Literature DB >> 5586087

Congenital primary hypomagnesemia, an inborn error of metabolism?

D Skyberg, J H Stromme, R Nesbakken, K Harnaes.   

Abstract

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Year:  1967        PMID： 5586087     DOI： 10.1111/j.1651-2227.1967.tb05195.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN： 0001-656X


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  4 in total

1.  Clinical presentation and outcome in primary familial hypomagnesaemia.

Authors:  H Shalev; M Phillip; A Galil; R Carmi; D Landau
Journal:  Arch Dis Child       Date:  1998-02       Impact factor: 3.791

2.  Tetany due to hypomagnesaemia with secondary hypocalcaemia.

Authors:  M Vainsel; G Vandevelde; J Smulders; M Vosters; P Hubain; H Loeb
Journal:  Arch Dis Child       Date:  1970-04       Impact factor: 3.791

3.  Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpoint.

Authors:  M Chery; V Biancalana; C Philippe; G Malpuech; H Carla; S Gilgenkrantz; J L Mandel; A Hanauer
Journal:  Hum Genet       Date:  1994-05       Impact factor: 4.132

4.  Mice defective in Trpm6 show embryonic mortality and neural tube defects.

Authors:  Roxanne Y Walder; Baoli Yang; John B Stokes; Patricia A Kirby; Xiao Cao; Peijun Shi; Charles C Searby; Russell F Husted; Val C Sheffield
Journal:  Hum Mol Genet       Date:  2009-08-18       Impact factor: 6.150
  4 in total

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