Zobrazeno 1 - 10
of 165
pro vyhledávání: '"A, Quyou"'
Publikováno v:
Arab Gulf Journal of Scientific Research, 2023, Vol. 42, Issue 3, pp. 636-645.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/AGJSR-01-2023-0027
Autor:
Zghaid, Mustapha, Arfaoui, Amine, Tahri, Mounia, Ameran, Ismail, HardouZ, Houria, Quyou, Ali, Benchrif, Abdelfettah
Publikováno v:
Tanzania Journal of Health Research; Jul2024, Vol. 25 Issue 3, p1198-1210, 13p
Autor:
Bouabid, Bahia, El Yahyaoui, Ouafae, El Bakkali, Mohamed, Ouaaziz, Nabil Ait, Lrhorfi, Lalla Aicha, Quyou, Ali, Bengueddour, Rachid
Publikováno v:
Journal of Global Innovations in Agricultural Sciences; 2024, Vol. 12 Issue 3, p653-660, 8p
Akademický článek
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Autor:
Wang, Ping, Liao, Hong, Wang, Quyou, Xie, Hanbing, Xu, Bocheng, Xiang, Qinqin, Wang, He, Yang, Mei, Liu, Shanling
Publikováno v:
Clinical Genetics; May2024, Vol. 105 Issue 5, p549-554, 6p
Publikováno v:
The Pan African Medical Journal, Vol 36, Iss 381 (2020)
INTRODUCTION: This work aims to bring out the epidemiological characteristics of extrapulmonary tuberculosis (EPTB) in the province of Larache (Morocco) and to investigate the effect of gender and age on its localization and treatment outcome. METHOD
Externí odkaz:
https://doaj.org/article/ab1869562bdd423aa02ccda0642f0a48
Publikováno v:
Tanzania Journal of Health Research; Jan2024, Vol. 25 Issue 1, p524-542, 19p
Autor:
Ouaaziz, Nabil Ait, El Bakkali, Mohamed, El yahyaoui, Ouafae, Bouabid, Bahia, Derdaki, Mohamed, Arfaoui, Amine, El majid Soulaymani, Abd, Quyou, Ali
Publikováno v:
Tanzania Journal of Health Research; Jan2024, Vol. 25 Issue 1, p511-523, 13p
Publikováno v:
Arab Gulf Journal of Scientific Research.
PurposeThe present study aims to bring out the impact of consanguinity on spontaneous pregnancy loss (SPL) and on descendants’ health, among the population of north Morocco.Design/methodology/approachConvenience sampling was used for collecting dat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25da9f964758d83834247ecd2051e9c2
https://doi.org/10.1108/agjsr-01-2023-0027
https://doi.org/10.1108/agjsr-01-2023-0027
Publikováno v:
Reproductive Sciences. 29:768-780
L1 syndrome, a complex X-linked neurological disorder, is caused by mutations in the L1 cell adhesion molecule (L1CAM) gene. L1CAM molecule is a member of immunoglobulin (Ig) superfamily of neural cell adhesion molecules (CAMs), which plays a pivotal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f8064aa249b65713453ebf4eda6258c
https://doi.org/10.1007/s43032-021-00828-4
https://doi.org/10.1007/s43032-021-00828-4