Malattia di Hirschsprung (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Malattia di Hirschsprung" in Italian language version.

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G. Martucciello G, M. P. Bicocchi MP, P. Dodero P et al., Total colonic aganglionosis associated with interstitial deletion of the long arm of chromosome 10, in Ped. Surg. Int., vol. 7, n. 4, 1992, pp. 308-310, DOI:10.1007/BF00183991. URL consultato l'11 dicembre 2022 (archiviato dall'url originale l'11 aprile 2013).

doi.org

dx.doi.org

G. Martucciello G, M. P. Bicocchi MP, P. Dodero P et al., Total colonic aganglionosis associated with interstitial deletion of the long arm of chromosome 10, in Ped. Surg. Int., vol. 7, n. 4, 1992, pp. 308-310, DOI:10.1007/BF00183991. URL consultato l'11 dicembre 2022 (archiviato dall'url originale l'11 aprile 2013).
Alessio Pini Prato, Rossella Arnoldi e Ilaria Falconi, Congenital anomalies of the kidney and urinary tract in a cohort of 280 consecutive patients with Hirschsprung disease, in Pediatric Nephrology (Berlin, Germany), 9 aprile 2021, DOI:10.1007/s00467-021-05061-4. URL consultato il 1º luglio 2021.
Alessio Pini Prato, Rossella Arnoldi e Maria Grazia Faticato, Minimally Invasive Redo Pull-Throughs in Hirschsprung Disease, in Journal of Laparoendoscopic & Advanced Surgical Techniques. Part A, 21 luglio 2020, DOI:10.1089/lap.2020.0250. URL consultato il 31 luglio 2020.
Alessio Pini Prato, Rossella Arnoldi e Maria Pia Dusio, Totally robotic soave pull-through procedure for Hirschsprung's disease: lessons learned from 11 consecutive pediatric patients, in Pediatric Surgery International, vol. 36, n. 2, 2020-02, pp. 209–218, DOI:10.1007/s00383-019-04593-z. URL consultato il 31 luglio 2020.

nih.gov

ncbi.nlm.nih.gov

GeneRewiev
Lamont MA, Fitchett M, Dennis NR, Interstitial deletion of distal 13q associated with Hirschsprung's disease, in J. Med. Genet., vol. 26, n. 2, febbraio 1989, pp. 100–4, PMC 1015558, PMID 2918536.
Shanske A, Ferreira JC, Leonard JC, Fuller P, Marion RW, Hirschsprung disease in an infant with a contiguous gene syndrome of chromosome 13, in Am. J. Med. Genet., vol. 102, n. 3, agosto 2001, pp. 231–6, PMID 11484199.
Lurie IW, Supovitz KR, Rosenblum-Vos LS, Wulfsberg EA, Phenotypic variability of del(2) (q22-q23): report of a case with a review of the literature, in Genet. Couns., vol. 5, n. 1, 1994, pp. 11–4, PMID 8031530.
Mowat DR, Croaker GD, Cass DT, et al., Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23, in J. Med. Genet., vol. 35, n. 8, agosto 1998, pp. 617–23, PMC 1051383, PMID 9719364.
Martucciello G. (2008 Jun) "Hirschsprung's disease, one of the most difficult diagnoses in pediatric surgery: a review of the problems from clinical practice to the bench". Eur J Pediatr Surg. ;18(3):140-9. Review. PubMed PMID 18493886
Alessio Pini Prato, Rossella Arnoldi e Maria Grazia Faticato, Minimally Invasive Redo Pull-Throughs in Hirschsprung Disease, in Journal of Laparoendoscopic & Advanced Surgical Techniques. Part A, 21 luglio 2020, DOI:10.1089/lap.2020.0250. URL consultato il 31 luglio 2020.
Alessio Pini Prato, Rossella Arnoldi e Maria Pia Dusio, Totally robotic soave pull-through procedure for Hirschsprung's disease: lessons learned from 11 consecutive pediatric patients, in Pediatric Surgery International, vol. 36, n. 2, 2020-02, pp. 209–218, DOI:10.1007/s00383-019-04593-z. URL consultato il 31 luglio 2020.
Shim WK, Swenson O, Treatmentof congenital megacolon in 50 infants, in Pediatrics, vol. 38, n. 2, agosto 1966, pp. 185–93, PMID 5944153.
Swenson O, Congenital megacolon, in Pediatr. Clin. North Am., vol. 14, n. 1, febbraio 1967, pp. 187–96, PMID 6016070.
Steichen FM, Talbert JL, Ravitch MM, Primary side-to-side colorectal anastomosis in the Duhamel operation for Hirschsprung's disease, in Surgery, vol. 64, n. 2, agosto 1968, pp. 475–83, PMID 5691680.
Soave F, Extramucosal endorectal pull through, in Curr Probl Surg, vol. 15, n. 6, giugno 1978, pp. 77–93, PMID 401426.

pubmed.ncbi.nlm.nih.gov

(EN) Pini Prato A, Arnoldi R, Sgrò A, Felici E, Racca F, Nozza P, Hirschsprung Disease and Down Syndrome: From the Reappraisal of Risk Factors to the Impact of Surgery, su Journal of pediatric surgery, 2019 Sep. URL consultato il 22 maggio 2020.
Alessio Pini Prato, Rossella Arnoldi e Ilaria Falconi, Congenital anomalies of the kidney and urinary tract in a cohort of 280 consecutive patients with Hirschsprung disease, in Pediatric Nephrology (Berlin, Germany), 9 aprile 2021, DOI:10.1007/s00467-021-05061-4. URL consultato il 1º luglio 2021.

whonamedit.com

(EN) Ole Daniel Enersen, Malattia di Hirschsprung, in Who Named It?.