425 related articles for article (PubMed ID: 16107578)
1. Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia.
Schlingmann KP; Sassen MC; Weber S; Pechmann U; Kusch K; Pelken L; Lotan D; Syrrou M; Prebble JJ; Cole DE; Metzger DL; Rahman S; Tajima T; Shu SG; Waldegger S; Seyberth HW; Konrad M
J Am Soc Nephrol; 2005 Oct; 16(10):3061-9. PubMed ID: 16107578
[TBL] [Abstract][Full Text] [Related]
2. Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia.
Walder RY; Landau D; Meyer P; Shalev H; Tsolia M; Borochowitz Z; Boettger MB; Beck GE; Englehardt RK; Carmi R; Sheffield VC
Nat Genet; 2002 Jun; 31(2):171-4. PubMed ID: 12032570
[TBL] [Abstract][Full Text] [Related]
3. Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family.
Schlingmann KP; Weber S; Peters M; Niemann Nejsum L; Vitzthum H; Klingel K; Kratz M; Haddad E; Ristoff E; Dinour D; Syrrou M; Nielsen S; Sassen M; Waldegger S; Seyberth HW; Konrad M
Nat Genet; 2002 Jun; 31(2):166-70. PubMed ID: 12032568
[TBL] [Abstract][Full Text] [Related]
4. Resolving basal ganglia calcification in hereditary hypomagnesemia with secondary hypocalcemia due to a novel TRPM6 gene mutation.
Habeb AM; Al-Harbi H; Schlingmann KP
Saudi J Kidney Dis Transpl; 2012 Sep; 23(5):1038-42. PubMed ID: 22982920
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Neonatal seizures and familial hypomagnesemia with secondary hypocalcemia.
Visudhiphan P; Visudtibhan A; Chiemchanya S; Khongkhatithum C
Pediatr Neurol; 2005 Sep; 33(3):202-5. PubMed ID: 16139735
[TBL] [Abstract][Full Text] [Related]
7. Novel TRPM6 mutations in familial hypomagnesemia with secondary hypocalcemia.
Zhao Z; Pei Y; Huang X; Liu Y; Yang W; Sun J; Si N; Xing X; Li M; Wang O; Jiang Y; Zhang X; Xia W
Am J Nephrol; 2013; 37(6):541-8. PubMed ID: 23689795
[TBL] [Abstract][Full Text] [Related]
8. Hypomagnesemia due to two novel TRPM6 mutations.
Coulter M; Colvin C; Korf B; Messiaen L; Tuanama B; Crowley M; Crossman DK; McCormick K
J Pediatr Endocrinol Metab; 2015 Nov; 28(11-12):1373-8. PubMed ID: 26226117
[TBL] [Abstract][Full Text] [Related]
9. New TRPM6 missense mutations linked to hypomagnesemia with secondary hypocalcemia.
Lainez S; Schlingmann KP; van der Wijst J; Dworniczak B; van Zeeland F; Konrad M; Bindels RJ; Hoenderop JG
Eur J Hum Genet; 2014 Apr; 22(4):497-504. PubMed ID: 23942199
[TBL] [Abstract][Full Text] [Related]
10. New TRPM6 mutation and management of hypomagnesaemia with secondary hypocalcaemia.
Katayama K; Povalko N; Yatsuga S; Nishioka J; Kakuma T; Matsuishi T; Koga Y
Brain Dev; 2015 Mar; 37(3):292-8. PubMed ID: 24985022
[TBL] [Abstract][Full Text] [Related]
11. A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant.
Uddin MS; Alradhi AY; Alqathani FMN; Alessa OS; Alshammari ANM; Tripathy R; Alomari MA
Am J Case Rep; 2024 Mar; 25():e942498. PubMed ID: 38528672
[TBL] [Abstract][Full Text] [Related]
12. Hypomagnesemia with secondary hypocalcemia due to a missense mutation in the putative pore-forming region of TRPM6.
Chubanov V; Schlingmann KP; Wäring J; Heinzinger J; Kaske S; Waldegger S; Mederos y Schnitzler M; Gudermann T
J Biol Chem; 2007 Mar; 282(10):7656-67. PubMed ID: 17197439
[TBL] [Abstract][Full Text] [Related]
13. Renal TRPathies.
Dietrich A; Chubanov V; Gudermann T
J Am Soc Nephrol; 2010 May; 21(5):736-44. PubMed ID: 20395377
[TBL] [Abstract][Full Text] [Related]
14. A novel synonymous homozygous variant [c.2538G>A (p.Thr846Thr)] in
Acar S; Schlingmann KP; Nalbantoğlu Ö; Köprülü Ö; Arslan G; Özkaya B; Özkan B
J Pediatr Endocrinol Metab; 2021 Nov; 34(11):1481-1486. PubMed ID: 34261199
[TBL] [Abstract][Full Text] [Related]
15. Insight into the molecular regulation of the epithelial magnesium channel TRPM6.
Cao G; Hoenderop JG; Bindels RJ
Curr Opin Nephrol Hypertens; 2008 Jul; 17(4):373-8. PubMed ID: 18660673
[TBL] [Abstract][Full Text] [Related]
16. [Clinical features and TRPM6 mutations of an infant with hypomagnesemia with secondary hypocalcemia].
Yang Z; Wang Y; Chen G
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Aug; 36(8):834-836. PubMed ID: 31400140
[TBL] [Abstract][Full Text] [Related]
17. The epithelial Mg2+ channel transient receptor potential melastatin 6 is regulated by dietary Mg2+ content and estrogens.
Groenestege WM; Hoenderop JG; van den Heuvel L; Knoers N; Bindels RJ
J Am Soc Nephrol; 2006 Apr; 17(4):1035-43. PubMed ID: 16524949
[TBL] [Abstract][Full Text] [Related]
18. Hereditary hypomagnesemia with secondary hypocalcemia caused by a novel mutation in
Dokurel Çetin İ; Betül Gerik-Çelebi H; Demiral M; Çetin O
J Pediatr Endocrinol Metab; 2024 Feb; 37(2):184-188. PubMed ID: 38084506
[TBL] [Abstract][Full Text] [Related]
19. Novel mutations in TRPM6 gene associated with primary hypomagnesemia with secondary hypocalcemia. Case report.
Papez J; Starha J; Slaba K; Hubacek JA; Pecl J; Aulicka S; Urik M; Ceylaner S; Vesela P; Slaby O; Jabandziev P
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub; 2021 Nov; 165(4):454-457. PubMed ID: 34012148
[TBL] [Abstract][Full Text] [Related]
20. A case of hypomagnesemia with secondary hypocalcemia caused by Trpm6 gene mutation.
Apa H; Kayserili E; Agin H; Hizarcioglu M; Gulez P; Berdeli A
Indian J Pediatr; 2008 Jun; 75(6):632-4. PubMed ID: 18759094
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
