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Journal Abstract Search

164 related items for PubMed ID: 30504582

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  • 3. 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 26; 25():e942498. PubMed ID: 38528672
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  • 5. 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 23; 13(3):300-307. PubMed ID: 33565749
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  • 6. Hereditary hypomagnesemia with secondary hypocalcemia caused by a novel mutation in TRPM6 gene.
    Dokurel Çetin İ, Betül Gerik-Çelebi H, Demiral M, Çetin O.
    J Pediatr Endocrinol Metab; 2024 Feb 26; 37(2):184-188. PubMed ID: 38084506
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  • 9. 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 26; 75(6):632-4. PubMed ID: 18759094
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  • 10. Mild hypotonia and recurrent seizures in an 8-month-old boy: Answers.
    Özlü SG, Kasapkara CS, Ceylaner S, Erat Nergız M, Alan B, Yılmaz S, Çıtak Kurt AN.
    Pediatr Nephrol; 2019 Oct 26; 34(10):1729-1731. PubMed ID: 30903374
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  • 11. [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 10; 36(8):805-808. PubMed ID: 31400133
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  • 13. 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 10; 165(4):454-457. PubMed ID: 34012148
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  • 14. 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 10; 22(4):497-504. PubMed ID: 23942199
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  • 15. 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 Apr 10; 37(6):541-8. PubMed ID: 23689795
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  • 16. 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 10; 16(10):3061-9. PubMed ID: 16107578
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  • 17. Familial hypomagnesaemia with secondary hypocalcaemia.
    Patel S, Rayanagoudar G, Gelding S.
    BMJ Case Rep; 2016 Sep 13; 2016():. PubMed ID: 27624449
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  • 20. 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 02; 101(9):2894-9. PubMed ID: 14976260
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