Zobrazeno 1 - 10
of 371
pro vyhledávání: '"GH therapy"'
Autor:
Yuki Kawashima-Sonoyama, Keisuke Wada, Kei Yamamoto, Masanobu Fujimoto, Noriyuki Namba, Takeshi Taketani
Publikováno v:
Endocrine Journal, Vol 71, Iss 7, Pp 687-694 (2024)
Short stature with IGF-1 receptor (IGF1R) gene alteration is known as small-for-gestational-age (SGA) short stature with elevated serum IGF1 levels. Its prevalence and clinical characteristics remain unclear. No adapted treatment is available for sho
Externí odkaz:
https://doaj.org/article/ae4200e683cb4784a31394e6cc26d5e8
Autor:
Domenico Corica, Fabio Toscano, Mariacarla Moleti, Giorgia Pepe, Alfredo Campenni, Guido Fadda, Gianlorenzo Dionigi, Carmelo Romeo, Tommaso Aversa, Malgorzata Wasniewska
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Thyroid nodules in children are less common than in adults but they are approximately two- to three-fold more likely to be malignant in children. Among thyroid nodular diseases, Plummer's adenoma occurs very rarely in pediatrics, and currently, there
Externí odkaz:
https://doaj.org/article/6e971353be334c3fa09ab15055dbfa95
Autor:
Silvia Ventresca, Francesca Romana Lepri, Sabrina Criscuolo, Giorgia Bottaro, Antonio Novelli, Sandro Loche, Marco Cappa
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
Silver-Russell syndrome (SRS, OMIM, 180860) is a rare genetic disorder with a wide spectrum of symptoms. The most common features are intrauterine growth retardation (IUGR), poor postnatal development, macrocephaly, triangular face, prominent forehea
Externí odkaz:
https://doaj.org/article/fe77b3818f0d4050af2e8cc70eb4b504
Autor:
Takasawa K, Mabe H, Nagamatsu F, Amano N, Miyakawa Y, Sutani A, Kagawa R, Okada S, Tanahashi Y, Suzuki S, Hiroshima S, Nagasaki K, Dateki S, Takishima S, Takahashi I, Kashimada K
Publikováno v:
Patient Preference and Adherence, Vol Volume 17, Pp 1885-1894 (2023)
Kei Takasawa,1 Hiroyo Mabe,2 Fusa Nagamatsu,2 Naoko Amano,3 Yuichi Miyakawa,4 Akito Sutani,4 Reiko Kagawa,5 Satoshi Okada,5 Yusuke Tanahashi,6 Shigeru Suzuki,6 Shota Hiroshima,7 Keisuke Nagasaki,7 Sumito Dateki,8 Shigeru Takishima,9 Ikuko Takahashi,1
Externí odkaz:
https://doaj.org/article/58e77d3d592f4b5290409b0fabc518c1
Autor:
Graziano Grugni, Alessandro Sartorio, Davide Soranna, Antonella Zambon, Lucia Grugni, Giuseppe Zampino, Antonino Crinò
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionPrader-Willi syndrome (PWS) is a complex disorder resulting from the failure of expression of paternal alleles in the PWS region of chromosome 15. The PWS phenotype resembles that observed in the classic non-PWS GH deficiency (GHD), inclu
Externí odkaz:
https://doaj.org/article/b28bdd249df54442bbba2de1422ca6a0
Autor:
Aman Bhakti Pulungan, Fabian Yap, Mei-Chyn Chao, Kah Yin Loke, Chen Yang, Tianrong Ma, Leroy Ovbude, Pen-Hua Su
Publikováno v:
Paediatrica Indonesiana, Vol 62, Iss 2, Pp 79-85 (2022)
Background Non-objective assessments indicate poor patient adherence to growth hormone (GH) prescribed for growth failure, with sub-optimal growth response. The easypod™ connect device for GH administration enables real-time, objective assessment o
Externí odkaz:
https://doaj.org/article/b6887653e95748d8a4f78587a681667b
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
The Poirier–Bienvenu neurodevelopmental syndrome is an autosomal dominant disorder characterized by intellectual disability and epilepsy. The disease is caused by mutations in the CSNK2B gene, which encodes the beta subunit of casein kinase II, and
Externí odkaz:
https://doaj.org/article/06af96648e4d45528f0dcb3ad6e0b583
Autor:
Stefano Cianfarani
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Growth hormone (GH) therapy dates back to 1958 and, though has shown an excellent safety profile in the short-term, has never ceased to raise concern about potential long-term side effects. In the last decade, a number of observational studies in dif
Externí odkaz:
https://doaj.org/article/8b6de60b19824085b0ebee638a88f091
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