Stamou M - Search Results

1

Phenotypic continuum between Waardenburg syndrome and idiopathic hypogonadotropic hypogonadism in humans with SOX10 variants.

Rojas RA, Kutateladze AA, Plummer L, Stamou M, Keefe DL Jr, Salnikov KB, Delaney A, Hall JE, Sadreyev R, Ji F, Fliers E, Gambosova K, Quinton R, Merino PM, Mericq V, Seminara SB, Crowley WF Jr, Balasubramanian R. Rojas RA, et al. Among authors: stamou m. Genet Med. 2021 Apr;23(4):629-636. doi: 10.1038/s41436-020-01051-3. Epub 2021 Jan 13. Genet Med. 2021. PMID: 33442024 Free PMC article.

2

Discovering Genes Essential to the Hypothalamic Regulation of Human Reproduction Using a Human Disease Model: Adjusting to Life in the "-Omics" Era.

Stamou MI, Cox KH, Crowley WF Jr. Stamou MI, et al. Endocr Rev. 2015 Dec;36(6):603-21. doi: 10.1210/er.2015-1045. Epub 2015 Sep 22. Endocr Rev. 2015. Retraction in: Endocr Rev. 2020 Dec 1;41(6):bnaa019. doi: 10.1210/endrev/bnaa019. PMID: 26394276 Free PMC article. Retracted. Review.

3

Withdrawn: Discovering Genes Essential to the Hypothalamic Regulation of Human Reproduction Using a Human Disease Model: Adjusting to Life in the "-Omics" Era.

Stamou MI, Cox KH, Crowley WF Jr. Stamou MI, et al. Endocr Rev. 2016 Feb;2016(1):4-22. doi: 10.1210/er.2015-1045.2016.1.test. Endocr Rev. 2016. Retraction in: Endocr Rev. 2020 Dec 1;41(6):bnaa019. doi: 10.1210/endrev/bnaa019. PMID: 27454361 Free PMC article. Retracted. Review.

4

Isolated GNRH deficiency: genotypic and phenotypic characteristics of the genetically heterogeneous Greek population.

Stamou MI, Varnavas P, Kentrou M, Adamidou F, Voutetakis A, Jing J, Plummer L, Koika V, Georgopoulos NA. Stamou MI, et al. Eur J Endocrinol. 2017 Mar;176(3):L1-L5. doi: 10.1530/EJE-16-0505. Epub 2016 Nov 24. Eur J Endocrinol. 2017. PMID: 27884859 Free PMC article. No abstract available.

5

Kallmann syndrome: phenotype and genotype of hypogonadotropic hypogonadism.

Stamou MI, Georgopoulos NA. Stamou MI, et al. Metabolism. 2018 Sep;86:124-134. doi: 10.1016/j.metabol.2017.10.012. Epub 2017 Nov 3. Metabolism. 2018. PMID: 29108899 Free PMC article. Review.

6

Unilateral renal agenesis as an early marker for genetic screening in Kallmann syndrome.

Stamou MI, Plummer L, Galli-Tsinopoulou A, Stergidou D, Koika V, Georgopoulos NA. Stamou MI, et al. Hormones (Athens). 2019 Mar;18(1):103-105. doi: 10.1007/s42000-018-0061-1. Epub 2018 Sep 25. Hormones (Athens). 2019. PMID: 30255480 Free PMC article.

7

Next-generation sequencing refines the genetic architecture of Greek GnRH-deficient patients.

Stamou MI, Varnavas P, Plummer L, Koika V, Georgopoulos NA. Stamou MI, et al. Endocr Connect. 2019 May 1;8(5):468-480. doi: 10.1530/EC-19-0010. Endocr Connect. 2019. PMID: 30921766 Free PMC article.

8

A novel FGF8 mutation in a female patient with isolated congenital anosmia.

Stamou MI, Plummer L, Koika V, Galli-Tsinopoulou A, Georgopoulos NA. Stamou MI, et al. Hormones (Athens). 2019 Jun;18(2):241-244. doi: 10.1007/s42000-019-00108-6. Epub 2019 May 13. Hormones (Athens). 2019. PMID: 31087283 Free PMC article. No abstract available.

9

A Balanced Translocation in Kallmann Syndrome Implicates a Long Noncoding RNA, RMST, as a GnRH Neuronal Regulator.

Stamou M, Ng SY, Brand H, Wang H, Plummer L, Best L, Havlicek S, Hibberd M, Khor CC, Gusella J, Balasubramanian R, Talkowski M, Stanton LW, Crowley WF. Stamou M, et al. J Clin Endocrinol Metab. 2020 Mar 1;105(3):e231-44. doi: 10.1210/clinem/dgz011. J Clin Endocrinol Metab. 2020. PMID: 31628846 Free PMC article.

10

Hypothalamic Ceramides and the Ovarian Sympathetic System: At the Crossroads of Obesity and Puberty.

Stamou MI, Balasubramanian R. Stamou MI, et al. Cell Metab. 2021 Jan 5;33(1):6-8. doi: 10.1016/j.cmet.2020.11.012. Epub 2020 Dec 1. Cell Metab. 2021. PMID: 33264644 Free PMC article.

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