Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Andrés E. Muy-Pérez"'
Autor:
David Araújo-Vilar, Antía Fernández-Pombo, Gemma Rodríguez-Carnero, Miguel Ángel Martínez-Olmos, Ana Cantón, Rocío Villar-Taibo, Álvaro Hermida-Ameijeiras, Alicia Santamaría-Nieto, Carmen Díaz-Ortega, Carmen Martínez-Rey, Antonio Antela, Elena Losada, Andrés E. Muy-Pérez, Blanca González-Méndez, Sofía Sánchez-Iglesias
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background Lipodystrophy syndromes are a group of disorders characterized by a loss of adipose tissue once other situations of nutritional deprivation or exacerbated catabolism have been ruled out. With the exception of the HIV-associated li
Externí odkaz:
https://doaj.org/article/8461b38fdc1c400c8b434208e4dcf593
Autor:
Carmen Díaz-Ortega, Antía Fernández-Pombo, Alicia Santamaría-Nieto, Gemma Rodriguez-Carnero, David Araújo-Vilar, Antonio Antela, M.A. Martinez-Olmos, Blanca González-Méndez, Elena Losada, Sofía Sánchez-Iglesias, Rocío Villar-Taibo, Carmen Martínez-Rey, Andrés E. Muy-Pérez, Álvaro Hermida-Ameijeiras, Ana Canton
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Lipodystrophy syndromes are a group of disorders characterized by a loss of adipose tissue once other situations of nutritional deprivation or exacerbated catabolism have been ruled out. With the exception of the HIV-associated lipodystrop