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 The attenuated end of the phenotypic spectrum in MPS III: from late-onset stable cognitive impairment to a non-neuronopathic phenotype Stephanie C. M. Nijmeijer, L. Ingeborg van den Born, Anneke J. A. Kievit, Karolina M. Stepien, Janneke Langendonk, Jan Pieter Marchal, Susanne Roosing, Frits A. Wijburg and Margreet A. E. M. Wagenmakers Orphanet Journal of Rare Diseases 2019, 14:249 | Published on: 12 November 2019 Full Text | PDF RESEARCH Clinical characteristics and prognosis of Chinese patients with hereditary transthyretin amyloid cardiomyopathy Shan He, Zhuang Tian, Hongzhi Guan, Jian Li, Quan Fang and Shuyang Zhang Orphanet Journal of Rare Diseases 2019, 14:251 | Published on: 12 November 2019 Full Text | PDF

Follow BMC on: For further information or enquiries please use our contact page details. BMC respects your privacy and does not disclose, sell or rent your personal information to any non-affliated third parties with your consent. Privacy policy. BioMed Central Ltd The Campus, 4 Crinan Street, London, N1 9XW, United Kingdom

© 2019 BioMed Central Limited unless otherwise stated. Part of Springer Nature.