POEMS Syndrome Complicated by Extensive Calciphylaxis: A Remarkable Recovery.

Measuring participation in children with disabilities using the Assessment of Life Habits. Dev Med Child Neurol (2007) 1.93

Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans. PLoS Biol (2012) 1.80

Predictors of disrupted social participation in myotonic dystrophy type 1. Arch Phys Med Rehabil (2008) 1.51

The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum. Nat Genet (2002) 1.51

Epidemiological surveillance of amyotrophic lateral sclerosis in Saguenay region. Can J Neurol Sci (2013) 1.42

Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy. Ann Neurol (2005) 1.29

Genes, maternal smoking, and the offspring brain and body during adolescence: design of the Saguenay Youth Study. Hum Brain Mapp (2007) 1.19

Clinical, electrophysiologic, and genetic study of non-dystrophic myotonia in French-Canadians. Neuromuscul Disord (2008) 1.05

Hereditary motor and sensory neuropathy with agenesis of the corpus callosum. Ann Neurol (2003) 1.05

Sleep complaints in patients with myotonic dystrophy. J Sleep Res (2004) 0.99

Usefulness of clinical and electrocardiographic data for predicting adverse cardiac events in patients with myotonic dystrophy. Can J Cardiol (2009) 0.98

Efficacy and tolerability of a 20-mg dose of methylphenidate for the treatment of daytime sleepiness in adult patients with myotonic dystrophy type 1: a 2-center, randomized, double-blind, placebo-controlled, 3-week crossover trial. Clin Ther (2012) 0.98

Founder SH3TC2 mutations are responsible for a CMT4C French-Canadians cluster. Neuromuscul Disord (2008) 0.86

Towards an integrative approach to the management of myotonic dystrophy type 1. J Neurol Neurosurg Psychiatry (2007) 0.85

Prevalence of lifestyle risk factors in myotonic dystrophy type 1. Can J Neurol Sci (2013) 0.83

Fatigue and daytime sleepiness in patients with myotonic dystrophy type 1: to lump or split? Neuromuscul Disord (2009) 0.81

Clinical, psychosocial, and central correlates of quality of life in myotonic dystrophy type 1 patients. Eur Neurol (2013) 0.81

C9orf72 hexanucleotide repeat expansions as the causative mutation for chromosome 9p21-linked amyotrophic lateral sclerosis and frontotemporal dementia. Arch Neurol (2012) 0.81

Clinical presentation and early evolution of spastic ataxia of Charlevoix-Saguenay. Mov Disord (2013) 0.79

Life habits in myotonic dystrophy type 1. J Rehabil Med (2007) 0.79

DOK7 mutations presenting as a proximal myopathy in French Canadians. Neuromuscul Disord (2010) 0.78

Standardized finger-nose test validity for coordination assessment in an ataxic disorder. Can J Neurol Sci (2004) 0.77

The potential of disease management for neuromuscular hereditary disorders. Rehabil Nurs (2009) 0.77

[Severe neuropathy with agenesis of the corpus callosum]. Med Sci (Paris) (2003) 0.77

Psychosocial impact of predictive testing for myotonic dystrophy type 1. Am J Med Genet A (2004) 0.77

Anticipation in myotonic dystrophy type 1 parents with small CTG expansions. Am J Med Genet A (2015) 0.76

Measurement of participation in myotonic dystrophy: reliability of the LIFE-H. Neuromuscul Disord (2006) 0.76

Intergenerational contraction of the CTG repeats in 2 families with myotonic dystrophy type 1. Neurology (2009) 0.76

Presence of palmar xanthomas in myotonic dystrophy identifies different patterns of linkage disequilibrium between the apolipoprotein E and myotonic dystrophy protein kinase loci. Genet Med (2005) 0.75

Stanford Chronic Disease Self-Management Program in myotonic dystrophy: New opportunities for occupational therapists: Stanford Chronic Disease Self-Management Program dans la dystrophie myotonique : De nouvelles opportunités pour les ergothérapeutes. Can J Occup Ther (2016) 0.75

Fine mapping the candidate region for peripheral neuropathy with or without agenesis of the corpus callosum in the French Canadian population. Eur J Hum Genet (2002) 0.75

Capecitabine-induced inflammation of actinic keratosis: case report and literature review. J Cutan Med Surg (2012) 0.75

Autosomal recessive spastic ataxia of Charlevoix-Saguenay: upper extremity aptitudes, functional independence and social participation. Int J Rehabil Res (2004) 0.75

An approach to the treatment of vulvar lymphedema. J Cutan Med Surg (2011) 0.75

Role for the central motor system in fibromyalgia: pain resolution after pontine infarction. Joint Bone Spine (2009) 0.75