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 Early start of growth hormone is associated with positive effects on auxology and metabolism in Prader-Willi-syndrome Lucy Magill, Constanze Laemmer, Joachim Woelfle, Rolf Fimmers and Bettina Gohlke Orphanet Journal of Rare Diseases 2020, 15:283 | Published on: 12 October 2020 Full Text | PDF RESEARCH The urgent need to empower rare disease organizations in China: an interview-based study Xuefeng Li, Zijuan Lu, Jianyong Zhang, Xiangyu Zhang, Shu Zhang, Jincheng Zhou, Bingzhe Li and Li Ou Orphanet Journal of Rare Diseases 2020, 15:282 | Published on: 12 October 2020 Full Text | PDF RESEARCH Type 1 tyrosinemia in Finland: a nationwide study Linnea Äärelä, Pauliina Hiltunen, Tea Soini, Nina Vuorela, Heini Huhtala, Pasi I. Nevalainen, Markku Heikinheimo, Laura Kivelä and Kalle Kurppa Orphanet Journal of Rare Diseases 2020, 15:281 | Published on: 12 October 2020 Full Text | PDF

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