Kristiina Makkonen
kristiina.makkonen@utu.fi |
- Kilpirauhassairaus voi johtua geeneistä – milloin ne kannattaa tutkia? (2025)
- LääkärilehtiEndocrine Abstracts
- Very-Early Onset Autoimmune Hypothyroidism: A Report of Two Cases with STAT3 Gain-Of-Function Variant (2025)
- European thyroid journal
- Altered skull and bone morphology in hyperthyroid knock-in mice with TSHR M453T and D633H mutations2024
- Decoding SLC26A7'S role in congenital hypothyroidism: delayed onset, very large goiters, and thyrotropin dependent basolateral expressionIdentification of a stat3 mutation, P.THR716MET in two cases of very early-onset autoimmune hypothyroidism (2024)
- Endocrine Abstracts
- (2024)
- Endocrine Abstracts
- Mechanisms of thyrotropin receptor-mediated phenotype variability deciphered by gene mutations and M453T-knockin model (2024)
- JCI Insight
- Screening for Mutations in Isolated Central Hypothyroidism Reveals a Novel Mutation in Insulin Receptor Substrate 4 (2021)
- Frontiers in Endocrinology
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