Literature DB >> 15795603

A novel mutation of Na+/glucose cotransporter in a Turkish newborn with congenital glucose-galactose malabsorption.

Faysal Gok1, Halil I Aydin, Ismail Kurt, Erdal Gokcay, Mari Maeda, Michihiro Kasahara.   

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Year:  2005        PMID： 15795603     DOI： 10.1097/01.mpg.0000153097.73083.a3

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN： 0277-2116            Impact factor:   2.839


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  3 in total

1.  Congenital glucose-galactose malabsorption: a novel deletion within the SLC5A1 gene.

Authors:  L Vallaeys; S Van Biervliet; G De Bruyn; B Loeys; A S Moring; E Van Deynse; L Cornette
Journal:  Eur J Pediatr       Date:  2012-07-29       Impact factor: 3.183

2.  Nephrocalcinosis in glucose-galactose malabsorption: nephrocalcinosis and proximal tubular dysfunction in a young infant with a novel mutation of SGLT1.

Authors:  Ozlem Bekem Soylu; Ciğdem Ecevit; Serdar Altinöz; Aysel Aydoğan Oztürk; Ali Kemal Temizkan; Mari Maeda; Michihiro Kasahara
Journal:  Eur J Pediatr       Date:  2008-02-21       Impact factor: 3.183

Review 3.  Diagnosing and Treating Intolerance to Carbohydrates in Children.

Authors:  Roberto Berni Canani; Vincenza Pezzella; Antonio Amoroso; Tommaso Cozzolino; Carmen Di Scala; Annalisa Passariello
Journal:  Nutrients       Date:  2016-03-10       Impact factor: 5.717
  3 in total

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