Literature DB >> 5425829

[Demonstration of the familial nature of chronic congenital hypomagnesemia].

J Salet, C Polonovki, J P Fournet, F de Gouyon, P Aymard, G Pean, J L Taillemite.   

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Year:  1970        PMID： 5425829

Source DB:  PubMed          Journal:  Arch Fr Pediatr        ISSN： 0003-9764


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  5 in total

1.  Primary hypomagnesemia. I. Absorption Studies.

Authors:  I Lombeck; F Ritzl; H G Schnippering; H Michael; H J Bremer; L E Feinendegen; W Kosenow
Journal:  Z Kinderheilkd       Date:  1975

2.  Primary hypomagnesaemia. A case report and literature review.

Authors:  K I Dudin; A S Teebi
Journal:  Eur J Pediatr       Date:  1987-05       Impact factor: 3.183

3.  Studies in primary hypomagnesaemia: evidence for defective carrier-mediated small intestinal transport of magnesium.

Authors:  P J Milla; P J Aggett; O H Wolff; J T Harries
Journal:  Gut       Date:  1979-11       Impact factor: 23.059

4.  Genetic regulation of plasma and red blood cell magnesium concentrations in man. I. Univariate and bivariate path analyses.

Authors:  P Darlu; D C Rao; J G Henrotte; J M Lalouel
Journal:  Am J Hum Genet       Date:  1982-11       Impact factor: 11.025

5.  Magnesium transport defect with hypercalcaemia.

Authors:  H M Nutbeam; L Sinclair; V G Oberholzer
Journal:  J R Soc Med       Date:  1979-12       Impact factor: 18.000
  5 in total

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