Familial hyperzincaemia: a rare entity.

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作者信息

Selimoglu M A, Ertekin V, Yildirim Z K, Altinkaynak S

出版信息

Int J Clin Pract. 2006 Jan;60(1):108-9. doi: 10.1111/j.1368-5031.2005.00684.x.

DOI:10.1111/j.1368-5031.2005.00684.x

PMID:16409438

Abstract

摘要

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Familial hyperzincaemia: a rare entity.

Int J Clin Pract. 2006 Jan;60(1):108-9. doi: 10.1111/j.1368-5031.2005.00684.x.

Effects of cyclosporine A in hyperzincaemia and hypercalprotectinaemia.

Acta Paediatr. 2006 Jul;95(7):857-60. doi: 10.1080/08035250500482255.

Disorders of mineral metabolism.

Clin Gastroenterol. 1982 Jan;11(1):87-117.

[Familial hypomagnesemia in a girl].

Pediatr Pol. 1980 Sep;55(9):1083-6.

[Iron overload in hereditary atransferrinemia].

Bol Med Hosp Infant Mex. 1986 Feb;43(2):99-101.

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

J Inherit Metab Dis. 1991;14(3):397-9. doi: 10.1007/BF01811713.

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An Esp Pediatr. 1999 Dec;51(6):723-5.

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Science. 1976 Aug 6;193(4252):496-8. doi: 10.1126/science.941021.

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Eur J Neurol. 2001 Sep;8(5):495-9. doi: 10.1046/j.1468-1331.2001.00274.x.

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Ann Clin Lab Sci. 1999 Jan-Mar;29(1):24-32.

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