Works matching Glucose-galactose malabsorption
Results: 63
Nephrocalcinosis in glucose-galactose malabsorption, association with renal tubular acidosis.
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- Pediatric Nephrology, 2005, v. 20, n. 9, p. 1336, doi. 10.1007/s00467-005-1885-x
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- Article
SLC5A1 Variants in Turkish Patients with Congenital Glucose-Galactose Malabsorption.
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- Genes, 2023, v. 14, n. 7, p. 1359, doi. 10.3390/genes14071359
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Congenital glucose‐galactose malabsorption: A case report with a novel SLC5A1 mutation.
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- Clinical Case Reports, 2019, v. 7, n. 1, p. 51, doi. 10.1002/ccr3.1913
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Nephrocalcinosis in glucose-galactose malabsorption: nephrocalcinosis and proximal tubular dysfunction in a young infant with a novel mutation of SGLT1.
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- 2008
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- journal article
Fructose Metabolism and Its Effect on Glucose-Galactose Malabsorption Patients: A Literature Review.
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- Diagnostics (2075-4418), 2023, v. 13, n. 2, p. 294, doi. 10.3390/diagnostics13020294
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- Article
Konjenital Glukoz-Galaktoz Malabsorbsiyonu ve Tekrarlayan Sepsis Atakları Olan Yenidoğan Olgusu.
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- Journal of Current Pediatrics / Guncel Pediatri, 2013, v. 11, n. 2, p. 85, doi. 10.4274/Jcp.11.21931
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Nephrolithiasis in a child with glucose-galactose malabsorption.
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- Pediatric Nephrology, 2004, v. 19, n. 2, p. 244, doi. 10.1007/s00467-003-1327-6
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Two Cases of Mistaken Polyuria and Nephrocalcinosis in Infants with Glucose-Galactose Malabsorption: A Possible Role of 1,25(OH)<sub>2</sub>D<sub>3</sub>.
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- Hormone Research in Paediatrics, 2017, v. 87, n. 4, p. 277, doi. 10.1159/000454951
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Long-Term Dietary Changes in Subjects with Glucose Galactose Malabsorption Secondary to Biallelic Mutations of SLC5A1.
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- Digestive Diseases & Sciences, 2021, v. 66, n. 12, p. 4414, doi. 10.1007/s10620-020-06792-4
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- Article
Dziedziczne zaburzenie wchłaniania glukozy i galaktozy.
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- Gastroenterologia Polska / Gastroenterology, 2008, v. 15, n. 4, p. 241
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- Article
Structural Insights into Genetic Variants of Na/Glucose Cotransporter SGLT1 Causing Glucose-Galactose Malabsorption: vSGLT as a Model Structure.
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- Cell Biochemistry & Biophysics, 2012, v. 63, n. 2, p. 151, doi. 10.1007/s12013-012-9352-3
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GLUCOSE-GALACTOSE MALABSORPTION.
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- Nutrition Reviews, 1974, v. 32, n. 5, p. 132, doi. 10.1111/j.1753-4887.1974.tb06301.x
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- Article
SLC5A1 Mutations in Saudi Arabian Patients With Congenital Glucose-Galactose Malabsorption.
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- 2018
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- journal article
The Molecular Basis of Glucose Galactose Malabsorption in a Large Swedish Pedigree.
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- Function, 2021, v. 2, n. 5, p. 1, doi. 10.1093/function/zqab040
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Congenital glucose-galactose malabsorption: a novel deletion within the SLC5A1 gene.
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- European Journal of Pediatrics, 2013, v. 172, n. 3, p. 409, doi. 10.1007/s00431-012-1802-9
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Literature review on congenital glucose–galactose malabsorption from 2001 to 2019.
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- Journal of Paediatrics & Child Health, 2020, v. 56, n. 11, p. 1779, doi. 10.1111/jpc.14702
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Congenital Glucose-Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene.
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- 2017
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- journal article
Multiple sequence variations in SLC5A1 gene are associated with glucose-galactose malabsorption in a large cohort of Old Order Amish.
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- Clinical Genetics, 2011, v. 79, n. 1, p. 86, doi. 10.1111/j.1399-0004.2010.01440.x
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Neonatal nephrocalcinosis in association with glucose-galactose malabsorption.
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- Pediatric Nephrology, 2003, v. 18, n. 7, p. 700, doi. 10.1007/s00467-003-1155-8
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Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter.
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- Nature, 1991, v. 350, n. 6316, p. 354
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Glucose-Galactose Malabsorption: A Study on the Transfer of Glucose Across the Red Cell Membrane.
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- Scandinavian Journal of Clinical & Laboratory Investigation, 1970, v. 25, n. 2, p. 145, doi. 10.3109/00365517009049196
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PRENATAL IDENTIFICATION OF A HETEROZYGOUS STATUS IN TWO FETUSES AT RISK FOR GLUCOSE-GALACTOSE MALABSORPTION.
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- Prenatal Diagnosis, 1996, v. 16, n. 5, p. 458, doi. 10.1002/(SICI)1097-0223(199605)16:5<458::AID-PD873>3.0.CO;2-U
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Five Arab children with glucose-galactose malabsorption.
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- Paediatrics & International Child Health, 2013, v. 33, n. 2, p. 108, doi. 10.1179/2046905513Y.0000000055
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Congenital glucose-galactose malabsorption diagnosed from macrohematuria in an infant.
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- Pediatrics International, 2016, v. 58, n. 12, p. 1365, doi. 10.1111/ped.13047
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GLUCOSE-GALACTOSE MALABSORPTION.
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- Acta Paediatrica, 1969, v. 58, n. S188, p. 3, doi. 10.1111/j.1651-2227.1969.tb06045.x
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GLUCOSE-GALACTOSE MALABSORPTION.
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- Acta Paediatrica, 1969, v. 58, n. S188, p. 19, doi. 10.1111/j.1651-2227.1969.tb06046.x
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GLUCOSE-GALACTOSE MALABSORPTION A Study with Biopsy of the Small Intestinal Mucosa.
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- Acta Paediatrica, 1968, v. 57, n. 4, p. 273, doi. 10.1111/j.1651-2227.1968.tb07291.x
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Congenital Glucose-Galactose Malabsorption in a Child.
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- 2022
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- Letter
Diagnosis of congenital glucose-galactose malabsorption by measuring sugar- and amino acid-evoked potential differences in jejunum in vivo.
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- 1986
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- journal article
Digestion and absorption rates of lactose, glucose, galactose, and fructose in three infants with congenital glucose-galactose malabsorption: perfusion studies.
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- 1985
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Congenital Glucose-Galactose Malabsorption in a Neonate with Hyperbilirubinemia and Hypernatremia.
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- 2023
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- Letter
DIAGNOSTIC PROBLEMS IN GLUCOSE-GALACTOSE MALABSORPTION: A Case Report.
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- Acta Paediatrica, 1970, v. 59, n. 2, p. 214, doi. 10.1111/j.1651-2227.1970.tb08992.x
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GLUCOSE-GALACTOSE MALABSORPTION.
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- Acta Paediatrica, 1970, v. 59, n. 1, p. 74, doi. 10.1111/j.1651-2227.1970.tb15517.x
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A Case of Glucose-Galactose Malabsorption.
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- Pediatrics International, 1977, v. 19, n. 2, p. 37, doi. 10.1111/j.1442-200X.1977.tb00092.x
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Ensiling and hydrothermal pretreatment of grass: consequences for enzymatic biomass conversion and total monosaccharide yields.
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- Biotechnology for Biofuels, 2014, v. 7, n. 1, p. 2, doi. 10.1186/1754-6834-7-95
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A novel mutation of Na+/glucose cotransporter in a Turkish newborn with congenital glucose-galactose malabsorption.
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- 2005
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- journal article
A Novel Mutation of Na+/Glucose Cotransporter in a Turkish Newborn with Congenital Glucose-Galactose Malabsorption.
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- Journal of Pediatric Gastroenterology & Nutrition, 2005, v. 40, n. 4, p. 508, doi. 10.1097/01.MPG.0000153097.73083.A3
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Congenital glucose-galactose malabsorption in Arab children.
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- 1996
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Congenital fructose-glucose-galactose malabsorption.
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- 1995
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19 GLUCOSE-GALACTOSE MALABSORPTION ASSOCIATED WITH MULTIPLE MUTATIONS IN THE Na<sup>+</sup>/GLUCOSE COTRANSPORTER.
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- Journal of Pediatric Gastroenterology & Nutrition, 1994, v. 19, n. 3, p. 334
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Konjenital glukoz-galaktoz malabsorpsiyonu: Bir yenidoğan vakası.
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- Cocuk Sagligi ve Hastaliklari Dergisi, 2015, v. 58, n. 1, p. 28
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Glucose transporters in the small intestine in health and disease.
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- Pflügers Archiv: European Journal of Physiology, 2020, v. 472, n. 9, p. 1207, doi. 10.1007/s00424-020-02439-5
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Importance of Early Genetic Sequencing in Neonates Admitted to NICU with Recurrent Hypernatremia: Results of a Prospective Cohort Study.
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- Neonatology (16617800), 2022, v. 119, n. 1, p. 103, doi. 10.1159/000519634
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Active sugar transport in health and disease.
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- Journal of Internal Medicine, 2007, v. 261, n. 1, p. 32, doi. 10.1111/j.1365-2796.2006.01746.x
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Diagnosing and Treating Intolerance to Carbohydrates in Children.
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- Nutrients, 2016, v. 8, n. 3, p. 157, doi. 10.3390/nu8030157
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What does sodium‐glucose co‐transporter 1 inhibition add: Prospects for dual inhibition.
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- Diabetes, Obesity & Metabolism, 2019, v. 21, p. 43, doi. 10.1111/dom.13630
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Prokaryotic Solute/Sodium Symporters: Versatile Functions and Mechanisms of a Transporter Family †.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 4, p. 1880, doi. 10.3390/ijms22041880
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Enteroendocrine Dysfunction in Two Saudi Sisters.
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- Case Reports in Gastroenterology, 2021, v. 15, n. 1, p. 290, doi. 10.1159/000511761
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Lactose malabsorption in young Lithuanian children with atopic dermatitis.
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- Acta Paediatrica, 2004, v. 93, n. 4, p. 482
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Antidepressant binding site in a bacterial homologue of neurotransmitter transporters.
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- Nature, 2007, v. 448, n. 7156, p. 952, doi. 10.1038/nature06038
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