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Pediatric Nephrology (Berlin, Germany)|July 11, 2018
Expert consensus guidelines for the genetic diagnosis of Alport syndromeJudy Savige, Francesca Ariani, Francesca Mari, et al.
Journal of the American Society of Nephrology : JASN|November 23, 2013
Evidence for activation of the unfolded protein response in collagen IV nephropathiesMyrtani Pieri, Charalambos Stefanou, Apostolos Zaravinos, et al.
Lancet (London, England)|August 31, 2010
Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritisDaniel P Gale, Elena Goicoechea de Jorge, H Terence Cook, et al.
Scientific Reports|November 18, 2024
biobank.cy: the Biobank of Cyprus past, present and futureEleni M Loizidou, Maria Kyratzi, Maria A Tsiarli, et al.
Genetic Testing and Molecular Biomarkers|October 7, 2014
Molecular investigation of distal renal tubular acidosis in Tunisia, evidence for founder mutationsMajdi Nagara, Konstantinos Voskarides, Sonia Nouira, et al.
Journal of the American Society of Nephrology : JASN|April 23, 2003
Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney diseaseRiccardo Magistroni, Ning He, Kairong Wang, et al.
Journal of the American Society of Nephrology : JASN|July 10, 2010
Genetic variation of DKK3 may modify renal disease severity in ADPKDMichelle Liu, Sally Shi, Sean Senthilnathan, et al.
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