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 REVIEW Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a review Michael Pugliese, Kylie Tingley, Andrea Chow, Nicole Pallone, Maureen Smith, Alvi Rahman, Pranesh Chakraborty, Michael T. Geraghty, Julie Irwin, Laure Tessier, Stuart G. Nicholls, Martin Offringa, Nancy J. Butcher, Ryan Iverson, Tammy J. Clifford, Sylvia Stockler… Orphanet Journal of Rare Diseases 2020, 15:12 | Published on: 14 January 2020 Full Text | PDF RESEARCH Out-of-pocket expenses for myasthenia gravis patients in China: a study on patients insured by basic medical insurance in China, 2013–2015 Tao-yu Lin, Xiao-yan Zhang, Peng-qian Fang and Rui Min Orphanet Journal of Rare Diseases 2020, 15:13 | Published on: 14 January 2020 Full Text | PDF RESEARCH Mutational spectrum of autosomal recessive limb-girdle muscular dystrophies in a cohort of 112 Iranian patients and reporting of a possible founder effect Marzieh Mojbafan, Reza Bahmani, Samira Dabbagh Bagheri, Zohreh Sharifi and Sirous Zeinali Orphanet Journal of Rare Diseases 2020, 15:14 | Published on: 14 January 2020 Full Text | PDF

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