Zobrazeno 1 - 10
of 1 092
pro vyhledávání: '"hypergonadotropic hypogonadism"'
Publikováno v:
European Journal of Case Reports in Internal Medicine (2024)
We report a case of primary hypogonadism induced by amiodarone and review the relevant literature. Amiodarone has a well-established and extensive profile of side effects including thyroid toxicity, corneal deposits and skin discoloration. In rare ca
Externí odkaz:
https://doaj.org/article/117543564ba94eeb82334d49adda9bcd
Autor:
Romana Chowdhury, Mohammad Azmain Iktidar, Mushfiq Newaz Ahmed, Mohammad Mehedi Hasan, Md. Mazharul Hoque Tapan, Sheikh Saiful Islam Shaheen, Atiar Rahman, Ayesha Khatun
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss 3, Pp 350-357 (2023)
Introduction: Hypogonadism is one of the most frequent complications in transfusion-dependent thalassemia patients and early recognition and treatment is the core element in restoring impaired gonadal function. Despite the high burden of disease, rel
Externí odkaz:
https://doaj.org/article/2b828e9c8dc34775a0d2c6858c6eae59
Autor:
Letizia Canu, Clotilde Sparano, Lara Naletto, Giuseppina De Filpo, Giulia Cantini, Elena Rapizzi, Serena Martinelli, Tonino Ercolino, Francesca Cioppi, Alessandro Fantoni, Lorenzo Zanatta, Alessandro Terreni, Massimo Mannelli, Michaela Luconi, Mario Maggi, Francesco Lotti
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2024)
PurposeAdrenocortical carcinoma (ACC) is a rare and aggressive tumor. ACC male patients under adjuvant mitotane therapy (AMT) frequently develop hypogonadism, however sexual function has never been assessed in this setting. The aim of this retrospect
Externí odkaz:
https://doaj.org/article/c80ae0ff8c364ee99c9961898ea05a70
Autor:
Tarik Elhadd, Ahmad Majzoub, Charlotte Wilson, Laura McCreight, Muna S. Mohamed, Fiona C. Green, Andrew J. Collier
Publikováno v:
BMC Endocrine Disorders, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Background Hypogonadism in older men is often considered as late onset hypogonadism. However, this clinical condition results from primary testicular failure which could be of genetic origin with Klinefelter syndrome being the most common ch
Externí odkaz:
https://doaj.org/article/6b70206e095b4b68a35067825e456c0b
Autor:
Giulio Frontino, Raffaella Di Tonno, Marianna Rita Stancampiano, Francesca Arrigoni, Andrea Rigamonti, Elisa Morotti, Daniele Canarutto, Riccardo Bonfanti, Gianni Russo, Graziano Barera, Lorenzo Piemonti
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
AimsWolfram Syndrome Spectrum Disorder (WFS1-SD), in its “classic” form, is a rare autosomal recessive disease with poor prognosis and wide phenotypic spectrum. Insulin dependent diabetes mellitus (DM), optic atrophy (OA) diabetes insipidus (DI)
Externí odkaz:
https://doaj.org/article/7ef22ef30a0c4d089676d73777b582f9
Publikováno v:
African Journal of Urology, Vol 27, Iss 1, Pp 1-4 (2021)
Abstract Background Male sex reversal syndrome is a rare genetic cause of male infertility with an overall incidence of 1/20,000–1/100,000 males. There is mismatching between the genetic make-up and the apparent clinical features. The clinical pres
Externí odkaz:
https://doaj.org/article/b4c60ad344b0400cb392532cf2e8e332
Publikováno v:
Репродуктивная эндокринология, Vol 0, Iss 53, Pp 87-93 (2020)
Despite the relatively small portion in the structure of the infertility causes, hypergonadotropic hypogonadism (HH) is one of the greatest challenges in reproductive medicine. Diagnosis of HH chromosomal causes often occurs with a significant delay.
Externí odkaz:
https://doaj.org/article/425f5514d4134b27a334c32cb8ca04bc
Autor:
Rey Rodolfo A.
Publikováno v:
Advances in Laboratory Medicine, Vol 1, Iss 2, Pp 879-90 (2020)
Externí odkaz:
https://doaj.org/article/b804a5a402cd419aaca93cfee88fe63a
Autor:
Diego Yeste, Maria Irene Valenzuela, Rosangela Tomasini, Maria Grazia Clemente, Paula Fernández-Alvarez, Laura Sayol-Torres
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 15:205-209
Prolyl endopeptidase-like (PREPL) deficiency (MIM#616224) is a rare congenital disorder characterised by neonatal hypotonia and feeding difficulties, growth hormone (GH) deficiency and hypergonadotropic hypogonadism. This syndrome is an autosomal rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5be43545fa75479ea7707216e62eec31
https://doi.org/10.4274/jcrpe.galenos.2021.2021.0128
https://doi.org/10.4274/jcrpe.galenos.2021.2021.0128
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.