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Refinado por: Nome da Publicação: Journal Of Pediatric Endocrinology And Metabolism remover
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1
Outcomes and experiences of adults with congenital hypogonadism can inform improvements in the management of delayed puberty
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Outcomes and experiences of adults with congenital hypogonadism can inform improvements in the management of delayed puberty

Howard, Sasha R. ; Quinton, Richard

Journal of Pediatric Endocrinology & Metabolism, 2024-01, Vol.37 (1), p.1-7 [Periódico revisado por pares]

Germany: De Gruyter

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2
Clinical characteristics and molecular genetic analysis of a cohort with idiopathic congenital hypogonadism
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Clinical characteristics and molecular genetic analysis of a cohort with idiopathic congenital hypogonadism

Turkyilmaz, Ayberk ; Cayir, Atilla ; Yarali, Oguzhan ; Kurnaz, Erdal ; Kartal Baykan, Emine ; Arslan Ates, Esra ; Demirbilek, Huseyin

Journal of Pediatric Endocrinology & Metabolism, 2021-06, Vol.34 (6), p.771-780 [Periódico revisado por pares]

Germany: De Gruyter

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3
Hypothalamic-pituitary dysfunction in Sturge–Weber syndrome: case report and review of the literature
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Hypothalamic-pituitary dysfunction in Sturge–Weber syndrome: case report and review of the literature

Hadid, Somar A. ; Noor, Laila ; Baer, Tamar ; Jacobson, Ronald I. ; Brutsaert, Erika

Journal of Pediatric Endocrinology and Metabolism, 2024-01, Vol.37 (1), p.80-83 [Periódico revisado por pares]

Germany: De Gruyter

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4
Gonadotropins for testicular descent in cryptorchid congenital hypogonadotropic hypogonadism males beyond infancy
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Gonadotropins for testicular descent in cryptorchid congenital hypogonadotropic hypogonadism males beyond infancy

Sharma, Shreya ; Shah, Ravikumar ; Patil, Virendra ; Lila, Anurag R. ; Sarathi, Vijaya ; Shah, Nalini ; Bandgar, Tushar

Journal of Pediatric Endocrinology & Metabolism, 2021-07, Vol.34 (7), p.917-924 [Periódico revisado por pares]

Germany: De Gruyter

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5
Molecular genetic and clinical delineation of 22 patients with congenital hypogonadotropic hypogonadism
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Molecular genetic and clinical delineation of 22 patients with congenital hypogonadotropic hypogonadism

Aoyama, Kohei ; Mizuno, Haruo ; Tanaka, Tatsushi ; Togawa, Takao ; Negishi, Yutaka ; Ohashi, Kei ; Hori, Ikumi ; Izawa, Masako ; Hamajima, Takashi ; Saitoh, Shinji

Journal of Pediatric Endocrinology & Metabolism, 2017-10, Vol.30 (10), p.1111-1118 [Periódico revisado por pares]

Germany: De Gruyter

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6
Turner syndrome and pituitary adenomas: a case report and review of literature
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Turner syndrome and pituitary adenomas: a case report and review of literature

Yeh, Tiffany ; Soto, Angela Ganan ; Quintos, Jose Bernardo ; Topor, Lisa Swartz

Journal of Pediatric Endocrinology & Metabolism, 2017-02, Vol.30 (2), p.231-235 [Periódico revisado por pares]

Germany: De Gruyter

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7
A novel DAX-1 mutation in two male siblings presenting with precocious puberty and late-onset hypogonadotropic hypogonadism
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A novel DAX-1 mutation in two male siblings presenting with precocious puberty and late-onset hypogonadotropic hypogonadism

Liu, Yanxia ; Yuan, Jinlei ; Zhang, Huijuan ; Jiang, Yanyan ; Qin, Guijun

Journal of Pediatric Endocrinology & Metabolism, 2017-03, Vol.30 (3), p.349-353 [Periódico revisado por pares]

Germany: De Gruyter

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8
A de novo mutation of DAX1 in a boy with congenital adrenal hypoplasia without hypogonadotropic hypogonadism
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A de novo mutation of DAX1 in a boy with congenital adrenal hypoplasia without hypogonadotropic hypogonadism

Wang, Chun Lin ; Fen, Zhu Wei ; Liang, Li

Journal of Pediatric Endocrinology and Metabolism, 2014-03, Vol.27 (3-4), p.343-347 [Periódico revisado por pares]

Germany

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9
Normosmic idiopathic hypogonadotropic hypogonadism: update on the genetic background and future challenges
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Normosmic idiopathic hypogonadotropic hypogonadism: update on the genetic background and future challenges

Fathi, Aws K. ; Luo, Xiaoping

Journal of Pediatric Endocrinology and Metabolism, 2013, Vol.26 (5), p.405-415 [Periódico revisado por pares]

Germany: De Gruyter

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10
Late onset X-linked adrenal hypoplasia congenita with hypogonadotropic hypgonadism due to a novel 4-bp deletion in exon 2 of NR0B1
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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 NR0B1

Ali, Johari Mohd ; Jalaludin, Muhammad Yazid ; Harun, Fatimah

Journal of Pediatric Endocrinology & Metabolism, 2014-11, Vol.27 (11), p.1189-1192 [Periódico revisado por pares]

Germany: De Gruyter

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