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Material Type: Artigo
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Outcomes and experiences of adults with congenital hypogonadism can inform improvements in the management of delayed pubertyHoward, Sasha R. ; Quinton, RichardJournal of Pediatric Endocrinology & Metabolism, 2024-01, Vol.37 (1), p.1-7 [Periódico revisado por pares]Germany: De GruyterTexto completo disponível |
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Material Type: Artigo
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Clinical characteristics and molecular genetic analysis of a cohort with idiopathic congenital hypogonadismTurkyilmaz, Ayberk ; Cayir, Atilla ; Yarali, Oguzhan ; Kurnaz, Erdal ; Kartal Baykan, Emine ; Arslan Ates, Esra ; Demirbilek, HuseyinJournal of Pediatric Endocrinology & Metabolism, 2021-06, Vol.34 (6), p.771-780 [Periódico revisado por pares]Germany: De GruyterTexto completo disponível |
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3 |
Material Type: Artigo
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Hypothalamic-pituitary dysfunction in Sturge–Weber syndrome: case report and review of the literatureHadid, Somar A. ; Noor, Laila ; Baer, Tamar ; Jacobson, Ronald I. ; Brutsaert, ErikaJournal of Pediatric Endocrinology and Metabolism, 2024-01, Vol.37 (1), p.80-83 [Periódico revisado por pares]Germany: De GruyterTexto completo disponível |
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4 |
Material Type: Artigo
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Gonadotropins for testicular descent in cryptorchid congenital hypogonadotropic hypogonadism males beyond infancySharma, Shreya ; Shah, Ravikumar ; Patil, Virendra ; Lila, Anurag R. ; Sarathi, Vijaya ; Shah, Nalini ; Bandgar, TusharJournal of Pediatric Endocrinology & Metabolism, 2021-07, Vol.34 (7), p.917-924 [Periódico revisado por pares]Germany: De GruyterTexto completo disponível |
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5 |
Material Type: Artigo
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Molecular genetic and clinical delineation of 22 patients with congenital hypogonadotropic hypogonadismAoyama, Kohei ; Mizuno, Haruo ; Tanaka, Tatsushi ; Togawa, Takao ; Negishi, Yutaka ; Ohashi, Kei ; Hori, Ikumi ; Izawa, Masako ; Hamajima, Takashi ; Saitoh, ShinjiJournal of Pediatric Endocrinology & Metabolism, 2017-10, Vol.30 (10), p.1111-1118 [Periódico revisado por pares]Germany: De GruyterTexto completo disponível |
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6 |
Material Type: Artigo
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Turner syndrome and pituitary adenomas: a case report and review of literatureYeh, Tiffany ; Soto, Angela Ganan ; Quintos, Jose Bernardo ; Topor, Lisa SwartzJournal of Pediatric Endocrinology & Metabolism, 2017-02, Vol.30 (2), p.231-235 [Periódico revisado por pares]Germany: De GruyterTexto completo disponível |
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7 |
Material Type: Artigo
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A novel DAX-1 mutation in two male siblings presenting with precocious puberty and late-onset hypogonadotropic hypogonadismLiu, Yanxia ; Yuan, Jinlei ; Zhang, Huijuan ; Jiang, Yanyan ; Qin, GuijunJournal of Pediatric Endocrinology & Metabolism, 2017-03, Vol.30 (3), p.349-353 [Periódico revisado por pares]Germany: De GruyterTexto completo disponível |
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8 |
Material Type: Artigo
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A de novo mutation of DAX1 in a boy with congenital adrenal hypoplasia without hypogonadotropic hypogonadismWang, Chun Lin ; Fen, Zhu Wei ; Liang, LiJournal of Pediatric Endocrinology and Metabolism, 2014-03, Vol.27 (3-4), p.343-347 [Periódico revisado por pares]GermanyTexto completo disponível |
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9 |
Material Type: Artigo
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Normosmic idiopathic hypogonadotropic hypogonadism: update on the genetic background and future challengesFathi, Aws K. ; Luo, XiaopingJournal of Pediatric Endocrinology and Metabolism, 2013, Vol.26 (5), p.405-415 [Periódico revisado por pares]Germany: De GruyterTexto completo disponível |
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10 |
Material Type: Artigo
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Late onset X-linked adrenal hypoplasia congenita with hypogonadotropic hypgonadism due to a novel 4-bp deletion in exon 2 of NR0B1Ali, Johari Mohd ; Jalaludin, Muhammad Yazid ; Harun, FatimahJournal of Pediatric Endocrinology & Metabolism, 2014-11, Vol.27 (11), p.1189-1192 [Periódico revisado por pares]Germany: De GruyterTexto completo disponível |