Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis

[1]  V. D’Agati.  Podocyte injury in focal segmental glomerulosclerosis: Lessons from animal models (a play in five acts). , 2008, Kidney international.

[2]  R. Dalton,et al.  C1q nephropathy in association with Gitelman syndrome: a case report , 2006, Pediatric Nephrology.

[3]  M. Konrad,et al.  Late-onset manifestation of antenatal Bartter syndrome as a result of residual function of the mutated renal Na+-K+-2Cl- co-transporter. , 2006, Journal of the American Society of Nephrology : JASN.

[4]  A. Edefonti,et al.  Simultaneous Mutations in the CLCNKB and SLC12A3 Genes in Two Siblings with Phenotypic Heterogeneity in Classic Bartter Syndrome , 2005, Pediatric Research.

[5]  H. Omran,et al.  Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure , 2001, Nature Genetics.

[6]  M. Konrad,et al.  Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness. , 2001, Pediatrics.

[7]  A. Fogo,et al.  Progression and potential regression of glomerulosclerosis. , 2001, Kidney international.

[8]  R. Lifton,et al.  Bartter syndrome and focal segmental glomerulosclerosis: a possible link between two diseases , 2000, Pediatric Nephrology.

[9]  G. Casari,et al.  Phenotypic variability in Bartter syndrome type I , 2000, Pediatric Nephrology.

[10]  J. Balfe,et al.  Non-steroidal anti-inflammatory drug-associated nephrotoxicity in Bartter syndrome , 1998, Pediatric Nephrology.

[11]  K. Çağlar,et al.  Association of Gitelman’s Syndrome and Focal Glomerulosclerosis , 1998, Nephron.

[12]  T. Mansfield,et al.  Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III , 1997, Nature Genetics.

[13]  R. Lifton,et al.  Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMK , 1996, Nature Genetics.

[14]  R. Lifton,et al.  Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2. , 1996, Nature genetics.

[15]  J. V. Van Wyk,et al.  Reversal of Bartter's syndrome by renal transplantation in a child with focal, segmental glomerular sclerosis. , 1985, The American journal of the medical sciences.