169 related articles for article (PubMed ID: 18759094)
1. 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]
2. 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]
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; 25():e942498. PubMed ID: 38528672
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [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]
6. [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]
7. Case of hypomagnesemia with secondary hypocalcemia with a novel
Lal N; Bhardwaj S; Lalgudi Ganesan S; Sharma R; Jain P
Neurol India; 2018; 66(6):1795-1800. PubMed ID: 30504582
[No Abstract] [Full Text] [Related]
8. 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]
9. Exome sequencing identifies a novel frameshift variant causing hypomagnesemia with secondary hypocalcemia.
Azim MK; Mehnaz A; Ahmed JZ; Mujtaba G
CEN Case Rep; 2019 Feb; 8(1):42-47. PubMed ID: 30144020
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
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; 165(4):454-457. PubMed ID: 34012148
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation.
Yücel H; Genç Sel Ç; Kasapkara ÇS; Karacan Küçükali G; Savas Erdeve S; Öztoprak Ü; Ceylaner S; Şenel S; Akçaboy M
J Clin Res Pediatr Endocrinol; 2021 Feb; 13(1):114-118. PubMed ID: 32302086
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Long-term follow-up of a patient with primary hypomagnesaemia and secondary hypocalcaemia due to a novel TRPM6 mutation.
Esteban-Oliva D; Pintos-Morell G; Konrad M
Eur J Pediatr; 2009 Apr; 168(4):439-42. PubMed ID: 18548273
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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]
[Next] [New Search]