319 related articles for article (PubMed ID: 26136118)
21. A Novel Mutation in CLDN16 Gene Causing Familial Hypomagnesemia, Hypercalciuria, Nephrocalcinosis in An Iranian Family.
Malakoutian T; Madadi B; Saber S
Iran J Kidney Dis; 2022 May; 16(3):209-213. PubMed ID: 35714216
[TBL] [Abstract][Full Text] [Related]
22. A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings.
Alparslan C; Öncel EP; Akbay S; Alaygut D; Mutlubaş F; Tatlı M; Konrad M; Yavaşcan Ö; Kasap-Demir B
Turk J Pediatr; 2018; 60(1):76-80. PubMed ID: 30102483
[TBL] [Abstract][Full Text] [Related]
23. Deletion of claudin-10 rescues claudin-16-deficient mice from hypomagnesemia and hypercalciuria.
Breiderhoff T; Himmerkus N; Drewell H; Plain A; Günzel D; Mutig K; Willnow TE; Müller D; Bleich M
Kidney Int; 2018 Mar; 93(3):580-588. PubMed ID: 29129401
[TBL] [Abstract][Full Text] [Related]
24. Atypical presentation of familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a patient with a new claudin-16 gene mutation.
Vianna JGP; Simor TG; Senna P; De Bortoli MR; Costalonga EF; Seguro AC; Luchi WM
Clin Nephrol Case Stud; 2019; 7():27-34. PubMed ID: 31119091
[TBL] [Abstract][Full Text] [Related]
25. Identification of a Novel Homozygous Missense Mutation in the CLDN16 Gene to Decipher the Ambiguous Clinical Presentation Associated with Autosomal Dominant Hypocalcaemia and Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis in an Indian Family.
Thapa R; Roy A; Nayek K; Basu A
Calcif Tissue Int; 2024 Feb; 114(2):110-118. PubMed ID: 38078932
[TBL] [Abstract][Full Text] [Related]
26. A novel
Zhang H; Ling C; Liu X
Clin Nephrol; 2019 Aug; 92(2):95-97. PubMed ID: 31232269
[TBL] [Abstract][Full Text] [Related]
27. Claudin-19 localizes to the thick ascending limb where its expression is required for junctional claudin-16 localization.
Dimke H; Griveau C; Ling WE; Brideau G; Cheval L; Muthan P; Müller D; Al-Shebel A; Houillier P; Prot-Bertoye C
Ann N Y Acad Sci; 2023 Aug; 1526(1):126-137. PubMed ID: 37344378
[TBL] [Abstract][Full Text] [Related]
28. Retrospective cohort study of familial hypomagnesaemia with hypercalciuria and nephrocalcinosis due to CLDN16 mutations.
Sikora P; Zaniew M; Haisch L; Pulcer B; Szczepańska M; Moczulska A; Rogowska-Kalisz A; Bieniaś B; Tkaczyk M; Ostalska-Nowicka D; Zachwieja K; Hyla-Klekot L; Schlingmann KP; Konrad M
Nephrol Dial Transplant; 2015 Apr; 30(4):636-44. PubMed ID: 25477417
[TBL] [Abstract][Full Text] [Related]
29. Haplotype analysis of CLDN19 single nucleotide polymorphisms in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Martin-Nuñez E; Cordoba-Lanus E; Gonzalez-Acosta H; Oliet A; Izquierdo E; Claverie-Martin F
World J Pediatr; 2015 Aug; 11(3):272-5. PubMed ID: 25410674
[TBL] [Abstract][Full Text] [Related]
30. Familial hypomagnesaemia, Hypercalciuria and Nephrocalcinosis associated with a novel mutation of the highly conserved leucine residue 116 of Claudin 16 in a Chinese patient with a delayed diagnosis: a case report.
Lu J; Zhao X; Paiardini A; Lang Y; Bottillo I; Shao L
BMC Nephrol; 2018 Jul; 19(1):181. PubMed ID: 30005619
[TBL] [Abstract][Full Text] [Related]
31. Claudin-16 and claudin-19 interact and form a cation-selective tight junction complex.
Hou J; Renigunta A; Konrad M; Gomes AS; Schneeberger EE; Paul DL; Waldegger S; Goodenough DA
J Clin Invest; 2008 Feb; 118(2):619-28. PubMed ID: 18188451
[TBL] [Abstract][Full Text] [Related]
32. Heterogeneity is a common ground in familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by CLDN19 gene mutations.
Vall-Palomar M; Burballa C; Claverie-Martín F; Meseguer A; Ariceta G
J Nephrol; 2021 Dec; 34(6):2053-2062. PubMed ID: 33929692
[TBL] [Abstract][Full Text] [Related]
33. A novel PCLN-1 gene mutation in familial hypomagnesemia with hypercalciuria and atypical phenotype.
Sanjad SA; Hariri A; Habbal ZM; Lifton RP
Pediatr Nephrol; 2007 Apr; 22(4):503-8. PubMed ID: 17123117
[TBL] [Abstract][Full Text] [Related]
34. Targeted deletion of murine Cldn16 identifies extra- and intrarenal compensatory mechanisms of Ca2+ and Mg2+ wasting.
Will C; Breiderhoff T; Thumfart J; Stuiver M; Kopplin K; Sommer K; Günzel D; Querfeld U; Meij IC; Shan Q; Bleich M; Willnow TE; Müller D
Am J Physiol Renal Physiol; 2010 May; 298(5):F1152-61. PubMed ID: 20147368
[TBL] [Abstract][Full Text] [Related]
35. The role of tight junctions in paracellular ion transport in the renal tubule: lessons learned from a rare inherited tubular disorder.
Haisch L; Almeida JR; Abreu da Silva PR; Schlingmann KP; Konrad M
Am J Kidney Dis; 2011 Feb; 57(2):320-30. PubMed ID: 21186073
[TBL] [Abstract][Full Text] [Related]
36. Hypomagnesemia with hypercalciuria and nephrocalcinosis: case report and a family study.
Tasic V; Dervisov D; Koceva S; Weber S; Konrad M
Pediatr Nephrol; 2005 Jul; 20(7):1003-6. PubMed ID: 15856319
[TBL] [Abstract][Full Text] [Related]
37. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: blocking endocytosis restores surface expression of a novel Claudin-16 mutant that lacks the entire C-terminal cytosolic tail.
Müller D; Kausalya PJ; Meij IC; Hunziker W
Hum Mol Genet; 2006 Apr; 15(7):1049-58. PubMed ID: 16501001
[TBL] [Abstract][Full Text] [Related]
38. Familial Hypomagnesemia, Hypercalciuria and Nephrocalcinosis with Novel Mutation.
Margabandhu S; Doshi M
Indian J Nephrol; 2019; 29(1):57-61. PubMed ID: 30814796
[TBL] [Abstract][Full Text] [Related]
39. Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis (FHHNC): compound heterozygous mutation in the claudin 16 (CLDN16) gene.
Hampson G; Konrad MA; Scoble J
BMC Nephrol; 2008 Sep; 9():12. PubMed ID: 18816383
[TBL] [Abstract][Full Text] [Related]
40. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis in 2 sisters.
Al-Elq AH
Saudi Med J; 2008 Mar; 29(3):447-51. PubMed ID: 18327378
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
