Research & Literature

Polymicrogyria in a 10-month-old boy with Mowat-Wilson syndrome.

Murray SB, Spangler BB, Helm BM, Vergano SS

American journal of medical genetics. Part A 2015; (167A(10)):2402-5 doi:10.1002/ajmg.a.37171.

Association Analysis of SLC6A20 Polymorphisms With Hirschsprung Disease.

Lee JS, Oh JT, Kim JH, et al.

Journal of pediatric gastroenterology and nutrition 2016; (62(1)):64-70 doi:10.1097/MPG.0000000000000880.

RET gene is a major risk factor for Hirschsprung's disease: a meta-analysis.

Tomuschat C, Puri P

Pediatric surgery international 2015; (31(8)):701-10 doi:10.1007/s00383-015-3731-y.

Familial Hirschsprung's disease: a systematic review.

Mc Laughlin D, Puri P

Pediatric surgery international 2015; (31(8)):695-700 doi:10.1007/s00383-015-3730-z.

Distal Rectal Skip-Segment Hirschsprung Disease and the Potential for False-Negative Diagnosis.

Coe A, Avansino JR, Kapur RP

Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2016; (19(2)):123-31 doi:10.2350/15-08-1686-OA.1.

Quality of Life and Anxiety in Parents of Children with an Anorectal Malformation or Hirschsprung Disease: The First Year after Diagnosis.

Witvliet MJ, Bakx R, Zwaveling S, et al.

European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie 2016; (26(1)):2-6 doi:10.1055/s-0035-1559885.

Anti-Glypican 3, a Novel Ancillary Maker in the Histological Assessment of Hirschsprung's Disease.

Ludwig K, Volpe A, Guzzardo V, et al.

Journal of pediatric gastroenterology and nutrition 2016; (62(5)):692-7 doi:10.1097/MPG.0000000000001020.

Aganglionosis with the absence of hypertrophied nerve fibres predicts disease proximal to rectosigmoid colon.

Narayanan SK, Soundappan SS, Kwan E, et al.

Pediatric surgery international 2016; (32(3)):221-6 doi:10.1007/s00383-015-3835-4.

Inactivation of Geminin in neural crest cells affects the generation and maintenance of enteric progenitor cells, leading to enteric aganglionosis.

Stathopoulou A, Natarajan D, Nikolopoulou P, et al.

Developmental biology 2016; (409(2)):392-405.

Hirschsprung disease with debut in adult age as acute intestinal obstruction: case report.

López Ruiz JA, Tallón Aguilar L, Sánchez Moreno L, et al.

Revista espanola de enfermedades digestivas 2016; (108(11)):742-746 doi:10.17235/reed.2016.3841/2015.

Hirschsprung disease is associated with an L286P mutation in the fifth transmembrane domain of the endothelin-B receptor in the N-ethyl-N-nitrosourea-induced mutant line.

Chen B, Ouyang HL, Wang WH, et al.

Experimental animals 2016; (65(3)):245-51 doi:10.1538/expanim.15-0110.

Cumulative Risk Impact of RET, SEMA3, and NRG1 Polymorphisms Associated With Hirschsprung Disease in Han Chinese.

Li Q, Zhang Z, Diao M, et al.

Journal of pediatric gastroenterology and nutrition 2017; (64(3)):385-390 doi:10.1097/MPG.0000000000001263.

Maternal Risk Factors and Perinatal Characteristics for Hirschsprung Disease.

Löf Granström A, Svenningsson A, Hagel E, et al.

Pediatrics 2016; (138(1)).

A genome-wide association analysis of chromosomal aberrations and Hirschsprung disease.

Bae JS, Koh I, Cheong HS, et al.

Translational research : the journal of laboratory and clinical medicine 2016; (177()):31-40.e6 doi:10.1016/j.trsl.2016.06.001.

Morphometric profile of large intestinal neuronal plexuses in normal perinatal autopsies and Hirschsprung disease.

Subramanian H, Badhe BA, Toi PC, Sambandan K

Neurogastroenterology and motility 2017; (29(3)) doi:10.1111/nmo.12939.

Analysis of Enteric Neural Crest Cell Migration Using Heterotopic Grafts of Embryonic Guts.

Soret R, Pilon N

Bio-protocol 2016; (6(17)):1-6 doi:10.21769/bioprotoc.1924.

Spectrum of Clinicopathological Deviations in Long-Segment Hirschsprung Disease Compared With Short-Segment Hirschsprung Disease: A Single-Institution Study.

Alnajar H, Murro D, Alsadi A, Jakate S

International journal of surgical pathology 2017; (25(3)):216-221 doi:10.1177/1066896916675729.

Guidelines for the diagnosis and management of Hirschsprung-associated enterocolitis.

Gosain A, Frykman PK, Cowles RA, et al.

Pediatric surgery international 2017; (33(5)):517-521 doi:10.1007/s00383-017-4065-8.

Bowel Function and Quality of Life After Transanal Endorectal Pull-through for Hirschsprung Disease: Controlled Outcomes up to Adulthood.

Neuvonen MI, Kyrklund K, Rintala RJ, Pakarinen MP

Annals of surgery 2017; (265(3)):622-629 doi:10.1097/SLA.0000000000001695.

Guidelines for the management of postoperative obstructive symptoms in children with Hirschsprung disease.

Langer JC, Rollins MD, Levitt M, et al.

Pediatric surgery international 2017; (33(5)):523-526 doi:10.1007/s00383-017-4066-7.

Single-stage transanal endorectal pull-through procedure for correction of Hirschsprung disease in neonates and nonneonates: A multicenter study.

Lu C, Hou G, Liu C, et al.

Journal of pediatric surgery 2017; (52(7)):1102-1107 doi:10.1016/j.jpedsurg.2017.01.061.

Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease.

Yang D, Yang J, Li S, et al.

Scientific reports 2017; (7()):43222 doi:10.1038/srep43222.

A Scoring System to Predict the Severity of Hirschsprung Disease at Diagnosis and Its Correlation With Molecular Genetics.

Núñez-Ramos R, Fernández RM, González-Velasco M, et al.

Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2017; (20(1)):28-37 doi:10.1177/1093526616683883.

Correction of Hirschsprung-Associated Mutations in Human Induced Pluripotent Stem Cells Via Clustered Regularly Interspaced Short Palindromic Repeats/Cas9, Restores Neural Crest Cell Function.

Lai FP, Lau ST, Wong JK, et al.

Gastroenterology 2017; (153(1)):139-153.e8 doi:10.1053/j.gastro.2017.03.014.

[Hirschsprung-associated enterocolitis: Observational study in a paediatric emergency care unit].

Sellers M, Udaondo C, Moreno B, et al.

Anales de pediatria 2018; (88(6)):329-334 doi:10.1016/j.anpedi.2017.07.002.

Hirschsprung Disease Diagnosis: Calretinin Marker Role in Determining the Presence or Absence of Ganglion Cells.

Rakhshani N, Araste M, Imanzade F, et al.

Iranian journal of pathology 2016; (11(4)):409-415.

Inflammatory bowel disease in patients with Hirschsprung's disease: a systematic review and meta-analysis.

Nakamura H, Lim T, Puri P

Pediatric surgery international 2018; (34(2)):149-154 doi:10.1007/s00383-017-4182-4.

Anorectal Manometry May Reduce the Number of Rectal Suction Biopsy Procedures Needed to Diagnose Hirschsprung Disease.

Meinds RJ, Trzpis M, Broens PMA

Journal of pediatric gastroenterology and nutrition 2018; (67(3)):322-327 doi:10.1097/MPG.0000000000002000.

Functional outcomes in Hirschsprung disease patients after transabdominal Soave and Duhamel procedures.

Widyasari A, Pavitasari WA, Dwihantoro A, Gunadi

BMC gastroenterology 2018; (18(1)):56 doi:10.1186/s12876-018-0783-1.

Advances in understanding the association between Down syndrome and Hirschsprung disease (DS-HSCR).

Moore SW

Pediatric surgery international 2018; (34(11)):1127-1137 doi:10.1007/s00383-018-4344-z.

Atypical onset of total colonic Hirschsprung disease in a small female infant: A case report.

Mărginean CO, Meliţ LE, Gozar H, et al.

Medicine 2018; (97(38)):e12315 doi:10.1097/MD.0000000000012315.

The long-term quality of life outcomes in adolescents with Hirschsprung disease.

Sood S, Lim R, Collins L, et al.

Journal of pediatric surgery 2018; (53(12)):2430-2434 doi:10.1016/j.jpedsurg.2018.08.036.

Reliability of the Hirschsprung-Associated Enterocolitis Score in Clinical Practice.

Dore M, Vilanova Sanchez A, Triana Junco P, et al.

European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie 2019; (29(1)):132-137 doi:10.1055/s-0038-1677046.

Long-term Outcome of Hirschsprung Disease: Impact on Quality of Life and Social Condition at Adult Age.

Drissi F, Meurette G, Baayen C, et al.

Diseases of the colon and rectum 2019; (62(6)):727-732 doi:10.1097/DCR.0000000000001363.

Factors influencing the incidence of Hirschsprung associated enterocolitis (HAEC).

Le-Nguyen A, Righini-Grunder F, Piché N, et al.

Journal of pediatric surgery 2019; (54(5)):959-963 doi:10.1016/j.jpedsurg.2019.01.026.

Hirschsprung disease and Down syndrome: From the reappraisal of risk factors to the impact of surgery.

Pini Prato A, Arnoldi R, Sgrò A, et al.

Journal of pediatric surgery 2019; (54(9)):1838-1842 doi:10.1016/j.jpedsurg.2019.01.053.

High Levels of Interest in Reproductive Genetic Information in Parents of Children and Adults With Hirschsprung Disease.

Berrios CD, Chakravarti A, Biesecker BB

Journal of pediatric gastroenterology and nutrition 2019; (69(3)):299-305 doi:10.1097/MPG.0000000000002392.

Clinical Outcomes After Staged and Primary Laparotomy Soave Procedure for Total Colonic Aganglionosis: a Single-Center Experience from 2007 to 2017.

Yan J, Chen Y, Ding C, Chen Y

Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract 2020; (24(7)):1673-1681 doi:10.1007/s11605-019-04319-5.

What is new about the genetic background of Hirschsprung disease?

Luzón-Toro B, Villalba-Benito L, Torroglosa A, et al.

Clinical genetics 2020; (97(1)):114-124 doi:10.1111/cge.13615.

Unexpected gap between intraoperative caliber change of the intestine and normoganglia in patients with intestinal aganglionosis.

Sekioka A, Fukumoto K, Miyake H, et al.

Pediatric surgery international 2019; (35(10)):1115-1121 doi:10.1007/s00383-019-04534-w.

A Metagenomics Study on Hirschsprung's Disease Associated Enterocolitis: Biodiversity and Gut Microbial Homeostasis Depend on Resection Length and Patient's Clinical History.

Pini Prato A, Bartow-McKenney C, Hudspeth K, et al.

Frontiers in pediatrics 2019; (7()):326 doi:10.3389/fped.2019.00326.

Hirschsprung's disease: the importance of early diagnosis.

Neumann AF, de Lima PP, de Melo AMAGP

Autopsy & case reports 2013; (3(3)):59-66 doi:10.4322/acr.2013.030.

Concurrent Hirschsprung's disease and anorectal malformation: a systematic review.

Nakamura H, Puri P

Pediatric surgery international 2020; (36(1)):21-24 doi:10.1007/s00383-019-04580-4.

Adult congenital megacolon with acute fecal obstruction and diabetic nephropathy: A case report.

Zhang M, Ding K

Experimental and therapeutic medicine 2019; (18(4)):2726-2730 doi:10.3892/etm.2019.7852.

Hirschsprung disease: Insights on genes, penetrance, and prenatal diagnosis.

Wang XJ, Camilleri M

Neurogastroenterology and motility 2019; (31(11)):e13732 doi:10.1111/nmo.13732.

Are We Underdiagnosing Hirschsprung Disease?

Kapur RP, Ambartsumyan L, Smith C

Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2020; (23(1)):60-71 doi:10.1177/1093526619889434.

Diagnosis of Hirschsprung Disease.

Ambartsumyan L, Smith C, Kapur RP

Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2020; (23(1)):8-22 doi:10.1177/1093526619892351.

Prospective study reveals a microbiome signature that predicts the occurrence of post-operative enterocolitis in Hirschsprung disease (HSCR) patients.

Tang W, Su Y, Yuan C, et al.

Gut microbes 2020; (11(4)):842-854 doi:10.1080/19490976.2020.1711685.

Waardenburg-Shah syndrome (WS type IV): a rare case from Pakistan.

Khan TA, Safdar CA, Zameer S, Khushdil A

Perioperative medicine (London, England) 2020; (9()):4 doi:10.1186/s13741-019-0135-x.

Bowel function after transanal endorectal pull-through for Hirschsprung disease - does outcome improve over time?

Fosby MV, Stensrud KJ, Bjørnland K

Journal of pediatric surgery 2020; (55(11)):2375-2378 doi:10.1016/j.jpedsurg.2020.04.010.

Quality of life of patients with Hirschsprung disease after Duhamel and Soave pull-through procedures: A mixed-methods sequential explanatory cohort study.

Saysoo MR, Dewi FST, Gunadi

Annals of medicine and surgery (2012) 2020; (56()):34-37 doi:10.1016/j.amsu.2020.05.043.

Identification of New Potential LncRNA Biomarkers in Hirschsprung Disease.

Torroglosa A, Villalba-Benito L, Fernández RM, et al.

International journal of molecular sciences 2020; (21(15)) doi:10.3390/ijms21155534.

Ultrashort-segment Hirschsprung disease in a 4-year-old female.

Rodas A, Barillas S, Ardebol J

Journal of surgical case reports 2020; (2020(9)):rjaa320 doi:10.1093/jscr/rjaa320.

Barium enema findings in total colonic aganglionosis: a single-center, retrospective study.

Yan J, Sun J, Wu R, et al.

BMC pediatrics 2020; (20(1)):499 doi:10.1186/s12887-020-02403-3.

Modified Duhamel with lateral anal sphincterotomy and coloanal stump for adult Hirschsprung's disease: A case series.

Handaya AY, Fauzi AR, Andrew J, Hanif AS

International journal of surgery case reports 2020; (77()):174-177 doi:10.1016/j.ijscr.2020.10.066.

Analysis of enteric nervous system and intestinal epithelial barrier to predict complications in Hirschsprung's disease.

Dariel A, Grynberg L, Auger M, et al.

Scientific reports 2020; (10(1)):21725 doi:10.1038/s41598-020-78340-z.

Reevaluation of concurrent acetylcholinesterase and hematoxylin and eosin staining for Hirschsprung's disease.

Yoshimaru K, Matsuura T, Yanagi Y, et al.

Pediatrics international : official journal of the Japan Pediatric Society 2021; (63(9)):1095-1102 doi:10.1111/ped.14596.

Reducing Underdiagnosis of Hirschsprung-Associated Enterocolitis: A Novel Scoring System.

Lewit RA, Veras LV, Cowles RA, et al.

The Journal of surgical research 2021; (261()):253-260 doi:10.1016/j.jss.2020.12.030.

Functional outcomes of patients with short-segment Hirschsprung disease after transanal endorectal pull-through.

Gunadi , Ivana G, Mursalin DA, et al.

BMC gastroenterology 2021; (21(1)):85 doi:10.1186/s12876-021-01668-x.

NOX5 is expressed aberrantly but not a critical pathogenetic gene in Hirschsprung disease.

Wang J, Xiao J, Meng X, et al.

BMC pediatrics 2021; (21(1)):153 doi:10.1186/s12887-021-02611-5.

A Case Report of a Prenatally Missed Mowat-Wilson Syndrome With Isolated Corpus Callosum Agenesis.

Şenbil N, Arslan Z, Sayın Kocakap DB, Bilgili Y

Child neurology open 2021; (8()):2329048X211006511 doi:10.1177/2329048X211006511.

Diet plays a central role in parental self-treatment of children with Hirschsprung's disease-a qualitative study.

Telborn L, Tofft L, Kristensson Hallström I, et al.

Acta paediatrica (Oslo, Norway : 1992) 2021; (110(9)):2610-2617 doi:10.1111/apa.15952.

Risk factors for enterocolitis in patients with Hirschsprung disease: A retrospective observational study.

Roorda D, Oosterlaan J, van Heurn E, Derikx JPM

Journal of pediatric surgery 2021; (56(10)):1791-1798 doi:10.1016/j.jpedsurg.2021.04.020.

Psychosocial factors affecting quality of life in patients with anorectal malformation and Hirschsprung disease-a qualitative systematic review.

Svetanoff WJ, Kapalu CL, Lopez JJ, et al.

Journal of pediatric surgery 2022; (57(3)):387-393 doi:10.1016/j.jpedsurg.2021.05.004.

Development of Clinical Referral Score Model for Early Diagnosis of Hirschsprung's Disease in Suspected Pediatric Patients.

Khorana J, Phiromkanchanasak P, Kumsattra J, et al.

Healthcare (Basel, Switzerland) 2021; (9(6)) doi:10.3390/healthcare9060678.

The impact of botulinum injection for hospitalized children with Hirschsprung-associated enterocolitis.

Svetanoff WJ, Lopez J, Aguayo P, et al.

Pediatric surgery international 2021; (37(10)):1467-1472 doi:10.1007/s00383-021-04966-3.

Optimal timing for Soave primary pull-through in short-segment Hirschsprung disease: A meta-analysis.

Westfal ML, Okiemy O, Chung PHY, et al.

Journal of pediatric surgery 2022; (57(4)):719-725 doi:10.1016/j.jpedsurg.2021.07.007.

Can Propofol Be Used to Assess the Presence of the Rectoanal Inhibitory Reflex During Anorectal Manometry Studies?

Arbizu RA, Amicangelo M, Rodriguez L, Nurko S

Journal of pediatric gastroenterology and nutrition 2022; (74(1)):33-37 doi:10.1097/MPG.0000000000003283.

Association between ABHD1 and DOK6 polymorphisms and susceptibility to Hirschsprung disease in Southern Chinese children.

Lan C, Wu Y, Wang N, et al.

Journal of cellular and molecular medicine 2021; (25(20)):9609-9616 doi:10.1111/jcmm.16905.

Rare Variant Hirschsprung Disease Presenting as Large Bowel Obstruction in Adulthood: Hypoganglionosis in the Anorectal Canal.

Lee RY, Li H, White RV, et al.

ACG case reports journal 2021; (8(5)):e00610 doi:10.14309/crj.0000000000000610.

Robotic Soave pull-through procedure for Hirschsprung's disease in children under 12-months: long-term outcomes.

Delgado-Miguel C, Camps JI

Pediatric surgery international 2022; (38(1)):51-57 doi:10.1007/s00383-021-05018-6.

Outpatient Botulinum Injections for Early Obstructive Symptoms in Patients with Hirschsprung Disease.

Svetanoff WJ, Briggs K, Fraser JA, et al.

The Journal of surgical research 2022; (269()):201-206 doi:10.1016/j.jss.2021.07.017.

Functional Outcomes After Surgery for Total Colonic, Long-Segment, Versus Rectosigmoid Segment Hirschsprung Disease.

Verkuijl SJ, Meinds RJ, van der Steeg AFW, et al.

Journal of pediatric gastroenterology and nutrition 2022; (74(3)):348-354 doi:10.1097/MPG.0000000000003355.

Forty-Year Experience Alleviating Postoperative Hirschsprung-Associated Enterocolitis by Complete Full-Thickness Posterior Rectal Cuff Excision. The Anorectal Line Eliminates Problematic Anastomoses.

Takeda M, Miyano G, Nakazawa-Tanaka N, et al.

Journal of laparoendoscopic & advanced surgical techniques. Part A 2021; (31(12)):1436-1444 doi:10.1089/lap.2021.0340.

Submucosal Nerve Diameter in the Rectum Increases With Age: An Important Consideration for the Diagnosis of Hirschsprung Disease.

Conces MR, Beach S, Pierson CR, Prasad V

Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2022; (25(3)):263-269 doi:10.1177/10935266211049689.

Alterations of Gut Bacteria in Hirschsprung Disease and Hirschsprung-Associated Enterocolitis.

Chantakhow S, Khorana J, Tepmalai K, et al.

Microorganisms 2021; (9(11)) doi:10.3390/microorganisms9112241.

Outcome analysis of single-stage transanal endorectal pull through in selected patients with hirschsprung disease.

Gandhi S, Makan A, Shenoy NS, et al.

African journal of paediatric surgery : AJPS 2022; (19(1)):56-59 doi:10.4103/ajps.AJPS_137_20.

Advanced Management Protocol of Transanal Irrigation in Order to Improve the Outcome of Pediatric Patients with Fecal Incontinence.

Caruso AM, Milazzo MPM, Bommarito D, et al.

Children (Basel, Switzerland) 2021; (8(12)) doi:10.3390/children8121174.

Sonographic findings of total colonic aganglionosis in a neonate with Haddad syndrome: A case report.

Lim YJ, Jung HK

Journal of clinical ultrasound : JCU 2022; (50(6)):810-813 doi:10.1002/jcu.23147.

Hirschsprung-Associated Enterocolitis: Transformative Research from Bench to Bedside.

Zhang Z, Li B, Jiang Q, et al.

European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie 2022; (32(5)):383-390 doi:10.1055/s-0042-1745780.

Current understanding of Hirschsprung-associated enterocolitis: Pathogenesis, diagnosis and treatment.

Lewit RA, Kuruvilla KP, Fu M, Gosain A

Seminars in pediatric surgery 2022; (31(2)):151162 doi:10.1016/j.sempedsurg.2022.151162.

The utilization of botulinum toxin for Hirschsprung disease.

Svetanoff WJ, Lim-Beutal IIP, Wood RJ, et al.

Seminars in pediatric surgery 2022; (31(2)):151161 doi:10.1016/j.sempedsurg.2022.151161.

The science of Hirschsprung disease: What we know and where we are headed.

Mueller JL, Goldstein AM

Seminars in pediatric surgery 2022; (31(2)):151157 doi:10.1016/j.sempedsurg.2022.151157.

Transanal full-thickness pull-through approach in the treatment of anastomotic leakage after operation for Hirschsprung disease.

Jiao C, Zhuansun D, He Y, et al.

Pediatric surgery international 2022; (38(9)):1263-1271 doi:10.1007/s00383-022-05164-5.

Can Infant Dyschezia Be a Suspect of Rectosigmoid Redundancy?

Noviello C, Nobile S, Romano M, et al.

Children (Basel, Switzerland) 2022; (9(7)) doi:10.3390/children9071097.

A pilot study characterizing longitudinal changes in fecal microbiota of patients with Hirschsprung-associated enterocolitis.

Parker KD, Mueller JL, Westfal M, et al.

Pediatric surgery international 2022; (38(11)):1541-1553 doi:10.1007/s00383-022-05191-2.

One-stage transanal endorectal pull-through for Hirschsprung disease: experience with 229 neonates.

Zhang Y, Liu Z, Li S, et al.

Pediatric surgery international 2022; (38(11)):1533-1540 doi:10.1007/s00383-022-05198-9.

Laparoscopic Management of Intestinal Obstruction due to a Tight Muscular Cuff Following Transanal Endorectal Pull-through for Hirschsprung's Disease.

Villamil V, Sanchez Morote JM, Aranda Garcia MJ, et al.

Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2022; (32(8)):S177-S179 doi:10.29271/jcpsp.2022.Supp2.S177.

Risk factors for Hirschsprung-associated enterocolitis following Soave: a retrospective study over a decade.

Xie C, Yan J, Zhang Z, et al.

BMC pediatrics 2022; (22(1)):654 doi:10.1186/s12887-022-03692-6.

Comprehensive characterization of the genetic landscape of familial Hirschsprung's disease.

Xiao J, Hao LW, Wang J, et al.

World journal of pediatrics : WJP 2023; (19(7)):644-651 doi:10.1007/s12519-023-00686-x.

Pediatric Bowel Management Options and Organizational Aspects.

Bokova E, Svetanoff WJ, Levitt MA, Rentea RM

Children (Basel, Switzerland) 2023; (10(4)) doi:10.3390/children10040633.

State of the Art Bowel Management for Pediatric Colorectal Problems: Anorectal Malformations.

Bokova E, Svetanoff WJ, Lopez JJ, et al.

Children (Basel, Switzerland) 2023; (10(5)) doi:10.3390/children10050846.

State of the Art Bowel Management for Pediatric Colorectal Problems: Functional Constipation.

Bokova E, Svetanoff WJ, Rosen JM, et al.

Children (Basel, Switzerland) 2023; (10(6)) doi:10.3390/children10061078.

State of the Art Bowel Management for Pediatric Colorectal Problems: Hirschsprung Disease.

Bokova E, Prasade N, Janumpally S, et al.

Children (Basel, Switzerland) 2023; (10(8)) doi:10.3390/children10081418.

Long-Term Functional Outcomes and Multidisciplinary Management after Ileorectal Duhamel Pull-Through for Total Colonic Aganglionosis-20-Year Experience in a Tertiary Surgical Center.

Bhandarkar K, De Coppi P, Cross K, et al.

European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie 2024; (34(5)):423-429 doi:10.1055/a-2181-2065.

Hirschsprung disease.

Montalva L, Cheng LS, Kapur R, et al.

Nature reviews. Disease primers 2023; (9(1)):54 doi:10.1038/s41572-023-00465-y.

Duhamel Versus Swenson Pull-Through for Total Colonic Aganglionosis: A Multi-Institutional Study.

Halaweish I, Srinivas S, Farooqui Z, et al.

Journal of pediatric surgery 2024; (59(2)):216-219 doi:10.1016/j.jpedsurg.2023.10.017.

Hirschsprung Disease and Intestinal Neuronal Dysplasia Type B: Is There a Difference in the Clinical Presentation of These Two Diseases?

Cesar Gonçalves A, Camargo de Oliveira B, Patti Sanches Coelho M, et al.

Cureus 2023; (15(12)):e50618 doi:10.7759/cureus.50618.

PHOX2B: a diagnostic cornerstone in neurocristopathies and neuroblastomas.

Windels ML, Cordier F, Van Dorpe J, et al.

Journal of clinical pathology 2024; (77(6)):378-382 doi:10.1136/jcp-2023-209047.

Clinical Relevance of Pathological Diagnosis of Hirschsprung's Disease with Acetylcholine-Esterase Histochemistry or Calretinin Immunohistochemistry.

Romero P, Burger A, Wennberg E, et al.

Children (Basel, Switzerland) 2024; (11(4)) doi:10.3390/children11040428.

Ernica Clinical Consensus Statements on Total Colonic and Intestinal Aganglionosis.

Granström AL, Irvine W, Hoel AT, et al.

Journal of pediatric surgery 2024; (59(10)):161565 doi:10.1016/j.jpedsurg.2024.04.019.

Bowel Management in Hirschsprung Disease-Pre-, Peri- and Postoperative Care for Primary Pull-Through.

Lindert J, Schulze F, Märzheuser S

Children (Basel, Switzerland) 2024; (11(5)) doi:10.3390/children11050588.

Chronic Constipation Unmasking as Hirschsprung Disease in a Preadolescent: Delayed Presentation or Delayed Diagnosis?

Bhargava A, Khedkar K

Cureus 2024; (16(5)):e60315 doi:10.7759/cureus.60315.

Timing for reconstructive surgery in Hirschsprung disease.

Pini Prato A, Felici E

Minerva pediatrics 2025; (77(1)):87-93 doi:10.23736/S2724-5276.24.07508-6.

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