Zobrazeno 1 - 10
of 14 334
pro vyhledávání: '"hormone deficiency"'
Autor:
Akhtar S, Berg B, Medina J, Gonczi MN, Hamilton S, Hildebrand E, Kelepouris N, Neergaard JS, Sværke C, Ter-Borch G, Rasmussen NK
Publikováno v:
Medical Devices: Evidence and Research, Vol Volume 17, Pp 427-439 (2024)
Shahid Akhtar,1 Birgitte Berg,2 Johan Medina,3 Maya Nicole Gonczi,4 Sophie Hamilton,5 Emily Hildebrand,4 Nicky Kelepouris,6 Jesper Skov Neergaard,7 Claus Sværke,8 Gitte Ter-Borch,2 Niklas Kahr Rasmussen3 1Devices & Digital Health, Novo Nordisk A/S,
Externí odkaz:
https://doaj.org/article/6a5c5a7dfa7a42059cd6600944db9b4b
Autor:
Lukas Plachy, Petra Dusatkova, Klara Maratova, Shenali Anne Amaratunga, Dana Zemkova, Vit Neuman, Stanislava Kolouskova, Barbora Obermannova, Marta Snajderova, Zdenek Sumnik, Jan Lebl, Stepanka Pruhova
Publikováno v:
Endocrine Connections, Vol 13, Iss 10, Pp 1-8 (2024)
Because the causes of combined pituitary hormone deficiency (CPHD) are complex, the etiology of congenital CPHD remains unknown in most cases. The aim of the study was to identify the genetic etiology of CPHD in a well-defined single-center cohort. I
Externí odkaz:
https://doaj.org/article/bd019d5695e14abdacc13ff0b6d850ca
Publikováno v:
Endocrines, Vol 5, Iss 3, Pp 341-353 (2024)
Growth hormone deficiency (GHD) is the most frequent pituitary hormone deficiency in childhood, with an incidence of 1 in 4000–10,000 live births. GHD can be congenital (genetic or due to hypothalamic/pituitary abnormalities) or acquired and can be
Externí odkaz:
https://doaj.org/article/50c95fa1d5504c9ea8e0a3aed78832ff
Publikováno v:
Caspian Journal of Internal Medicine, Vol 15, Iss 4, Pp 570-578 (2024)
Background: In Permanent congenital hypothyroidism (PCH) is a lifelong condition characterized by a deficiency in thyroid hormone, leading to various neurodevelopmental complications. Early clinical signs are often nonspecific and easily overlooked,
Externí odkaz:
https://doaj.org/article/440680e863f14e8caeb3ddd2e5f86739
Altered individual-level morphological similarity network in children with growth hormone deficiency
Autor:
Yanglei Cheng, Liping Lin, Weifeng Hou, Huaqiong Qiu, Chengfen Deng, Zi Yan, Long Qian, Wei Cui, Yanbing Li, Zhiyun Yang, Qiuli Chen, Shu Su
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 16, Iss 1, Pp 1-13 (2024)
Abstract Background Accumulating evidences indicate regional grey matter (GM) morphology alterations in pediatric growth hormone deficiency (GHD); however, large-scale morphological brain networks (MBNs) undergo these patients remains unclear. Object
Externí odkaz:
https://doaj.org/article/9c48c35222ef49bca086993f7b41e459
Publikováno v:
Zdorovʹe Rebenka, Vol 19, Iss 4, Pp 190-194 (2024)
Background. The significance of this study lies in the fact that short stature is highly prevalent among children, affecting 1–5 % of the population and having diverse causes. The child’s growth potential in the long term is largely depends on
Externí odkaz:
https://doaj.org/article/7aa51911615747fa8183950c0475cfca
Autor:
Gülsüm Yitik Tonkaz, Atilla Çayır
Publikováno v:
JCRPE, Vol 16, Iss 2, Pp 177-184 (2024)
INTRODUCTION: The aim of this study was to evaluate executive function (EF), such as inhibition and working memory, in children with isolated growth hormone deficiency (IGHD) using performance-based tests and parent-report scales. METHODS: A total o
Externí odkaz:
https://doaj.org/article/e8ed5c6eb2894ea280d8cc36f961b5c5
Autor:
Patricia García Navas, María Yolanda Ruíz del Prado, Pablo Villoslada Blanco, Emma Recio Fernández, María Ruíz del Campo, Patricia Pérez Matute
Publikováno v:
Anales de Pediatría, Vol 100, Iss 6, Pp 404-411 (2024)
Resumen: Introducción: La hormona de crecimiento (GH) y el factor de crecimiento similar a la insulina tipo 1 (IGF-1) tienen efecto modulador sobre la funcionalidad intestinal y la microbiota. Nuestro objetivo fue investigar si los pacientes con dé
Externí odkaz:
https://doaj.org/article/8e4c1867a4f14d609d304e84e9bbb31f
Autor:
Xiaozhen Huang, Hong Chen, Huakun Shangguan, Wenyong Wu, Zhuanzhuan Ai, Zhifeng Chen, Ruimin Chen
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
BackgroundIsolated growth hormone deficiency type II (IGHD II) is an autosomal dominant disorder characterized by a GH1 gene variant resulting in a significant reduction in growth hormone (GH) secretion and a subsequent decrease of plasma insulin-lik
Externí odkaz:
https://doaj.org/article/48b49923f03845f89fd8209d571ba1a4