Erratum for "IGSF1 Deficiency: Lessons From an Extensive Case Series and Recommendations for Clinical Management".
出版信息
J Clin Endocrinol Metab. 2017 Jun 1;102(6):2125. doi: 10.1210/jc.2017-00903.
Abstract
摘要
相似文献
1
Erratum for "IGSF1 Deficiency: Lessons From an Extensive Case Series and Recommendations for Clinical Management".
J Clin Endocrinol Metab. 2017 Jun 1;102(6):2125. doi: 10.1210/jc.2017-00903.
2
Pituitary Hormone Secretion Profiles in IGSF1 Deficiency Syndrome.IGSF1 缺乏综合征中的垂体激素分泌谱
Neuroendocrinology. 2016;103(3-4):408-16. doi: 10.1159/000439433. Epub 2015 Aug 25.
3
Identification of an IGSF1-specific deletion in a five-generation pedigree with X-linked Central Hypothyroidism without macroorchidism.在一个五代家系中鉴定出IGSF1特异性缺失，该家系患有X连锁性中枢性甲状腺功能减退且无巨睾症。
Clin Endocrinol (Oxf). 2016 Oct;85(4):609-15. doi: 10.1111/cen.13094. Epub 2016 Jun 9.
4
Spatial and temporal expression of immunoglobulin superfamily member 1 in the rat.大鼠免疫球蛋白超家族成员1的时空表达
J Endocrinol. 2015 Sep;226(3):181-91. doi: 10.1530/JOE-15-0204. Epub 2015 Jul 10.
5
Familial Central Hypothyroidism Caused by a Novel IGSF1 Gene Mutation.由新型IGSF1基因突变引起的家族性中枢性甲状腺功能减退症
Thyroid. 2016 Dec;26(12):1693-1700. doi: 10.1089/thy.2015.0672. Epub 2016 Jul 25.
6
Mild deficits in attentional control in patients with the IGSF1 deficiency syndrome.IGSF1 缺乏综合征患者存在轻度注意力控制缺陷。
Clin Endocrinol (Oxf). 2016 Jun;84(6):896-903. doi: 10.1111/cen.12947. Epub 2015 Oct 15.
7
IGSF1 variants in boys with familial delayed puberty.患有家族性青春期延迟男孩中的IGSF1变异体
Eur J Pediatr. 2015 May;174(5):687-92. doi: 10.1007/s00431-014-2445-9. Epub 2014 Oct 30.
8
9
TRH Action Is Impaired in Pituitaries of Male IGSF1-Deficient Mice.TRH作用在雄性IGSF1缺陷小鼠的垂体中受损。
Endocrinology. 2017 Apr 1;158(4):815-830. doi: 10.1210/en.2016-1788.
10
Combined Growth Hormone and Thyroid-Stimulating Hormone Deficiency in a Japanese Patient with a Novel Frameshift Mutation in IGSF1.一名日本患者因IGSF1基因发生新型移码突变导致生长激素和促甲状腺激素联合缺乏
Horm Res Paediatr. 2015;84(5):349-54. doi: 10.1159/000438672. Epub 2015 Aug 19.
Zotero 插件