» Authors » Claire Dagorno

Claire Dagorno

Explore the profile of Claire Dagorno including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 6
Citations 10
Followers 0
Related Specialties
Top 10 Co-Authors
Published In
Affiliations
Soon will be listed here.
Recent Articles
1.
Dagorno C, Montalva L, Capito C, Lavrand F, Guinot A, De Napoli Cocci S, et al.
J Pediatr Surg . 2024 Oct; 60(1):161909. PMID: 39368852
Objectives: Short Bowel Syndrome (SBS), secondary to various underlying diseases, is one of the main causes of intestinal failure in children. Surgical management by serial transverse enteroplasty (STEP), is feasible...
2.
Dagorno C, Marique L, Korrel M, de Graaf N, Thouny C, Renault G, et al.
Surg Endosc . 2023 Dec; 38(2):769-779. PMID: 38052888
Background: Three randomized controlled trials have reported improved functional recovery after Laparoscopic pancreatoduodenectomy (LPD), as compared to open pancreatoduodenectomy (OPD). Long-term results regarding quality of life (QoL) are lacking. The...
3.
Dagorno C, Montalva L, Ali L, Brustia R, Paye-Jaquen A, Pio L, et al.
J Pediatr Surg . 2021 May; 56(12):2157-2164. PMID: 34030881
Objective: Enhanced recovery after surgery (ERAS) has been widely implemented after minimally invasive surgeries (MIS) in adults. The aim of this study was to evaluate the current evidence available on...
4.
Dagorno C, Sarsam M, Brun A, Longchampt E, Sage E, Chapelier A, et al.
Ann Thorac Surg . 2021 Apr; 113(2):e95-e97. PMID: 33930359
We present the case of a 20-year-old male patient presenting a right lower intralobar pulmonary "horseshoe" sequestration extending into the left cavity supplied by 4 aberrant arteries from the thoracic...
5.
DeAngelis N, Beghdadi N, Bianchi G, Brunetti F, Dagorno C
Colorectal Dis . 2020 Dec; 23(3):768-769. PMID: 33340197
No abstract available.
6.
Dagorno C, Pio L, Capri Y, Ali L, Giurgea I, Qoshe L, et al.
Pediatr Surg Int . 2020 Sep; 36(11):1309-1315. PMID: 32980962
Aim Of The Study: Mowat Wilson syndrome (MWS) is a complex genetic disorder due to mutation or deletion of the ZEB2 gene (ZFHX1B), including multiple clinical features. Hirschsprung disease is...