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Items: 1 to 20 of 111

1.

Noninvasive diagnosis of hypolactasia with 4-Galactosylxylose (Gaxilose): a multicentre, open-label, phase IIB-III nonrandomized trial.

Aragón JJ, Hermida C, Martínez-Costa OH, Sánchez V, Martín I, Sánchez JJ, Codoceo R, Cano JM, Cano A, Crespo L, Torres Y, García FJ, Fernández-Mayoralas A, Solera J, Martínez P.

J Clin Gastroenterol. 2014 Jan;48(1):29-36. doi: 10.1097/MCG.0b013e318297fb10.

PMID:
23722657
2.

Phase I and phase IB clinical trials for the noninvasive evaluation of intestinal lactase with 4-galactosylxylose (gaxilose).

Hermida C, Guerra P, Martínez-Costa OH, Sánchez V, Sánchez JJ, Solera J, Fernández-Mayoralas A, Codoceo R, Frías J, Aragón JJ.

J Clin Gastroenterol. 2013 Jul;47(6):501-8. doi: 10.1097/MCG.0b013e318272f507.

PMID:
23328304
3.

Improvement and validation of d-xylose determination in urine and serum as a new tool for the noninvasive evaluation of lactase activity in humans.

Hermida C, Martínez-Costa OH, Corrales G, Teruel C, Sánchez V, Sánchez JJ, Sarrión D, Ariza MJ, Codoceo R, Calvo I, Fernández-Mayoralas A, Aragón JJ.

J Clin Lab Anal. 2014 Nov;28(6):478-86. doi: 10.1002/jcla.21713. Epub 2014 Mar 22.

PMID:
24659338
4.

Noninvasive evaluation of intestinal lactase with 4-galactosylxylose: comparison with 3- and 2-galactosylxylose and optimization of the method in rats.

Hermida C, Corrales G, Martínez-Costa OH, Fernández-Mayoralas A, Aragón JJ.

Clin Chem. 2006 Feb;52(2):270-7. Epub 2005 Dec 29.

5.

Genetic testing improves the diagnosis of adult type hypolactasia in the Mediterranean population of Sardinia.

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

Eur J Clin Nutr. 2007 Oct;61(10):1220-5. Epub 2007 Feb 21.

PMID:
17311063
6.
7.

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
8.

Primary hypolactasia diagnosis: Comparison between the gaxilose test, shortened lactose tolerance test, and clinical parameters corresponding to the C/T-13910 polymorphism.

Domínguez Jiménez JL, Fernández Suárez A, Muñoz Colmenero AÚ, Fatela Cantillo D, López Pelayo I.

Clin Nutr. 2016 Jan 20. pii: S0261-5614(16)00008-X. doi: 10.1016/j.clnu.2016.01.006. [Epub ahead of print]

PMID:
26847948
9.

A comparison between lactose breath test and quick test on duodenal biopsies for diagnosing lactase deficiency in patients with self-reported lactose intolerance.

Furnari M, Bonfanti D, Parodi A, Franzè J, Savarino E, Bruzzone L, Moscatelli A, Di Mario F, Dulbecco P, Savarino V.

J Clin Gastroenterol. 2013 Feb;47(2):148-52. doi: 10.1097/MCG.0b013e31824e9132.

PMID:
22495813
10.

Quick test: a new test for the diagnosis of duodenal hypolactasia.

Ojetti V, La Mura R, Zocco MA, Cesaro P, De Masi E, La Mazza A, Cammarota G, Gasbarrini G, Gasbarrini A.

Dig Dis Sci. 2008 Jun;53(6):1589-92.

PMID:
17932760
11.

Lactase persistence/non-persistence variants, C/T_13910 and G/A_22018, as a diagnostic tool for lactose intolerance in IBS patients.

Bernardes-Silva CF, Pereira AC, de Fátima Alves da Mota G, Krieger JE, Laudanna AA.

Clin Chim Acta. 2007 Nov-Dec;386(1-2):7-11. Epub 2007 Jul 19.

PMID:
17706627
12.

A diagnostic approach to patients with suspected lactose malabsorption.

Perets TT, Shporn E, Aizic S, Kelner E, Levy S, Bareli Y, Pakanaev L, Niv Y, Dickman R.

Dig Dis Sci. 2014 May;59(5):1012-6. doi: 10.1007/s10620-013-2980-7. Epub 2013 Dec 20.

PMID:
24357185
13.

Comparison of a real-time polymerase chain reaction assay for lactase genetic polymorphism with standard indirect tests for lactose maldigestion.

Szilagyi A, Malolepszy P, Hamard E, Xue X, Hilzenrat N, Ponniah M, MacNamara E, Chong G.

Clin Gastroenterol Hepatol. 2007 Feb;5(2):192-6. Epub 2006 Jul 28.

PMID:
16876487
15.

Comparison of quick point-of-care test for small-bowel hypolactasia with biochemical lactase assay in children.

Rao P, Rao N, Jordinson M, Scott C, Hinchcliffe C, Campbell D.

J Pediatr Gastroenterol Nutr. 2012 Mar;54(3):401-3. doi: 10.1097/MPG.0b013e318231eb30.

PMID:
21857246
16.

A genetic test which can be used to diagnose adult-type hypolactasia in children.

Rasinperä H, Savilahti E, Enattah NS, Kuokkanen M, Tötterman N, Lindahl H, Järvelä I, Kolho KL.

Gut. 2004 Nov;53(11):1571-6.

17.

A biopsy-based quick test in the diagnosis of duodenal hypolactasia in upper gastrointestinal endoscopy.

Kuokkanen M, Myllyniemi M, Vauhkonen M, Helske T, Kääriäinen I, Karesvuori S, Linnala A, Härkönen M, Järvelä I, Sipponen P.

Endoscopy. 2006 Jul;38(7):708-12. Epub 2006 Jun 6.

PMID:
16761211
18.

Concordance of genetic and breath tests for lactose intolerance in a tertiary referral centre.

Krawczyk M, Wolska M, Schwartz S, Gruenhage F, Terjung B, Portincasa P, Sauerbruch T, Lammert F.

J Gastrointestin Liver Dis. 2008 Jun;17(2):135-9.

19.

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
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