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 Safety of antithrombotic therapy in subjects with hereditary hemorrhagic telangiectasia: prospective data from a multidisciplinary working group Eleonora Gaetani, Fabiana Agostini, Angelo Porfidia, Igor Giarretta, Daniela Feliciani, Luigi Di Martino, Annalisa Tortora, Antonio Gasbarrini and Roberto Pola Orphanet Journal of Rare Diseases 2019, 14:298 | Published on: 26 December 2019 Full Text | PDF RESEARCH Retinal hyperreflective foci in Fabry disease Yevgeniya Atiskova, Rahman Rassuli, Anja Friederike Koehn, Amir Golsari, Lars Wagenfeld, Marcel du Moulin, Nicole Muschol and Simon Dulz Orphanet Journal of Rare Diseases 2019, 14:296 | Published on: 26 December 2019 Full Text | PDF RESEARCH Primary hypertrophic osteoarthropathy related gastrointestinal complication has distinctive clinical and pathological characteristics: two cases report and review of the literature Qiang Wang, Ying-he Li, Guo-le Lin, Yue Li, Wei-xun Zhou, Jia-ming Qian, Wei-bo Xia and Dong Wu Orphanet Journal of Rare Diseases 2019, 14:297 | Published on: 26 December 2019 Full Text | PDF

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