Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases

The following new articles have just been published in Orphanet Journal of Rare Diseases RESEARCH Profiling of patient-specific myocytes identifies altered gene expression in the ophthalmoplegic subphenotype of myasthenia gravis Melissa Nel, Sharon Prince and Jeannine M. Heckmann Orphanet Journal of Rare Diseases 2019, 14:24 | Published on: 29 January 2019 Full Text | PDF RESEARCH Assessing disease experience across the life span for individuals with osteogenesis imperfecta: challenges and opportunities for patient-reported outcomes (PROs) measurement: a pilot study Laura L. Tosi, Marianne K. Floor, Christina M. Dollar, Austin P. Gillies, Tracy S. Hart, David D. Cuthbertson, V. Reid Sutton and Jeffrey P. Krischer Orphanet Journal of Rare Diseases 2019, 14:23 | Published on: 29 January 2019 Full Text | PDF

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