Article, Ajoutée
le 27/01/2018 19:07
Introduction: Étudier le profil épidémiologique, clinique et paraclinique de la PKAD chez des patients diagnostiqués au CNHU de Cotonou et
évaluer l'intérêt d'un dépistage chez les patients à risque. Méthodes: Il s'agit d'une étude transversale comp [...]
AGBOTON BRUNO LEOPOLD [1],
VIGAN JACQUES [2],
AZONBAKIN SIMON [3],
YEKPE PATRICIA [4],
AWEDE BEAUNAVENTURE [6],
LALEYE ANATOLE [6],
DARBOUX RAPHAEL [6],
Article, Ajoutée
le 01/02/2018 16:39
Autosomal dominant polycystic kidney disease in University Clinic of Nephrology and Haemodialysis
of Cotonou: Clinical and genetical findings: Autosomal dominant polycystic kidney disease (ADPKD) is the most
common hereditary kidney disease, but po [...]
LALEYE Y ANATOLE [1],
AWEDE B [2],
AGBOTON BRUNO LEOPOLD [3],
AZONBAKIN SIMON [4],
BIAOU OLIVIER [5],
SAGBO G [6],
ADJAGBA M [6],
AUDREZET MP [6],
Article, Ajoutée
le 01/02/2018 22:42
Background: Rheumatoïd arthritis (RA) is characterized by a multifactorial aetiology and a complex genetic background, with the major histocompatibility complex (MHC) region playing a major role.
Aim of the work: To detect the genetic susceptibility [...]
ZOMALHETO ZAVIER [1],
ASSOGBA MICHEE [2],
AVOHOU GERMAINE [3],
AZONBAKIN SIMON [4],
LALEYE ANATOLE [5],
Article, Ajoutée
le 19/02/2018 15:31
Background. Several studies have reported theimplication of HLA-DR/DQ loci in the susceptibility totype 1 diabetes (T1D). Since no such study has yet been performed in Benin, this pilot one aimed at assessing HLA class II allele, haplotype, and genot [...]
FAGBEMI KAOSSARATH [1],
MEDEHOUENOU THIERRY COMLAN MARC [1],
AZONBAKIN SIMON [3],
ADJAGBA MARIUS [4],
OSSENI RAZACK [5],
AHOUEYA JOCELYNE [6],
AGBALINSOU ARNAUD [7],
DARBOUX RAPHAËL BARTHÉLÉMY [8],
BABA-MOUSSA LAMINE SAÏD [3],
LALEYE OLABISSI ANATOLE A. [3],
Article, Ajoutée
le 18/02/2020 20:33
L’anévrysme de la veine de Galien est une malformation artério-veineuse intracrânienne rare, com-plexe, associant une dilatation pseudo-anévrysmale de l’ampoule de Galien à une ou plusieurs fis-tules artério-veineuses. Le pronostic est souvent mauvai [...]
GANDAHO HUGUES JEAN-THIERRY [1],
AZONBAKIN SIMON [2],
LALEYE C.M. [3],
GANGBO ÉPSE HOUNDJO FLORE ARMANDE [4],
LALEYE OLABISSI ANATOLE A. [5],
Article, Ajoutée
le 18/02/2020 20:34
The aim of this study was to determine the threshold values of pelvimetry by scanning and to
evaluate the ability of the pelvimetry alone to diagnose a fetal-pelvic disproportion.
It was an observational retrospective study on 410 pregnant women wh [...]
LALEYE C.M. [1],
AZONBAKIN SIMON [2],
DELMAS VINCENT [3],
AGOSSOU-VOYEME AUGUSTIN KARL [4],
DOUARD RICHARD [5],
HOUNNOU GERVAIS MARTIAL [6],
Article, Ajoutée
le 19/02/2020 17:09
Abstract
The 48 XXYY syndrome is a distinct clinical and genetic entity with an incidence
of 1/40000 to 1/18000. A 15-month-old child was admitted in genetic clinics for
psycho-motor delayed management. The patient disclosed a dysmorphism with
hy [...]
AZONBAKIN SIMON [1],
ADJAGBA MARIUS MARIUS [2],
NBOUKE NATACHA [3],
ADOVOEKPE DIANE [4],
AGBALINSOU ARNAUD [5],
ALAO MODJÉRÉ OLA MAROUFOU JULES [6],
GANGBO FLORE [7],
LALEYE OLABISSI ANATOLE A. [8],