103 related articles for article (PubMed ID: 5425829)
1. [Demonstration of the familial nature of chronic congenital hypomagnesemia].
Salet J; Polonovki C; Fournet JP; de Gouyon F; Aymard P; Pean G; Taillemite JL
Arch Fr Pediatr; 1970 May; 27(5):550-1. PubMed ID: 5425829
[No Abstract] [Full Text] [Related]
2. [Primary and chronic congenital hypomagnesemia with magnesium-dependent hypocalcemia].
Pouillaude JM; Frederich A; François B; Racle P; Pernod J; François R
Arch Fr Pediatr; 1971 Dec; 28(10):1021-40. PubMed ID: 5150491
[No Abstract] [Full Text] [Related]
3. 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]
4. Chronic hypomagnesemia with magnesium-dependent hypocalcemia. I. A new syndrome with intestinal magnesium malabsorption.
Nordio S; Donath A; Macagno F; Gatti R
Acta Paediatr Scand; 1971 Jul; 60(4):441-8. PubMed ID: 5556386
[No Abstract] [Full Text] [Related]
5. Chronic hypomagnesemia with magnesium-dependent hypocalcemia. II. A study of the relationship between magnesium, calcium and strontium.
Nordio S; Donath A; Macagno F; Gatti R
Acta Paediatr Scand; 1971 Jul; 60(4):449-55. PubMed ID: 5556387
[No Abstract] [Full Text] [Related]
6. Neonatal hypomagnesemia with selective malabsorption of magnesium--a clinical entity.
Skyberg D; Stromme JH; Nesbakken R; Harnaes K
Scand J Clin Lab Invest; 1968; 21(4):355-63. PubMed ID: 5704707
[No Abstract] [Full Text] [Related]
7. [Congenital primary hypomagnesemia as a cause of spastic states in 2 infants].
Getlík A; Hruskovic I; Sasinka M; Páleníková O; Benko J
Cesk Pediatr; 1971 Aug; 26(8):380-2. PubMed ID: 5095992
[No Abstract] [Full Text] [Related]
8. Congenital primary hypomagnesemia, an inborn error of metabolism?
Skyberg D; Stromme JH; Nesbakken R; Harnaes K
Acta Paediatr Scand; 1967; ():Suppl 177:26-7. PubMed ID: 5586087
[No Abstract] [Full Text] [Related]
9. Inherited hypomagnesemia.
Meij IC; van den Heuvel LP; Knoers NV
Adv Nephrol Necker Hosp; 2000; 30():163-76. PubMed ID: 11068641
[No Abstract] [Full Text] [Related]
10. Fluid and electrolyte disorders. Magnesium.
Brenton DP; Gordon TE
Br J Hosp Med; 1984 Aug; 32(2):60, 64-6, 68-9. PubMed ID: 6536360
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Case of hypomagnesemia with hypocalciuria.
Murunga E; Zawada ET; McMillin JM
S D Med; 2006 May; 59(5):199-201. PubMed ID: 16729652
[No Abstract] [Full Text] [Related]
13. Isolated magnesium malabsorption in a 10-year-old boy.
Romero R; Meacham LR; Winn KT
Am J Gastroenterol; 1996 Mar; 91(3):611-3. PubMed ID: 8633527
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [Primary hypomagnesemia with hypocalcemia. A cause of disease in a child].
Stojanov Lj; Filipović D; Marjanović B; Vulović D; Zamurović D
Srp Arh Celok Lek; 1982 Apr; 110(4):437-44. PubMed ID: 7163892
[No Abstract] [Full Text] [Related]
16. 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]
17. [Familial hypomagnesemia in a girl].
Pronicka E; Kowalewska-Kantecka B; Gruszczyńska B; Sliwińska J; Kraińska L
Pediatr Pol; 1980 Sep; 55(9):1083-6. PubMed ID: 7422421
[No Abstract] [Full Text] [Related]
18. [Malabsorption syndromes in childhood].
Mei V
Clin Pediatr (Bologna); 1967 Dec; 49(12):733-76. PubMed ID: 4878228
[No Abstract] [Full Text] [Related]
19. [The significance of magnesium in medicine. (II) Disturbances of magnesium metabolism and their treatment (author's transl)].
Peerenboom H; Keck E
MMW Munch Med Wochenschr; 1980 Sep; 122(39):1328-32. PubMed ID: 6780810
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
