Jukka Kero

Decoding SLC26A7'S role in congenital hypothyroidism: delayed onset, very large goiters, and thyrotropin dependent basolateral expression (2024)

Endocrine Abstracts

Ojala Johanna; Niuro Laura; Ravi Rowmika; Melnyk Vladyslav; Linnossuo Veli; Makkonen Kristiina; Jääskelainen Jarmo; Danner Emmi; Huopio Hanna; Niinikoski Harri; Viikari Liisa; Miettinen Paivi; Schoenmakers Nadia; Pat Reeve Mary; Kero Jukka

(Konferenssiposteri)

Identification of a stat3 mutation, P.THR716MET in two cases of very early-onset autoimmune hypothyroidism (2024)

Endocrine Abstracts

Ravi Rowmika; Nuutinen Anita; Makkonen Kristiina; Toppari Jorma; Kero Jukka

(Konferenssiposteri)

Mechanisms of thyrotropin receptor-mediated phenotype variability deciphered by gene mutations and M453T-knockin model (2024)

JCI Insight

Makkonen Kristiina, Jännäri Meeri, Crisostomo Luis, Kuusi Matilda, Patyra Konrad, Melnyk Vladyslav, Linnossuo Veli, Ojala Johanna, Ravi Rowmika, Löf Christoffer, Makela Juho-Antti, Miettinen Paivi, Laakso Saila, Ojaniemi Marja, Jaaskelainen Jarmo, Laakso Markku, Bossowski Filip, Sawicka Beata, Stozek Karolina, Bossowski Artur, Kleinau Gunnar, Scheerer Patrick; FinnGen, Reeve Mary Pat, Kero Jukka

(Vertaisarvioitu alkuperäisartikkeli tai data-artikkeli tieteellisessä aikakauslehdessä (A1))

Altered skull and bone morphology in hyperthyroid knock-in mice with TSHR M453T and D633H mutations (2024)

Endocrine Abstracts

Makkonen Kristiina; Määttä Jorma; Ivaska Kaisa; Patyra Konrad; Melnyk Vladyslav; Linnossuo Veli; Ojala Johanna; Ravi Rowmika; Jaschke Holger; Undeutsch Julian; Kero Jukka

(O2 Muu julkaisu )

Higher initial levothyroxine doses and very early treatment start may lead to better cognitive outcomes in children with congenital hypothyroidism (2024)

Acta Paediatrica

Danner, Emmi; Niuro, Laura; Lapinoja, Sonja; Huopio, Hanna; Viikari, Liisa A.; Kero, Jukka; Jääskeläinen, Jarmo; Niinikoski, Harri

(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )

Comorbidity in Congenital Hypothyroidism—A Nationwide, Population-based Cohort Study (2023)

Journal of Clinical Endocrinology and Metabolism

Danner Emmi, Jääskeläinen Jarmo, Niuro Laura, Huopio Hanna, Niinikoski Harri, Viikari Liisa, Kero Jukka, Sund Reijo

(Vertaisarvioitu alkuperäisartikkeli tai data-artikkeli tieteellisessä aikakauslehdessä (A1))

Incidence of primary congenital hypothyroidism over 24 years in Finland (2023)

Pediatric Research

Danner Emmi, Niuro Laura, Huopio Hanna, Niinikoski Harri, Viikari Liisa, Kero Jukka, Jääskeläinen Jarmo

(A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )

Activation of mitogen-activated protein kinase signaling and development of papillary thyroid carcinoma in thyroid-stimulating hormone receptor D633H knockin mice (2023)

European thyroid journal

Eszlinger Markus, Stephenson Alexandra, Mirhadi Shideh, Patyra Kondrad, Moran Michael F., Khalil Moosa, Kero Jukka, Paschke Ralf

(Vertaisarvioitu alkuperäisartikkeli tai data-artikkeli tieteellisessä aikakauslehdessä (A1))

INnoVative trial design for testing the Efficacy, Safety and Tolerability of 6-month treatment with incretin-based therapy to prevent type 1 DIAbetes in autoantibody positive participants: A protocol for three parallel double-blind, randomised controlled trials (INVESTDIA) (2022)

Diabetic Medicine

Kero Jukka, Koskenniemi Jaakko J., Karsikas Sara, Pokka Tytti, Lou Olivia, Toppari Jorma, Veijola Riitta

(Vertaisarvioitu alkuperäisartikkeli tai data-artikkeli tieteellisessä aikakauslehdessä (A1))

Exploring Minimally Invasive Approach to Define Stages of Type 1 Diabetes Remotely (2022)

Diabetes Technology and Therapeutics

Kontola Helena, Alanko Inka, Koskenniemi Jaakko J, Löyttyniemi Eliisa, Itoshima Saori, Knip Mikael, Veijola Riitta, Toppari Jorma, Kero Jukka

(Vertaisarvioitu alkuperäisartikkeli tai data-artikkeli tieteellisessä aikakauslehdessä (A1))

Ota yhteyttä

Julkaisut

Järjestä:

Decoding SLC26A7'S role in congenital hypothyroidism: delayed onset, very large goiters, and thyrotropin dependent basolateral expression (2024)

Identification of a stat3 mutation, P.THR716MET in two cases of very early-onset autoimmune hypothyroidism (2024)

Mechanisms of thyrotropin receptor-mediated phenotype variability deciphered by gene mutations and M453T-knockin model (2024)

Altered skull and bone morphology in hyperthyroid knock-in mice with TSHR M453T and D633H mutations (2024)

Higher initial levothyroxine doses and very early treatment start may lead to better cognitive outcomes in children with congenital hypothyroidism (2024)

Comorbidity in Congenital Hypothyroidism—A Nationwide, Population-based Cohort Study (2023)

Incidence of primary congenital hypothyroidism over 24 years in Finland (2023)

Activation of mitogen-activated protein kinase signaling and development of papillary thyroid carcinoma in thyroid-stimulating hormone receptor D633H knockin mice (2023)

INnoVative trial design for testing the Efficacy, Safety and Tolerability of 6-month treatment with incretin-based therapy to prevent type 1 DIAbetes in autoantibody positive participants: A protocol for three parallel double-blind, randomised controlled trials (INVESTDIA) (2022)

Exploring Minimally Invasive Approach to Define Stages of Type 1 Diabetes Remotely (2022)