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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1909 2
1913 3
1914 1
1916 1
1917 1
1918 1
1919 2
1923 1
1925 1
1926 1
1928 2
1929 1
1930 4
1931 1
1932 3
1933 1
1935 2
1936 2
1938 1
1939 1
1940 1
1945 3
1946 6
1947 10
1948 6
1949 12
1950 15
1951 18
1952 33
1953 19
1954 24
1955 26
1956 30
1957 28
1958 23
1959 24
1960 15
1961 24
1962 34
1963 30
1964 47
1965 43
1966 34
1967 52
1968 43
1969 38
1970 63
1971 54
1972 41
1973 41
1974 23
1975 51
1976 45
1977 40
1978 53
1979 58
1980 52
1981 60
1982 64
1983 67
1984 89
1985 85
1986 103
1987 91
1988 67
1989 110
1990 74
1991 82
1992 87
1993 88
1994 125
1995 117
1996 131
1997 133
1998 158
1999 137
2000 128
2001 136
2002 145
2003 151
2004 123
2005 146
2006 163
2007 163
2008 147
2009 168
2010 163
2011 181
2012 187
2013 216
2014 229
2015 245
2016 276
2017 247
2018 242
2019 281
2020 289
2021 310
2022 298
2023 274
2024 297
2025 15

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7,692 results

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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. ...Up to one third of patients develop Hirschsprung's-associated enterocolitis, a significant cause of mortality. Patient
Hirschsprung's disease (congenital megacolon) is caused by the failed migration of colonic ganglion cells during
[Congenital megacolon].
SOSTEGNI A, STRAMINGNONI G. SOSTEGNI A, et al. Minerva Pediatr. 1952 Mar 31;4(6):195. Minerva Pediatr. 1952. PMID: 14956920 Undetermined Language. No abstract available.
Congenital megacolon.
Swenson O. Swenson O. Pediatr Clin North Am. 1967 Feb;14(1):187-96. doi: 10.1016/s0031-3955(16)31950-2. Pediatr Clin North Am. 1967. PMID: 6016070 No abstract available.
KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon.
Almannai M, AlAbdi L, Maddirevula S, Alotaibi M, Alsaleem BM, Aljadhai YI, Alsaif HS, Abukhalid M, Alkuraya FS. Almannai M, et al. Hum Genet. 2023 Mar;142(3):399-405. doi: 10.1007/s00439-022-02513-1. Epub 2022 Dec 23. Hum Genet. 2023. PMID: 36564622
Human disorders of the enteric nervous system (ENS), e.g., Hirschsprung's disease, are rarely associated with major central nervous system involvement. We describe two families each segregating a different homozygous truncating variant in KIF26A with a unique conste …
Human disorders of the enteric nervous system (ENS), e.g., Hirschsprung's disease, are rarely associated with major central ne …
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. ...The inheritance of HSCR …
Disorders that arise as a consequence of defective neural crest cell development are termed neurocristopathies. One such disorder is Hirs
Congenital megacolon (Hirschsprung's disease).
KEEFER GP, MOKROHISKY JF. KEEFER GP, et al. Radiology. 1954 Aug;63(2):157-75. doi: 10.1148/63.2.157. Radiology. 1954. PMID: 13194867 No abstract available.
Congenital aganglionic megacolon.
AXELROD H. AXELROD H. Am J Surg. 1955 Jul;90(1):18-25. doi: 10.1016/0002-9610(55)90653-x. Am J Surg. 1955. PMID: 14388171 No abstract available.
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
7,692 results