Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Conny J.H.M. Meeussen"'
Autor:
Alice S. Brooks, Robert van der Helm, Bianca M. de Graaf, Erwin Brosens, Conny J.H.M. Meeussen, Laura E. Kuil, Robert M.W. Hofstra, Thuy Linh Le, Anwarul Karim, Annelies de Klein, Rene M. H. Wijnen, Cornelius E. J. Sloots, Paul K.H. Tam, Maria M. Alves, Yolande van Bever, Clara S. Tang, Maria-Mercè Garcia-Barceló, Jeanne Amiel, Jonathan D. Windster, Katherine C. MacKenzie, Dick Tibboel, Stanislas Lyonnet
Publikováno v:
PLoS Genetics, Vol 17, Iss 8, p e1009698 (2021)
PLoS Genetics, 17(8):1009698. Public Library of Science
PLoS Genetics
PLoS Genetics, 17(8):1009698. Public Library of Science
PLoS Genetics
Hirschsprung disease (HSCR) is a complex genetic disease characterized by absence of ganglia in the intestine. HSCR etiology can be explained by a unique combination of genetic alterations: rare coding variants, predisposing haplotypes and Copy Numbe
Autor:
Conny J.H.M. Meeussen, Cornelis P. van de Ven, Rene M. H. Wijnen, Cornelius E. J. Sloots, Claudia M. G. Keyzer-Dekker, Mirjam Ploeg, John Vlot
Publikováno v:
European Journal of Pediatric Surgery, 29(5), 443-448. Thieme Medical Publishers
Background In 2011, we implemented a new video-based system for quality control of laparoscopic pyloromyotomy. More than 3 years later, we evaluated how the implementation had gone and assessed its usability in predicting postoperative outcomes. Mate
Autor:
Erwin Brosens, van der Helm R, Alice S. Brooks, van Bever Y, Conny J.H.M. Meeussen, Windster Jd, Laura E. Kuil, Stanislas Lyonnet, Cornelius E. J. Sloots, Wijnen Rmh, Maria-Mercè Garcia-Barceló, Dick Tibboel, Maria M. Alves, Thuy-Linh Le, de Graaf Bm, MacKenzie Kc, Clara S. Tang, Paul Kh Tam, R Hofstra, de Klein A, Jeanne Amiel, Anwarul Karim
BackgroundHirschsprung disease (HSCR) is characterized by absence of ganglia in the intestine. Approximately 18% of patients have additional anatomical malformations or neurological symptoms (HSCR-AAM). HSCR is a complex genetic disease in which the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba9197a3b38c67c1737236746383b2f7
https://doi.org/10.1101/2020.11.02.20221481
https://doi.org/10.1101/2020.11.02.20221481
Autor:
Irene K. Schokker-van Linschoten, Katharina Biermann, Claudia M. G. Keyzer-Dekker, Conny J.H.M. Meeussen, Cornelius E. J. Sloots, Michael Doukas
Publikováno v:
European Journal of Pediatric Surgery, 26(1), 100-105. Thieme Medical Publishers
Introduction Rectal suction biopsy (RSB) is performed on clinical and radiological suspicion of Hirschsprung disease (HD). Positive histochemical staining for acetylcholinesterase in the lamina propria mucosa and muscularis mucosa together with the a
Autor:
Nanko de Graaf, Maarten Thomeer, Morteza Meradji, Conny J.H.M. Meeussen, Annick S. Devos, Maarten H. Lequin, Ivo de Blaauw, Cornelius E. J. Sloots
Publikováno v:
European Radiology
European Radiology, 25, 3472-9
European Radiology, 25(12), 3472-3479. Springer-Verlag
European Radiology, 25, 12, pp. 3472-9
European Radiology, 25, 3472-9
European Radiology, 25(12), 3472-3479. Springer-Verlag
European Radiology, 25, 12, pp. 3472-9
Contains fulltext : 152293.pdf (Publisher’s version ) (Open Access) OBJECTIVE: To compare MRI and colostography/fistulography in neonates with anorectal malformations (ARM), using surgery as reference standard. METHODS: Thirty-three neonates (22 bo
Autor:
Gerard C. Madern, Dick Tibboel, Conny J.H.M. Meeussen, Marten J. Poley, Richard Keijzer, Marie-Chantal Struijs
Publikováno v:
Journal of Pediatric Surgery, 47(4), 658-664. W.B. Saunders
Background: Surgeons prefer to close ostomies at least 6 weeks after the primary operation because of the anticipated postoperative abdominal adhesions. Limited data support this habit. Our aim was to evaluate adhesion formation-together with an anal
Publikováno v:
European Journal of Pediatric Surgery, 24(1), 61-69. Thieme Medical Publishers
IntroductionThe aim of this article is to identify the ideal type and location of colostomy in children with colorectal disease. Patients and MethodsA retrospective case study of children with an anorectal malformation who received a colostomy, born
Autor:
Saskia J. Gischler, Hanneke IJsselstijn, Rene M. H. Wijnen, Cornelius E. J. Sloots, Conny J.H.M. Meeussen, Desiree van den Hondel
Publikováno v:
Journal of Pediatric Surgery, 48, 818-25
Journal of Pediatric Surgery, 48, 4, pp. 818-25
Journal of Pediatric Surgery, 48(4), 818-825. W.B. Saunders
Journal of Pediatric Surgery, 48, 4, pp. 818-25
Journal of Pediatric Surgery, 48(4), 818-825. W.B. Saunders
Item does not contain fulltext BACKGROUND/PURPOSE: To evaluate growth and development in children with anorectal malformations and to analyze effects of type of malformation and comorbidities. METHODS: Non-syndromal children with anorectal malformati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13191193be0b0e3aed6e5403693ab1cd
http://hdl.handle.net/2066/144807
http://hdl.handle.net/2066/144807