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Items: 1 to 20 of 305

1.

Hirschsprung's disease in Arab siblings with Bardet-Biedl syndrome.

Cherian MP, Al-Sanna'a NA, Al-Mulhim SI.

J Pediatr Surg. 2008 Jun;43(6):1213-7. doi: 10.1016/j.jpedsurg.2008.02.013.

PMID:
18558212
2.

Hirschsprung's disease.

Kenny SE, Tam PK, Garcia-Barcelo M.

Semin Pediatr Surg. 2010 Aug;19(3):194-200. doi: 10.1053/j.sempedsurg.2010.03.004. Review.

PMID:
20610192
3.

Many faces of Hirschsprung's disease.

Godbole K.

Indian Pediatr. 2004 Nov;41(11):1115-23. Review.

4.

Clinical spectrum of Bardet-Biedl syndrome among four Saudi Arabian families.

Cherian MP, Al-Sanna'a NA.

Clin Dysmorphol. 2009 Oct;18(4):188-94. doi: 10.1097/MCD.0b013e32832e4657.

PMID:
19707123
5.

Long-term outcome of total colonic aganglionosis.

Raboei EH.

Eur J Pediatr Surg. 2008 Oct;18(5):300-2. doi: 10.1055/s-2008-1038495. Epub 2008 Oct 14.

PMID:
18855314
6.

Imperforate anus, malrotation, and Hirschsprung's disease with double zonal aganglionosis: an extremely rare combination.

Oshio T.

J Pediatr Surg. 2008 Jan;43(1):222-6. doi: 10.1016/j.jpedsurg.2007.09.005.

PMID:
18206486
7.

Early diagnosis and treatment of Hirschsprung's disease in New Mexico.

Kosloske AM, Goldthorn JF.

Surg Gynecol Obstet. 1984 Mar;158(3):233-7.

PMID:
6701735
8.

Hirschsprung's disease, colonic atresia, and absent hand: a new triad.

Croaker GD, Harvey JG, Cass DT.

J Pediatr Surg. 1997 Sep;32(9):1368-70. Review.

PMID:
9314266
9.

Concomitant existence of total bowel aganglionosis and congenital central hypoventilation syndrome in a neonate with PHOX2B gene mutation.

Ou-Yang MC, Yang SN, Hsu YM, Ou-Yang MH, Haung HC, Lee SY, Hsieh WS, Su YN, Liu CA.

J Pediatr Surg. 2007 Feb;42(2):e9-11.

PMID:
17270534
10.

Congenital aganglionic megacolon in Nigerian adults: two case reports and review of the literature.

Bakari AA, Gali BM, Ibrahim AG, Nggada HA, Ali N, Dogo D, Abubakar AM.

Niger J Clin Pract. 2011 Apr-Jun;14(2):249-52. doi: 10.4103/1119-3077.84032. Review.

11.

Concordant expression of Hirschsprung's disease in monozygous twins.

Mohammed AA, Gahukamble DB.

Saudi Med J. 2000 Feb;21(2):200-1.

PMID:
11533767
12.

[Clinical study of multiple zonal aganglionosis in long segment Hirschsprung's disease].

Yang HY, Liu QL, Wang JX, Xu HF.

Zhonghua Yi Xue Za Zhi. 2005 Oct 19;85(39):2772-4. Chinese.

PMID:
16324319
13.

Familial Hirschsprung's disease--a report of 22 affected siblings in four families.

Schiller M, Levy P, Shawa RA, Abu-Dalu K, Gorenstein A, Katz S.

J Pediatr Surg. 1990 Mar;25(3):322-5.

PMID:
2313502
14.

A review of the literature of Bardet-Biedl disease and report of three cases associated with metabolic syndrome and diagnosed after the age of fifty.

Iannello S, Bosco P, Cavaleri A, Camuto M, Milazzo P, Belfiore F.

Obes Rev. 2002 May;3(2):123-35. Review.

PMID:
12120419
15.

Gastroschisis, ileal atresia, and Hirschsprung's disease in a newborn: the first reported case.

Goslin B, Brown A, Robertson D.

J Pediatr Surg. 2012 Nov;47(11):2134-6. doi: 10.1016/j.jpedsurg.2012.09.040.

PMID:
23164011
16.

Aganglionosis of the small intestine: a rare form of Hirschsprung's disease.

Rayhorn NJ, Ingebo KR.

Gastroenterol Nurs. 1999 Jul-Aug;22(4):164-6. Review.

PMID:
10745745
17.

Clinical and genetic differences in total colonic aganglionosis in Hirschsprung's disease.

Moore SW, Zaahl M.

J Pediatr Surg. 2009 Oct;44(10):1899-903. doi: 10.1016/j.jpedsurg.2009.04.026.

PMID:
19853744
18.

Chromosomal and related Mendelian syndromes associated with Hirschsprung's disease.

Moore SW.

Pediatr Surg Int. 2012 Nov;28(11):1045-58. doi: 10.1007/s00383-012-3175-6. Epub 2012 Sep 23. Review.

PMID:
23001136
19.

Phenotypic overlap of McKusick-Kaufman syndrome with bardet-biedl syndrome: a literature review.

Slavotinek AM, Biesecker LG.

Am J Med Genet. 2000 Nov 27;95(3):208-15. Review.

PMID:
11102925
20.

Hirschsprung's disease associated with alopecia universalis congenita: a case report.

Malik S, Singhal M, Jadhav SS, Korday CS, Nayak CS.

J Med Case Rep. 2016 Sep 15;10(1):250. doi: 10.1186/s13256-016-1035-z.

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