Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Congenital Growth Hormone Deficiency"'
Publikováno v:
Clinical Endocrinology. 94:392-398
Background Random growth hormone (GH) levels have been used in the neonate to investigate congenital growth hormone deficiency (GHD). The cut-off value for use in this diagnosis is yet to be established. Methods This is a retrospective chart review o
Autor:
Rafael Loch Batista, Valéria Aparecida Costa Hong, Ivo J.P. Arnhold, Luiz Aparecido Bortolotto, Isabela Peixoto Biscotto, Luciani R. Carvalho, Berenice B. Mendonca
Publikováno v:
Pituitary. 24:216-228
To evaluated the metabolic profiles and vascular properties in congenital growth hormone (GH) deficiency (GHD) and its replacement in adults. Cross-sectional study conducted in a single tertiary center for pituitary diseases. Eighty-one adult subject
Autor:
Chenxi Yu, Bobo Xie, Zhengye Zhao, Sen Zhao, Lian Liu, Xi Cheng, Xiaoxin Li, Bingyan Cao, Jiashen Shao, Jiajia Chen, Hengqiang Zhao, Zihui Yan, Chang Su, Yuchen Niu, Yanning Song, Liya Wei, Yi Wang, Xiaoya Ren, Lijun Fan, Beibei Zhang, Chuan Li, Baoheng Gui, Yuanqiang Zhang, Lianlei Wang, Shaoke Chen, Jianguo Zhang, Zhihong Wu, Chunxiu Gong, Xin Fan, Nan Wu
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Frontiers in Endocrinology
Frontiers in Endocrinology
PurposeCongenital growth hormone deficiency (GHD) is a rare and etiologically heterogeneous disease. We aim to screen disease-causing mutations of GHD in a relatively sizable cohort and discover underlying mechanisms via a candidate gene-based mutati
Autor:
Anshul Kumar, Rahul Sahlot, Himanshu Sharma, Umesh Garg, Naincy Purwar, Sandeep Kumar Mathur, Balram Sharma
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEMReferences. 34(7)
Objectives Congenital idiopathic growth hormone deficiency (GHD) is associated with various MRI abnormalities, including sellar and extrasellar abnormalities. However, it remains contentious whether MRI brain findings could provide an additional aven
Publikováno v:
Clinical endocrinologyREFERENCES. 94(4)
Objective: Growth hormone deficiency (GHD) is usually treated with recombinant human GH (rhGH), and this has been rarely associated with hip disorders. We analysed the clinical data of patients with congenital GHD receiving rhGH who had associated hi
Publikováno v:
American Journal of Medical Genetics Part A. 173:2261-2267
Congenital growth hormone deficiency is a rare disorder with an incidence of approximately 1 in 4,000 live births. Pituitary development is under the control of a multitude of spatiotemporally regulated signaling molecules and transcription factors.
Publikováno v:
Journal of the Endocrine Society
Growth hormone deficiency (GHD) is the commonest pituitary hormone deficiency and may require treatment with recombinant human GH (rhGH) for a variable period, ranging from a few years to lifelong. In this respect, surveillance for the long-term side
Autor:
Sandeep Kumar Mathur, Himanshu Sharma, Naincy Purwar, Anshul Kumar, Balram Sharma, Nitish Mathur
Publikováno v:
Journal of the Endocrine Society. 5:A683-A683
Background and Objectives: Congenital idiopathic growth hormone deficiency(GHD) is associated with various MRI abnormalities, including both sellar anomalies such as pituitary hypoplasia, ectopic pituitary, empty sella and abnormalities of the pituit
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Akademický článek
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