viernes, 21 de agosto de 2020

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

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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