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 Orthopaedic phenotyping of NGLY1 deficiency using an international, family-led disease registry Eli M. Cahan and Steven L. Frick Orphanet Journal of Rare Diseases 2019, 14:148 | Published on: 19 June 2019 Full Text | PDF RESEARCH Ovarian primary primitive neuroectodermal tumor: a review of cases at PUMCH and in the published literature Xiaopei Chao, Yalan Bi and Lei Li Orphanet Journal of Rare Diseases 2019, 14:147 | Published on: 19 June 2019 Full Text | PDF REVIEW Treatment of Satoyoshi syndrome: a systematic review Julián Solís-García del Pozo, Carlos de Cabo and Javier Solera Orphanet Journal of Rare Diseases 2019, 14:146 | Published on: 19 June 2019 Full Text | PDF

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