Miettinen PJ - Search Results

1

Presentation and diagnosis of childhood-onset combined pituitary hormone deficiency: A single center experience from over 30 years.

Hietamäki J, Kärkinen J, Iivonen AP, Vaaralahti K, Tarkkanen A, Almusa H, Huopio H, Hero M, Miettinen PJ, Raivio T. Hietamäki J, et al. Among authors: miettinen pj. EClinicalMedicine. 2022 Jul 18;51:101556. doi: 10.1016/j.eclinm.2022.101556. eCollection 2022 Sep. EClinicalMedicine. 2022. PMID: 35875813 Free PMC article.

2

Glioneuroma associated with colobomatous dysplasia of the anterior uvea and retina. A case simulating medulloepithelioma.

Kivelä T, Kauniskangas L, Miettinen P, Tarkkanen A. Kivelä T, et al. Ophthalmology. 1989 Dec;96(12):1799-808. doi: 10.1016/s0161-6420(89)32652-2. Ophthalmology. 1989. PMID: 2622623

3

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: miettinen pj. Pediatr Res. 2016 May;79(5):705-9. doi: 10.1038/pr.2015.278. Epub 2015 Dec 31. Pediatr Res. 2016. PMID: 26720605

4

Circulating makorin ring finger protein 3 levels decline in boys before the clinical onset of puberty.

Varimo T, Dunkel L, Vaaralahti K, Miettinen PJ, Hero M, Raivio T. Varimo T, et al. Among authors: miettinen pj. Eur J Endocrinol. 2016 Jun;174(6):785-90. doi: 10.1530/EJE-15-1193. Epub 2016 Mar 29. Eur J Endocrinol. 2016. PMID: 27025240 Clinical Trial.

5

Clinical, Genetic, and Biochemical Characteristics of Early-Onset Diabetes in the Finnish Population.

Huopio H, Miettinen PJ, Ilonen J, Nykänen P, Veijola R, Keskinen P, Näntö-Salonen K, Vangipurapu J, Raivo J, Stančáková A, Männistö J, Kuulasmaa T, Knip M, Otonkoski T, Laakso M. Huopio H, et al. Among authors: miettinen pj. J Clin Endocrinol Metab. 2016 Aug;101(8):3018-26. doi: 10.1210/jc.2015-4296. Epub 2016 May 11. J Clin Endocrinol Metab. 2016. PMID: 27167055

6

Congenital hypogonadotropic hypogonadism, functional hypogonadotropism or constitutional delay of growth and puberty? An analysis of a large patient series from a single tertiary center.

Varimo T, Miettinen PJ, Känsäkoski J, Raivio T, Hero M. Varimo T, et al. Among authors: miettinen pj. Hum Reprod. 2017 Jan;32(1):147-153. doi: 10.1093/humrep/dew294. Epub 2016 Dec 6. Hum Reprod. 2017. PMID: 27927844

7

Precocious Puberty or Premature Thelarche: Analysis of a Large Patient Series in a Single Tertiary Center with Special Emphasis on 6- to 8-Year-Old Girls.

Varimo T, Huttunen H, Miettinen PJ, Kariola L, Hietamäki J, Tarkkanen A, Hero M, Raivio T. Varimo T, et al. Among authors: miettinen pj. Front Endocrinol (Lausanne). 2017 Aug 23;8:213. doi: 10.3389/fendo.2017.00213. eCollection 2017. Front Endocrinol (Lausanne). 2017. PMID: 28878739 Free PMC article.

8

GnRH receptor gene mutations in adolescents and young adults presenting with signs of partial gonadotropin deficiency.

Hietamäki J, Hero M, Holopainen E, Känsäkoski J, Vaaralahti K, Iivonen AP, Miettinen PJ, Raivio T. Hietamäki J, et al. Among authors: miettinen pj. PLoS One. 2017 Nov 28;12(11):e0188750. doi: 10.1371/journal.pone.0188750. eCollection 2017. PLoS One. 2017. PMID: 29182666 Free PMC article.

9

Disorders of sex development: timing of diagnosis and management in a single large tertiary center.

Kohva E, Miettinen PJ, Taskinen S, Hero M, Tarkkanen A, Raivio T. Kohva E, et al. Among authors: miettinen pj. Endocr Connect. 2018 Apr;7(4):595-603. doi: 10.1530/EC-18-0070. Epub 2018 Mar 26. Endocr Connect. 2018. PMID: 29581155 Free PMC article.

10

The Role of KCNQ1 Mutations and Maternal Beta Blocker Use During Pregnancy in the Growth of Children With Long QT Syndrome.

Huttunen H, Hero M, Lääperi M, Känsäkoski J, Swan H, Hirsch JA, Miettinen PJ, Raivio T. Huttunen H, et al. Among authors: miettinen pj. Front Endocrinol (Lausanne). 2018 Apr 24;9:194. doi: 10.3389/fendo.2018.00194. eCollection 2018. Front Endocrinol (Lausanne). 2018. PMID: 29740400 Free PMC article.

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