Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Katia Allal-Taouli"'
Autor:
Nawel Kaddour, Farah Benyettou, Kawtar Moulai, Abdelouahab Mebarki, Katia Allal-Taouli, Rose Ghemrawi, Jamie Whelan, Hafida Merzouk, Ali Trabolsi, Nassima Amel Mokhtari-Soulimane
Publikováno v:
Heliyon, Vol 10, Iss 9, Pp e30450- (2024)
Complications associated with Type 1 diabetes (T1D) have complex origins that revolve around chronic hyperglycemia; these complications involve hemostasis disorders, coagulopathies, and vascular damage. Our study aims to develop innovative approaches
Externí odkaz:
https://doaj.org/article/230a5703294a4b6bb22858365dd43afc
Autor:
Ilhem Nassour-Mokhtari, Bouchra Loukidi, Abdellatif Moussouni, Reda Bettioui, Riad Benhabib, Hafida Merzouk, Amaria Aouar, Katia Allal-Taouli
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
Abstract Background Recurrent pregnancy loss (RPL) is a common disorder that affects around 3 to 5% of pregnant women. It has different causes, and in about 50%, it is of unknown etiology. Thrombophilia might increase the risk of RPL by adversely aff
Externí odkaz:
https://doaj.org/article/9c72bfe508f74e939983c512ae72ea44
Autor:
Riad Benhabib, Hafida Merzouk, Ilhem Nassour-Mokhtari, Abdellatif Moussouni, Reda Bettioui, Bouchra Loukidi, Katia Allal-Taouli, Amaria Aouar
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
Background Recurrent pregnancy loss (RPL) is a common disorder that affects around 3 to 5% of pregnant women. It has different causes, and in about 50%, it is of unknown etiology. Thrombophilia might increase the risk of RPL by adversely affecting th
Publikováno v:
Transfusion Clinique et Biologique. 24:350-351
Introduction Des tests specifiques sont pratiques pour la recherche du phenotype D faible, notamment chez les donneurs de sang «negatifs» afin d’eviter la formation d’anticorps anti-D chez les receveurs. But de l’etude L’objectif de cette e
Autor:
Nassour-Mokhtari, Ilhem1 (AUTHOR), Loukidi, Bouchra1 (AUTHOR), Moussouni, Abdellatif2,3 (AUTHOR) abdellatif.moussouni@gmail.com, Bettioui, Reda3 (AUTHOR), Benhabib, Riad4 (AUTHOR), Merzouk, Hafida1 (AUTHOR), Aouar, Amaria3 (AUTHOR), Allal-Taouli, Katia1,5 (AUTHOR)
Publikováno v:
Egyptian Journal of Medical Human Genetics. 8/17/2020, Vol. 21 Issue 1, pN.PAG-N.PAG. 1p.