• "Recurrent Papillary Necrosis and Nephrocalcinosis Induced by Nonsteroidal Anti-Inflammatory Drugs for Gouty Arthritis Associated with Congenital Chloride-Losing Diarrhea: A Major Risk for Kidney Loss"
• A Case of Congenital Tufting Enteropathy with <em>EpCAM</em> Gene Complex Heterozygous Mutation (c.491+1G&gt;A; c.352_353ins CACC)
• A missense mutation in SLC26A3 is associated with human male subfertility and impaired activation of CFTR
• A novel de novo SLC26A3 mutation causing congenital chloride diarrhea in a Japanese neonate
• A novel missense mutation Q495K of SLC26A3 gene identified in a Chinese child with congenital chloride-losing diarrhoea
• A Potential Treatment of Congenital Sodium Diarrhea in Patients With Activating GUCY2C Mutations
• Acquired long QT syndrome due to antiemetics, COVID-19 and <em>Blastocystis hominis</em> induced exacerbation of congenital chloride losing diarrhoea
• Approach to Congenital Diarrhea and Enteropathies (CODEs)
• Bartter Syndrome-Related Variants Distribution: Brazilian Data and Its Comparison with Worldwide Cohorts
• Bicarbonate secretion and acid/base sensing by the intestine
• Bowel Dilation Diagnosed Prenatally
• Captopril in congenital chloride diarrhoea: a case study
• Case Report on a Rare Disease in Lithuania: Congenital Chloride Diarrhea
• Causes Of Chronic Non-Infectious Diarrhoea In Infants Less Than 6 Months Of Age: Rarely Recognized Entities
• Clinical features and MYO5B mutations of a family affected by microvillus inclusion disease
• Clinical Features, Molecular Genetics, and Long-Term Outcome in Congenital Chloride Diarrhea: A Nationwide Study in Japan
• Clinical Practice Guideline: Maintenance Intravenous Fluids in Children
• Congenital Chloride Diarrhea - Novel Mutation in SLC26A3 Gene
• Congenital Chloride Diarrhea (CCD): A Case Report of CCD Suspected by Prenatal Ultrasonography and Magnetic Resonance Imaging (MRI)
• Congenital Chloride Diarrhea and Childhood Inflammatory Bowel Disease: A Multicenter Case Series
• Congenital chloride diarrhea and Pendred syndrome: case report of siblings with two rare recessive disorders of SLC26 family genes
• Congenital chloride diarrhea clinical features and management: a systematic review
• Congenital chloride diarrhea in a Japanese neonate with a novel SLC26A3 mutation
• Congenital chloride diarrhea in dizygotic twins
• Congenital chloride diarrhea in Korean children: novel mutations and genetic characteristics
• Congenital chloride diarrhea in patient with SLC26A2 mutation - analysis of the clinical phenotype and differential diagnosis
• Congenital chloride diarrhea in patient with SLC26A2 mutation - analysis of the clinical phenotype and differential diagnosis
• Congenital chloride diarrhea mimicking meconium ileus in newborn
• Congenital chloride diarrhea misdiagnosed as pseudo-Bartter syndrome
• Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndrome
• Congenital chloride diarrhea presenting as dilated fetal bowel loops
• Congenital chloride diarrhea presenting in newborn as a rare cause of meconium ileus
• Congenital chloride diarrhea: a review of twelve Arabian children
• Congenital Chloride Diarrhea: Accurate Prenatal Diagnosis Using Color Doppler Sonography to Show the Passage of Diarrhea
• Congenital Chloride Diarrhea: Diagnosis by Easy-Accessible Chloride Measurement in Feces
• Congenital chloride diarrhoea
• Congenital chloride diarrhoea in a Chinese infant with a compound heterozygous SLC26A3 mutation
• Congenital chloride losing diarrhea: A single center experience in a highly consanguineous population
• Congenital chloride-losing diarrhea in a Mexican child with the novel homozygous SLC26A3 mutation G393W
• Congenital chloride-losing diarrhoea and Crohn's disease: a diagnostic and therapeutic challenge
• Congenital disorders of intestinal digestion and absorption (sugars, proteins, lipids, ions)
• Congenital Sodium Diarrhea by mutation of the SLC9A3 gene
• Delayed Diagnosis in a Male With Congenital Chloride Losing Diarrhea
• Development of Crohn's Disease in a Child With <em>SLC26A3</em>-related Congenital Chloride Diarrhea: Report of the First Case in East Asia and a Novel Missense Variant
• Development of Crohn's Disease in a Child With SLC26A3-related Congenital Chloride Diarrhea: Report of the First Case in East Asia and a Novel Missense Variant
• Diagnostic Challenge of Congenital Chloride Diarrhea and Ulcerative Colitis Overlap in an Adult Misdiagnosed with Bartter Syndrome: Case Report and Literature Review
• Differential diagnosis of perinatal Bartter, Bartter and Gitelman syndromes
• Establishment of a congenital chloride diarrhea-associated SLC26A3 c.392C&gt;G (p.P131R) polymorphism-expressing cell model and a preliminary analysis of its mechanism of action
• Establishment of a congenital chloride diarrhea-associated SLC26A3 c.392C>G (p.P131R) polymorphism-expressing cell model and a preliminary analysis of its mechanism of action
• Exome Sequencing in Clinical Hepatology
• Expression pattern of congenital chloride diarrhea pathogenic gene Slc26a3 in the reproductive tract of male rodents
• Favorable Effects of Octreotide in Congenital Chloride Diarrhea Associated With CKD
• Fecal microbiota in congenital chloride diarrhea and inflammatory bowel disease
• Functional characterization of SLC26A3 c.392C&gt;G (p.P131R) mutation in intestinal barrier function using CRISPR/CAS9-created cell models
• Functional interaction of the cystic fibrosis transmembrane conductance regulator with members of the SLC26 family of anion transporters (SLC26A8 and SLC26A9): physiological and pathophysiological relevance
• Genetic investigation confirmed the clinical phenotype of congenital chloride diarrhea in a Hungarian patient: a case report
• Genotype-dependency of butyrate efficacy in children with congenital chloride diarrhea
• Glucocorticoids and myosin5b loss of function induce heightened PKA signaling in addition to membrane traffic defects
• Honeycomb fetal abdomen: characteristic sign of congenital chloride diarrhea
• Improvement Of Congenital Chloride Diarrhea With Corticosteroids: An Incidental Finding
• Improvement of delayed growth after treatment in child with congenital chloride diarrhea
• Inflammatory Bowel Disease in Patients with Congenital Chloride Diarrhoea
• Inherited salt-losing tubulopathy: An old condition but a new category of tubulopathy
• Japanese neonate with congenital chloride diarrhea caused by SLC26A3 mutation
• Late Diagnosis of Congenital Chloride Diarrhea Mimicking Hirschsprung's Disease
• Loss of the anion exchanger DRA (Slc26a3), or PAT1 (Slc26a6), alters sulfate transport by the distal ileum and overall sulfate homeostasis
• Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis
• Molecular analysis of human solute carrier SLC26 anion transporter disease-causing mutations using 3-dimensional homology modeling
• Monogenic mutations in four cases of neonatal-onset watery diarrhea and a mutation review in East Asia
• Mucosal Abnormalities in Children With Congenital Chloride Diarrhea-An Underestimated Phenotypic Feature?
• NGS Gene Panel Analysis Revealed Novel Mutations in Patients with Rare Congenital Diarrheal Disorders
• Novel SLC26A3 mutation in an infant with congenital chloride-losing diarrhea initially misdiagnosed as Bartter's syndrome
• Novel solute carrier family 26, member 3 mutation in a prenatal recurrent case with congenital chloride diarrhea
• Prenatal and Postnatal Manifestations of Congenital Chloride Diarrhea Due to a Heterozygote Variant of the <em>SLC26A3</em> Gene: A Case Report
• Prenatal and Postnatal Manifestations of Congenital Chloride Diarrhea Due to a Heterozygote Variant of the SLC26A3 Gene: A Case Report
• Prenatal biochemical diagnosis of two forms of congenital diarrheal disorders (congenital chloride diarrhea and congenital sodium diarrhea): A series of 12 cases
• Prenatal diagnosis of congenital chloride diarrhea by whole exome sequencing in four Chinese families and prenatal genotype-phenotype association study
• Prenatal diagnosis of congenital chloride diarrhea: A case report
• Rare mutation in the SLC26A3 transporter causes life-long diarrhoea with metabolic alkalosis
• Recurrent Metabolic Alkalosis in a Cystic Fibrosis Patient: Coexistence with Congenital Chloride Diarrhea
• Regulation of kidney on potassium balance and its clinical significance
• Segmental differences in Slc26a3-dependent Cl^- absorption and HCO₃^- secretion in the mouse large intestine in vitro in Ussing chambers
• Segmental maternal uniparental disomy of chromosome 7q in a patient with congenital chloride diarrhea
• Slc26 Family of Anion Transporters in the Gastrointestinal Tract: Expression, Function, Regulation, and Role in Disease
• Slc26a3 deficiency is associated with epididymis dysplasia and impaired sperm fertilization potential in the mouse
• Slc26a3 deletion alters pH-microclimate, mucin biosynthesis, microbiome composition and increases the TNFα expression in murine colon
• SLC26A3 gene mutations in Tunisian patients with congenital chloride diarrhea
• SLC26A3 mutation in Turkish neonate and her sibling with congenital chloride diarrhea
• Sonographic findings of transient marked proximal bowel dilatation in a growth-restricted fetus at 35 weeks' gestation
• Step-Up Approach for Sodium Butyrate Treatment in Children With Congenital Chloride Diarrhea
• Suicide attempt using potassium tablets for congenital chloride diarrhea: A case report
• Sulfate secretion and chloride absorption are mediated by the anion exchanger DRA (Slc26a3) in the mouse cecum
• Surgical consequences in infants with delayed diagnosis of congenital chloride diarrhea
• The first cases of genetically confirmed congenital diarrhea with chloride loss in Slovakia
• The utility of next generation sequencing in the correct diagnosis of congenital hypochloremic hypokalemic metabolic alkalosis
• Tumor necrosis factor-α acts reciprocally with solute carrier family 26, member 3, (downregulated-in-adenoma) and reduces its expression, leading to intestinal inflammation
• Twelve Novel Mutations in the SLC26A3 Gene in 17 Sporadic Cases of Congenital Chloride Diarrhea
• Type IV neonatal Bartter syndrome complicated with congenital chloride diarrhea
• Updates on bone health in children with gastrointestinal diseases
• Upregulation of antimicrobial peptide expression in slc26a3-/- mice with colonic dysbiosis and barrier defect