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Fondazione Telethon and Unione Italiana Lotta alla Distrofia Muscolare, a successful partnership for neuromuscular healthcare research of value for patients.
Orphanet J Rare Dis. 2021 Oct 2;16(1):408. doi: 10.1186/s13023-021-02047-1.
Orphanet J Rare Dis. 2021.
PMID: 34600567
Free PMC article.
Review.
The IRDiRC Chrysalis Task Force: making rare disease research attractive to companies.
Beaverson KL, Julkowska D, Letinturier MCV, Aartsma-Rus A, Austin J, Bueren J, Frost S, Hamamura M, Larkindale J, LaRosa G, Magenheim R, Merico A, Gerdina Pasmooij AM, Pirard V, Ekow Thomford N, Wada M, Wong-Rieger D, Hartman AL.
Beaverson KL, et al. Among authors: merico a.
Ther Adv Rare Dis. 2023 Jul 29;4:26330040231188979. doi: 10.1177/26330040231188979. eCollection 2023 Jan-Dec.
Ther Adv Rare Dis. 2023.
PMID: 37529076
Free PMC article.
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A second pathway to degrade pyrimidine nucleic acid precursors in eukaryotes.
Andersen G, Björnberg O, Polakova S, Pynyaha Y, Rasmussen A, Møller K, Hofer A, Moritz T, Sandrini MP, Merico AM, Compagno C, Akerlund HE, Gojković Z, Piskur J.
Andersen G, et al. Among authors: merico am.
J Mol Biol. 2008 Jul 18;380(4):656-66. doi: 10.1016/j.jmb.2008.05.029. Epub 2008 May 17.
J Mol Biol. 2008.
PMID: 18550080
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