Cristiane Kopacek Zilz,Juliana Keller Brenner,Regina Helena Elnecave
Cristiane Kopacek Zilz
Backgrounds/aims: Turner syndrome is not usually associated with thrombotic events. The aim of this study is to report 3 Turner syndrome patients with portal vein thrombosis and, in 2 of them, high factor VIII. These find...
Case Reports
Hormone research. 2006;66(2):89-93. DOI:10.1159/000093693 2006
Obestatin, acylated and total ghrelin concentrations in the perinatal rat pancreas [0.03%]
大鼠围产期胰腺中obestatin、酰化和总ghrelin的浓度
Jean-Pierre Chanoine,Alfred C K Wong,Vicente Barrios
Jean-Pierre Chanoine
Background: Ghrelin and obestatin are encoded by the preproghrelin gene and originate from posttranslational processing of the preproghrelin peptide. The fetal rat pancreas contains acylated and desacylated ghrelin peptid...
Congenital hyperreninemic hypoaldosteronism: are there different forms? [0.03%]
先天性肾素过高皮质醇过低血症：有不同类型吗？
Michael Peter
Michael Peter
Congenital hyperreninemic hypoaldosteronism in Israel: sequence analysis of CYP11B2 gene [0.03%]
以色列先天性肾素过高皮质醇合成酶缺乏症患者的CYP11B2基因序列分析
Esther Leshinsky-Silver,Zohar Landau,Sema Unlubay et al.
Esther Leshinsky-Silver et al.
Background/aims: Isolated aldosterone biosynthesis defect causing congenital hyperreninemic hypoaldosteronism with otherwise normal adrenal function usually results from aldosterone synthase deficiency. Patients present w...
Case Reports
Hormone research. 2006;66(2):73-8. DOI:10.1159/000093583 2006
Use of the low-dose corticotropin stimulation test for the monitoring of children with asthma treated with inhaled corticosteroids [0.03%]
低剂量促肾上腺皮质激素刺激试验用于监测吸入型糖皮质激素治疗的哮喘儿童的应用
M C Raux Demay,J P Magny,N Idrès et al.
M C Raux Demay et al.
Objective: Subnormal hypothalamic-pituitary-adrenal (HPA) function and rare cases of adrenal crisis have been reported in asthmatic children treated with inhaled corticosteroids. We investigated subnormal HPA activity and...
Controlled Clinical Trial
Hormone research. 2006;66(2):51-60. DOI:10.1159/000093468 2006
Karine Clément
Karine Clément
A two-base deletion -439delGC in the melanocortin-4 receptor promoter associated with early-onset obesity [0.03%]
与早发性肥胖相关的色素类皮质素受体-4启动子-439delGC双核苷酸缺失变异
Kaisa Valli-Jaakola,Jorma J Palvimo,Marita Lipsanen-Nyman et al.
Kaisa Valli-Jaakola et al.
Background/aims: Mutations in melanocortin-4 receptor (MC4R) are the most common genetic cause of human obesity. Mutations in MC4R promoter could also underlie obesity, but have so far not been reported. Transcription fac...
Case Reports
Hormone research. 2006;66(2):61-9. DOI:10.1159/000093469 2006
Mansour Siavash Dastjerdi,Mahin Hashemipour,Hasan Rezvanian et al.
Mansour Siavash Dastjerdi et al.
Background: Iodine deficiency produces the spectrum of iodine deficiency disorders (IDDs): endemic goiter, hypothyroidism, cretinism, and congenital anomalies. Other factors, including goitrogens and micronutrient deficie...
Fluorine-18 L-3,4-dihydroxyphenylalanine positron emission tomography: improving surgery and outcome in focal hyperinsulinism. Commentary to Mohnike et al.: Proposal for a standardized protocol for F-DOPA-PET (PET/CT) in congenital hyperinsulinism (Horm Res 2006;66:40-42) [0.03%]
18F-FDOPA PET（PET/CT）在先天性高胰岛素血症局灶性病变中的应用：评Mohnike等人的文章及高胰岛素血症中18F-FDOPA-PET（PET/CT）标准化方案的建议
Julian P H Shield
Julian P H Shield
Proposal for a standardized protocol for 18F-DOPA-PET (PET/CT) in congenital hyperinsulinism [0.03%]
关于先天性高胰岛素血症18F-DOPA-PET（PET/CT）的标准化方案建议
K Mohnike,O Blankenstein,H T Christesen et al.
K Mohnike et al.