Growth-hormone deficiency in mitochondrial disorders

被引：2
|
作者：
Finsterer, Josef [1 ]
Frank, Marlies [2 ]
机构：
[1] Krankenanstalt Rudolfstiftung Wien, Postfach 20, A-1180 Vienna, Austria
[2] Krankenanstalt Rudolfstiftung Wien, Med Dept 1, Vienna, Austria
来源：
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | 2017年 / 30卷 / 04期
关键词：
epilepsy; gene; Leigh syndrome; MELAS; mitochondrial disorder; mtDNA; seizures; stroke; stroke-like episode; stroke-like lesion; KEARNS-SAYRE-SYNDROME; DNA DELETION; DIABETES-MELLITUS; PEARSON-SYNDROME; MELAS SYNDROME; PATIENT; CYTOPATHY; MUTATION; ACIDOSIS; THERAPY;
D O I：
10.1515/jpem-2016-0418
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：479 / 481
页数：3
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