Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Bouchard, Gérard
1991.
Mobile populations, stable communities: social and demographic processes in the rural parishes of the Saguenay, 1840–1911.
Continuity and Change,
Vol. 6,
Issue. 1,
p.
59.
Dao, To‐Nga
Mathieu, Jean
Bouchard, Jean‐Pierrs
and
Braekeleer, Marc De
1992.
Fertility in myotonic dystrophy in Saguenay‐Lac‐St‐Jean: a historical perspective.
Clinical Genetics,
Vol. 42,
Issue. 5,
p.
234.
Dao, To‐Nga
Mathieu, Jean
Bouchard, Jean‐Pierre
and
de Braekeleer, Marc
1993.
Infant mortality in myotonic dystrophy in Saguenay‐Lac‐St‐Jean: a historical perspective.
Clinical Genetics,
Vol. 43,
Issue. 1,
p.
25.
Magzhanov, R. V.
Akhmadeeva, L. R.
Khusnutdinova, Е. К.
Tunik, V. F.
Fatkhlislamova, R. I.
Farrakhov, Е. Z.
and
Semenov, Е. К.
1997.
Clinical genetic analysis of myotonia dystrophica in the republic of bashkortostan.
Neurology Bulletin,
Vol. XXIX,
Issue. 1-2,
p.
78.
Waring, J. D.
and
Korneluk, R. G.
1998.
Trinucleotide Diseases and Instability.
Vol. 21,
Issue. ,
p.
77.
Sizhong, Zhang
Hui, Wu
Agen, Pan
Cuiying, Xiao
Ge, Zhang
Yiping, Hou
and
Jiayou, Chu
2000.
Low incidence of myotonic dystrophy in Chinese Hans is associated with a lower number of CTG trinucleotide repeats.
American Journal of Medical Genetics,
Vol. 96,
Issue. 3,
p.
425.
Ortega Calvo, M.
Cayuela Domínguez, A.
Macías Pérez, V.
and
González Álvarez, M.
2004.
Distrofias miotónicas congénitas en un área de salud rural.
Atención Primaria,
Vol. 33,
Issue. 1,
p.
53.
ASHIZAWA, TETSUO
and
HARPER, PETER S.
2006.
Genetic Instabilities and Neurological Diseases.
p.
21.
Amenabar, F.
Jorquera, H.
Acuña, M.
and
Cifuentes, L.
2009.
CTG repeats at the myotonic protein kinase gene in a healthy Chilean population sample.
Acta Neurologica Scandinavica,
Vol. 119,
Issue. 5,
p.
321.
Vanlinthout, L. E. H.
Booij, L. H. D. J.
Van Egmond, J.
and
Robertson, E. N.
2010.
Comparison of mechanomyography and acceleromyography for the assessment of rocuronium induced neuromuscular block in myotonic dystrophy type 1.
Anaesthesia,
Vol. 65,
Issue. 6,
p.
601.
Suominen, Tiina
Bachinski, Linda L
Auvinen, Satu
Hackman, Peter
Baggerly, Keith A
Angelini, Corrado
Peltonen, Leena
Krahe, Ralf
and
Udd, Bjarne
2011.
Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland.
European Journal of Human Genetics,
Vol. 19,
Issue. 7,
p.
776.
Chapron, Kevin
Bouchard, Kevin
Duchesne, Elise
and
Gaboury, Sebastien
2017.
Transportable and scalable system for activities and exercises recognition in real-time.
p.
1.
Murillo-Melo, N.M.
Márquez-Quiróz, L.C.
Gómez, R.
Orozco, L.
Mendoza-Caamal, E.
Tapia-Guerrero, Y.S.
Camacho-Mejorado, R.
Cortés, H.
López-Reyes, A.
Santana, C.
Noris, G.
Hernández-Hernández, O.
Cisneros, B.
and
Magaña, J.J.
2017.
Origin of the myotonic dystrophy type 1 mutation in Mexican population and influence of Amerindian ancestry on CTG repeat allelic distribution.
Neuromuscular Disorders,
Vol. 27,
Issue. 12,
p.
1106.
Wenninger, Stephan
Montagnese, Federica
and
Schoser, Benedikt
2018.
Core Clinical Phenotypes in Myotonic Dystrophies.
Frontiers in Neurology,
Vol. 9,
Issue. ,
Chapron, Kévin
Plantevin, Valère
Thullier, Florentin
Bouchard, Kévin
Duchesne, Elise
and
Gaboury, Sébastien
2018.
A More Efficient Transportable and Scalable System for Real-Time Activities and Exercises Recognition.
Sensors,
Vol. 18,
Issue. 1,
p.
268.
Khadilkar, Satish V.
Yadav, Rakhil S.
and
Patel, Bhagyadhan A.
2018.
Neuromuscular Disorders.
p.
197.
Lamacie, Mariana M.
Warman-Chardon, Jodi
Crean, Andrew M.
Florian, Anca
and
Wahbi, Karim
2019.
The Added Value of Cardiac Magnetic Resonance in Muscular Dystrophies.
Journal of Neuromuscular Diseases,
Vol. 6,
Issue. 4,
p.
389.
Roussel, Marie-Pier
Hébert, Luc J.
and
Duchesne, Elise
2020.
Strength-training effectively alleviates skeletal muscle impairments in myotonic dystrophy type 1.
Neuromuscular Disorders,
Vol. 30,
Issue. 4,
p.
283.
Roussel, Marie-Pier
Fiset, Marie-Michèle
Gauthier, Laurie
Lavoie, Claudia
McNicoll, Émilie
Pouliot, Laurie
Gagnon, Cynthia
and
Duchesne, Elise
2021.
Assessment of muscular strength and functional capacity in the juvenile and adult myotonic dystrophy type 1 population: a 3-year follow-up study.
Journal of Neurology,
Vol. 268,
Issue. 11,
p.
4221.
Lapointe, Patrick
Chapron, Kévin
Lessard, Isabelle
Bouchard, Kevin
Lavoie, Mélissa
Gagnon, Cynthia
Duchesne, Elise
and
Gaboury, Sébastien
2022.
Monitoring changes in physical activity data during strength training of people with myotonic dystrophy type 1.
Procedia Computer Science,
Vol. 198,
Issue. ,
p.
51.