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2,163 results

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Quoted phrase not found in phrase index: "Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease"
Page 1
Hirschsprung's disease: diagnosis and management.
Kessmann J. Kessmann J. Am Fam Physician. 2006 Oct 15;74(8):1319-22. Am Fam Physician. 2006. PMID: 17087425 Free article. Review.
Hirschsprung's disease (congenital megacolon) is caused by the failed migration of colonic ganglion cells during gestation. ...Patients should be monitored closely for enterocolitis for years after surgical treatment of Hirschsprung's disease. With pro
Hirschsprung's disease (congenital megacolon) is caused by the failed migration of colonic ganglion cells during gestation. ..
Hirschsprung disease.
Montalva L, Cheng LS, Kapur R, Langer JC, Berrebi D, Kyrklund K, Pakarinen M, de Blaauw I, Bonnard A, Gosain A. Montalva L, et al. Nat Rev Dis Primers. 2023 Oct 12;9(1):54. doi: 10.1038/s41572-023-00465-y. Nat Rev Dis Primers. 2023. PMID: 37828049 Review.
Hirschsprung disease (HSCR) is a rare congenital intestinal disease that occurs in 1 in 5,000 live births. ...Syndromes associated with HSCR include trisomy 21, Mowat-Wilson syndrome, congenital central hypoventilation syndrome
Hirschsprung disease (HSCR) is a rare congenital intestinal disease that occurs in 1 in 5,000 live births. ...Sy
Hirschsprung's Disease-Recent Understanding of Embryonic Aspects, Etiopathogenesis and Future Treatment Avenues.
Klein M, Varga I. Klein M, et al. Medicina (Kaunas). 2020 Nov 13;56(11):611. doi: 10.3390/medicina56110611. Medicina (Kaunas). 2020. PMID: 33202966 Free PMC article. Review.
Hirschsprung's disease is a neurocristopathy, caused by defective migration, proliferation, differentiation and survival of neural crest cells, leading to gut aganglionosis. ...From the diagnostic perspective, researchers also focused on "Variants of Hirschsprung
Hirschsprung's disease is a neurocristopathy, caused by defective migration, proliferation, differentiation and survival of ne
The science of Hirschsprung disease: What we know and where we are headed.
Mueller JL, Goldstein AM. Mueller JL, et al. Semin Pediatr Surg. 2022 Apr;31(2):151157. doi: 10.1016/j.sempedsurg.2022.151157. Epub 2022 Apr 18. Semin Pediatr Surg. 2022. PMID: 35690468 Review.
Congenital or acquired disruption of ENS development leads to various neurointestinal diseases. Hirschsprung disease is a congenital neurocristopathy, a disease of the neural crest. It is characterized by a variable length of distal colonic aganglionosis due …
Congenital or acquired disruption of ENS development leads to various neurointestinal diseases. Hirschsprung disease is a cong …
The developmental etiology and pathogenesis of Hirschsprung disease.
Butler Tjaden NE, Trainor PA. Butler Tjaden NE, et al. Transl Res. 2013 Jul;162(1):1-15. doi: 10.1016/j.trsl.2013.03.001. Epub 2013 Mar 22. Transl Res. 2013. PMID: 23528997 Free PMC article. Review.
Disorders that arise as a consequence of defective neural crest cell development are termed neurocristopathies. One such disorder is Hirschsprung disease (HSCR), also known as congenital megacolon or intestinal aganglionosis. HSCR occurs in 1/5000 live births …
Disorders that arise as a consequence of defective neural crest cell development are termed neurocristopathies. One such disorder is Hirs
ERNICA guidelines for the management of rectosigmoid Hirschsprung's disease.
Kyrklund K, Sloots CEJ, de Blaauw I, Bjørnland K, Rolle U, Cavalieri D, Francalanci P, Fusaro F, Lemli A, Schwarzer N, Fascetti-Leon F, Thapar N, Johansen LS, Berrebi D, Hugot JP, Crétolle C, Brooks AS, Hofstra RM, Wester T, Pakarinen MP. Kyrklund K, et al. Orphanet J Rare Dis. 2020 Jun 25;15(1):164. doi: 10.1186/s13023-020-01362-3. Orphanet J Rare Dis. 2020. PMID: 32586397 Free PMC article. Review.
BACKGROUND: Hirschsprung's disease (HSCR) is a serious congenital bowel disorder with a prevalence of 1/5000. ...
BACKGROUND: Hirschsprung's disease (HSCR) is a serious congenital bowel disorder with a prevalence of 1/5000. ...
PTEN Immunohistochemistry.
Terra SA, de Arruda Lourenção PLT, Rodrigues MAM. Terra SA, et al. Arch Pathol Lab Med. 2022 May 1;147(5):577-583. doi: 10.5858/arpa.2021-0424-OA. Arch Pathol Lab Med. 2022. PMID: 35943858 Free article.
.-: To analyze the applicability of PTEN immunohistochemistry in the diagnosis of IND B and to compare with control cases and cases of Hirschsprung disease (HD). DESIGN.-: PTEN immunohistochemical expression was analyzed in colorectal samples from 29 cases of IND B …
.-: To analyze the applicability of PTEN immunohistochemistry in the diagnosis of IND B and to compare with control cases and cases of Hi
Hirschsprung Disease.
Mahon M, Khlevner J. Mahon M, et al. Pediatr Rev. 2021 Dec 1;42(12):714-716. doi: 10.1542/pir.2020-004912. Pediatr Rev. 2021. PMID: 36017952 No abstract available.
Hirschsprung disease outcomes.
Short SS, Durham MM, Rollins MD. Short SS, et al. Semin Pediatr Surg. 2022 Apr;31(2):151160. doi: 10.1016/j.sempedsurg.2022.151160. Epub 2022 Apr 8. Semin Pediatr Surg. 2022. PMID: 35690462
Hirschsprung disease (HD) is a complex surgical and medical problem that appears to have varied health and social outcomes with the age and neurodevelopmental state of patients. ...
Hirschsprung disease (HD) is a complex surgical and medical problem that appears to have varied health and social outcomes wit
Hirschsprung disease.
Langer JC. Langer JC. Curr Opin Pediatr. 2013 Jun;25(3):368-74. doi: 10.1097/MOP.0b013e328360c2a0. Curr Opin Pediatr. 2013. PMID: 23615177 Review.
PURPOSE OF REVIEW: Hirschsprung disease is relatively common in children. Surgical techniques are available to remove the aganglionic bowel and reconstruct the intestinal tract. ...SUMMARY: Pediatricians and primary care physicians have an important role to play in …
PURPOSE OF REVIEW: Hirschsprung disease is relatively common in children. Surgical techniques are available to remove the agan …
2,163 results