Zobrazeno 1 - 10
of 124
pro vyhledávání: '"P. Y. Mure"'
Publikováno v:
EMC - Pediatría. 58:1-7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dedefa931f3ce75a4ea7f0d5879cca39
https://doi.org/10.1016/s1245-1789(23)47446-x
https://doi.org/10.1016/s1245-1789(23)47446-x
Publikováno v:
African Journal of Paediatric Surgery, Vol 15, Iss 3, Pp 142-145 (2018)
Background: Several surgical approaches or modifications of existing techniques have been described for the repair of hypospadias. In Sub-Saharan Africa, a two-stage approach is the preferred option in proximal cases with severe penile curvature. Obj
Externí odkaz:
https://doaj.org/article/8a1eebae17754154a01e2ec14a1e1c17
Autor:
L. O. Mbouché, G. Ondobo Andzé, A. S. Nwaha Makon, D. Nyanit Bob, E. Njuma Tamufor, A. L. Amenglé, F. F. Mouafo Tambo, P. Y. Mure, J. Zé Mikandé, F. F. Angwafo
Publikováno v:
Case Reports in Urology, Vol 2019 (2019)
Urinary stones are uncommon in children. Urethral location of calculi can give rise to various clinical manifestations. We report three cases of urethral lithiasis presenting with acute urinary retention in children.
Externí odkaz:
https://doaj.org/article/2f0398b372b843f291938566565792da
Autor:
F F Mouafo Tambo, S Dahoun, C Kamadjou, A S Nwaha Makon, G Fossi, O G Andze, M A Sosso, P Y Mure
Publikováno v:
African Journal of Paediatric Surgery, Vol 13, Iss 3, Pp 145-149 (2016)
Mixed gonadal dysgenesis is characterised by unilateral chromosomal abnormality, which is probably the result of anaphase lag during mitosis. The 45, XO/46, XY karyotype is the most common form of mosaicism involving the Y chromosome. It is a rare cl
Externí odkaz:
https://doaj.org/article/ee9da52493de4799809cec65e433eacc
Publikováno v:
Archives de Pédiatrie. 29:153-156
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a430fb590b4db25170b1c7369c21024
https://doi.org/10.1016/j.arcped.2021.11.013
https://doi.org/10.1016/j.arcped.2021.11.013
Autor:
Mouafo Tambo Faustin Felicien, A S Nwaha Makon, C Kamadjou, G Fossi, C Le Coultre, O G Andze, M A Sosso, P Y Mure
Publikováno v:
African Journal of Paediatric Surgery, Vol 13, Iss 4, Pp 193-195 (2016)
Background: In parts of Africa, routine circumcision is practised and sometimes even on children with hypospadias. The lack of preputial foreskin renders urethroplasty more difficult and often requires to use of a mucosal graft as described by Bracka
Externí odkaz:
https://doaj.org/article/aca516deba9044f2ba411ded79fd80fd
Autor:
F F Mouafo Tambo, C Kamadjou, T Djeumi, A S Nwaha Makon, G Fossi, C Le Coultre, O G Andze, M A Sosso, P Y Mure
Publikováno v:
African Journal of Paediatric Surgery, Vol 13, Iss 3, Pp 152-154 (2016)
Syringocele or dilatation of the duct of the bulbo-urethral (Cowper′s) gland is usually of congenital origin but can be acquired. It is a very rare deformity,
Externí odkaz:
https://doaj.org/article/43a6f77863b9445ca84500333d5931ca
Autor:
F. F. Mouafo Tambo, G. Fossi kamga, C. Kamadjou, L. Mbouche, A. S. Nwaha Makon, J. Birraux, O. G. Andze, F. F. Angwafo, P. Y. Mure
Publikováno v:
Case Reports in Urology, Vol 2016 (2016)
Introduction. Urethral strictures in boys denote narrowing of the urethra which can be congenital or acquired. In case of acquired strictures, the etiology is iatrogenic or traumatic and rarely infectious or inflammatory. The aim of this study was to
Externí odkaz:
https://doaj.org/article/f11ede2f436b4762ba9f827afad515aa
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 29(2)
Congenital mesoblastic nephroma is a rare pediatric renal tumor and has been reported in patients presenting with palpable abdominal mass, arterial hypertension, hematuria, polyuria, or hypercalcemia. Here we present the case of a 1-month-old neonate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b594a93c1f6ebc9ee96dcd10588f64c2
https://pubmed.ncbi.nlm.nih.gov/35039190
https://pubmed.ncbi.nlm.nih.gov/35039190