Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Zahra Sadr"'
Autor:
Zahra Sadr, Seyyed Amir Yasin Ahmadi, Batool Tayefi, Sedigheh Yousefzadegan, Soheila Mahdavynia, Ramin Zare Mahmoudabadi, Kourosh Kabir, Zahra Rampisheh, Neda SoleimanvandiAzar, Ali Tayebi, Ali Mehrabi, Marzieh Nojomi
Publikováno v:
BMC Medical Education, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract Background and objective One of the most important aspects of health is social health. Addressing social health and social accountability is possible by education of social determinants of health (SDH) to medical students. The aim of current
Externí odkaz:
https://doaj.org/article/3c5c2a195d5544dfa65a838f6b5f42e3
Publikováno v:
بهداشت در عرصه, Vol 12, Iss 1 (2024)
زمینه و اهداف: دخانیات یکی از عوامل خطر قابل پیشگیری بیماریها بوده که سالانه باعث مرگ بسیاری از افراد میشود. شناسایی چالشهای مرتبط با
Externí odkaz:
https://doaj.org/article/3ed2cd7c73ff4b689ce63c2ded251707
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-6 (2022)
Abstract Variegate Porphyria (VP) is an inherited rare disorder that is caused by mutations in the protoporphyrinogen oxidase (PPOX) gene. This deficiency is associated with the accumulation of porphyrins and porphyrin precursors in the body, which,
Externí odkaz:
https://doaj.org/article/63d36937226b4ac189a7b54f8d413aba
Autor:
Zahra Sadr, Mehrnaz Jamali Moghaddam, Hamideh Sabet Rouhani, Nadia Sani’ee, Maryam Biglari Abhari
Publikováno v:
Journal of Preventive Epidemiology, Vol 6, Iss 2, Pp e32-e32 (2021)
Breast cancer is one of the most common cancers and is one of the biggest health threats in women around the world. Since the systematic review study in Iran has not been conducted so far, this study was designed to determine the role of family physi
Externí odkaz:
https://doaj.org/article/9f02915a76694674ad3a07681490e888
NMNAT1 and hereditary spastic paraplegia (HSP): expanding the phenotypic spectrum of NMNAT1 variants
Publikováno v:
Neuromuscular Disorders. 33:295-301
Publikováno v:
Neurological Sciences.
Publikováno v:
Italian journal of pediatrics. 48(1)
Variegate Porphyria (VP) is an inherited rare disorder that is caused by mutations in the protoporphyrinogen oxidase (PPOX) gene. This deficiency is associated with the accumulation of porphyrins and porphyrin precursors in the body, which, in turn,
Publikováno v:
BMC Nutrition, Vol 10, Iss 1, Pp 1-11 (2024)
Abstract Introduction Overweight and obesity are common problems among teenagers regardless of ethnicity, race, and socio-economic status. Therefore, this study aims to explore the social and environmental factors impacting adolescents motivation for
Externí odkaz:
https://doaj.org/article/2847f0069e6a46af938f44bbc721cefd
Autor:
Axel Leblanc, Chotivut Tangchingchai, Zahra Sadre Momtaz, Elyjah Kiyooka, Jean-Michel Hartmann, Gonzalo Troncoso Fernandez-Bada, Zoltán Scherübl, Boris Brun, Vivien Schmitt, Simon Zihlmann, Romain Maurand, Étienne Dumur, Silvano De Franceschi, François Lefloch
Publikováno v:
Physical Review Research, Vol 6, Iss 3, p 033281 (2024)
Hybrid superconductor(S)-semiconductor(Sm) devices bring a range of functionalities into superconducting circuits. In particular, hybrid parity-protected qubits and Josephson diodes were recently proposed and experimentally demonstrated. Such devices
Externí odkaz:
https://doaj.org/article/07ed69861f244ad4a7579e7221af082b
Publikováno v:
Journal of Molecular Neuroscience. 65:444-455
Neuroblastoma (NB) remains the critical challenge in pediatric oncology. It has the highest rate of spontaneous regression among all human cancers. Aurora kinase B (AURKB), a crucial regulator of malignant mitosis, is involved in chromosome segregati