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Presentation and diagnosis of childhood-onset combined pituitary hormone deficiency: A single center experience from over 30 years.
EClinicalMedicine. 2022 Jul 18;51:101556. doi: 10.1016/j.eclinm.2022.101556. eCollection 2022 Sep.
EClinicalMedicine. 2022.
PMID: 35875813
Free PMC article.
The aetiology of extreme tall stature in a screened Finnish paediatric population.
Kärkinen J, Sorakunnas E, Miettinen PJ, Raivio T, Hero M.
Kärkinen J, et al.
EClinicalMedicine. 2021 Nov 20;42:101208. doi: 10.1016/j.eclinm.2021.101208. eCollection 2021 Dec.
EClinicalMedicine. 2021.
PMID: 34849478
Free PMC article.
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Etiology of severe short stature below -3 SDS in a screened Finnish population.
Kärkinen J, Miettinen PJ, Raivio T, Hero M.
Kärkinen J, et al.
Eur J Endocrinol. 2020 Nov;183(5):481-488. doi: 10.1530/EJE-20-0313.
Eur J Endocrinol. 2020.
PMID: 33107436
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Kallmann syndrome in a patient with Weiss-Kruszka syndrome and a de novo deletion in 9q31.2.
Iivonen AP, Kärkinen J, Yellapragada V, Sidoroff V, Almusa H, Vaaralahti K, Raivio T.
Iivonen AP, et al. Among authors: karkinen j.
Eur J Endocrinol. 2021 May 21;185(1):57-66. doi: 10.1530/EJE-20-1387.
Eur J Endocrinol. 2021.
PMID: 33909591
Free PMC article.
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Central precocious puberty in boys: secular trend and clinical features.
Huttunen H, Kärkinen J, Varimo T, Miettinen PJ, Raivio T, Hero M.
Huttunen H, et al. Among authors: karkinen j.
Eur J Endocrinol. 2024 Mar 2;190(3):211-219. doi: 10.1093/ejendo/lvae021.
Eur J Endocrinol. 2024.
PMID: 38523472
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Congenital hypogonadotropic hypogonadism in a patient with a de novo POGZ mutation.
Eskici N, Madhusudan S, Vaaralahti K, Yellapragada V, Gomez-Sanchez C, Kärkinen J, Almusa H, Brandstack N, Miettinen PJ, Wang Y, Raivio T.
Eskici N, et al. Among authors: karkinen j.
Eur J Endocrinol. 2023 Aug 2;189(2):271-280. doi: 10.1093/ejendo/lvad111.
Eur J Endocrinol. 2023.
PMID: 37619992
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