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Journal of the American Society of Nephrology, ISSN 1046-6673, 12/2017, Volume 29, Issue 3, pp. ASN.2017060600 - 739
Renal tubulopathies provide insights into the inner workings of the kidney, yet also pose therapeutic challenges. Because of the central nature of sodium in... 
Cell & Transport Physiology | Gitelman-s syndrome | Bartter-s syndrome | Up Front Matters | kidney tubule | children
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 8/2013, Volume 28, Issue 8, pp. 1153 - 1156
Journal Article
Journal Article
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, ISSN 0031-6768, 06/2019, Volume 471, Issue 6, pp. 817 - 818
Journal Article
Journal of the American Society of Nephrology, ISSN 1046-6673, 03/2018, Volume 29, Issue 3, pp. 727 - 739
Renal tubulopathies provide insights into the inner workings of the kidney, yet also pose therapeutic challenges. Because of the central nature of sodium in... 
ANTENATAL BARTTERS-SYNDROME | SENSORINEURAL DEAFNESS | UROLOGY & NEPHROLOGY | HYPOKALEMIC ALKALOSIS | CHLORIDE CHANNEL | NEPHROGENIC DIABETES-INSIPIDUS | SODIUM-PHOSPHATE COTRANSPORTER | PROXIMAL TUBULE | THICK ASCENDING LIMB | RENAL FANCONI SYNDROME | SYNDROME TYPE-IV
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 5/2019, Volume 34, Issue 5, pp. 751 - 762
Kidney disease is a global problem with around three million people diagnosed in the UK alone and the incidence is rising. Research is critical to develop... 
Pediatrics | Animal model | Renal diseases | Nephrology | Medicine & Public Health | Acute kidney injury | Zebrafish | Chronic kidney disease | Urology | Kidney | Polycystic kidney disease | SYSTEM | PHENOTYPES | IDENTIFICATION | GENOME | GENETIC SCREEN | RETINOIC ACID | UROLOGY & NEPHROLOGY | PEDIATRICS | INSERTIONAL MUTAGENESIS | MUTATIONS | EXPRESSION | TOOL | Animal models | Animal welfare | Filtration | Kidneys | Kidney diseases | Review
Journal Article
Archives of Disease in Childhood, ISSN 0003-9888, 06/2019, Volume 104, Issue Suppl 3, p. A324
Background and aimsGitelman syndrome (GS) is a rare renal channelopathy with an autosomal recessive type of inheritance, caused by homozygous or compound... 
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 04/2012, Volume 366, Issue 16, pp. 1508 - 1514
Three patients with homozygous mutations in the integrin α3 gene, a transmembrane integrin receptor subunit, were found to have disrupted basement-membrane... 
Congenital diseases | Kidneys | Epidermolysis bullosa | Laboratories | Lung diseases | Genes | Nephrotic syndrome | Patients | Peritoneal dialysis | Radiography | Babies | Pathology | Parents & parenting | Microscopy | Biopsy | Rodents | Skin diseases | Skin | Mutation | Age
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 12/2019, Volume 34, Issue 12, pp. 2539 - 2540
Journal Article
Journal Article
Nature, ISSN 0028-0836, 02/2012, Volume 482, Issue 7383, pp. 98 - 102
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 10/2019
Journal Article