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| Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience | |
| Sun-Jeong Shin, Yeonah Sul, Ja Hye Kim, Ja Hyang Cho, Gu-Hwan Kim, Jae Hyun Kim, Jin-Ho Choi, Han-Wook Yoo | |
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Ann Pediatr Endocrinol Metab. 2015;20(1):27-33. Published online March 31, 2015 DOI: https://doi.org/10.6065/apem.2015.20.1.27 |
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Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience Annals of Pediatric Endocrinology & Metabolism. 2015;20(1):27  Clinical features and ovulation induction in women with idiopathic hypogonadotropic hypogonadism or kallmann syndrome Fertility and Sterility. 2007;88:S177 Vol. 39: Kallmann Syndrome and Hypogonadotropic Hypogonadism Acta Paediatrica. 2010;99(12):1914-1914 Novel FGFR1 mutations in Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: evidence for the involvement of an alternatively spliced isoform Fertility and Sterility. 2015;104(5):1261-1267.e1 Kallmann syndrome: phenotype and genotype of hypogonadotropic hypogonadism Metabolism. 2018;86:124-134 Kallmann’s syndrome and normosmic isolated hypogonadotropic hypogonadism: two largely overlapping manifestations of one rare disorder Journal of Endocrinological Investigation. 2014;37(5):499-500 Kallmann's Syndrome and Idiopathic Hypogonadotropic Hypogonadism Encyclopedia of Endocrine Diseases. 2004;119-124 The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome Fertility and Sterility. 2011;96(6):1424-1430.e6 Reversal of congenital hypogonadotropic hypogonadism in a man with Kallmann syndrome due toSOX10mutation Clinical Endocrinology. 2016;85(6):988-989 The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome Molecular and Cellular Endocrinology. 2011;346(1-2):74-83 |
