Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Leyla Bagheri"'
Publikováno v:
Journal of Nephropathology, Vol 13, Iss 3, Pp e17130-e17130 (2024)
Primary hyperoxaluria is a rare congenital autosomal recessive disorder disrupting the glyoxylate metabolism pathway in the liver. Type1 primary hyperoxaluria is caused by a deficiency in a specific liver enzyme namely, alanine glyoxylate-aminotransf
Externí odkaz:
https://doaj.org/article/25f0497506fe40b6a9624ccf721542d8
Autor:
Leyla Bagheri, Hoda Kavosi, Nasim Shokouhi, Shila Aghayani, Khosro Sadeghniiat Haghighi, Seyed Reza Najafizadeh
Publikováno v:
European Journal of Translational Myology (2024)
We aimed to investigate sleep disorders in patients with systemic scleroderma (SSc) and its relationship with socio-demographic and medical factors and to provide a suitable solution to better control the disease and improve the quality of life in th
Externí odkaz:
https://doaj.org/article/d5c3ad7b8e564c3baf8347a8e1c3da39
Publikováno v:
Journal of Biological Engineering, Vol 16, Iss 1, Pp 1-14 (2022)
Abstract Background According to recent studies, electrospun Poly (Ɛ-caprolactone) (PCL) is an absorbing candidate for the formulation of biocompatible scaffolds used in tissue engineering. Tissue engineering is a set of techniques for producing or
Externí odkaz:
https://doaj.org/article/42f952ef1bf24ffca931ae89e169eb69
Autor:
Leyla Bagheri, Davoud Jafari-Gharabaghlou, Hasan Valizadeh, Abolfazl Barzegari, Nosratollah Zarghami
Publikováno v:
Journal of Biomaterials Science, Polymer Edition. :1-20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fe1ca6cea24cc94dc45490503bd104e
https://doi.org/10.1080/09205063.2023.2170675
https://doi.org/10.1080/09205063.2023.2170675
Autor:
Leyla Bagheri, Fatemeh Rahimi, Sara Besharat, Mohammad Fathi, Alireza Zali, Sasan Tavana, Farzad Esmaeili Tarki, Nasser Malekpour Alamdari, Seyed Sina Naghibi Irvani, Siamak Afaghi, Fatemeh Pourmotahari, Ali Dabbagh, Seyed Ali Mousavi
Publikováno v:
The Tohoku journal of experimental medicine. 252(1)
The Coronavirus Disease 2019 (COVID-19) pandemic has killed many people worldwide since December 2019, and Iran has been among the most affected countries. In this retrospective study, we aimed to determine the prognostic factors associated with mort
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c101fbc0621f1cfb520c8721bff63037
https://pubmed.ncbi.nlm.nih.gov/32908083
https://pubmed.ncbi.nlm.nih.gov/32908083
Publikováno v:
Journal of Nephropathology.
Primary hyperoxaluria is a rare congenital autosomal recessive disorder disrupting the glyoxylate metabolism pathway in the liver. Type1 primary hyperoxaluria is caused by a deficiency in a specific liver enzyme namely, alanine glyoxylate-aminotransf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef2769412f66fe4cbb736cd3fc962763
https://doi.org/10.34172/jnp.2022.17130
https://doi.org/10.34172/jnp.2022.17130
Autor:
leyla bagheri, Marina Milyavskaya
This paper investigates the plausibility of novelty–variety as a potential basic psychological need in a series of three studies. Using criteria proposed by Baumeister and Leary (Psychol Bull 117:497–529, 1995) and Ryan and Deci (in Self-determin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c17f8627347e8571e34920284a4e502
https://doi.org/10.31234/osf.io/jv5d7
https://doi.org/10.31234/osf.io/jv5d7
