miércoles, 30 de enero de 2019

Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases | Home page



New Articles For BioMed Central:

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

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

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