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Genetics of congenital hypogonadotropic hypogonadism in Denmark.
Tommiska J, Känsäkoski J, Christiansen P, Jørgensen N, Lawaetz JG, Juul A, Raivio T. Tommiska J, et al. Among authors: kansakoski j. Eur J Med Genet. 2014 Jul;57(7):345-8. doi: 10.1016/j.ejmg.2014.04.002. Epub 2014 Apr 13. Eur J Med Genet. 2014. PMID: 24732674
Childhood growth in boys with congenital hypogonadotropic hypogonadism.
Varimo T, Hero M, Laitinen EM, Miettinen PJ, Tommiska J, Känsäkoski J, Juul A, Raivio T. Varimo T, et al. Among authors: kansakoski j. Pediatr Res. 2016 May;79(5):705-9. doi: 10.1038/pr.2015.278. Epub 2015 Dec 31. Pediatr Res. 2016. PMID: 26720605
Neuron-Derived Neurotrophic Factor Is Mutated in Congenital Hypogonadotropic Hypogonadism.
Messina A, Pulli K, Santini S, Acierno J, Känsäkoski J, Cassatella D, Xu C, Casoni F, Malone SA, Ternier G, Conte D, Sidis Y, Tommiska J, Vaaralahti K, Dwyer A, Gothilf Y, Merlo GR, Santoni F, Niederländer NJ, Giacobini P, Raivio T, Pitteloud N. Messina A, et al. Among authors: kansakoski j. Am J Hum Genet. 2020 Jan 2;106(1):58-70. doi: 10.1016/j.ajhg.2019.12.003. Epub 2019 Dec 26. Am J Hum Genet. 2020. PMID: 31883645 Free PMC article.
PROKR2 mutations in autosomal recessive Kallmann syndrome.
Tommiska J, Toppari J, Vaaralahti K, Känsäkoski J, Laitinen EM, Noisa P, Kinnala A, Niinikoski H, Raivio T. Tommiska J, et al. Among authors: kansakoski j. Fertil Steril. 2013 Mar 1;99(3):815-8. doi: 10.1016/j.fertnstert.2012.11.003. Epub 2012 Nov 29. Fertil Steril. 2013. PMID: 23200691 Free article.
Gonadotropin-releasing hormone receptor mutations in ageing men.
Tommiska J, Känsäkoski J, Pitteloud N, Wu F, Raivio T. Tommiska J, et al. Among authors: kansakoski j. Clin Endocrinol (Oxf). 2016 Jan;84(1):150-1. doi: 10.1111/cen.12833. Epub 2015 Jul 1. Clin Endocrinol (Oxf). 2016. PMID: 26044071 No abstract available.
25 results