Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Shahira Elshafie"'
Publikováno v:
African Journal of Biological Sciences. 18:59-74
Publikováno v:
Fayoum University Medical Journal. 5:41-45
Publikováno v:
Fayoum University Medical Journal. 1:19-35
Autor:
Livia Parodi, Khalid Hamid El Hachimi, Stéphane Zuily, Marine Legendre, Diana Rodriguez, Dario Saracino, Aleksandra Trifunovic, Silvina Perin, Nicolas Villain, Marijana Croon, Thierry Kuntzer, Mahmoud Y. Issa, Fanny Mochel, Filippo M. Santorelli, Foudil Lamari, Priscilla Thomas, Cyril Goizet, Chantal Tse, Claire Ewenczyk, Florence Fellmann, Maha S. Zaki, Arnaud Mourier, Patrick Giavalisco, Laurent Le Corre, Aurélien Trimouille, Emilie Blond, Milica Popovic, Frédéric Darios, Anastasia D. Gazi, Cyril Mignot, Isabelle Kemlin, Sophie M. Steculorum, Cécilia Marelli-Tosi, Joseph G. Gleeson, Mathilde Renaud, Claire Pujol, Jean-Luc Boucher, S. Mathieu, Shahira Elshafie, Anne Legrand, Serge Picaud, Alexandra Durr, Giulia Coarelli, Giovanni Stevanin, Manon Valet, Daniele Galatolo, Rana Alkouri, Alexandre Seyer
Publikováno v:
Journal of Experimental Medicine
Journal of Experimental Medicine, Rockefeller University Press, 2021, 218 (11), pp.e20210846. ⟨10.1084/jem.20210846⟩
J Exp Med
Journal of Experimental Medicine, 2021, 218 (11), pp.e20210846. ⟨10.1084/jem.20210846⟩
Journal of Experimental Medicine, Rockefeller University Press, 2021, 218 (11), pp.e20210846. ⟨10.1084/jem.20210846⟩
J Exp Med
Journal of Experimental Medicine, 2021, 218 (11), pp.e20210846. ⟨10.1084/jem.20210846⟩
International audience; Hereditary spastic paraplegias are heterogeneous neurodegenerative disorders. Understanding of their pathogenicmechanisms remains sparse, and therapeutic options are lacking. We characterized a mouse model lacking the Cyp2u1 g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::469946ff71d85dcc23b62485c5694fca
https://hal-pasteur.archives-ouvertes.fr/pasteur-03434224
https://hal-pasteur.archives-ouvertes.fr/pasteur-03434224
Publikováno v:
Laboratory Medicine
Objective Because of the rapidly emerging SARS-CoV-2 pandemic and its wide public health challenges, rapid diagnosis is essential to decrease the spread. Antigen-based rapid detection tests are available; however, insufficient data about their perfor
Autor:
Shahira Elshafie
Publikováno v:
Fayoum University Medical journal. 1:24-27
– The purpose of this paper is to explore the challenges facing medical education system in Egypt particularly in the area of education quality. It builds upon several existing studies conducted in Egypt to make the case for improving education out
Autor:
Heba M. Zein Elabdin, Sara A. Taha, Ahmed Salah Aldin Hassan, Shahira Elshafie, Maher A. Al-Amir
Publikováno v:
The Egyptian Journal of Internal Medicine, Vol 29, Iss 3, Pp 112-116 (2017)
Background Hepcidin is a small peptide that is produced by hepatocytes and circulates in the plasma. It plays a central role in regulating the iron status in the body. Aim The aim of this study was to measure serum hepcidin levels in maintenance hemo
Publikováno v:
Comparative Clinical Pathology. 24:1223-1230
Multiple sclerosis has a clinically significant heritable component. The interleukin 7 receptor alpha (IL-7RA) has been recognized as a susceptibility gene for multiple sclerosis (MS). It is known that demographic, environmental factors, as well as p
Autor:
Al‐Kassem Ahmed Al‐Gamil, Mona Gamal Mostafa El Nahhas, Ahmed Ali Badie Sady, Abeer Mohamed Abdelrazik, Manal Niazi El Said, Shahira Elshafie, Ghada M. Ezzat Ahmed
Publikováno v:
Transfusion. 56(9)
BACKGROUND β-Thalassemia is considered the most common chronic hemolytic anemia in Egypt. Alloimmunization can lead to serious clinical complications in transfusion-dependent patients. The objective of this study was to determine the frequency and t
Publikováno v:
Transfusion.
Background Rh discrepancies are a problem during routine testing because of partial and weak D phenotypes. Some blood units with weak and partial D expression may escape detection by serology. Limitations of serology can be overcome by molecular typi