Vilma-Lotta Lehtokari
7PUBLICATIONS
40CO-AUTHORS
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Publications (7)
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|Nov 28, 2025
Characterization of novel CASQ1 variants in two families with unusual phenotypic features.Milla Laarne, Manu Jokela, Fang Zhao
|Jun 14, 2025
Structural variation in nebulin and its impact on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletions.Lydia Sagath, Kirsi Kiiski, Kireshnee Naidu
|May 21, 2025
A homozygous single-nucleotide variant in TNNT1 causes abnormal troponin T isoform expression in a patient with severe nemaline myopathy: A case report.Milla Laarne, Ali Oghabian, Jenni Laitila
|Feb 20, 2025
Nutritional status of patients with nemaline myopathy and related congenital myopathies in Finland: A pilot study.Vilma-Lotta Lehtokari, Minna Similä, Marianne Tammepuu
|Jan 13, 2025
Structural variation in nebulin and its implications on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletions.Lydia Sagath, Kirsi Kiiski, Kireshnee Naidu
|Dec 01, 2023
Self-reported functioning among patients with ultra-rare nemaline myopathy or a related disorder in Finland: a pilot study.Vilma-Lotta Lehtokari, Minna Similä, Marianne Tammepuu
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Frequent Collaborators
5 joint publications
Katarina Pelin
4 joint publications
Lydia Sagath
4 joint publications
Milla Laarne
3 joint publications
Kirsi Kiiski
2 joint publications
Alan H Beggs
2 joint publications
Per Harald Jonson
2 joint publications
Susan T Iannaccone
2 joint publications
Marco Savarese
2 joint publications
Maureen Kelly Galindo
1 joint publications
Peter Hackman
