Hasil Pencarian - Sini Weckström

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  1. 1
    Successful palliative resection of giant epimyocardial lymphatic malformation with 14 years of follow-up: a case report

    Successful palliative resection of giant epimyocardial lymphatic malformation with 14 years of follow-up: a case report oleh Krista Heliö, Sini Weckström, Sari Kivistö, Jouko Lohi, Tiina Heliö

    Diterbitkan 2023-08-01
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  2. 2
    Timing of pacemaker and ICD implantation in LMNA mutation carriers

    Timing of pacemaker and ICD implantation in LMNA mutation carriers oleh Kjell Nikus, Laura Helena Ollila, Hannu Parikka, Sini Weckström, Heliö Tiina

    Diterbitkan 2021-06-01
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  3. 3
    MYH7 Genotype–Phenotype Correlation in a Cohort of Finnish Patients

    MYH7 Genotype–Phenotype Correlation in a Cohort of Finnish Patients oleh Teemu Vepsäläinen, Tiina Heliö, Catalina Vasilescu, Laura Martelius, Sini Weckström, Juha Koskenvuo, Anita Hiippala, Tiina Ojala

    Diterbitkan 2022-03-01
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  4. 4
    DSP p.(Thr2104Glnfs*12) variant presents variably with early onset severe arrhythmias and left ventricular cardiomyopathy

    DSP p.(Thr2104Glnfs*12) variant presents variably with early onset severe arrhythmias and left ventricular cardiomyopathy oleh Krista Heliö, Tiia Kangas-Kontio, Sini Weckström, Sari U. M. Vanninen, Katriina Aalto-Setälä, Tero-Pekka Alastalo, Samuel Myllykangas, Tiina M. Heliö, Juha W. Koskenvuo

    Diterbitkan 2020-01-01
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  5. 5
    DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma

    DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma oleh Krista Heliö, Eveliina Brandt, Satu Vaara, Sini Weckström, Liisa Harjama, Riina Kandolin, Johanna Järviö, Katariina Hannula-Jouppi, Katariina Hannula-Jouppi, Tiina Heliö, Miia Holmström, Juha W. Koskenvuo

    Diterbitkan 2023-03-01
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  6. 6
    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 oleh Krista Heliö, Mikko I. Mäyränpää, Inka Saarinen, Saija Ahonen, Heidi Junnila, Johanna Tommiska, Sini Weckström, Miia Holmström, Mia Toivonen, Kjell Nikus, Kjell Nikus, Julie Hathaway, Pauli Siivonen, Mikko Muona, Johanna Sistonen, Pertteli Salmenperä, Massimiliano Gentile, Jussi Paananen, Samuel Myllykangas, Tero-Pekka Alastalo, Tiina Heliö, Juha Koskenvuo

    Diterbitkan 2021-11-01
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  7. 7
    Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathy.

    Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathy. oleh Juha W Koskenvuo, Inka Saarinen, Saija Ahonen, Johanna Tommiska, Sini Weckström, Eija H Seppälä, Sari Tuupanen, Tiia Kangas-Kontio, Jennifer Schleit, Krista Heliö, Julie Hathaway, Anders Gummesson, Pia Dahlberg, Tiina H Ojala, Ville Vepsäläinen, Ville Kytölä, Mikko Muona, Johanna Sistonen, Pertteli Salmenperä, Massimiliano Gentile, Jussi Paananen, Samuel Myllykangas, Tero-Pekka Alastalo, Tiina Heliö

    Diterbitkan 2021-01-01
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