Publications by authors named "Tuuli Mustonen"

Claim this Profile
H
Hearing problems in patients with hereditary gelsolin amyloidosis.
Tuuli Mustonen, Ville Sivonen, Sari Atula, Sari Kiuru-Enari, Saku T Sinkkonen

Orphanet J Rare Dis· October 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Cardiac manifestations in Finnish gelsolin amyloidosis patients.
Tuuli Mustonen, Arttu Holkeri, Miia Holmström, Sari Atula, Sami Pakarinen

Amyloid· September 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Finnish gelsolin amyloidosis causes significant disease burden but does not affect survival: FIN-GAR phase II study.
Eeva-Kaisa Schmidt, Tuuli Mustonen, Sari Kiuru-Enari, Tero T Kivelä, Sari Atula

Orphanet J Rare Dis· January 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Myocardial tissue characterization in patients with hereditary gelsolin (AGel) amyloidosis using novel cardiovascular magnetic resonance techniques.
Lauri Lehmonen, Touko Kaasalainen, Sari Atula, Tuuli Mustonen, Miia Holmström

Int J Cardiovasc Imaging· February 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Common origin of the gelsolin gene variant in 62 Finnish AGel amyloidosis families.
Tuuli Mustonen, Eeva-Kaisa Schmidt, Miko Valori, Pentti J Tienari, Sari Atula

Eur J Hum Genet· January 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis