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Lancet neurology, ISSN 1474-4422, 2015, Volume 14, Issue 10, pp. 992 - 1001
Journal Article
Journal Article
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by Abarca-Gómez, Leandra and Abdeen, Ziad A and Acosta-Cazares, Benjamin and Acuin, Cecilia and Adams, Robert J and Aekplakorn, Wichai and Afsana, Kaosar and Aguilar-Salinas, Carlos A and Agyemang, Charles and Ahrens, Wolfgang and Ajlouni, Kamel and Al-Hazzaa, Hazzaa M and Al-Othman, Amani Rashed and Al-Raddadi, Rajaa and Al Buhairan, Fadia and Al Dhukair, Shahla and Alkerwi, Ala'a and Aly, Eman and Amuzu, Antoinette and Andersen, Lars Bo and Anderssen, Sigmund A and Ängquist, Lars H and Aounallah-Skhiri, Hajer and Araújo, Joana and Aryal, Krishna K and Azevedo, Ana and Babu, Bontha V and Balakrishna, Nagalla and Bamoshmoosh, Mohamed and Barbagallo, Carlo M and Barkat, Amina and Barros, Aluisio JD and Bata, Iqbal and Batieha, Anwar M and Batista, Rosangela L and Baur, Louise A and Romdhane, Habiba Ben and Benedics, Judith and Benet, Mikhail and Bennett, James E and Bernabe-Ortiz, Antonio and Bettiol, Heloisa and Bhagyalaxmi, Aroor and Bharadwaj, Sumit and Bhutta, Zulfiqar A and Bi, Hongsheng and Bi, Yufang and Bikbov, Mukharram and Bjelica, Dusko J and Bjerregaard, Peter and Blokstra, Anneke and Bo, Simona and Boeing, Heiner and Bonaccio, Marialaura and Bragt, Marjolijn CE and Brajkovich, Imperia and Branca, Francesco and Breckenkamp, Juergen and Brenner, Hermann and Brinduse, Lacramioara and Bruno, Graziella and Cai, Hui and Cameron, Christine and Can, Günay and Cardoso, Viviane C and Carvalho, Maria J and Casanueva, Felipe F and Chaturvedi, Himanshu K and Chaturvedi, Nishi and Chen, Chien-Jen and Chen, Zhengming and Cheng, Ching-Yu and Chikova-Iscener, Ekaterina and Chiolero, Arnaud and Cho, Belong and Cinteza, Eliza and Clays, Els and Concin, Hans and Confortin, Susana C and Coppinger, Tara C and Costanzo, Simona and Cowell, Chris and d'Orsi, Eleonora and Dallongeville, Jean and Damasceno, Albertino and Damsgaard, Camilla T and Danaei, Goodarz and Dankner, Rachel and Dantoft, Thomas M and Dauchet, Luc and Davletov, Kairat and De Backer, Guy and De Bacquer, Dirk and De Henauw, Stefaan and de Oliveira, Paula Duarte and De Ridder, Karin and De Smedt, Delphine and Dehghan, Abbas and Dias-da-Costa, Juvenal Soares and Djalalinia, Shirin and ... and NCD Risk Factor Collaboration (NCD-RisC) and Institutionen för medicin, avdelningen för samhällsmedicin och folkhälsa and Institute of Medicine, Department of Molecular and Clinical Medicine and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy and Sahlgrenska akademin and Institutionen för medicin, avdelningen för molekylär och klinisk medicin and Institute of Medicine, Department of Public Health and Community Medicine
The Lancet (British edition), ISSN 0140-6736, 12/2017, Volume 390, Issue 10113, pp. 2627 - 2642
Journal Article
Przeglad lekarski, ISSN 0033-2240, 2009, Volume 66, Issue 12, p. 1065
Myotonic dystrophy (MD) is a genetically determined disease with autosomal dominant mode of inheritance... 
Heart Diseases - etiology | Respiratory Tract Diseases - etiology | Death, Sudden - etiology | Myotonic Dystrophy - complications | Myotonic Dystrophy - diagnosis | Humans | Sleep Wake Disorders - etiology
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