Hypoganglionose als Ursache chronischer Obstipation

Author:

Bruder E.,Meier-Ruge W.A.

Publisher

Springer Science and Business Media LLC

Subject

Pathology and Forensic Medicine

Reference38 articles.

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2. Farrugia MK, Alexander N, Clarke S et al. (2003) Does transitional zone pull-through in Hirschsprung’s disease imply a poor prognosis? J Pediatr Surg 38: 1766–1769

3. Faussone-Pellegrini MS, Infantino A, Matini P et al. (1999) Neuronal anomalies and normal muscle morphology at the hypomotile ileocecocolonic region of patients affected by idiopathic chronic constipation. Histol Histopathol 14: 1119–1134

4. Gabriel SB, Salomon R, Pelet A et al. (2002) Segregation at three loci explains familial and population risk in Hirschsprung disease. Nat Genet 31: 89–93

5. Gershon MD, Ratcliffe EM (2004) Developmental biology of the enteric nervous system: pathogenesis of Hirschsprung’s disease and other congenital dysmotilities. Semin Pediatr Surg 13: 224–235

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1. Chronische Obstipation und Stuhlentleerungsstörung – Diagnostik und Therapie aus Sicht des Chirurgen;coloproctology;2024-06-27

2. HIPOGANGLIONOSE MIMETIZANDO SÍNDROME DE WILKIE: RELATO DE CASO;Revista Contemporânea;2024-01-31

3. Variant Hirschsprung’s Disease;Pediatric Surgery;2023

4. Stuhlentleerungsstörung;Allgemeinmedizin up2date;2022-11

5. Congenital Myenteric Hypoganglionosis;American Journal of Surgical Pathology;2021-01-22

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