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Tuuli Mustonen
Tuuli Mustonen
University of Helsinki
Amyloidosis
Gelsolin
Internal medicine
Medicine
Biology
5
Papers
20
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Hearing problems in patients with hereditary gelsolin amyloidosis.
2021
Orphanet Journal of Rare Diseases
Tuuli Mustonen
Ville Sivonen
Sari Atula
Sari Kiuru-Enari
Saku T. Sinkkonen
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Cardiac manifestations in Finnish gelsolin amyloidosis patients.
2021
Amyloid
Tuuli Mustonen
Arttu Holkeri
Miia Holmström
Sari Atula
Sami Pakarinen
Lauri Lehmonen
Sari Kiuru-Enari
Aapo L. Aro
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Finnish gelsolin amyloidosis causes significant disease burden but does not affect survival: FIN-GAR phase II study.
2020
Orphanet Journal of Rare Diseases
Eeva-Kaisa Schmidt
Tuuli Mustonen
Sari Kiuru-Enari
Tero Kivelä
Sari Atula
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Citations (8)
Myocardial tissue characterization in patients with hereditary gelsolin (AGel) amyloidosis using novel cardiovascular magnetic resonance techniques
2019
International Journal of Cardiovascular Imaging
Lauri Lehmonen
Touko Kaasalainen
Sari Atula
Tuuli Mustonen
Miia Holmström
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Common origin of the gelsolin gene variant in 62 Finnish AGel amyloidosis families
2018
European Journal of Human Genetics
Tuuli Mustonen
Eeva-Kaisa Schmidt
Miko Valori
Pentti J. Tienari
Sari Atula
Sari Kiuru-Enari
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Citations (5)
1