Recurrent urinary tract infection and nephrocalcinosis: Answers
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00467-020-04650-z.pdf
Reference12 articles.
1. Hou J, Goodenough DA (2010) Claudin-16 and claudin-19 function in the thick ascending limb. Curr Opin Nephrol Hypertens 19(5):483–488. https://doi.org/10.1097/MNH.0b013e32833b7125
2. Manz F, Schärer K, Janka P, Lombeck J (1978) Renal magnesium wasting, incomplete tubular acidosis, hypercalciuria, and nephrocalcinosis in siblings. Eur J Pediatr 128(2):67–79. https://doi.org/10.1007/BF00496992
3. Claverie-Martin F (2015) Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: Clinical and molecular characteristics. Clin Kidney J 8(6):656–664. https://doi.org/10.1093/ckj/sfv081
4. Claverie-Martin F, Garcia-Nieto V, Loris C, Ariceta G, Nadal I, Espinosa L, Fernandez-Maseda A, Anton-Gamero M, Avila A, Madrid A, Gonzzlez-Acosta H, Cordoba-Lanus E, Santos F, Gil-Calvo M, Espino M, Garcia-Martinez E, Sanchez A, Mulye R (2013) Claudin-19 mutations and clinical phenotype in Spanish patients with Familial Hypomagnesemia with hypercalciuria and nephrocalcinosis. PLoS One 8(1):e53151. https://doi.org/10.1371/journal.pone.0053151
5. Godron A, Harambat J, Boccio V, Mensire A, May A, Rigothier C, Couzi L, Barrou B, Godin M, Chauveau D, Faguer S, Vallet M, Cochat P, Eckart P, Guest G, Guigonis V, Houillier H, Blanchard A, Jeunemaitre X, Vargas-Poussou R (2012) Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: Phenotype-Genotype Correlation and Outcome in 32 patients with CLDN16 or CLDN19 mutations. Clin J Am Soc Nephrol 7(5):801–809. https://doi.org/10.2215/CJN.12841211
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