"Weckström, Sini" - Selaus tekijän mukaan TUNICRIS-julkaisut

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

      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 (25.11.2021)
      article
      <p>Background: Familial dilated cardiomyopathy (DCM) is a monogenic disorder typically inherited in an autosomal dominant pattern. We have identified two Finnish families with familial cardiomyopathy that is not ...

    • Timing of pacemaker and ICD implantation in LMNA mutation carriers 

      Ollila, Laura Helena; Nikus, Kjell; Parikka, Hannu; Weckström, Sini; Tiina, Heliö (2021)
      article
      <p>Aims LMNA-cardiomyopathy is often associated with pathology in the cardiac conduction system necessitating device implantations. The aim was to study the timing and types of device implantations and need for ...