271 related articles for article (PubMed ID: 30576809)
21. 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]
22. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Vall-Palomar M; Madariaga L; Ariceta G
Pediatr Nephrol; 2021 Oct; 36(10):3045-3055. PubMed ID: 33595712
[TBL] [Abstract][Full Text] [Related]
23. Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes.
Guran T; Akcay T; Bereket A; Atay Z; Turan S; Haisch L; Konrad M; Schlingmann KP
Nephrol Dial Transplant; 2012 Feb; 27(2):667-73. PubMed ID: 21669885
[TBL] [Abstract][Full Text] [Related]
24. Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features.
Eltan M; Yavas Abali Z; Turkyilmaz A; Gokce I; Abali S; Alavanda C; Arman A; Kirkgoz T; Guran T; Hatun S; Bereket A; Turan S
Calcif Tissue Int; 2022 Apr; 110(4):441-450. PubMed ID: 34761296
[TBL] [Abstract][Full Text] [Related]
25. A novel mutation of the claudin 16 gene in familial hypomagnesemia with hypercalciuria and nephrocalcinosis mimicking rickets.
Kasapkara CS; Tumer L; Okur I; Hasanoglu A
Genet Couns; 2011; 22(2):187-92. PubMed ID: 21848011
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. A novel mutation in CLDN16 results in rare familial hypomagnesaemia with hypercalciuria and nephrocalcinosis in a Chinese family.
Lv F; Xu XJ; Wang JY; Liu Y; Jiang Y; Wang O; Xia WB; Xing XP; Li M
Clin Chim Acta; 2016 Jun; 457():69-74. PubMed ID: 27067446
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. 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]
31. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN16 mutations.
Kang JH; Choi HJ; Cho HY; Lee JH; Ha IS; Cheong HI; Choi Y
Pediatr Nephrol; 2005 Oct; 20(10):1490-3. PubMed ID: 16047219
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. 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]
34. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis in three siblings having the same genetic lesion but different clinical presentations.
Seeley HH; Loomba-Albrecht LA; Nagel M; Butani L; Bremer AA
World J Pediatr; 2012 May; 8(2):177-80. PubMed ID: 21633858
[TBL] [Abstract][Full Text] [Related]
35. Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis: clinical and molecular characteristics.
Claverie-Martin F
Clin Kidney J; 2015 Dec; 8(6):656-64. PubMed ID: 26613020
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. Claudins in Renal Physiology and Pathology.
Prot-Bertoye C; Houillier P
Genes (Basel); 2020 Mar; 11(3):. PubMed ID: 32164158
[TBL] [Abstract][Full Text] [Related]
39. Hypomagnesemia and nephrocalcinosis in a patient with two heterozygous mutations in the CLDN16 gene.
Staiger K; Staiger H; Haas C; Thamer C; Risler T; Machicao F; Häring HU
J Nephrol; 2007; 20(1):107-10. PubMed ID: 17347984
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
