Sort   by:  
 Page size 
UnknownAdult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation.
Not available
S-EPMC4542621 | biostudies-literature
UnknownNovel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians.
Not available
S-EPMC7078025 | biostudies-literature
UnknownStudy protocol for the Sino-Canadian Healthy Life Trajectories Initiative (SCHeLTI): a multicentre, cluster-randomised, parallel-group, superiority trial of a multifaceted community-family-mother-child intervention to prevent childhood overweight and obesity.
Not available
S-EPMC8021741 | biostudies-literature
UnknownA stepwise approach to designing and delivering the SCHeLTI trial community-family-mother-child obesity prevention intervention.
Not available
S-EPMC12274767 | biostudies-literature
UnknownRevisiting the link between oropharyngeal dysphagia and cancer in autoimmune myositis: a descriptive study.
Not available
S-EPMC12613458 | biostudies-literature
UnknownExpanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay.
Not available
S-EPMC6323608 | biostudies-literature
UnknownConvalescent plasma for hospitalized patients with COVID-19: an open-label, randomized controlled trial.
Not available
S-EPMC8604729 | biostudies-literature
UnknownBi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes.
Not available
S-EPMC6408318 | biostudies-literature
Sort   by:  
 Page size