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For: Friedmacher F, Puri P. Classification and diagnostic criteria of variants of Hirschsprung's disease. Pediatr Surg Int. 2013;29:855-872. [PMID: 23943250 DOI: 10.1007/s00383-013-3351-3] [Cited by in Crossref: 50] [Cited by in F6Publishing: 34] [Article Influence: 6.3] [Reference Citation Analysis]
Number Citing Articles
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8 Budianto IR, Obata S, Kinoshita Y, Yoshimaru K, Yanagi Y, Miyata J, Nagata K, Ieiri S, Taguchi T. Reevaluation of acetylcholinesterase staining for the diagnosis of Hirschsprung disease and allied disorders. J Pediatr Gastroenterol Nutr 2015;60:606-12. [PMID: 25522309 DOI: 10.1097/MPG.0000000000000664] [Cited by in Crossref: 11] [Cited by in F6Publishing: 2] [Article Influence: 1.8] [Reference Citation Analysis]
9 Zhu J, Zhang Y, Wang Y, Yu S, Chen Y, Guo Z, Zhao Y. Dysmorphic Neurofilament-Positive Ganglion Cells in the Myenteric Plexus at the Proximal Resection Margin Indicate Worse Postoperative Prognosis in Hirschsprung’s Disease. Pediatr Dev Pathol 2020;23:222-9. [DOI: 10.1177/1093526619878083] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
10 Lourenção PLTA, Ortolan EVP, Rosa LLM, Angelini MC, Cassettari VMG, Terra SA, Rodrigues MAM. What should be the treatment for intestinal neuronal dysplasia type B? A comparative long-term follow-up study. J Pediatr Surg 2021;56:1611-7. [PMID: 33279216 DOI: 10.1016/j.jpedsurg.2020.11.019] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
11 Terra SA, Gonçalves AC, Lourenção PLTA, Rodrigues MAM. Challenges in the diagnosis of intestinal neuronal dysplasia type B: A look beyond the number of ganglion cells. World J Gastroenterol 2021; 27(44): 7649-7660 [PMID: 34908804 DOI: 10.3748/wjg.v27.i44.7649] [Reference Citation Analysis]
12 Watanabe Y, Sumida W, Takasu H, Oshima K, Kanamori Y, Uchida K, Taguchi T. Early jejunostomy creation in cases of isolated hypoganglionosis: verification of our own experience based on a national survey. Surg Today 2015;45:1509-12. [DOI: 10.1007/s00595-015-1114-6] [Cited by in Crossref: 8] [Article Influence: 1.1] [Reference Citation Analysis]
13 Watanabe S, Matsudera S, Yamaguchi T, Tani Y, Ogino K, Nakajima M, Yamaguchi S, Sasaki K, Suzumura H, Tsuchioka T. Waardenburg syndrome with isolated deficiency of myenteric ganglion cells at the sigmoid colon and rectum. Pediatr Rep 2018;10:7500. [PMID: 30069293 DOI: 10.4081/pr.2018.7500] [Reference Citation Analysis]
14 Yoshimaru K, Kinoshita Y, Yanagi Y, Obata S, Jimbo T, Iwanaka T, Takahashi Y, Esumi G, Miyata JA, Matsuura T, Izaki T, Taguchi T. The evaluation of rectal mucosal punch biopsy in the diagnosis of Hirschsprung’s disease: a 30-year experience of 954 patients. Pediatr Surg Int 2017;33:173-9. [DOI: 10.1007/s00383-016-4010-2] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
15 Takahashi J, Seki H, Inoue K, Murase R, Ideno S, Morisaki H. A case of Hirschsprung disease recognized during anesthesia induction with nitrous oxide. Paediatr Anaesth 2017;27:869-71. [PMID: 28685986 DOI: 10.1111/pan.13191] [Cited by in Crossref: 1] [Article Influence: 0.2] [Reference Citation Analysis]
16 Gfroerer S, Rolle U. Pediatric intestinal motility disorders. World J Gastroenterol 2015; 21(33): 9683-9687 [PMID: 26361414 DOI: 10.3748/wjg.v21.i33.9683] [Cited by in CrossRef: 17] [Cited by in F6Publishing: 17] [Article Influence: 2.4] [Reference Citation Analysis]
17 Obata S, Yoshimaru K, Kirino K, Izaki T, Ieiri S, Yamataka A, Koshinaga T, Iwai J, Ikeda H, Matsufuji H, Oda Y, Taguchi T. Acquired isolated hypoganglionosis as a distinct entity: results from a nationwide survey. Pediatr Surg Int 2019;35:215-20. [PMID: 30456687 DOI: 10.1007/s00383-018-4398-y] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
18 Miura Y, Watanabe T, Uchida T, Nawa T, Endo N, Fukuzawa T, Ohkubo R, Takeyama J, Sasaki A, Hayasaka K. A novel PHOX2B gene mutation in an extremely low birth weight infant with congenital central hypoventilation syndrome and variant Hirschsprung's disease. Eur J Med Genet 2019;62:103541. [PMID: 30227298 DOI: 10.1016/j.ejmg.2018.09.008] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
19 Lee RY, Li H, White RV, Shin BJ, Birkholz JH. Rare Variant Hirschsprung Disease Presenting as Large Bowel Obstruction in Adulthood: Hypoganglionosis in the Anorectal Canal. ACG Case Rep J 2021;8:e00610. [PMID: 34549071 DOI: 10.14309/crj.0000000000000610] [Reference Citation Analysis]
20 Lourenção PLTA, Ortolan EVP, Rosa LLM, Angelini MC, Terra SA, Rodrigues MAM. Long-term follow-up of patients with intestinal neuronal dysplasia type B: Protocol for an observational, ambispective, and comparative study. Medicine (Baltimore) 2017;96:e7485. [PMID: 28700491 DOI: 10.1097/MD.0000000000007485] [Cited by in Crossref: 2] [Article Influence: 0.4] [Reference Citation Analysis]
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22 Muto M, Matsufuji H, Taguchi T, Tomomasa T, Nio M, Tamai H, Tamura M, Sago H, Toki A, Nosaka S, Kuroda T, Yoshida M, Nakajima A, Kobayashi H, Sou H, Masumoto K, Watanabe Y, Kanamori Y, Hamada Y, Yamataka A, Shimojima N, Kubota A, Ushijima K, Haruma K, Fukudo S, Araki Y, Kudo T, Obata S, Sumita W, Watanabe T, Fukahori S, Fujii Y, Yamada Y, Jimbo K, Kawai F, Fukuoka T, Onuma S, Morizane T, Ieiri S, Esumi G, Jimbo T, Yamasaki T. Japanese clinical practice guidelines for allied disorders of Hirschsprung's disease, 2017. Pediatr Int 2018;60:400-10. [PMID: 29878629 DOI: 10.1111/ped.13559] [Cited by in Crossref: 12] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
23 Taguchi T, Kobayashi H, Kanamori Y, Segawa O, Yamataka A, Sugiyama M, Iwanaka T, Shimojima N, Kuroda T, Nakazawa A. Isolated intestinal neuronal dysplasia Type B (IND-B) in Japan: results from a nationwide survey. Pediatr Surg Int. 2014;30:815-822. [PMID: 25052255 DOI: 10.1007/s00383-014-3542-6] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 1.6] [Reference Citation Analysis]
24 Das K, Mohanty S. Hirschsprung Disease - Current Diagnosis and Management. Indian J Pediatr 2017;84:618-23. [PMID: 28600660 DOI: 10.1007/s12098-017-2371-8] [Cited by in Crossref: 20] [Cited by in F6Publishing: 19] [Article Influence: 4.0] [Reference Citation Analysis]
25 Zheng Y, Lan C, Wang N, Xu X, Hu T, Wu Q, Xie X, Wang Z, Zhang Y, Li C. Significant Association of rs2147555 Genetic Polymorphism in the EDNRB Gene with Hirschsprung Disease in Southern Chinese Children. Biomed Res Int 2020;2020:5956412. [PMID: 33178831 DOI: 10.1155/2020/5956412] [Reference Citation Analysis]
26 Sergi CM, Caluseriu O, McColl H, Eisenstat DD. Hirschsprung's disease: clinical dysmorphology, genes, micro-RNAs, and future perspectives. Pediatr Res 2017;81:177-91. [PMID: 27682968 DOI: 10.1038/pr.2016.202] [Cited by in Crossref: 30] [Cited by in F6Publishing: 28] [Article Influence: 5.0] [Reference Citation Analysis]
27 Subramanian H, Badhe BA, Toi PC, Sambandan K. Morphometric profile of large intestinal neuronal plexuses in normal perinatal autopsies and Hirschsprung disease. Neurogastroenterol Motil 2017;29:e12939. [DOI: 10.1111/nmo.12939] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
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29 Kapur RP, Ambartsumyan L, Smith C. Are We Underdiagnosing Hirschsprung Disease? Pediatr Dev Pathol. 2020;23:60-71. [PMID: 31747832 DOI: 10.1177/1093526619889434] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
30 Zhi Z, Zhu H, Lv X, Lu C, Li Y, Wu F, Zhou L, Li H, Tang W. IGF2-derived miR-483-3p associated with Hirschsprung's disease by targeting FHL1. J Cell Mol Med 2018;22:4913-21. [PMID: 30073757 DOI: 10.1111/jcmm.13756] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
31 Kawai H, Satomi K, Morishita Y, Murata Y, Sugano M, Nakano N, Noguchi M. Developmental markers of ganglion cells in the enteric nervous system and their application for evaluation of Hirschsprung disease: Markers of Hirschsprung disease. Pathol Int 2014;64:432-42. [DOI: 10.1111/pin.12191] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 0.8] [Reference Citation Analysis]
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33 Braczynski AK, Gfroerer S, Beschorner R, Harter PN, Baumgarten P, Rolle U, Mittelbronn M. Cholinergic innervation and ganglion cell distribution in Hirschsprung's disease. BMC Pediatr 2020;20:399. [PMID: 32838761 DOI: 10.1186/s12887-020-02299-z] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
34 Khorana J, Phiromkanchanasak P, Kumsattra J, Klinoun S, Aksorn S, Chantakhow S, Tepmalai K, Singhavejsakul J. Development of Clinical Referral Score Model for Early Diagnosis of Hirschsprung's Disease in Suspected Pediatric Patients. Healthcare (Basel) 2021;9:678. [PMID: 34200020 DOI: 10.3390/healthcare9060678] [Reference Citation Analysis]
35 Sreedher G, Garrison A, Novak R, Keisling M, Ganapathy SS. Congenital intestinal hypoganglionosis: A radiologic mimic of Hirschsprung's disease. Radiol Case Rep 2019;14:171-4. [PMID: 30416639 DOI: 10.1016/j.radcr.2018.10.007] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
36 Tomuschat C, Puri P. RET gene is a major risk factor for Hirschsprung's disease: a meta-analysis. Pediatr Surg Int 2015;31:701-10. [PMID: 26164711 DOI: 10.1007/s00383-015-3731-y] [Cited by in Crossref: 27] [Cited by in F6Publishing: 21] [Article Influence: 3.9] [Reference Citation Analysis]
37 Klein M, Varga I. Hirschsprung's Disease-Recent Understanding of Embryonic Aspects, Etiopathogenesis and Future Treatment Avenues. Medicina (Kaunas) 2020;56:E611. [PMID: 33202966 DOI: 10.3390/medicina56110611] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]