119 related articles for article (PubMed ID: 3436090)
1. Isolated autosomal recessive renal magnesium loss in two sisters.
Geven WB; Monnens LA; Willems JL; Buijs W; Hamel CJ
Clin Genet; 1987 Dec; 32(6):398-402. PubMed ID: 3436090
[TBL] [Abstract][Full Text] [Related]
2. Renal magnesium wasting in two families with autosomal dominant inheritance.
Geven WB; Monnens LA; Willems HL; Buijs WC; ter Haar BG
Kidney Int; 1987 May; 31(5):1140-4. PubMed ID: 3298795
[TBL] [Abstract][Full Text] [Related]
3. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Kari JA; Farouq M; Alshaya HO
Pediatr Nephrol; 2003 Jun; 18(6):506-10. PubMed ID: 12720080
[TBL] [Abstract][Full Text] [Related]
4. Hereditary isolated renal magnesium loss maps to chromosome 11q23.
Meij IC; Saar K; van den Heuvel LP; Nuernberg G; Vollmer M; Hildebrandt F; Reis A; Monnens LA; Knoers NV
Am J Hum Genet; 1999 Jan; 64(1):180-8. PubMed ID: 9915957
[TBL] [Abstract][Full Text] [Related]
5. Primary idiopathic hypomagnesemia in two female siblings.
Challa A; Papaefstathiou I; Lapatsanis D; Tsolas O
Acta Paediatr; 1995 Sep; 84(9):1075-8. PubMed ID: 8652964
[TBL] [Abstract][Full Text] [Related]
6. Dominant isolated renal magnesium loss is caused by misrouting of the Na+,K+-ATPase gamma-subunit.
Meij IC; Koenderink JB; De Jong JC; De Pont JJ; Monnens LA; Van Den Heuvel LP; Knoers NV
Ann N Y Acad Sci; 2003 Apr; 986():437-43. PubMed ID: 12763862
[TBL] [Abstract][Full Text] [Related]
7. Magnesium metabolism in childhood.
Geven WB; Monnens LA; Willems JL
Miner Electrolyte Metab; 1993; 19(4-5):308-13. PubMed ID: 8264518
[TBL] [Abstract][Full Text] [Related]
8. Genetic heterogeneity in tubular hypomagnesemia-hypokalemia with hypocalcuria (Gitelman's syndrome).
Bettinelli A; Bianchetti MG; Borella P; Volpini E; Metta MG; Basilico E; Selicorni A; Bargellini A; Grassi MR
Kidney Int; 1995 Feb; 47(2):547-51. PubMed ID: 7723239
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Familial hypomagnesemia-hypercalciuria in 2 siblings.
Kuwertz-Bröking E; Fründ S; Bulla M; Kleta R; August C; Kisters K
Clin Nephrol; 2001 Aug; 56(2):155-61. PubMed ID: 11522093
[TBL] [Abstract][Full Text] [Related]
11. [5 children with hypokalemia, hypomagnesemia and hypocalciuria (Gitelman syndrome) in one family].
Schweizer JJ; van Collenburg JJ
Ned Tijdschr Geneeskd; 1997 Aug; 141(35):1698-701. PubMed ID: 9543787
[TBL] [Abstract][Full Text] [Related]
12. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Praga M; Vara J; González-Parra E; Andrés A; Alamo C; Araque A; Ortiz A; Rodicio JL
Kidney Int; 1995 May; 47(5):1419-25. PubMed ID: 7637271
[TBL] [Abstract][Full Text] [Related]
13. Familial hypomagnesemia--a follow-up examination of three patients after 9 to 12 years of treatment.
Strømme JH; Steen-Johnsen J; Harnaes K; Hofstad F; Brandtzaeg P
Pediatr Res; 1981 Aug; 15(8):1134-9. PubMed ID: 7267188
[TBL] [Abstract][Full Text] [Related]
14. Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes.
Bettinelli A; Bianchetti MG; Girardin E; Caringella A; Cecconi M; Appiani AC; Pavanello L; Gastaldi R; Isimbaldi C; Lama G
J Pediatr; 1992 Jan; 120(1):38-43. PubMed ID: 1731022
[TBL] [Abstract][Full Text] [Related]
15. Recent advances in molecular genetics of hereditary magnesium-losing disorders.
Konrad M; Weber S
J Am Soc Nephrol; 2003 Jan; 14(1):249-60. PubMed ID: 12506158
[TBL] [Abstract][Full Text] [Related]
16. Severe hypomagnesemia in a neonate with isolated renal magnesium loss.
Meij I; Illy KE; Monnens L
Nephron; 2000 Feb; 84(2):198. PubMed ID: 10657728
[No Abstract] [Full Text] [Related]
17. HNF1B mutations associate with hypomagnesemia and renal magnesium wasting.
Adalat S; Woolf AS; Johnstone KA; Wirsing A; Harries LW; Long DA; Hennekam RC; Ledermann SE; Rees L; van't Hoff W; Marks SD; Trompeter RS; Tullus K; Winyard PJ; Cansick J; Mushtaq I; Dhillon HK; Bingham C; Edghill EL; Shroff R; Stanescu H; Ryffel GU; Ellard S; Bockenhauer D
J Am Soc Nephrol; 2009 May; 20(5):1123-31. PubMed ID: 19389850
[TBL] [Abstract][Full Text] [Related]
18. A familial disorder characterized by hypokalemia and hypomagnesemia.
Gitelman HJ; Graham JB; Welt LG
Ann N Y Acad Sci; 1969 Aug; 162(2):856-64. PubMed ID: 5259575
[No Abstract] [Full Text] [Related]
19. CNNM2, encoding a basolateral protein required for renal Mg2+ handling, is mutated in dominant hypomagnesemia.
Stuiver M; Lainez S; Will C; Terryn S; Günzel D; Debaix H; Sommer K; Kopplin K; Thumfart J; Kampik NB; Querfeld U; Willnow TE; Němec V; Wagner CA; Hoenderop JG; Devuyst O; Knoers NV; Bindels RJ; Meij IC; Müller D
Am J Hum Genet; 2011 Mar; 88(3):333-43. PubMed ID: 21397062
[TBL] [Abstract][Full Text] [Related]
20. Hypomagnesemia: an evidence-based approach to clinical cases.
Assadi F
Iran J Kidney Dis; 2010 Jan; 4(1):13-9. PubMed ID: 20081299
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]