Consensus-based care recommendations for adults with myotonic dystrophy type 1

PURPOSE OF REVIEW: Myotonic dystrophy type 1 (DM1) is a severe, progressive genetic disease that affects between 1 in 3,000 and 8,000 individuals globally. No evidence-based guideline exists to inform the care of these patients, and most do not have access to multidisciplinary care centers staffed b...

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Bibliografiset tiedot
Julkaisussa:Neurol Clin Pract
Päätekijät: Ashizawa, Tetsuo, Gagnon, Cynthia, Groh, William J., Gutmann, Laurie, Johnson, Nicholas E., Meola, Giovanni, Moxley, Richard, Pandya, Shree, Rogers, Mark T., Simpson, Ericka, Angeard, Nathalie, Bassez, Guillaume, Berggren, Kiera N., Bhakta, Deepak, Bozzali, Marco, Broderick, Ann, Byrne, Janice L.B., Campbell, Craig, Cup, Edith, Day, John W., De Mattia, Elisa, Duboc, Denis, Duong, Tina, Eichinger, Katy, Ekstrom, Anne-Berit, van Engelen, Baziel, Esparis, Belen, Eymard, Bruno, Ferschl, Marla, Gadalla, Shahinaz M., Gallais, Benjamin, Goodglick, Todd, Heatwole, Chad, Hilbert, James, Holland, Venessa, Kierkegaard, Marie, Koopman, Wilma J., Lane, Kari, Maas, Daphne, Mankodi, Ami, Mathews, Katherine D., Monckton, Darren G., Moser, David, Nazarian, Saman, Nguyen, Linda, Nopoulos, Peg, Petty, Richard, Phetteplace, Janel, Puymirat, Jack, Raman, Subha, Richer, Louis, Roma, Elisabetta, Sampson, Jacinda, Sansone, Valeria, Schoser, Benedikt, Sterling, Laurie, Statland, Jeffrey, Subramony, S.H., Tian, Cuixia, Trujillo, Careniña, Tomaselli, Gordon, Turner, Chris, Venance, Shannon, Verma, Aparajitha, White, Molly, Winblad, Stefan
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Lippincott Williams & Wilkins 2018
Aiheet:
Review
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6294540/
https://ncbi.nlm.nih.gov/pubmed/30588381
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/CPJ.0000000000000531
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