https://doi.org/10.1177/10815589221143485
https://doi.org/10.1177/10815589221143485
Autor:
David Araujo-Vilar, Antía Fernández-Pombo, Silvia Cobelo-Gómez, Ana I. Castro, Sofía Sánchez-Iglesias
Publikováno v:
Endocrinología, Diabetes y Nutrición. 70:290-292
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a2295c006fc68673b6612ec70e302b5
https://doi.org/10.1016/j.endinu.2022.12.009
https://doi.org/10.1016/j.endinu.2022.12.009
Publikováno v:
Diabetologia Hungarica. 28:16-17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::562cd52ec9605e03b4b74f5ac2c4d5ca
https://doi.org/10.24121/dh.2020.s1.7
https://doi.org/10.24121/dh.2020.s1.7
Publikováno v:
Diabetologia Hungarica. 28:83-84
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50b6d83ee73679627a02d0ec7ea0a782
https://doi.org/10.24121/dh.2020.s1.56
https://doi.org/10.24121/dh.2020.s1.56
Autor:
Keziah Cook, Anna Stears, David Araujo-Vilar, Ferruccio Santini, Stephen O'Rahilly, Giovanni Ceccarini, Shruti Tibrewala, Pamela Bradt, Corinne Vigouroux, Camille Vatier, David B Savage
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa0e7cef0edbf5e9f9ef5ca8ca9426c4
https://doi.org/10.1530/endoabs.63.p586
https://doi.org/10.1530/endoabs.63.p586
Autor:
David Araujo-Vilar
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24dbba8a979423dd4c73cf175b796110
https://doi.org/10.1530/endoabs.56.s20.3
https://doi.org/10.1530/endoabs.56.s20.3
Publikováno v:
Nucleus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a79e104342fcb4ad8749ea503388869
https://doi.org/10.1080/19491034.2018.1515606
https://doi.org/10.1080/19491034.2018.1515606
Autor:
Isabel Castro Piedras, Jesús Martin Calamata, Berta Victoria, Ignacio Bernabeú Moron, María Teresa Calvo, Fernando Palos Paz, Olga Barca Mallo, David Araujo Vilar, Roberto Peinó, Diego Peteiro, Joaquin Lado Abeal, Ramón Albero Gamboa
Publikováno v:
Medicina Clínica. 137:551-554
Fundamento y objetivo La resistencia a la accion de las hormonas tiroideas (SRHT) es un sindrome causado mayoritariamente por mutaciones en el gen receptor beta de las hormonas tiroideas (THRB). Se estudian cinco familias con fenotipo de SRHT. Pacien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29a52901625f9f87306a454f34db1397
https://doi.org/10.1016/j.medcli.2010.11.037
https://doi.org/10.1016/j.medcli.2010.11.037
Autor:
Joaquin, Lado Abeal, Ramón, Albero Gamboa, David, Araujo Vilar, Olga, Barca Mallo, Ignacio, Bernabeú Moron, María Teresa, Calvo, Isabel, Castro Piedras, Jesús, Martin Calamata, Fernando, Palos Paz, Roberto, Peinó, Diego, Peteiro, Berta, Victoria
Publikováno v:
Medicina clinica. 137(12)
Resistance to thyroid hormone (RTH) is a syndrome mostly caused by mutations in thyroid hormone receptor beta gen (THRB). We present five families with RTH phenotype.THRB gene sequencing. In vitro studies to evaluate the mutants response to thyroid h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::90288c3b05fbeb82eb514391e6515a27
https://pubmed.ncbi.nlm.nih.gov/21703645
https://pubmed.ncbi.nlm.nih.gov/21703645