Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Hazar Lahlou"'
Autor:
A. Jakar, A. El Kartouti, M. Er-Rami, Salma Benjelloun, M. El Haouri, A. Khalloufi, A. Zeroual, Hazar Lahlou
Publikováno v:
Pathologie Biologie. 61:49-53
An increase in the number of cases of cutaneous leishmaniasis has been observed, in recent years, in Morocco. We tried, through a series of 49 cases collected from the dermatology department at the military hospital Moulay Ismail of Meknes, to clarif
Autor:
Fatima El Boukhrissi, Mohamed El Haouri, Salma Benjelloun, Hazar Lahlou, Moncef Amrani Hassani, Ghita Yahyaoui, Imane Tlamçani, Youssef Bamou, Mohamed Karim Moudden, L. Balouch, Mohamed Baaj
Publikováno v:
Annales de biologie clinique. 72(4)
Angioedema is a rare but may be serious (laryngeal edema). This is a recurrent edema, subcutaneous and/or submucosal, whose cause is a hereditary or acquired deficiency in C1 inhibiteur (C1 inhibitor fraction of complement). We present the case of a
Autor:
S. Rabhi, Wafaa Bono, Meryem Alami, Moncef Hassani Amrani, Rhizlane Berrady, Hazar Lahlou, Ahmed B Filali
Publikováno v:
BMC Research Notes
BMC Research Notes, Vol 4, Iss 1, p 389 (2011)
BMC Research Notes, Vol 4, Iss 1, p 389 (2011)
Background Visceral leishmaniasis is a notifiable parasitic disease that had increased in incidence in our region on the past few years. It is common in children. In adults, it occurs more on a background of immunodeficiency, and frequently with inco
Autor:
Moncef Amrani, Hassani, Meryem, Alami, Ahmed Filali, Baba, Hazar, Lahlou, Abdeladim, Baba Khouya, Zahra, Akoudad, Samir, Atmani, Mustapha, Hida
Publikováno v:
Annales de biologie clinique. 68(6)
The Niemann Pick disease is a rare lysosomal storage disease responsible for numerous cytological abnormalities of blood cells and bone marrow. The diagnosis requires enzymatic dosages, which can be long and difficult. In this context, the detection
Publikováno v:
Annales de Dermatologie et de Vénéréologie. 139:171-172