Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Abdelhakim Ourrai"'
Autor:
Aomar Agadr, Amal Hassani, Rachid Abilkassem, Abdelhakim Ourrai, Abdelilah Radi, Jihane El Mahi, Ghita Hachim
Publikováno v:
Journal of Advances in Medical and Pharmaceutical Sciences. :8-13
Hyper-IgE syndrome (HIES) is a primary immunodeficiency disorder characterized by eczema, cold abscesses, pneumonia, eosinophilia, and a very high serum IgE concentration. An association with celiac disease is rare. Immunodeficiency and autoimmunity
Autor:
Aomar Agadr, Amal Hassani, Rihane El Mohtarim, Rachid Abilkassem, Najat Lamalmi, Abdelilah Radi, Abdelhakim Ourrai, Ghita Hachim
Publikováno v:
Asian Journal of Pediatric Research. :21-25
Autoimmune Hepatitis (AIH) pathogenesis is still unknown. However, among patients who have a genetic susceptibility, some viral infections appear to be triggers for AIH. We report a case of a child who developed type 2 autoimmune hepatitis as a resul
Publikováno v:
Asian Journal of Pediatric Research. :6-10
We report the case of a female child with congenital isolated malabsorption of folic acid. The patient was referred to our hospital for pancytopenia and a tendency to various infections, but with no neurological disturbances. A bone marrow aspiration
Autor:
Abdelilah Radi, Aomar Agadr, Abdelhakim Ourrai, Nadia Mebrouk, Mohamed Selouti, A. Hassani, Rachid Abilkassem, M. Kmari
Publikováno v:
Asian Journal of Pediatric Research. :1-5
Factor VII (FVII) deficiency is the most common among rare inherited autosomal recessive bleeding disorders. It is a multifaceted disease because of the lack of a direct correlation between plasma levels of coagulation FVII and bleeding manifestation
Autor:
Rachid Abilkassem, Mohamed Sellouti, Aomar Agadr, Karima Laarbi Ouassou, Abdelhakim Ourrai, Amale Hassani
Publikováno v:
Open Journal of Pharmacology and Pharmacotherapeutics. :001-003
Inhalation therapy involves two types of adherence: adherence to the drug and adherence to the procedures for the inhalation device. Recent increases in the range of inhaled medications available have expanded treatment options
Autor:
Aomar Agadr, Mohamed Sellouti, Rachid Abilkassem, Abdelhakim Elyajouri, Amale Hassani, Abdelhakim Ourrai
Publikováno v:
International Journal of Medical Reviews and Case Reports. 4:1
Glycogen storage disease (GSD) IV is a rare autosomal recessive inherited disorder caused by mutations in the gene coding for glycogen branching enzyme(GBE). The clinical spectrum is wide ranging from isolated non-progressive hepathopathy, neuromuscu