These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 30504582)

  • 21. 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]  

  • 22. 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]  

  • 23. A functional study for verifying the pathogenicity of a TRPM6 variant of uncertain significance: A novel non-canonical splicing-site variant in primary hypomagnesemia with secondary hypocalcemia.
    Wang P; Qian Y; Gu C; Zhi X; Pu L; Yan D; Shu J; Lv L; Cai C
    Clin Chim Acta; 2021 Dec; 523():469-475. PubMed ID: 34755648
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. 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]  

  • 26. 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]  

  • 27. 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]  

  • 28. Rare cause of recurrent hypocalcaemia and functional hypoparathyroidism due to hypomagnesaemia caused by
    Khadse S; Takalikar VS; Ghildiyal R; Shah N
    BMJ Case Rep; 2024 Feb; 17(2):. PubMed ID: 38413141
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. [Familial congenital hypomagnesemia revealed by neonatal convulsions].
    Ndiaye M; Toffa DH; Sow AD; Sène MS; Basse AM; Fall AL; Seck LB; Touré K; Diop AG; Sow HD; Ndiaye MM
    Arch Pediatr; 2013 Nov; 20(11):1212-1218. PubMed ID: 24090669
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Inherited forms of renal hypomagnesemia: an update.
    Knoers NV
    Pediatr Nephrol; 2009 Apr; 24(4):697-705. PubMed ID: 18818955
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Familial Hypomagnesemia with Secondary Hypocalcemia Mimicking Neurodegenerative Disorder.
    Kamate M; Singh N; Patil S
    Indian Pediatr; 2015 Jun; 52(6):521-2. PubMed ID: 26121732
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Transient receptor potential melastatin 6 knockout mice are lethal whereas heterozygous deletion results in mild hypomagnesemia.
    Woudenberg-Vrenken TE; Sukinta A; van der Kemp AW; Bindels RJ; Hoenderop JG
    Nephron Physiol; 2011; 117(2):p11-9. PubMed ID: 20814221
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Renal diseases that course with hypomagnesemia. Comments on a new hereditary hypomagnesemic tubulopathy.
    Garcia-Nieto VM; Claverie-Martin F; Moraleda-Mesa T; Perdomo-Ramírez A; Fraga-Rodríguez GM; Luis-Yanes MI; Ramos-Trujillo E;
    Nefrologia (Engl Ed); 2024; 44(1):23-31. PubMed ID: 38350738
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Hypomagnesemia related to the use of omeprazole with negative result for mutation in the TRPM6 gene].
    Fernández-Fernández FJ; Sesma P; Caínzos-Romero T; Ferreira L
    Med Clin (Barc); 2011 Jul; 137(4):188-9. PubMed ID: 21047658
    [No Abstract]   [Full Text] [Related]  

  • 36. 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]  

  • 37. TRPM6 forms the Mg2+ influx channel involved in intestinal and renal Mg2+ absorption.
    Voets T; Nilius B; Hoefs S; van der Kemp AW; Droogmans G; Bindels RJ; Hoenderop JG
    J Biol Chem; 2004 Jan; 279(1):19-25. PubMed ID: 14576148
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Familial hypomagnesemia with hypocalcemia: a rare cause of infantile seizures.
    Srinivasan R; Ninama AC; Krishna S; Vasudevan A
    CEN Case Rep; 2023 May; 12(2):139-145. PubMed ID: 36131192
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Familial hypomagnesaemia with secondary hypocalcaemia as a cause of seizures in children].
    Thorsteinsson K; Thaarup J; Hagstrøm S
    Ugeskr Laeger; 2019 Apr; 181(15):. PubMed ID: 30990164
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.