Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Rodolfo A. Rey"'
Autor:
Lourdes Correa Brito, Ana Keselman, Florencia Villegas, Paula Scaglia, María Esnaola Azcoiti, Sebastián Castro, Nora Sanguineti, Agustín Izquierdo, Marianela Maier, Ignacio Bergadá, Claudia Arberas, Rodolfo A. Rey, María Gabriela Ropelato
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Pubertal delay can be due to hypogonadotropic hypogonadism (HH), which may occur in association with anosmia or hyposmia and is known as Kallmann syndrome (OMIM #308700). Recently, hypogonadotropic hypogonadism has been suggested to overlap with Witt
Externí odkaz:
https://doaj.org/article/5ca50093384a43658714a0fd86450d05
Autor:
Rodolfo A. Rey, Romina P. Grinspon
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
Anti-Müllerian hormone (AMH) is a Sertoli cell-secreted glycoprotein involved in male fetal sex differentiation: it provokes the regression of Müllerian ducts, which otherwise give rise to the Fallopian tubes, the uterus and the upper part of the v
Externí odkaz:
https://doaj.org/article/a659135c2c3c47b6876c439a1fdb2f98
Autor:
Jimena Lopez Dacal, Silvina Prada, Lourdes Correa Brito, Maria Gabriela Ropelato, Maria Gabriela Ballerini, Maria Eugenia Rodriguez, Marcela E. Gutiérrez, Marcela Soria, Lorena Morán, Cristina Ferraro, Patricia Bedecarrás, Guillermo Drelichman, Luis Aversa, Ignacio Bergadá, Rodolfo A. Rey, Romina P. Grinspon
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionHematopoietic malignancies are the most frequent type of cancer in childhood. Recent advances in cancer treatment have significantly improved survival until adulthood. There is an extensive literature on the effects of cancer treatment on
Externí odkaz:
https://doaj.org/article/90fd11805aba42bdbb3919b3b1f997db
Autor:
Rodolfo A. Rey
Publikováno v:
Biomedicine Hub, Vol 7, Iss 1, Pp 48-53 (2022)
Externí odkaz:
https://doaj.org/article/2020ba4c814a4064a29ef643911f59ad
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/24137181b4d946039db5b1041e8318b0
Autor:
Sebastián Castro, Franco G. Brunello, Gabriela Sansó, Paula Scaglia, María Esnaola Azcoiti, Agustín Izquierdo, Florencia Villegas, Ignacio Bergadá, María Gabriela Ropelato, Marcelo A. Martí, Rodolfo A. Rey, Romina P. Grinspon
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Pubertal delay in males is frequently due to constitutional delay of growth and puberty, but pathologic hypogonadism should be considered. After general illnesses and primary testicular failure are ruled out, the main differential diagnosis is centra
Externí odkaz:
https://doaj.org/article/ccc7fd59ba5648a2a4803ec51b501e54
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Anti-Müllerian hormone (AMH) is a distinctive biomarker of the immature Sertoli cell. AMH expression, triggered by specific transcription factors upon fetal Sertoli cells differentiation independently of gonadotropins or sex steroids, drives Müller
Externí odkaz:
https://doaj.org/article/0f5666b8be134d18a373831f3ea7a925
Autor:
Rodolfo A. Rey
Publikováno v:
Therapeutic Advances in Endocrinology and Metabolism, Vol 13 (2022)
Clinical manifestations and the need for treatment varies according to age in males with hypogonadism. Early foetal-onset hypogonadism results in disorders of sex development (DSD) presenting with undervirilised genitalia whereas hypogonadism establi
Externí odkaz:
https://doaj.org/article/f85f4e7b790d4ee9b5badf76a7f15831
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Disorders of Sex Development (DSD) are anomalies occurring in the process of fetal sexual differentiation that result in a discordance between the chromosomal sex and the sex of the gonads and/or the internal and/or external genitalia. Congenital dis
Externí odkaz:
https://doaj.org/article/4c62dcad96aa4280abb2400af8cf0820
Publikováno v:
Biomedicines, Vol 10, Iss 10, p 2506 (2022)
This article reviews the main findings on anti-Müllerian hormone (AMH) and its involvement in the pathogenesis of polycystic ovary syndrome (PCOS) and its male equivalent. In women, AMH is produced by granulosa cells from the mid-fetal life to menop
Externí odkaz:
https://doaj.org/article/a7fbd53ba12249b5aa37384a3296fda8