Výsledky vyhledávání - "Precocious pubarche"

Akademický článek

Differences in hormonal levels between heterozygous CYP21A2 pathogenic variant carriers, non-carriers, and females with non-classic congenital hyperplasia

Autor: Rita Santos Silva, Berta Carvalho, Jorge Pedro, Cíntia Castro-Correia, Davide Carvalho, Filipa Carvalho, Manuel Fontoura

Publikováno v: Archives of Endocrinology and Metabolism, Vol 66, Iss 2, Pp 168-175 (2022)

ABSTRACT Objective: CYP21A2 mutation heterozygote carriers seem to have an increased risk of hyperandrogenism. However, the clinical relevance of the heterozygote carrier status and the reliability of hormonal testing in discriminating a carrier from

Externí odkaz: https://doaj.org/article/e54a369761f94b82b21abaf1fbcd0947

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Effects of half-dose spiomet treatment in girls with early puberty and accelerated bone maturation: a multicenter, randomized, placebo-controlled study protocol

Autor: Judit Bassols, Francis de Zegher, Marta Diaz, Gemma Carreras-Badosa, Cristina Garcia-Beltran, Elsa Puerto-Carranza, Cora Oliver-Vila, Paula Casano, Céline Alicia Franco, Rita Malpique, Abel López-Bermejo, Lourdes Ibáñez

Publikováno v: Trials. 24

Background A “mismatch” sequence of less prenatal weight gain and more postnatal weight gain may lead to ectopic lipid accumulation, and trigger the development of early adrenarche/pubarche and the activation of the gonadotropic axis resulting in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6b122dff22addc2882e6bb845a9fbef
https://doi.org/10.1186/s13063-022-07050-w

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Akademický článek

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Akademický článek

NON CLASSIC 21 HYDROXYLASE DEFICIENT ADRENAL HYPERPLASIA IN PATIENTS WITH ISOLATED PRECOCIOUS PUBARCHE

Autor: H. Moayeri, A. Rabbani

Publikováno v: Acta Medica Iranica, Vol 41, Iss 3, Pp 171-174 (2003)

Precocious Pubarche (PP) is most often a benign condition secondary to the early appearance of adrenarche. However, PP may be a manifestation of mild errors of steroidogenesis in particular non classic 21 hydroxylase deficiency (NC210HD). The inciden

Externí odkaz: https://doaj.org/article/e6ee46c18ec940a0b7878330945ba335

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Nutritional, Gastrointestinal and Endo-Metabolic Traps in the Management of Children with Spinal Muscular Atrophy Type 1

Autor: Anna Mandelli, Dario Dilillo, Ruggiero Francavilla, Antonio Corsello, Valeria Calcaterra, V. Fabiano, Annalisa Govoni, Gloria Pelizzo, Elena Zoia, Sara Vizzuso, Alessandra Bosetti, Gian Vincenzo Zuccotti, Flavia Indrio, Lorenzo Scatigno, Elvira Verduci, Martina Pascuzzi

The management of patients with spinal muscular atrophy type 1 (SMA1) is constantly evolving. In just a few decades the medical approach has switched from an exclusively palliative therapy to a targeted therapy, transforming the natural history of th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ae5d083a87b4b4a5278fe7505ba3511

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Clinical and biochemical signs of polycystic ovary syndrome in young women born preterm

Autor: Marja Vääräsmäki, Hanna-Maria Matinolli, Marika Paalanne, Marjaana Tikanmäki, Marjo-Riitta Järvelin, Laure Morin-Papunen, Sanna Mustaniemi, Eero Kajantie, Karoliina Wehkalampi, Johan G. Eriksson

Publikováno v: European Journal of Endocrinology

Objective It has been suggested that adverse early life exposures increase the risk of developing polycystic ovary syndrome (PCOS) in later life. We hypothesized that women born preterm would have more biochemical and clinical signs of PCOS than wome

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a889c9d593176011ee80f5ccbf3b621d
https://pubmed.ncbi.nlm.nih.gov/34081616

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Cardiometabolic risk profile among young adult females with a history of premature adrenarche

Autor: Liimatta, Jani, Utriainen, Pauliina, Laitinen, Tomi, Voutilainen, Raimo, Jääskeläinen, Jarmo

Context: Premature adrenarche (PA) is associated with childhood overweight and hyperinsulinemia; the long-term cardiometabolic outcome is unknown. Objective: To study cardiometabolic profile in adult women with previous PA. Design and participants: T

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1593::6343ec5d4fd36d98c1de1bec5820cee2
http://hdl.handle.net/10138/327621

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Nutritional, Gastrointestinal and Endo-Metabolic Challenges in the Management of Children with Spinal Muscular Atrophy Type 1

Autor: Ruggiero Francavilla, Antonio Corsello, Alessandra Bosetti, Dario Dilillo, Gloria Pelizzo, Lorenzo Scatigno, Flavia Indrio, V. Fabiano, Gian Vincenzo Zuccotti, Anna Mandelli, Sara Vizzuso, Annalisa Govoni, Elena Zoia, Valeria Calcaterra, Elvira Verduci, Martina Chiara Pascuzzi

Publikováno v: Nutrients, Vol 13, Iss 2400, p 2400 (2021)
Nutrients

The management of patients with spinal muscular atrophy type 1 (SMA1) is constantly evolving. In just a few decades, the medical approach has switched from an exclusively palliative therapy to a targeted therapy, transforming the natural history of t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e8668aa9ad8b6474bb7bc6d57770f1a
https://doi.org/10.3390/nu13072400

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