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Laron-type dwarfism (hereditary somatomedin deficiency): a review.

作者信息

Laron Z

出版信息

Ergeb Inn Med Kinderheilkd. 1984;51:117-50. doi: 10.1007/978-3-642-69070-9_3.

DOI:10.1007/978-3-642-69070-9_3
PMID:6317375
Abstract
摘要

相似文献

1
Laron-type dwarfism (hereditary somatomedin deficiency): a review.
Ergeb Inn Med Kinderheilkd. 1984;51:117-50. doi: 10.1007/978-3-642-69070-9_3.
2
[Severe dwarfism with high plasma hGH levels and no somatomedin acitvity: Laron's syndrome (author's transl)].严重侏儒症伴高血浆人生长激素水平且无生长调节素活性:拉龙综合征(作者译)
Sem Hop. 1980;56(43-44):1853-6.
3
Deficiencies of growth hormone and somatomedins in man.
Spec Top Endocrinol Metab. 1983;5:149-99.
4
[Nanism with high values of GH and no generation of somatomedin after hGH (Laron's syndrome). Clinico-biochemical study of 8 cases].[生长激素水平高但生长激素释放激素(hGH)后未产生生长调节素的侏儒症(拉伦综合征)。8例临床生化研究]
An Esp Pediatr. 1985 Feb;22(2):113-22.
5
Genetic pituitary dwarfism with high serum concentation of growth hormone--a new inborn error of metabolism?伴有高血清生长激素浓度的遗传性垂体性侏儒症——一种新的先天性代谢紊乱?
Isr J Med Sci. 1966 Mar-Apr;2(2):152-5.
6
Pituitary dwarfism with high serum levels of growth hormone.
Isr J Med Sci. 1968 Jul-Aug;4(4):883-94.
7
Defect of human growth hormone receptors in the liver of two patients with Laron-type dwarfism.两名拉伦氏侏儒症患者肝脏中人类生长激素受体的缺陷。
Isr J Med Sci. 1984 Jan;20(1):8-11.
8
Pseudohypopituitary dwarfism with normal plasma growth hormone and low serum sulfation factor.血浆生长激素正常但血清硫酸化因子水平低的假性垂体性侏儒症
J Pediatr. 1972 Apr;80(4):620-6. doi: 10.1016/s0022-3476(72)80059-3.
9
[Activity of blood somatomedin during childhood in normal subjects and in delayed growth].
Ann Biol Clin (Paris). 1976;34(1):11-8.
10
Current concepts of somatomedin and other biologically related growth factors.生长调节素及其他生物学相关生长因子的当前概念。
Diabetes. 1976 Oct;25(10):994-1004. doi: 10.2337/diab.25.10.994.

引用本文的文献

1
Disabilities and Handicaps of Patients with Laron Syndrome.拉龙综合征患者的残疾与障碍
Children (Basel). 2025 Sep 22;12(9):1271. doi: 10.3390/children12091271.
2
Branding of subjects affected with genetic syndromes of severe short stature in developing countries.发展中国家患有严重身材矮小遗传综合征患者的特征描述
BMJ Case Rep. 2020 Feb 9;13(2):e231737. doi: 10.1136/bcr-2019-231737.
3
Growth Hormone and Insulin-Like Growth Factor Action in Reproductive Tissues.生长激素和胰岛素样生长因子在生殖组织中的作用
Front Endocrinol (Lausanne). 2019 Nov 12;10:777. doi: 10.3389/fendo.2019.00777. eCollection 2019.
4
Recombinant Human Insulin-Like Growth Factor-1 Treatment: Prime Time or Timeout? [Commentary on "Recombinant Human Insulin Like Growth Factor-1 Treatment: Ready for Prime Time" by Bright GM, Mendoza JR, Rosenfeld RG, Endocrinol Metab Clin N Am 2009; 38:625-38].重组人生长激素-1治疗:黄金时机还是暂停?[对Bright GM、Mendoza JR、Rosenfeld RG所著《重组人生长激素-1治疗:准备进入黄金时期》的评论,发表于《北美内分泌与代谢临床》2009年;38:625 - 38]
Int J Pediatr Endocrinol. 2009;2009:429684. doi: 10.1155/2009/429684. Epub 2010 Feb 8.
5
Laron syndrome abnormalities: spinal stenosis, os odontoideum, degenerative changes of the atlanto-odontoid joint, and small oropharynx.拉伦综合征异常表现:椎管狭窄、齿突骨、寰枢关节退变以及小咽腔。
AJNR Am J Neuroradiol. 2002 Apr;23(4):625-31.
6
Insulin-like growth factor 1 (IGF-1): a growth hormone.胰岛素样生长因子1(IGF-1):一种生长激素。
Mol Pathol. 2001 Oct;54(5):311-6. doi: 10.1136/mp.54.5.311.
7
Growth hormone: roles in male reproduction.生长激素:在男性生殖中的作用。
Endocrine. 2000 Dec;13(3):243-50. doi: 10.1385/ENDO:13:3:243.
8
Renal function in Laron syndrome patients treated by insulin-like growth factor-I.
Pediatr Nephrol. 1994 Dec;8(6):684-8. doi: 10.1007/BF00869089.
9
Somatomedin-1 (insulin-like growth factor-I) in clinical use. Facts and potential.临床应用中的生长调节素-1(胰岛素样生长因子-I)。事实与潜力。
Drugs. 1993 Jan;45(1):1-8. doi: 10.2165/00003495-199345010-00001.
10
Structural and functional characterization of the human T lymphocyte receptor for insulin-like growth factor I in vitro.人胰岛素样生长因子I T淋巴细胞受体的体外结构与功能特性研究
J Clin Invest. 1988 Sep;82(3):950-7. doi: 10.1172/JCI113703.