Zobrazeno 1 - 10
of 321
pro vyhledávání: '"Primary ovarian failure"'
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
BackgroundThe causal relationship between juvenile idiopathic arthritis (JIA) and primary ovarian failure (POF) remains uncertain. To elucidate this relationship, we employed a two-sample Mendelian randomization analysis.MethodsThe single nucleotide
Externí odkaz:
https://doaj.org/article/935dc7ee66cf43b5a7d1a32102bd6d4d
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Previous studies investigating the relationship between systemic lupus erythematosus (SLE) and primary ovarian failure (POF) generated conflicting results. To data, no mendelian randomization study has been applied to examine this associatio
Externí odkaz:
https://doaj.org/article/ed4d817e0268491ab1a13ef778cedbcf
Publikováno v:
Regenerative Therapy, Vol 25, Iss , Pp 10-23 (2024)
Premature ovarian insufficiency (POI), also known as premature ovarian failure (POF), is a complex endocrine disease that commonly affects women under the age of 40. It is characterized by the cessation of ovarian function before the age of 40, leadi
Externí odkaz:
https://doaj.org/article/8001cb2176e540dfab634c578e1d75ec
Akademický článek
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Akademický článek
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Autor:
Eleonora Ferrarini, Giuseppina De Marco, Francesca Orsolini, Elena Gianetti, Elena Benelli, Franca Fruzzetti, Tommaso Simoncini, Patrizia Agretti, Massimo Tonacchera
Publikováno v:
Journal of Ovarian Research, Vol 14, Iss 1, Pp 1-8 (2021)
Abstract Background Premature ovarian insufficiency (POI) is an ovarian defect characterized by primary or secondary amenorrhea, hypergonadotropism and hypoestrogenism which occurs before the age of 40 years with a major genetic component. In this st
Externí odkaz:
https://doaj.org/article/7a78316a3fda489c8dd7b6d58d1f6846
Publikováno v:
BMC Microbiology, Vol 20, Iss 1, Pp 1-13 (2020)
Abstract Background Primary ovarian failure (POF) is defined as follicular failure in women of reproductive age. Although many factors are speculated to contribute to the occurrence of POF, the exact aetiology remains unclear. Moreover, alterations i
Externí odkaz:
https://doaj.org/article/ccec5bade2f14c158bab985a8bcbb90e
Akademický článek
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Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 15:90-96
The tRNA methyltransferase 10 homologue A (TRMT10A) gene encodes a tRNA methyl transferase, and biallelic loss of function mutations cause a recessive syndrome of intellectual disability, microcephaly, short stature and diabetes. A case with intellec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5fd8bef6b2cb355016673c18459aa46
https://doi.org/10.4274/jcrpe.galenos.2021.2021.0110
https://doi.org/10.4274/jcrpe.galenos.2021.2021.0110
Publikováno v:
Journal of Clinical and Translational Endocrinology Case Reports, Vol 17, Iss , Pp 100068- (2020)
Blepharophimosis, ptosis and epicanthus inversus syndrome (BPES) is an extremely rare genetic developmental condition, with hallmark findings of ocular malformation. It has two subtypes, both of which include the eponymous oculofacial features. Type
Externí odkaz:
https://doaj.org/article/553651f16c3948dc9a8489b23a18f33d