Furosemide rescues hypercalciuria in familial hypomagnesaemia with hypercalciuria and nephrocalcinosis model

被引:1
|
作者
Mutig, Kerim
Kriuchkova, Natalia
Breiderhoff, Tilman
Muller, Dominik
Yilmaz, Duygu
Demirci, Hasan
Drewell, Hoora
Gunzel, Dorothee
Himmerkus, Nina
Bleich, Markus
Persson, Pontus
机构
关键词
TRPV5; claudin-16; distal calcium reabsorption;
D O I
10.1152/physiol.2023.38.S1.5791619
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
引用
收藏
页数:2
相关论文
共 50 条
  • [41] HYPERCALCIURIA AND NEPHROCALCINOSIS IN THE OCULOCEREBRORENAL SYNDROME
    SLIMAN, GA
    WINTERS, WD
    SHAW, DWW
    AVNER, ED
    [J]. JOURNAL OF UROLOGY, 1995, 153 (04): : 1244 - 1246
  • [42] Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene
    Stefanie Weber
    Katrin Hoffmann
    Nikola Jeck
    Kathrin Saar
    Martin Boeswald
    Eberhard Kuwertz-Broeking
    Ivan IC Meij
    Nine VAM Knoers
    Pierre Cochat
    Tereza Šuláková
    Klaus E Bonzel
    Marianne Soergel
    Friedrich Manz
    Karl Schaerer
    Hannsjoerg W Seyberth
    André Reis
    Martin Konrad
    [J]. European Journal of Human Genetics, 2000, 8 : 414 - 422
  • [43] Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene
    Weber, S
    Hoffmann, K
    Jeck, N
    Saar, K
    Boeswald, M
    Kuwertz-Broeking, E
    Meij, IIC
    Knoers, NVAM
    Cochat, P
    Suláková, T
    Bonzel, KE
    Soergel, M
    Manz, F
    Schaerer, K
    Seyberth, HW
    Reis, A
    Konrad, M
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2000, 8 (06) : 414 - 422
  • [44] Familial hypomagnesaemia-hypercalciuria and nephrocalcinosis in 2 siblings: 2 novel heterozygous mutations in the gene encoding Claudin-16
    Hampson, G
    McDonald, D
    Scoble, J
    Konrad, M
    [J]. JOURNAL OF BONE AND MINERAL RESEARCH, 2005, 20 (07) : 1295 - 1295
  • [45] Unusual presentation of familial hypomagnesemia with hypercalciuria and nephrocalcinosis over two generations
    Bojkovska, N. Ristoska
    Schaller, A.
    Gucev, Z.
    Konrad, M.
    Tasic, V.
    [J]. PEDIATRIC NEPHROLOGY, 2007, 22 (09) : 1494 - 1494
  • [46] Clinical and genetic studies in 17 families with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis
    Vargas-Poussou, R.
    Blanchard, A.
    Guest, G.
    Cochat, P.
    May, A.
    Godin, M.
    Horen, B.
    Vendrell, T.
    Houillier, P.
    Jeunemaitre, X.
    [J]. PEDIATRIC NEPHROLOGY, 2008, 23 (09) : 1588 - 1588
  • [47] Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN16 mutations
    Kang, JH
    Choi, HJ
    Cho, HY
    Lee, JH
    Ha, IS
    Cheong, HI
    Choi, Y
    [J]. PEDIATRIC NEPHROLOGY, 2005, 20 (10) : 1490 - 1493
  • [48] Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN16 mutations
    Ju Hyung Kang
    Hyun Jin Choi
    Hee Yeon Cho
    Joo Hoon Lee
    Il Soo Ha
    Hae Il Cheong
    Yong Choi
    [J]. Pediatric Nephrology, 2005, 20 : 1490 - 1493
  • [49] A novel CLDN16 mutation in familial hypomagnesemia with hypercalciuria and nephrocalcinosis
    Zhang, Hejia
    Ling, Chen
    Liu, Xiaorong
    [J]. CLINICAL NEPHROLOGY, 2019, 92 (02) : 95 - 97
  • [50] Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations (vol 54, pg 26, 2017)
    Yamaguti, P. M.
    Neves, F. D. A. R.
    Hotton, D.
    [J]. JOURNAL OF MEDICAL GENETICS, 2017, 54 (11) : 786 - 786