• <em>SLC5A1</em> Variants in Turkish Patients with Congenital Glucose-Galactose Malabsorption
• A 9-Day-Old With Weight Loss and Diarrhea
• A Case of Congenital Glucose Galactose Malabsorption with a New Mutation in the <em>SLC5A1</em> Gene
• A Case of Congenital Glucose Galactose Malabsorption with a New Mutation in the SLC5A1 Gene
• A case of neonatal diarrhoea caused by congenital glucose-galactose malabsorption
• A high-capacity membrane potential FRET-based assay for the sodium-coupled glucose co-transporter SGLT1
• A novel mutation of Na+/glucose cotransporter in a Turkish newborn with congenital glucose-galactose malabsorption
• A novel mutation within the lactase gene (LCT): the first report of congenital lactase deficiency diagnosed in Central Europe
• A Rare Cause of Intractable Diarrhea of Infancy
• A single amino acid change converts the sugar sensor SGLT3 into a sugar transporter
• Active sugar transport in health and disease
• Altered pancreatic islet morphology and function in SGLT1 knockout mice on a glucose-deficient, fat-enriched diet
• Antidepressant binding site in a bacterial homologue of neurotransmitter transporters
• Biology of human sodium glucose transporters
• Bitterness of glucose/galactose: novel mutations in the SLC5A1 gene
• Breath Hydrogen as a Biomarker for Glucose Malabsorption after Roux-en-Y Gastric Bypass Surgery
• Carbohydrate malabsorption mechanism for tumor formation in rats treated with the SGLT2 inhibitor canagliflozin
• Causes Of Chronic Non-Infectious Diarrhoea In Infants Less Than 6 Months Of Age: Rarely Recognized Entities
• Congenital Diarrhoea In A Neonate With Hypernatraemia And Dehydration
• Congenital diseases of the gastrointestinal tract
• Congenital disorders of intestinal digestion and absorption (sugars, proteins, lipids, ions)
• Congenital glucose galactose malabsorption
• Congenital glucose-galactose malabsorption diagnosed from macrohematuria in an infant
• Congenital Glucose-Galactose Malabsorption in a Child
• Congenital Glucose-Galactose Malabsorption in a Neonate with Hyperbilirubinemia and Hypernatremia
• Congenital Glucose-Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene
• Congenital Glucose-Galactose Malabsorption: A Case Report
• Congenital glucose-galactose malabsorption: A case report with a novel <em>SLC5A1</em> mutation
• Congenital glucose-galactose malabsorption: A case report with a novel SLC5A1 mutation
• Congenital Glucose-Galactose Malabsorption: A Case With a Novel SLC5A1 Mutation in a Saudi Infant
• Congenital glucose-galactose malabsorption: a descriptive study of clinical characteristics and outcome from Western Saudi Arabia
• Congenital glucose-galactose malabsorption: a novel deletion within the SLC5A1 gene
• Congenital glucose-galactose malabsorption: A rare and severe cause of infant diarrhea
• Coordinated Multi-Language Translation of A Validated Symptom Questionnaire for Carbohydrate Intolerances: A Practical Structured Procedure
• D28G mutation in congenital glucose-galactose malabsorption
• Development of SGLT1 and SGLT2 inhibitors
• Diagnosing and Treating Intolerance to Carbohydrates in Children
• Differential analysis of protein expression of Bifidobacterium grown on different carbohydrates
• Disaccharidase Deficiencies in Children With Chronic Abdominal Pain
• Enteroendocrine Dysfunction in Two Saudi Sisters
• Evolution of type 2 diabetes and carbohydrate intolerance following bariatric surgery in a Mexican mestizo population
• Exploring newer target sodium glucose transporter 2 for the treatment of diabetes mellitus
• Familial renal glucosuria and SGLT2: from a mendelian trait to a therapeutic target
• Five Arab children with glucose-galactose malabsorption
• Fructose Metabolism and Its Effect on Glucose-Galactose Malabsorption Patients: A Literature Review
• Genetic Variants in SGLT1, Glucose Tolerance, and Cardiometabolic Risk
• Glucose and galactose malabsorption: A new case in Spain
• Glucose Galactose Malabsorption complicated with Rickets and Nephrogenic Diabetes Insipidus
• Glucose transport families SLC5 and SLC50
• Glucose transport hereditary diseases
• Glucose transport into everted sacs of the small intestine of mice
• Glucose transporters in the small intestine in health and disease
• GLUT1 deficiency and other glucose transporter diseases
• History of Acquired Monosaccharide Intolerance in Houston, Texas
• Importance of Early Genetic Sequencing in Neonates Admitted to NICU with Recurrent Hypernatremia: Results of a Prospective Cohort Study
• Importance of genetic sequencing studies in managing chronic neonatal diarrhea: a case report of a novel variant in the glucose-galactose transporter SLC5A1
• Intestinal absorption in health and disease--sugars
• Lactose malabsorption in young Lithuanian children with atopic dermatitis
• Literature review on congenital glucose-galactose malabsorption from 2001 to 2019
• Long-Term Dietary Changes in Subjects with Glucose Galactose Malabsorption Secondary to Biallelic Mutations of SLC5A1
• Malabsorption of fermentable oligo-, di-, or monosaccharides and polyols (FODMAP) as a common cause of unclear abdominal discomfort
• Molecular basis for glucose-galactose malabsorption
• Multiple sequence variations in SLC5A1 gene are associated with glucose-galactose malabsorption in a large cohort of Old Order Amish
• Na(+)-D-glucose cotransporter SGLT1 is pivotal for intestinal glucose absorption and glucose-dependent incretin secretion
• Neonatal diarrhea due to congenital glucose-galactose malabsorption: report of seven cases
• Neonatal nephrocalcinosis in association with glucose-galactose malabsorption
• Nephrocalcinosis in glucose-galactose malabsorption, association with renal tubular acidosis
• Nephrocalcinosis in glucose-galactose malabsorption: nephrocalcinosis and proximal tubular dysfunction in a young infant with a novel mutation of SGLT1
• Nephrolithiasis in a child with glucose-galactose malabsorption
• NGS Gene Panel Analysis Revealed Novel Mutations in Patients with Rare Congenital Diarrheal Disorders
• Novel and Unexpected Functions of SGLTs
• Novel Mutation in the <em>SLC5A1</em> Gene Causing Glucose-Galactose Malabsorption: First Confirmed Case From Central America
• Novel Mutation in the SLC5A1 Gene Causing Glucose-Galactose Malabsorption: First Confirmed Case From Central America
• Nutrition management of congenital glucose-galactose malabsorption: Case report of a Chinese infant
• Prokaryotic Solute/Sodium Symporters: Versatile Functions and Mechanisms of a Transporter Family
• Proposed mechanism for the selection of lactase persistence in childhood
• Recurrent abdominal pain in children: a clinical approach
• Relevance of solute carrier family 5 transporter defects to inherited and acquired human disease
• Roles of Lactose and Fructose Malabsorption and Dietary Outcomes in Children Presenting with Chronic Abdominal Pain
• Selected disorders of malabsorption
• Significance of hydrogen breath tests in children with suspected carbohydrate malabsorption
• SLC5A1 Mutations in Saudi Arabian Patients With Congenital Glucose-Galactose Malabsorption
• SLC5A1 Variants in Turkish Patients with Congenital Glucose-Galactose Malabsorption
• Structural Basis of the Selective Sugar Transport in Sodium-Glucose Cotransporters
• Structural insights into genetic variants of Na(+)/glucose cotransporter SGLT1 causing glucose-galactose malabsorption: vSGLT as a model structure
• The apical localization of SGLT1 glucose transporter is determined by the short amino acid sequence in its N-terminal domain
• The glucose transporter families SGLT and GLUT: molecular basis of normal and aberrant function
• The malabsorption of commonly occurring mono and disaccharides: levels of investigation and differential diagnoses
• The Molecular Basis of Glucose Galactose Malabsorption in a Large Swedish Pedigree
• The Na(+)/glucose cotransporters: from genes to therapy
• The new functions of the gut in the control of glucose homeostasis
• The physiology of glucagon-like peptide-1 and its role in the pathophysiology of type 2 diabetes mellitus
• The role of fructose transporters in diseases linked to excessive fructose intake
• The sodium/glucose cotransport family SLC5
• To make a new intestinal mucosa
• Transmembrane IV of the high-affinity sodium-glucose cotransporter participates in sugar binding
• Two Cases of Mistaken Polyuria and Nephrocalcinosis in Infants with Glucose-Galactose Malabsorption: A Possible Role of 1,25(OH)2D3

• Two Cases of Mistaken Polyuria and Nephrocalcinosis in Infants with Glucose-Galactose Malabsorption: A Possible Role of 1,25(OH)2D3
• Valid Assessment of Carbohydrate Intolerance and the Need for a Distinction to Carbohydrate Malabsorption. Comment on "Roles of Lactose and Fructose Malabsorption and Dietary Outcomes in Children Presenting with Chronic Abdominal Pain.", <em&
• What does sodium-glucose co-transporter 1 inhibition add: Prospects for dual inhibition