Literature DB >> 1770801

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

E Pronicka1, B Gruszczyńska.   

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Year:  1991        PMID： 1770801     DOI： 10.1007/bf01811713

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  7 in total

Review 1.  Gene mapping of mineral metabolic disorders.

Authors:  R V Thakker; K E Davies; J L O'Riordan
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

2.  Primary infantile hypomagnesaemia; report of two cases and review of literature.

Authors:  Y M Abdulrazzaq; F C Smigura; G Wettrell
Journal:  Eur J Pediatr       Date:  1989-02       Impact factor: 3.183

3.  Primary hypomagnesaemia, an X-borne allele?

Authors:  A S Teebi
Journal:  Lancet       Date:  1983-03-26       Impact factor: 79.321

4.  Primary hypomagnesaemia, an autosomal recessive inherited disease?

Authors:  R C Hennekam; R A Donckerwolcke
Journal:  Lancet       Date:  1983-04-23       Impact factor: 79.321

Review 5.  [Magnesium deficiency in children].

Authors:  R Mettey; A Hoppeler
Journal:  Arch Fr Pediatr       Date:  1982-12

6.  Parathyroid hormone secretion and responsiveness to parathyroid hormone in primary hypomagnesemia.

Authors:  R Garty; A Alkalay; J L Bernheim
Journal:  Isr J Med Sci       Date:  1983-04

7.  [Primary hypomagnesemia. Clinical, diagnostic and therapeutic studies in three children (author's transl)].

Authors:  K Becker; I Lombeck; H J Bremer
Journal:  Monatsschr Kinderheilkd       Date:  1979-01
  7 in total

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