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Items: 1 to 20 of 102

1.

Congenital diarrheal disorders: an updated diagnostic approach.

Terrin G, Tomaiuolo R, Passariello A, Elce A, Amato F, Di Costanzo M, Castaldo G, Canani RB.

Int J Mol Sci. 2012;13(4):4168-85. doi: 10.3390/ijms13044168. Review.

2.

Recent progress in congenital diarrheal disorders.

Canani RB, Terrin G.

Curr Gastroenterol Rep. 2011 Jun;13(3):257-64. doi: 10.1007/s11894-011-0188-6. Review.

PMID:
21494839
3.

Extremely rare cause of congenital diarrhea: enteric anendocrinosis.

Sayar E, Islek A, Yilmaz A, Akcam M, Flanagan SE, Artan R.

Pediatr Int. 2013 Oct;55(5):661-3. doi: 10.1111/ped.12169.

PMID:
24134759
4.

Congenital diarrheal disorders: improved understanding of gene defects is leading to advances in intestinal physiology and clinical management.

Berni Canani R, Terrin G, Cardillo G, Tomaiuolo R, Castaldo G.

J Pediatr Gastroenterol Nutr. 2010 Apr;50(4):360-6. doi: 10.1097/MPG.0b013e3181d135ef. Review.

PMID:
20216094
5.

Congenital intestinal diarrhoeal diseases: A diagnostic and therapeutic challenge.

Posovszky C.

Best Pract Res Clin Gastroenterol. 2016 Apr;30(2):187-211. doi: 10.1016/j.bpg.2016.03.004. Review.

PMID:
27086885
6.

Exome sequencing finds a novel PCSK1 mutation in a child with generalized malabsorptive diarrhea and diabetes insipidus.

Yourshaw M, Solorzano-Vargas RS, Pickett LA, Lindberg I, Wang J, Cortina G, Pawlikowska-Haddal A, Baron H, Venick RS, Nelson SF, Martín MG.

J Pediatr Gastroenterol Nutr. 2013 Dec;57(6):759-67. doi: 10.1097/MPG.0b013e3182a8ae6c.

7.

Congenital diarrhoeal disorders: advances in this evolving web of inherited enteropathies.

Canani RB, Castaldo G, Bacchetta R, Martín MG, Goulet O.

Nat Rev Gastroenterol Hepatol. 2015 May;12(5):293-302. doi: 10.1038/nrgastro.2015.44. Review.

PMID:
25782092
8.

[Congenital diarrhoea].

Buda P, Friedman-Gruszczyńska J, Książyk J.

Med Wieku Rozwoj. 2011 Oct-Dec;15(4):477-86. Review. Polish.

9.

[Clinical studies of pediatric malabsorption syndromes].

Hosoyamada T.

Fukuoka Igaku Zasshi. 2006 Nov;97(11):322-50. Japanese.

PMID:
17228786
10.

[Thirty years of research on congenital glucose and galactose malabsorption: from phenotype to genotype].

Desjeux JF, Wright EM.

Bull Acad Natl Med. 1993 Jan;177(1):125-31; discussion 132-5. French.

PMID:
8319109
11.

Significance of molecular testing for congenital chloride diarrhea.

Lechner S, Ruemmele FM, Zankl A, Lausch E, Huber WD, Mihatsch W, Phillips AD, Lewindon P, Querfeld U, Heinz-Erian P, Müller T, Janecke AR.

J Pediatr Gastroenterol Nutr. 2011 Jul;53(1):48-54. doi: 10.1097/MPG.0b013e31820bc856.

PMID:
21694535
12.

Familial enteropathy: a syndrome of protracted diarrhea from birth, failure to thrive, and hypoplastic villus atrophy.

Davidson GP, Cutz E, Hamilton JR, Gall DG.

Gastroenterology. 1978 Nov;75(5):783-90.

PMID:
100367
13.

Mutant neurogenin-3 in congenital malabsorptive diarrhea.

Wang J, Cortina G, Wu SV, Tran R, Cho JH, Tsai MJ, Bailey TJ, Jamrich M, Ament ME, Treem WR, Hill ID, Vargas JH, Gershman G, Farmer DG, Reyen L, Martín MG.

N Engl J Med. 2006 Jul 20;355(3):270-80.

14.

[30 years' work on congenital glucose and galactose malabsorption: from phenotype to genotype].

Desjeux JF, Wright EM.

Ann Gastroenterol Hepatol (Paris). 1993 Oct;29(5):263-6; discussion 266-8. Review. French.

PMID:
8250522
15.

Congenital Sodium Diarrhea: A Form of Intractable Diarrhea, With a Link to Inflammatory Bowel Disease.

Janecke AR, Heinz-Erian P, Müller T.

J Pediatr Gastroenterol Nutr. 2016 Aug;63(2):170-6. doi: 10.1097/MPG.0000000000001139.

PMID:
26835907
16.

Nutrition management of congenital glucose-galactose malabsorption: a case study.

Abad-Sinden A, Borowitz S, Meyers R, Sutphen J.

J Am Diet Assoc. 1997 Dec;97(12):1417-21.

PMID:
9404340
17.

Congenital glucose galactose malabsorption.

Wickramasinghe P, Lamabadusuriya SP, Lalani HA.

Ceylon Med J. 2001 Mar;46(1):26-7. No abstract available.

PMID:
11569998
18.

Misdiagnosis of congenital chloride-losing diarrhea.

Khan SN, Yaish HM.

J Perinatol. 1992 Jun;12(2):112-4.

PMID:
1522426
19.

A paucity of colonic enteroendocrine and/or enterochromaffin cells characterizes a subset of patients with chronic unexplained diarrhea/malabsorption.

Ohsie S, Gerney G, Gui D, Kahana D, Martín MG, Cortina G.

Hum Pathol. 2009 Jul;40(7):1006-14. doi: 10.1016/j.humpath.2008.12.016.

PMID:
19297006
20.

[Intestinal malabsorption and genetic defects].

Porto JA, Mello Sda S, Junqueira A.

Arq Bras Endocrinol Metabol. 1969 Apr;18(1):5-23. Portuguese. No abstract available.

PMID:
5403667
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