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Laura Tanner

Showing results (11-20 of 28) with videos related to

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Orphanet Journal of Rare Diseases|May 1, 2026
Perinatal outcomes in 35 children with cartilage hair hypoplasiaEllamaija Kasanen, Sanna Toiviainen-Salo, Svetlana Vakkilainen, et al.
Cutis|November 4, 2021
Cutaneous ProtothecosisDana M Baigrie, Laura F Sandoval, Warren J White, et al.
Climatic Change|March 10, 2025
Bringing art and science together to address climate changeAllyza R Lustig, Allison R Crimmins, Michael O Snyder, et al.
Prenatal Diagnosis|May 25, 2022
Genetic spectrum of prenatally diagnosed skeletal dysplasias in a Finnish patient cohortKatri Rajala, Ellamaija Kasanen, Sanna Toiviainen-Salo, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|July 26, 2024
Infertility following trisomic pregnancies: A nationwide cohort studySatu Wedenoja, Mika Pihlajamäki, Mika Gissler, et al.
European Journal of Endocrinology|August 2, 2013
Insulin secretion and sensitivity in the prediction of type 1 diabetes in children with advanced β-cell autoimmunityHeli T Siljander, Robert Hermann, Anne Hekkala, et al.
Molecular Genetics and Metabolism|January 7, 2012
Exploring the transcriptomic variation caused by the Finnish founder mutation of lysinuric protein intolerance (LPI)Maaria Tringham, Johanna Kurko, Laura Tanner, et al.
Lifestyle Genomics|June 25, 2019
A Long-Term Follow-Up Study on Disclosing Genetic Risk Information (APOE) to Promote Healthy Lifestyles in FinlandHanna-Leena Hietaranta-Luoma, Maaria Tringham, Heli Karjalainen, et al.
Molecular Immunology|July 27, 2015
Dysfunction in macrophage toll-like receptor signaling caused by an inborn error of cationic amino acid transportJohanna Kurko, Mari Vähä-Mäkilä, Maaria Tringham, et al.
Emerging Infectious Diseases|July 9, 2016
Correction: Vol. 18, No. 2Mira Meriluoto, Lea Hedman, Laura Tanner, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Orphanet Journal of Rare Diseases|May 1, 2026
Perinatal outcomes in 35 children with cartilage hair hypoplasiaEllamaija Kasanen, Sanna Toiviainen-Salo, Svetlana Vakkilainen, et al.
Cutis|November 4, 2021
Cutaneous ProtothecosisDana M Baigrie, Laura F Sandoval, Warren J White, et al.
Climatic Change|March 10, 2025
Bringing art and science together to address climate changeAllyza R Lustig, Allison R Crimmins, Michael O Snyder, et al.
Prenatal Diagnosis|May 25, 2022
Genetic spectrum of prenatally diagnosed skeletal dysplasias in a Finnish patient cohortKatri Rajala, Ellamaija Kasanen, Sanna Toiviainen-Salo, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|July 26, 2024
Infertility following trisomic pregnancies: A nationwide cohort studySatu Wedenoja, Mika Pihlajamäki, Mika Gissler, et al.
European Journal of Endocrinology|August 2, 2013
Insulin secretion and sensitivity in the prediction of type 1 diabetes in children with advanced β-cell autoimmunityHeli T Siljander, Robert Hermann, Anne Hekkala, et al.
Molecular Genetics and Metabolism|January 7, 2012
Exploring the transcriptomic variation caused by the Finnish founder mutation of lysinuric protein intolerance (LPI)Maaria Tringham, Johanna Kurko, Laura Tanner, et al.
Lifestyle Genomics|June 25, 2019
A Long-Term Follow-Up Study on Disclosing Genetic Risk Information (APOE) to Promote Healthy Lifestyles in FinlandHanna-Leena Hietaranta-Luoma, Maaria Tringham, Heli Karjalainen, et al.
Molecular Immunology|July 27, 2015
Dysfunction in macrophage toll-like receptor signaling caused by an inborn error of cationic amino acid transportJohanna Kurko, Mari Vähä-Mäkilä, Maaria Tringham, et al.
Emerging Infectious Diseases|July 9, 2016
Correction: Vol. 18, No. 2Mira Meriluoto, Lea Hedman, Laura Tanner, et al.
Pageof 3