Jääskeläinen, Jarmo

Long-term outcome of classical 21-hydroxylase deficiency: diagnosis, complications and quality of life

Jääskeläinen, J., & Voutilainen, R. (2000) · Acta Paediatrica

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 89

Detection of Novel Gene Variants Associated with Congenital Hypothyroidism in a Finnish Patient Cohort

Löf, C., Patyra, K., Kuulasmaa, T., Vangipurapu, J., Undeutsch, H., Jaeschke, H., Pajunen, T., Kero, A., Krude, H., Biebermann, H., et al. (2016) · Thyroid®

Thyroid Disorders and TreatmentsGenomics and Rare Diseases

Cited by 81

Simultaneous analysis by LC–MS/MS of 22 ketosteroids with hydroxylamine derivatization and underivatized estradiol from human plasma, serum and prostate tissue

Häkkinen, M. R., Murtola, T., Voutilainen, R., Poutanen, M., Linnanen, T., Koskivuori, J., Lakka, T., Jääskeläinen, J., & Auriola, S. (2019) · Journal of Pharmaceutical and Biomedical Analysis

Analytical Methods in PharmaceuticalsAnalytical Chemistry and Chromatography

Cited by 74

Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism

Cangul, H., Liao, X.-H., Schoenmakers, E., Kero, J., Barone, S., Srichomkwun, P., Iwayama, H., Serra, E. G., Saglam, H., Eren, E., et al. (2018) · JCI Insight

Thyroid Disorders and TreatmentsChemical Analysis and Environmental Impact

Cited by 69

Interleukins 1α and 1β as regulators of steroidogenesis in human NCI-H295R adrenocortical cells

Tkachenko, I. V., Jääskeläinen, T., Jääskeläinen, J., Palvimo, J. J., & Voutilainen, R. (2011) · Steroids

Adrenal Hormones and DisordersStress Responses and Cortisol

Cited by 52