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Select item 64129021.

Congenital Lactase Deficiency: Mutations, Functional and Biochemical Implications, and Future Perspectives

Dalanda Wanes, Diab M. Husein, Hassan Y. Naim

Nutrients. 2019 Feb; 11(2): 461. Published online 2019 Feb 22. doi: 10.3390/nu11020461

PMCID:: PMC6412902

Abstract Article PDF–833K

Select item 45159292.

A novel mutation within the lactase gene (LCT): the first report of congenital lactase deficiency diagnosed in Central Europe

Walid Fazeli, Sigrid Kaczmarek, Martin Kirschstein, René Santer

BMC Gastroenterol. 2015; 15: 90. Published online 2015 Jul 28. doi: 10.1186/s12876-015-0316-0

PMCID:: PMC4515929

Abstract Article PDF–1.4M

Select item 44325173.

Congenital lactose intolerance is triggered by severe mutations on both alleles of the lactase gene

Lena Diekmann, Katrin Pfeiffer, Hassan Y Naim

BMC Gastroenterol. 2015; 15: 36. Published online 2015 Mar 21. doi: 10.1186/s12876-015-0261-y

PMCID:: PMC4432517

Abstract Article PDF–1.0M

Select item 26353694.

Four novel mutations in the lactase gene (LCT) underlying congenital lactase deficiency (CLD)

Suvi Torniainen, Roberta Freddara, Taina Routi, Carolien Gijsbers, Carlo Catassi, Pia Höglund, Erkki Savilahti, Irma Järvelä

BMC Gastroenterol. 2009; 9: 8. Published online 2009 Jan 22. doi: 10.1186/1471-230X-9-8

PMCID:: PMC2635369

Abstract Article PDF–549K

Select item 20202745.

Congenital Lactose Malabsorption

B. Levin, J. M. Abraham, E. Ann Burgess, Patricia G. Wallis

Arch Dis Child. 1970 Apr; 45(240): 173–177. doi: 10.1136/adc.45.240.173

PMCID:: PMC2020274

Summary Page Browse PDF–922K

Select item 16279626.

Congenital lactase deficiency. A clinical study on 16 patients.

E Savilahti, K Launiala, P Kuitunen

Arch Dis Child. 1983 Apr; 58(4): 246–252. doi: 10.1136/adc.58.4.246

PMCID:: PMC1627962

Summary Page Browse PDF–971K

Select item 13802407.

Mutations in the Translated Region of the Lactase Gene (LCT) Underlie Congenital Lactase Deficiency

Mikko Kuokkanen, Jorma Kokkonen, Nabil Sabri Enattah, Tero Ylisaukko-oja, Hanna Komu, Teppo Varilo, Leena Peltonen, Erkki Savilahti, Irma Järvelä

Am J Hum Genet. 2006 Feb; 78(2): 339–344. Published online 2005 Dec 15. doi: 10.1086/500053

PMCID:: PMC1380240

Abstract Article PDF–622K

Select item 13774968.

Assignment of the locus for congenital lactase deficiency to 2q21, in the vicinity of but separate from the lactase-phlorizin hydrolase gene.

I Järvelä, N S Enattah, J Kokkonen, T Varilo, E Savilahti, L Peltonen

Am J Hum Genet. 1998 Oct; 63(4): 1078–1085. doi: 10.1086/302064

PMCID:: PMC1377496

Summary PDF–630K

Select item 1111929.

Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis

John W Belmont, Barbara Reid, William Taylor, Susan S Baker, Warren H Moore, Michael C Morriss, Susan M Podrebarac, Nancy Glass, I David Schwartz

BMC Pediatr. 2002; 2: 4. Published online 2002 Apr 25. doi: 10.1186/1471-2431-2-4

PMCID:: PMC111192

Abstract Article PDF–679K

Select item 968568110.

Cow’s milk-induced gastrointestinal disorders: From infancy to adulthood

Mohammed Al-Beltagi, Nermin Kamal Saeed, Adel Salah Bediwy, Reem Elbeltagi

World J Clin Pediatr. 2022 Nov 9; 11(6): 437–454. Published online 2022 Nov 9. doi: 10.5409/wjcp.v11.i6.437

PMCID:: PMC9685681

Abstract Article PDF–622K

Select item 154596011.

Thyrotoxicosis in a neonate of a mother with no history of thyroid disease.

D S Brookfield, A E McCandless, C S Smith

Arch Dis Child. 1976 Apr; 51(4): 314–316. doi: 10.1136/adc.51.4.314

PMCID:: PMC1545960

Summary Page Browse PDF–658K

Select item 154543412.

Breath hydrogen test for detecting lactose malabsorption in infants and children. Prevalence of lactose malabsorption in Japanese children and adults.

O Nose, Y Iida, H Kai, T Harada, M Ogawa, H Yabuuchi

Arch Dis Child. 1979 Jun; 54(6): 436–440. doi: 10.1136/adc.54.6.436

PMCID:: PMC1545434

Summary Page Browse PDF–755K

Select item 1057357713.

Genotype Prevalence of Lactose Deficiency, Vitamin D Deficiency, and the Vitamin D Receptor in a Chilean Inflammatory Bowel Disease Cohort: Insights from an Observational Study

Tamara Pérez-Jeldres, M. Leonor Bustamante, Roberto Segovia-Melero, Nataly Aguilar, Fabien Magne, Gabriel Ascui, Denisse Uribe, Lorena Azócar, Cristián Hernández-Rocha, Ricardo Estela, Verónica Silva, Andrés De La Vega, Elizabeth Arriagada, Mauricio Gonzalez, Gian-Franco Onetto, Sergio Escobar, Pablo Baez, Alejandra Zazueta, Carolina Pavez-Ovalle, Juan Francisco Miquel, Manuel Álvarez-Lobos

Int J Mol Sci. 2023 Oct; 24(19): 14866. Published online 2023 Oct 3. doi: 10.3390/ijms241914866

PMCID:: PMC10573577

Abstract Article PDF–480K

Select item 1029887614.

A Comprehensive Look at the -13910 C>T LCT Gene Polymorphism as a Molecular Marker for Vitamin D and Calcium Levels in Young Adults in Central and Eastern Europe: A Preliminary Study

Magdalena Kowalówka, Grzegorz Kosewski, Daniel Lipiński, Juliusz Przysławski

Int J Mol Sci. 2023 Jun; 24(12): 10191. Published online 2023 Jun 15. doi: 10.3390/ijms241210191

PMCID:: PMC10298876

Abstract Article PDF–3.2M

Select item 923909815.

Short-Term Dairy Product Elimination and Reintroduction Minimally Perturbs the Gut Microbiota in Self-Reported Lactose-Intolerant Adults

Courtney J. Smith, Les Dethlefsen, Christopher Gardner, Linda Nguyen, Marcus Feldman, Elizabeth K. Costello, Oren Kolodny, David A. Relman

mBio. 2022 May-Jun; 13(3): e01051-22. Published online 2022 Jun 13. doi: 10.1128/mbio.01051-22

PMCID:: PMC9239098

Abstract Article PDF–2.1M

Select item 807071516.

Lactose Intolerance Assessed by Analysis of Genetic Polymorphism, Breath Test and Symptoms in Patients with Inflammatory Bowel Disease

Olga Maria Nardone, Francesco Manfellotto, Caterina D’Onofrio, Alba Rocco, Giovanni Annona, Francesca Sasso, Pasquale De Luca, Nicola Imperatore, Anna Testa, Roberto de Sire, Elio Biffali, Fabiana Castiglione

Nutrients. 2021 Apr; 13(4): 1290. Published online 2021 Apr 14. doi: 10.3390/nu13041290

PMCID:: PMC8070715

Abstract Article PDF–1.0M

Select item 755141617.

Genetics of Lactose Intolerance: An Updated Review and Online Interactive World Maps of Phenotype and Genotype Frequencies

Augusto Anguita-Ruiz, Concepción M. Aguilera, Ángel Gil

Nutrients. 2020 Sep; 12(9): 2689. Published online 2020 Sep 3. doi: 10.3390/nu12092689

PMCID:: PMC7551416

Abstract Article PDF–1.3M

Select item 737935718.

Type 2 diabetes susceptibility genes on mouse chromosome 11 under high sucrose environment

Misato Kobayashi, Hironori Ueda, Naru Babaya, Michiko Itoi-Babaya, Shinsuke Noso, Tomomi Fujisawa, Fumihiko Horio, Hiroshi Ikegami

BMC Genet. 2020; 21: 81. Published online 2020 Jul 23. doi: 10.1186/s12863-020-00888-6

PMCID:: PMC7379357

Abstract Article PDF–2.0M

Select item 732505119.

Evaluation of breath, plasma, and urinary markers of lactose malabsorption to diagnose lactase non-persistence following lactose or milk ingestion

Aahana Shrestha, Matthew P. G. Barnett, Jo K. Perry, David Cameron-Smith, Amber M. Milan

BMC Gastroenterol. 2020; 20: 204. Published online 2020 Jun 29. doi: 10.1186/s12876-020-01352-6

PMCID:: PMC7325051

Abstract Article PDF–714K

Select item 666905020.

Lactose digestion in humans: intestinal lactase appears to be constitutive whereas the colonic microbiome is adaptable

Richard A Forsgård

Am J Clin Nutr. 2019 Aug; 110(2): 273–279. Published online 2019 Jun 8. doi: 10.1093/ajcn/nqz104

PMCID:: PMC6669050

Abstract Article PDF–146K

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