FAMILIAL HYPOMAGNESEMIA WITH SECONDARY HYPOCALCEMIA - AUTOSOMAL OR X-LINKED INHERITANCE

被引：14

作者：

PRONICKA, E

GRUSZCZYNSKA, B

机构：

[1] Department of Metabolic Diseases, Memorial Child Health Centre, Warsaw

来源：

关键词：

D O I：

10.1007/BF01811713

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：397 / 399

页数：3

共 9 条

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WETTRELL, G
[J]. EUROPEAN JOURNAL OF PEDIATRICS, 1989, 148 (05) : 459 - 461
[2] BECKER K, 1979, MONATSSCHR KINDERH, V29, P37
[3] GARTY R, 1983, ISRAEL J MED SCI, V19, P345
[4] HENNEKAM RCM, 1983, LANCET, V1, P927
[5] METTEY R, 1982, ARCH FR PEDIATR, V39, P837
[6] MEYER M, 1978, REV FR ENDOCRINOL CL, V19, P101
[7] SALET J, 1966, ARCH FR PEDIATR, V23, P749
[8] TEEBI AS, 1983, LANCET, V1, P701
[9] GENE-MAPPING OF MINERAL METABOLIC DISORDERS
THAKKER, RV
DAVIES, KE
ORIORDAN, JLH
[J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1989, 12 : 231 - 246