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 Education and information needs for physicians about rare diseases in Spain Enrique Ramalle-Gómara, Elena Domínguez-Garrido, María Gómez-Eguílaz, María Eugenia Marzo-Sola, José Luis Ramón-Trapero and Josefa Gil-de-Gómez Orphanet Journal of Rare Diseases 2020, 15:18 | Published on: 17 January 2020 Full Text | PDF LETTER TO THE EDITOR Evaluation of retinal microvascular perfusion in hereditary angioedema: a case-control study Paola Triggianese, Massimo Cesareo, Maria Domenica Guarino, Paola Conigliaro, Maria Sole Chimenti, Francesca Cedola, Caterina Mazzeo, Carlo Nucci and Roberto Perricone Orphanet Journal of Rare Diseases 2020, 15:20 | Published on: 17 January 2020 Full Text | PDF RESEARCH Finnish gelsolin amyloidosis causes significant disease burden but does not affect survival: FIN-GAR phase II study Eeva-Kaisa Schmidt, Tuuli Mustonen, Sari Kiuru-Enari, Tero T. Kivelä and Sari Atula Orphanet Journal of Rare Diseases 2020, 15:19 | Published on: 17 January 2020 Full Text | PDF

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