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Training in minimally invasive surgery: experience of paediatric surgery trainees in Europe.
Markel M, Lacher M, Hall NJ, Martynov I, Siles Hinojosa A, de Augustin Asensio JC, Fortmann C, Hukkinen M, Mutanen A, Ford K, Glenisson M, Bonnard A, Dimitrios G, Zavras N, Malowiecka M, Patkowski D, Zambaiti E, Pelizzo G, Salo M, Wester T, Hoel AT, Bjornland K, Arni D, Wildhaber BE, Karagöz A, Topuzlu Tekant G, Barroso C, Correia-Pinto J, Gorter R, van Heurn E, Reusens H, Steyaert H, Dagilyte R, Strumila A, Arneitz C, Till H, Dotlaci V, Rygl M, Jukic M, Pogorelic Z, Enache T, Balanescu L, Cascio S, Zani A, Pio L. Markel M, et al. Among authors: wildhaber be. Br J Surg. 2023 Sep 6;110(10):1397-1399. doi: 10.1093/bjs/znad245. Br J Surg. 2023. PMID: 37527435 No abstract available.
Caroli disease, bilateral diffuse cystic renal dysplasia, situs inversus, postaxial polydactyly, and preauricular fistulas: a ciliopathy caused by a homozygous NPHP3 mutation.
Calinescu-Tuleasca AM, Bottani A, Rougemont AL, Birraux J, Gubler MC, Le Coultre C, Majno P, Mentha G, Girardin E, Belli D, Wildhaber BE. Calinescu-Tuleasca AM, et al. Among authors: wildhaber be. Eur J Pediatr. 2013 Jul;172(7):877-81. doi: 10.1007/s00431-011-1552-0. Epub 2011 Aug 16. Eur J Pediatr. 2013. PMID: 21845392
Adrenocortical oncocytoma in a child.
Gumy-Pause F, Bongiovanni M, Wildhaber B, Jenkins JJ, Chardot C, Ozsahin H. Gumy-Pause F, et al. Pediatr Blood Cancer. 2008 Mar;50(3):718-21. doi: 10.1002/pbc.21090. Pediatr Blood Cancer. 2008. PMID: 17091483
International registry of congenital porto-systemic shunts: a multi-centre, retrospective and prospective registry of neonates, children and adults with congenital porto-systemic shunts.
Korff S, Mostaguir K, Beghetti M, D'Antiga L, Debray D, Franchi-Abella S, Gonzales E, Guerin F, Hachulla AL, Lambert V, Makrythanasis P, Roduit N, Savale L, Senat MV, Spaltenstein J, van Steenbeek F, Wildhaber BE, Zwahlen M, McLin VA. Korff S, et al. Among authors: wildhaber be. Orphanet J Rare Dis. 2022 Jul 19;17(1):284. doi: 10.1186/s13023-022-02412-8. Orphanet J Rare Dis. 2022. PMID: 35854389 Free PMC article.
131 results