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 Genetic profiling and cardiovascular phenotypic spectrum in a Chinese cohort of Loeys-Dietz syndrome patients Hang Yang, Yanyun Ma, Mingyao Luo, Guoyan Zhu, Yinhui Zhang, Binbin Li, Chang Shu and Zhou Zhou Orphanet Journal of Rare Diseases 2020, 15:6 | Published on: 8 January 2020 Full Text | PDF REVIEW Hereditary haemorrhagic telangiectasia and pregnancy: a review of the literature Olivier Dupuis, Laura Delagrange and Sophie Dupuis-Girod Orphanet Journal of Rare Diseases 2020, 15:5 | Published on: 7 January 2020 Full Text | PDF REVIEW Future treatments for hereditary hemorrhagic telangiectasia Florian Robert, Agnès Desroches-Castan, Sabine Bailly, Sophie Dupuis-Girod and Jean-Jacques Feige Orphanet Journal of Rare Diseases 2020, 15:4 | Published on: 7 January 2020 Full Text | PDF

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