Familial hypomagnesaemia with secondary hypocalcaemia — Autosomal or X-linked inheritance?-Reference-Cited by-同舟云学术

Familial hypomagnesaemia with secondary hypocalcaemia — Autosomal or X-linked inheritance?

Published:1991-05 Issue:3 Volume:14 Page:397-399
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Pronicka E.,Gruszczyńska B.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://www.springerlink.com/index/pdf/10.1007/BF01811713

Reference9 articles.

1. Abdulrazzag, U. M., Smigura, F. and Wettrell, G. Primary infantile hypomagnesaemia; report of two cases and review of literature.Eur. J. Pediatr. 148 (1989) 459–461

2. Becker, K., Lombeck, I. and Bremer, H. J. Primäre hypomagnesiämie. Klinischer Verlauf, diagnostische und therapeutische Untersuchungen bei drei Kindern.Monatsschr. Kinderheilkd. 29 (1979) 37–42

3. Garty, R., Alkalag, A. and Bernheim, J. L. Parathyroid hormone in primary hypomagnesemia.Isr. J. Med. Sci. 19 (1983) 345–348

4. Hennekam, R. C. M. and Donckerwolcke, R. A. Primary hypomagnesaemia, an autosomal recessive inherited disease?Lancet 1 (1983) 927

5. Mettey, R. and Hoppeler, A. Les déficits magnésiens de l'enfant.Arch. Fr. Pediatr. 39 (1982) 837–844

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2. REFERENCES (GAMUTS);Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

3. Physiology of epithelial Ca2+ and Mg2+ transport;Reviews of Physiology, Biochemistry and Pharmacology;2007

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