Search Results - Helioe, T

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  1. 1
    No evidence for linkage between familial hypertriglyceridemia and apolipoprotein B, apolipoprotein C-III or lipoprotein lipase genes

    No evidence for linkage between familial hypertriglyceridemia and apolipoprotein B, apolipoprotein C-III or lipoprotein lipase genes by HELIÖ, T, PALOTIE, A, SANE, T, TIKKANEN, M. J, KONTULA, K

    Published in Human genetics
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  2. 2
    Finnish type of familial amyloidosis: Cosegregation of Asp sub(187) arrow right Asn mutation of gelsolin with the disease in three large families

    Finnish type of familial amyloidosis: Cosegregation of Asp sub(187) arrow right Asn mutation of gelsolin with the disease in three large families by Hiltunen, T, Kiuru, S, Hongell, V, Helioe, T, Palo, J, Peltonen, L

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  3. 3
    Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases

    Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericard... by Rapezzi, Claudio, Arbustini, Eloisa, Caforio, Alida L P, Charron, Philippe, Gimeno-Blanes, Juan, Heliö, Tiina, Linhart, Ales, Mogensen, Jens, Pinto, Yigal, Ristic, Arsen, Seggewiss, Hubert, Sinagra, Gianfranco, Tavazzi, Luigi, Elliott, Perry M

    Published in European heart journal
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  4. 4
    Start age of enzyme replacement therapy (ERT) did not effect ECG parameters in Fabry disease patients (FD) treated by ERT for 5 years

    Start age of enzyme replacement therapy (ERT) did not effect ECG parameters in Fabry disease patients (FD) treated by ERT for 5 years by Kantola, Ilkka, Annala, Antti-Pekka, Hietaharju, Aki, Helioe, Tiina M., Kantola, Taru-Tuuli, Kuusisto, Johanna, Effati, Paivi Pietila, Saarinen, Jukka, Taurio, Jyrki, Walls, Susanne, Valtola, Kati, Yliaska, Iina

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  5. 5
    GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy

    GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy by Heliö, Krista, Mäyränpää, Mikko I, Saarinen, Inka, Ahonen, Saija, Junnila, Heidi, Tommiska, Johanna, Weckström, Sini, Holmström, Miia, Toivonen, Mia, Nikus, Kjell, Hathaway, Julie, Siivonen, Pauli, Muona, Mikko, Sistonen, Johanna, Salmenperä, Pertteli, Gentile, Massimiliano, Paananen, Jussi, Myllykangas, Samuel, Alastalo, Tero-Pekka, Heliö, Tiina, Koskenvuo, Juha

    Published in Frontiers in genetics
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  6. 6
    Actin-microtubule cytoskeletal interplay mediated by MRTF-A/SRF signaling promotes dilated cardiomyopathy caused by LMNA mutations

    Actin-microtubule cytoskeletal interplay mediated by MRTF-A/SRF signaling promotes dilated cardiomyopathy caused by LMNA mutations by Le Dour, Caroline, Chatzifrangkeskou, Maria, Macquart, Coline, Magiera, Maria M., Peccate, Cécile, Jouve, Charlène, Virtanen, Laura, Heliö, Tiina, Aalto-Setälä, Katriina, Crasto, Silvia, Cadot, Bruno, Cardoso, Déborah, Mougenot, Nathalie, Adesse, Daniel, Di Pasquale, Elisa, Hulot, Jean-Sébastien, Taimen, Pekka, Janke, Carsten, Muchir, Antoine

    Published in Nature communications
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  7. 7
    Characteristics of Atrial Fibrillation and Comorbidities in Familial Atrial Fibrillation

    Characteristics of Atrial Fibrillation and Comorbidities in Familial Atrial Fibrillation by JURKKO, RAIJA, PALOJOKI, EEVA, HUTTUNEN, HANNA, HOLM, CHRISTIAN, LEHTO, MIKA, HELIÖ, TIINA, SWAN, HEIKKI, TOIVONEN, LAURI

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