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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
143 related items for PubMed ID: 7422421
1. [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]
2. Disorders of mineral metabolism. Hambidge KM, Walravens PA. Clin Gastroenterol; 1982 Jan; 11(1):87-117. PubMed ID: 6277535 [No Abstract] [Full Text] [Related]
3. Inherited forms of renal hypomagnesemia: an update. Knoers NV. Pediatr Nephrol; 2009 Apr; 24(4):697-705. PubMed ID: 18818955 [Abstract] [Full Text] [Related]
4. Inherited disorders of renal hypomagnesaemia. Konrad M, Schlingmann KP. Nephrol Dial Transplant; 2014 Sep; 29 Suppl 4():iv63-71. PubMed ID: 25165187 [Abstract] [Full Text] [Related]
6. 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 [Abstract] [Full Text] [Related]
7. Renal responsiveness to magnesium and parathormone in primary familial hypomagnesaemia. Pronicka E, Sliwińska J, Gruszczyńska B, Wieczorek E, Klimaszewski J, Urbanek M. Acta Med Pol; 1985 Jan; 26(1-2):37-42. PubMed ID: 4096262 [No Abstract] [Full Text] [Related]
8. Afebrile seizures in infants: Never forget magnesium! Minute M, Ventura G, Giorgi R, Faletra F, Costa P, Cozzi G. J Paediatr Child Health; 2018 Apr; 54(4):446-448. PubMed ID: 29411453 [No Abstract] [Full Text] [Related]
9. [Significance of magnesium in pediatrics]. Steidl L, Simková M, Volejník J. Cesk Pediatr; 1979 Jun; 34(6):349-52. PubMed ID: 378442 [No Abstract] [Full Text] [Related]
10. Chronic hypomagnesemia and hypokalemia due to renal wasting in siblings. Iwata F, Hanawa Y, Takashima H. Acta Paediatr Jpn; 1993 Jun; 35(3):252-7. PubMed ID: 8351995 [Abstract] [Full Text] [Related]
11. A GPHN point mutation leading to molybdenum cofactor deficiency. Reiss J, Lenz U, Aquaviva-Bourdain C, Joriot-Chekaf S, Mention-Mulliez K, Holder-Espinasse M. Clin Genet; 2011 Dec; 80(6):598-9. PubMed ID: 22040219 [No Abstract] [Full Text] [Related]
12. Genetics of hereditary disorders of magnesium homeostasis. Schlingmann KP, Konrad M, Seyberth HW. Pediatr Nephrol; 2004 Jan; 19(1):13-25. PubMed ID: 14634861 [Abstract] [Full Text] [Related]
13. [The treatment of hypomagnesemia]. Cornelissen EA, Knoers NV. Ned Tijdschr Geneeskd; 2002 Dec 07; 146(49):2387; author reply 2387-8. PubMed ID: 12510410 [No Abstract] [Full Text] [Related]
14. Neonatal hypomagnesemia with selective malabsorption of magnesium--a clinical entity. Skyberg D, Stromme JH, Nesbakken R, Harnaes K. Scand J Clin Lab Invest; 1968 Dec 07; 21(4):355-63. PubMed ID: 5704707 [No Abstract] [Full Text] [Related]
15. Familial hyperzincaemia: a rare entity. Selimoglu MA, Ertekin V, Yildirim ZK, Altinkaynak S. Int J Clin Pract; 2006 Jan 07; 60(1):108-9. PubMed ID: 16409438 [No Abstract] [Full Text] [Related]
16. [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 07; 20(11):1212-1218. PubMed ID: 24090669 [Abstract] [Full Text] [Related]
17. The familial magnesium-losing kidney. Hedemann L, Strunge P, Munck V. Acta Med Scand; 1986 Nov 07; 219(1):133-6. PubMed ID: 3953313 [Abstract] [Full Text] [Related]
18. [Renal tubular hypomagnesemia of familial origin]. Rapado A, Pedraza M, Torrijos A, Moreno F, Aparicio A, Sánchez-Alarcón J. Rev Clin Esp; 1985 Apr 07; 176(6):302-4. PubMed ID: 4001489 [No Abstract] [Full Text] [Related]
19. Familial hypomagnesemia--hypercalciuria and pseudotumor cerebri. Gregoric A, Bracic K, Marcun-Varda N. Wien Klin Wochenschr; 2001 Apr 07; 113 Suppl 3():59-61. PubMed ID: 15503623 [Abstract] [Full Text] [Related]