Interleukin 1 receptor antagonist as biomarker for disease flares in fibrodysplasia ossificans progressiva
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Elsevier BV
Reference16 articles.
1. A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva;Shore;Nat. Genet.,2006
2. The natural history of fibrodysplasia ossificans progressiva: a prospective, global 36-month study;Pignolo;Genet. Med. Off. J. Am. Coll. Med. Genet.,2022
3. Novel asymptomatic CNS findings in patients with ACVR1/ALK2 mutations causing fibrodysplasia ossificans progressiva;Severino;J. Med. Genet.,2016
4. Palovarotene for Fibrodysplasia Ossificans Progressiva (FOP): results of a randomized, placebo-controlled, double-blind phase 2 trial;Pignolo;J. Bone Miner. Res. Off. J. Am. Soc. Bone Miner. Res.,2022
5. Reduction of new heterotopic ossification (HO) in the open-label, phase 3 MOVE trial of Palovarotene for Fibrodysplasia Ossificans Progressiva (FOP);Pignolo;J. Bone Miner. Res. Off. J. Am. Soc. Bone Miner. Res.,2023
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