BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

490 related articles for article (PubMed ID: 12032570)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia.
    Chubanov V; Waldegger S; Mederos y Schnitzler M; Vitzthum H; Sassen MC; Seyberth HW; Konrad M; Gudermann T
    Proc Natl Acad Sci U S A; 2004 Mar; 101(9):2894-9. PubMed ID: 14976260
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 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. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Primary hypomagnesemia with secondary hypocalcemia. Report of a case and review of the world literature.
    Yamamoto T; Kabata H; Yagi R; Takashima M; Itokawa Y
    Magnesium; 1985; 4(2-3):153-64. PubMed ID: 2995735
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A Novel Homozygous Mutation in the Transient Receptor Potential Melastatin 6 Gene: A Case Report.
    Altıncık A; Schlingmann KP; Tosun MS
    J Clin Res Pediatr Endocrinol; 2016 Mar; 8(1):101-4. PubMed ID: 26759217
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Intestinal hypomagnesemia in an Iranian patient with a novel TRPM6 variant: a case report and review of the literature.
    Kamali F; Jamee M; Sayer JA; Sadeghi-Bojd S; Golchehre Z; Dehghanzad R; Keramatipour M; Mohkam M
    CEN Case Rep; 2023 Nov; 12(4):413-418. PubMed ID: 36967423
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Analysis of TRPM6 gene variant in a pedigree affected with hypocalcemia secondary to hypomagnesemia].
    Tan J; Yan T; Li Z; Huang J; Cai R
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Aug; 36(8):805-808. PubMed ID: 31400133
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic background of HSH in three Polish families and a patient with an X;9 translocation.
    Jalkanen R; Pronicka E; Tyynismaa H; Hanauer A; Walder R; Alitalo T
    Eur J Hum Genet; 2006 Jan; 14(1):55-62. PubMed ID: 16267500
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Long-term Clinical Follow-up of Patients with Familial Hypomagnesemia with Secondary Hypocalcemia.
    Bayramoğlu E; Keskin M; Aycan Z; Savaş-Erdeve Ş; Çetinkaya S
    J Clin Res Pediatr Endocrinol; 2021 Aug; 13(3):300-307. PubMed ID: 33565749
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 25.