Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Vida Yazdani"'
Autor:
Mehdi Rasti, Amir Hossein Parniaei, Leila Dehghani, Salar Nasr Esfahani, Hossein Mirhendi, Vida Yazdani, Vajihe Azimian Zavareh
Publikováno v:
Regenerative Therapy, Vol 26, Iss , Pp 281-289 (2024)
Introduction: The skin plays a crucial role as a protective barrier against external factors, but disruptions to its integrity can lead to wound formation and hinder the natural healing process. Scar formation and delayed wound healing present signif
Externí odkaz:
https://doaj.org/article/d1708a6dc67c461a81d3612c1f7b1a11
Autor:
Vida Yazdani, Sheida Zeraattalab-Motlagh, Ahmad Jayedi, Maryam Majdi, Amin Mirrafiei, Fahimeh Martami, Kurosh Djafarian, Sakineh Shab-Bidar
Publikováno v:
Public Health Nutrition, Vol 26, Pp 1609-1616 (2023)
Abstract Objective: Evidence on the relationship between sleep duration and irregularity in daily energy intake with diet quality in Iranian adults is scarce. We aimed to evaluate the association of sleep duration with diet quality and irregularity
Externí odkaz:
https://doaj.org/article/9b4b259e3b81406e9d1c667c913fdda9
Autor:
Narges Nouri, Nayereh Nouri, Samane Tirgar, Elham Soleimani, Vida Yazdani, Farzaneh Zahedi, Bagher Larijani
Publikováno v:
Journal of Medical Ethics and History of Medicine, Vol 10 (2017)
Consanguineous marriage, which is common in many regions in the world, has absorbed much attention as a causative factor in raising the incidence of genetic diseases. The adverse effects may be attributed to the expression of the genes received from
Externí odkaz:
https://doaj.org/article/a2cc89a303644b438b6aa8f839b443eb
Autor:
Erfan Khorram, Mohammad Amin Tabatabaiefar, Omid Yaghini, Mehdi Khorrami, Vida Yazdani, Fatemeh Fakhr, Masoomeh Amini, Majid Kheirollahi
Publikováno v:
Molecular Genetics and Genomics. 298:485-493
Autor:
Mojgan Rezaei, Majid Kheirollahi, Arash Hejazifar, Erfan Khorram, Maryam Riahinezhad, Omid Iravani, Mehdi Khorrami, Omid Yaghini, Vida Yazdani
Publikováno v:
Journal of molecular neuroscience : MNReferences. 71(11)
Vanishing white matter disease (VWM) is a rare autosomal recessive leukodystrophy caused by a mutation in any of the five gene encoding subunits of the translation initiation factors eIF2B1 to eIF2B5. Whole-exome sequencing was performed on a 7-year-