Zobrazeno 1 - 10
of 12
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:
Camilla Pellegrini, Marta Columbaro, Elisa Schena, Sabino Prencipe, Davide Andrenacci, Patricia Iozzo, Maria Angela Guzzardi, Cristina Capanni, Elisabetta Mattioli, Manuela Loi, David Araujo-Vilar, Stefano Squarzoni, Saverio Cinti, Paolo Morselli, Assuero Giorgetti, Laura Zanotti, Alessandra Gambineri, Giovanna Lattanzi
Publikováno v:
Experimental and Molecular Medicine, Vol 51, Iss 8, Pp 1-17 (2019)
Fat tissue disorders: Dysfunctional fat cell differentiation An abnormal distribution of fatty tissues associated with certain tissue disorders is driven by disrupted fat cell differentiation. Type 2 familial partial lipodystrophy (FPLD2) is a geneti
Externí odkaz:
https://doaj.org/article/acb5e923c2674727aca3ca4769ad4e1d
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
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
Publikováno v:
Diabetologia Hungarica. 28:16-17
Publikováno v:
Diabetologia Hungarica. 28:83-84
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.
Autor:
David Araujo-Vilar
Publikováno v:
Endocrine Abstracts.
Publikováno v:
Nucleus
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