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 LETTER TO THE EDITOR Screening for Fabry disease in unknown origin axonal polyneuropathy: to do or not to do, this is the question! Eugenia Rota, Marina Grandis, Alessia Di Sapio, Elisabetta Ghiglione, Pietro Fiorentino, Alessandra Repetto, Claudia Giliberto, Chiara Gemelli, Nicola Morelli, Angelo Schenone and Dario Cocito Orphanet Journal of Rare Diseases 2020, 15:216 | Published on: 20 August 2020 Full Text | PDF RESEARCH A novel prognostic model for adult patients with Hemophagocytic Lymphohistiocytosis Jun Zhou, Jing Zhou, Zhi-Qi Wu, Hemant Goyal and Hua-Guo Xu Orphanet Journal of Rare Diseases 2020, 15:215 | Published on: 20 August 2020 Full Text | PDF REVIEW Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update Morten Krogh Herlin, Michael Bjørn Petersen and Mats Brännström Orphanet Journal of Rare Diseases 2020, 15:214 | Published on: 20 August 2020 Full Text | PDF

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