Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mohamed, Benabadji"'
Autor:
Ghalia Khellaf, Ali Benziane, Louiza Kaci, Djouher Ait-Idir, Soumia Missoum, Mohamed Benabadji
Publikováno v:
Clinical Nephrology. 99:172-179
Autor:
Ghalia, Khellaf, Ali, Benziane, Louiza, Kaci, Soumia, Missoum, Mourad, Lahmar, Mohamed, Benabadji
Publikováno v:
Clinical Nephrology. 99:92-97
Lecithin-cholesterol acyltransferase (LCAT) deficiency is an autosomal recessive disorder that can reveal two different diseases: a very interesting nephrological picture of complete enzyme deficiency characterized by the association of dyslipidemia,
Publikováno v:
Nephrology Dialysis Transplantation. 37
BACKGROUND AND AIMS The aim of this study was to assess predictors of renal involvement and other factors secondary to FMF in renal and overall survival. METHOD We prospectively studied 57 Algerian patients admitted to our nephrology department from
Publikováno v:
Nephrology Dialysis Transplantation. 37
BACKGROUND AND AIMS There is podocyte involvement in corticosteroid-resistant nephrotic syndrome. A certain number of proteins play an essential role in the biology of the podocyte; the mutation of these proteins generates the aforementioned patholog
Publikováno v:
Clinical nephrology. 97(3)
AA renal amyloidosis is present in Algeria, often secondary to chronic infections, the most frequent being tuberculosis. We studied the evolution of the epidemiology of AA amyloidosis over a period of 20 years.We conducted a retrospective study of al
Autor:
Rowaida Z. Taha, Hatem El-Shanti, R. Sari-Hamidou, Ghalia Khellaf, Djouher Ait-Idir, Mustapha Benmansour, Farid Haddoum, Bahia Djerdjouri, Faiza Bouldjennet, Mohamed Benabadji
Publikováno v:
European journal of medical genetics. 60(3)
Familial Mediterranean fever (FMF, OMIM 249100) is the most common hereditary fever, resulting from mutations in MEFV. FMF is characterized by episodic febrile attacks and polyserositis. Renal AA-amyloidosis is a major complication, which often leads
Autor:
Philippe Lefevre-Witier, Mohamed Benabadji, Kristin L. Melvin, Pierre Darlu, Michael H. Crawford, Hadi Aireche, André Sevin
Publikováno v:
American Journal of Human Biology. 18:492-501
Blood samples were collected in Algeria from 4,444 army recruits and tested for 10 genetic polymorphic systems. These samples were collected from territorial Wilayas (administrative units of Algeria) from which the young soldiers had originated. Base
Protein 4.1, a principal component of the erythrocyte membrane skeleton, is thought to be important in regulating membrane stability through its interaction with spectrin and actin. A key role for protein 4.1 has been indicated in studies in which de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b0dd00a9b41df40e651b0d6d8400d73
https://europepmc.org/articles/PMC329534/
https://europepmc.org/articles/PMC329534/