Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Nadia Mahfouth"'
Autor:
Nacim Louhichi, Emna Bahloul, Slaheddine Marrakchi, Houda Ben Othman, Chahnez Triki, Kawthar Aloulou, Lobna Trabelsi, Nadia Mahfouth, Zeineb Ayadi-Mnif, Leila Keskes, Faiza Fakhfakh, Hamida Turki
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-8 (2019)
Abstract Background Chanarin-Dorfman syndrome (CDS) is a rare syndromic disease related to an accumulation of triacylglycerol in most organs. The aim of our study was to investigate various organs in a large series of CDS patients. Results We report
Externí odkaz:
https://doaj.org/article/2d57499c78b04551bfa10e55a114fbc3
Autor:
Chahnez Triki, Lobna Trabelsi, Nacim Louhichi, Emna Bahloul, Nadia Mahfouth, Leila Keskes, Faiza Fakhfakh, Houda Ben Othman, Slaheddine Marrakchi, Hamida Turki, Zeineb Ayadi-Mnif, Kawthar Aloulou
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-8 (2019)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Chanarin-Dorfman syndrome (CDS) is a rare syndromic disease related to an accumulation of triacylglycerol in most organs. The aim of our study was to investigate various organs in a large series of CDS patients. Results We report for the f