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pro vyhledávání: '"Henri B. Lottmann"'
Autor:
Nicolas Vinit, Antoine Khoury, Pauline Lopez, Laurence Heidet, Nathalie Botto, Olivier Traxer, Olivia Boyer, Thomas Blanc, Henri B. Lottmann
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Purpose: Cystinuria is a genetic disorder characterized by a defective reabsorption of cystine and dibasic amino acids leading to development of urinary tract calculi from childhood onward. Cystine lithiasis is known to be resistant to fragmentation.
Externí odkaz:
https://doaj.org/article/57c05c4cbab643ae8f5bb1ef5fc8de8b
Autor:
Venusia Fiorenza, Maria Hukkinen, Ilona Alova, Pauline Clermidi, Aline Broch, Nathalie Botto, Thomas Blanc, Henri B. Lottmann
Publikováno v:
Journal of Urology. 209:591-599
Since bladder neck dextranomer/hyaluronic acid copolymer (Deflux) injections can improve urinary incontinence of various etiologies, we hypothesized that incontinent children with bladder exstrophy-epispadias complex would benefit from dextranomer/hy
Autor:
Ilona Alova, Henri B. Lottmann
Publikováno v:
Archivos Españoles de Urología (Ed. impresa). 61
Two kinds of elimination disorders can be associated with Vesico Ureteral Reflux (VUR): pure bladder elimination disorders or combination of bladder and bowel elimination disorders. An elimination disorder is always a factor which worsens the prognos
Publikováno v:
Urology. 64(3)
Objectives To report our experience with the management of encrusted cystitis and pyelitis (EC and EP) in the pediatric population. EC and EP are well-known entities in adults but are rarely identified in children. They consist of mucosal encrustatio