Literature DB >> 6132241

Primary hypomagnesaemia, an autosomal recessive inherited disease?

R C Hennekam, R A Donckerwolcke.   

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Year:  1983        PMID： 6132241     DOI： 10.1016/s0140-6736(83)91352-1

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  5 in total

1.  Familial hypomagnesaemia with secondary hypocalcaemia--autosomal or X-linked inheritance?

Authors:  E Pronicka; B Gruszczyńska
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

2.  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

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.  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

5.  Long-term follow-up of a patient with primary hypomagnesaemia and secondary hypocalcaemia due to a novel TRPM6 mutation.

Authors:  Dolors Esteban-Oliva; Guillem Pintos-Morell; Martin Konrad
Journal:  Eur J Pediatr       Date:  2008-06-12       Impact factor: 3.183
  5 in total

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