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Results: 1 to 20 of 91

Similar articles for PubMed (Select 23211657)

1.

Association between celiac disease and primary lactase deficiency.

Basso MS, Luciano R, Ferretti F, Muraca M, Panetta F, Bracci F, Ottino S, Diamanti A.

Eur J Clin Nutr. 2012 Dec;66(12):1364-5. doi: 10.1038/ejcn.2012.153.

PMID:
23211657
2.

Genotyping of the lactase-phlorizin hydrolase c/t-13910 polymorphism by means of a new rapid denaturing high-performance liquid chromatography-based assay in healthy subjects and colorectal cancer patients.

Piepoli A, Schirru E, Mastrorilli A, Gentile A, Cotugno R, Quitadamo M, Merla A, Congia M, Usai Satta P, Perri F.

J Biomol Screen. 2007 Aug;12(5):733-9. Epub 2007 May 3.

PMID:
17478481
3.

Prevalence of adult-type hypolactasia as diagnosed with genetic and lactose hydrogen breath tests in Hungarians.

Nagy D, Bogácsi-Szabó E, Várkonyi A, Csányi B, Czibula A, Bede O, Tari B, Raskó I.

Eur J Clin Nutr. 2009 Jul;63(7):909-12. doi: 10.1038/ejcn.2008.74. Epub 2009 Jan 21.

PMID:
19156157
4.

High prevalence of celiac disease in patients with lactose intolerance.

Ojetti V, Nucera G, Migneco A, Gabrielli M, Lauritano C, Danese S, Zocco MA, Nista EC, Cammarota G, De Lorenzo A, Gasbarrini G, Gasbarrini A.

Digestion. 2005;71(2):106-10. Epub 2005 Mar 16.

PMID:
15775678
5.

Genetic testing for adult-type hypolactasia in Italian families.

Mottes M, Belpinati F, Milani M, Saccomandi D, Petrelli E, Calacoci M, Chierici R, Pignatti PF, Borgna-Pignatti C.

Clin Chem Lab Med. 2008;46(7):980-4. doi: 10.1515/CCLM.2008.189.

PMID:
18605960
6.

CD14 polymorphisms correlate with an augmented risk for celiac disease in Italian patients.

Catamo E, Segat L, Lenarduzzi S, Petix V, Morgutti M, Crovella S.

Genes Immun. 2012 Sep;13(6):489-95. doi: 10.1038/gene.2012.23. Epub 2012 May 31.

PMID:
22648004
7.

Frequencies of genetic polymorphisms of TLR4 and CD14 and of HLA-DQ genotypes in children with celiac disease, type 1 diabetes mellitus, or both.

Dezsofi A, Szebeni B, Hermann CS, Kapitány A, Veres G, Sipka S, Körner A, Madácsy L, Korponay-Szabó I, Rajczy K, Arató A.

J Pediatr Gastroenterol Nutr. 2008 Sep;47(3):283-7. doi: 10.1097/MPG.0b013e31816de885.

PMID:
18728522
8.

Evaluation of a new DNA test compared with the lactose hydrogen breath test for the diagnosis of lactase non-persistence.

Högenauer C, Hammer HF, Mellitzer K, Renner W, Krejs GJ, Toplak H.

Eur J Gastroenterol Hepatol. 2005 Mar;17(3):371-6.

PMID:
15716664
9.

Decline of lactase activity and c/t-13910 variant in Sardinian childhood.

Schirru E, Corona V, Usai-Satta P, Scarpa M, Cucca F, De Virgiliis S, Rossino R, Frau F, Macis MD, Jores RD, Congia M.

J Pediatr Gastroenterol Nutr. 2007 Oct;45(4):503-6.

PMID:
18030226
10.

A common CTLA4 polymorphism confers susceptibility to autoimmune thyroid disease in celiac children.

Tolone C, Cirillo G, Papparella A, Tolone S, Santoro N, Grandone A, Perrone L, del Giudice EM.

Dig Liver Dis. 2009 Jun;41(6):385-9. doi: 10.1016/j.dld.2008.09.001. Epub 2008 Oct 16.

PMID:
18929517
11.

Genetic test for lactase non-persistence and hydrogen breath test: is genotype better than phenotype to diagnose lactose malabsorption?

Di Stefano M, Terulla V, Tana P, Mazzocchi S, Romero E, Corazza GR.

Dig Liver Dis. 2009 Jul;41(7):474-9. doi: 10.1016/j.dld.2008.09.020. Epub 2008 Nov 14.

PMID:
19010095
12.

Genetic variation and lactose intolerance: detection methods and clinical implications.

Sibley E.

Am J Pharmacogenomics. 2004;4(4):239-45. Review.

PMID:
15287817
13.

Celiac disease in North Italian patients with autoimmune thyroid diseases.

Spadaccino AC, Basso D, Chiarelli S, Albergoni MP, D'Odorico A, Plebani M, Pedini B, Lazzarotto F, Betterle C.

Autoimmunity. 2008 Feb;41(1):116-21. doi: 10.1080/08916930701620209.

PMID:
18176874
14.

A family-based study does not confirm the association of MYO9B with celiac disease in the Italian population.

Giordano M, Marano C, Mellai M, Limongelli MG, Bolognesi E, Clerget-Darpoux F, Momigliano-Richiardi P, Greco L.

Genes Immun. 2006 Oct;7(7):606-8. Epub 2006 Aug 31.

PMID:
16943798
15.

Lactase persistence, dietary intake of milk, and the risk for prostate cancer in Sweden and Finland.

Torniainen S, Hedelin M, Autio V, Rasinperä H, Bälter KA, Klint A, Bellocco R, Wiklund F, Stattin P, Ikonen T, Tammela TL, Schleutker J, Grönberg H, Järvelä I.

Cancer Epidemiol Biomarkers Prev. 2007 May;16(5):956-61.

16.

CTLA-4 gene polymorphisms predispose to autoimmune endocrinopathies but not to celiac disease.

Dallos T, Avbelj M, Barák L, Zapletalová J, Pribilincová Z, Krajcírová M, Kostálová L, Battelino T, Kovács L.

Neuro Endocrinol Lett. 2008 Jun;29(3):334-40.

PMID:
18580850
17.

ATG16L1 and IL23R are associated with inflammatory bowel diseases but not with celiac disease in the Netherlands.

Weersma RK, Zhernakova A, Nolte IM, Lefebvre C, Rioux JD, Mulder F, van Dullemen HM, Kleibeuker JH, Wijmenga C, Dijkstra G.

Am J Gastroenterol. 2008 Mar;103(3):621-7. Epub 2007 Nov 28.

PMID:
18047540
18.

Celiac disease in North Italian patients with autoimmune Addison's disease.

Betterle C, Lazzarotto F, Spadaccino AC, Basso D, Plebani M, Pedini B, Chiarelli S, Albergoni M.

Eur J Endocrinol. 2006 Feb;154(2):275-9.

19.

Hydrogen breath testing versus LCT genotyping for the diagnosis of lactose intolerance: a matter of age?

Kerber M, Oberkanins C, Kriegshäuser G, Kollerits B, Dossenbach-Glaninger A, Fuchs D, Ledochowski M.

Clin Chim Acta. 2007 Aug;383(1-2):91-6. Epub 2007 May 10.

PMID:
17574225
20.

Molecular genetics of adult-type hypolactasia.

Järvelä IE.

Ann Med. 2005;37(3):179-85. Review.

PMID:
16019716
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