 |
|
Central precocious puberty in a patient with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome
Ji Won Koh, So Young Kang, Gu Hwan Kim, Han Wook Yoo, Jeesuk Yu
Ann Pediatr Endocrinol Metab. 2013;18(2):90-94. Published online 2013 Jun 30 DOI: https://doi.org/10.6065/apem.2013.18.2.90
|
|
Citations to this article as recorded by
 A rare case of central precocious puberty in a male infant with adrenal hypoplasia congenita
Aikaterini Mastoropoulou, Andrew H. Lane
Journal of Pediatric Endocrinology and Metabolism.2024; 37(12): 1086. CrossRef Precocious Puberty in Boys with NR0B1 Variants
Atsushi Hattori, Maki Fukami
Endocrines.2024; 5(4): 529. CrossRef Nuclear Receptor Gene Variants Underlying Disorders/Differences of Sex Development through Abnormal Testicular Development
Atsushi Hattori, Maki Fukami
Biomolecules.2023; 13(4): 691. CrossRef IL1RAPL1 Gene Deletion in a Female Patient with Developmental Delay and Continuous Spike-Wave during Sleep
Evan Jiang, Mark P. Fitzgerald, Katherine L. Helbig, Ethan M. Goldberg
Journal of Pediatric Epilepsy.2022; 11(01): 021. CrossRef Pleomorphism of the HPG axis with NR0B1 gene mutation — a case report of longitudinal follow-up of a proband with central precocious puberty
Jun Zhang, Qiuli Chen, Song Guo, Yanhong Li, Huamei Ma, Rujiang Zheng, Minlian Du
Journal of Pediatric Endocrinology and Metabolism.2022; 35(7): 962. CrossRef Identification of a novel point mutation in DAX-1 gene in a patient with adrenal hypoplasia congenita
Han Saem Choi, Ahreum Kwon, Hyun Wook Chae, Junghwan Suh, Kyung Chul Song, Jin-Sung Lee, Ho-Seong Kim
Annals of Pediatric Endocrinology & Metabolism.2021; 26(2): 126. CrossRef Central precocious puberty as a prelude of gonad dysplasia
Lele Li, Chunxiu Gong
Pediatric Investigation.2019; 3(1): 50. CrossRef Central precocious puberty as a prelude to hypogonadism in a patient with Klinefelter syndrome
Chunxiu Gong, Lele Li, Jiahui Chen, Wenjing Li
Pediatric Investigation.2019; 3(2): 127. CrossRef Gonadotropin- and Adrenocorticotropic Hormone-Independent Precocious Puberty of Gonadal Origin in a Patient with Adrenal Hypoplasia Congenita Due to DAX1 Gene Mutation – A Case Report and Review of the Literature: Implications for the Pathomechanism
Stella A. Nagel, Michaela F. Hartmann, Felix G. Riepe, Stefan A. Wudy, Martin Wabitsch
Hormone Research in Paediatrics.2019; 91(5): 336. CrossRef The Synaptic and Neuronal Functions of the X‐Linked Intellectual Disability Protein Interleukin‐1 Receptor Accessory Protein Like 1 (IL1RAPL1)
Caterina Montani, Laura Gritti, Stefania Beretta, Chiara Verpelli, Carlo Sala
Developmental Neurobiology.2019; 79(1): 85. CrossRef A novel DAX-1 mutation in two male siblings presenting with precocious puberty and late-onset hypogonadotropic hypogonadism
Yanxia Liu, Jinlei Yuan, Huijuan Zhang, Yanyan Jiang, Guijun Qin
Journal of Pediatric Endocrinology and Metabolism.2017;[Epub] CrossRef NR0B1 Frameshift Mutation in a Boy with Idiopathic Central Precocious Puberty
Hirohito Shima, Shuichi Yatsuga, Akie Nakamura, Shinichiro Sano, Takako Sasaki, Noriyuki Katsumata, Erina Suzuki, Kenichiro Hata, Kazuhiko Nakabayashi, Yukihide Momozawa, Michiaki Kubo, Kohji Okamura, Shigeo Kure, Yoichi Matsubara, Tsutomu Ogata, Satoshi
Sexual Development.2016; 10(4): 205. CrossRef Adrenal Hypoplasia Congenita: A Rare Cause of Primary Adrenal Insufficiency and Hypogonadotropic Hypogonadism
Marta Loureiro, Filipa Reis, Brígida Robalo, Carla Pereira, Lurdes Sampaio
Pediatric Reports.2015; 7(3): 5936. CrossRef
|