Patricia Delai
Hospital Israelita Albert Einstein(BR)Insper(BR)
Publications by Year
Research Areas
Medical Imaging and Pathology Studies, Heterotopic Ossification and Related Conditions, Parathyroid Disorders and Treatments, Bone Tumor Diagnosis and Treatments, Genetic Syndromes and Imprinting
Most-Cited Works
- → A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva(2006)1,212 cited
- → Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1(2008)444 cited
- → The Phenotype of Fibrodysplasia Ossificans Progressiva(2005)115 cited
- → Reduction of New Heterotopic Ossification ( HO ) in the Open‐Label , Phase 3 MOVE Trial of Palovarotene for Fibrodysplasia Ossificans Progressiva ( FOP )(2022)62 cited
- → Neurological symptoms in individuals with fibrodysplasia ossificans progressiva(2012)54 cited
- → Special considerations for clinical trials in fibrodysplasia ossificans progressiva (FOP)(2018)47 cited
- → Self-reported baseline phenotypes from the International Fibrodysplasia Ossificans Progressiva (FOP) Association Global Registry(2020)35 cited
- → The FOP Connection Registry: Design of an international patient-sponsored registry for Fibrodysplasia Ossificans Progressiva(2017)32 cited
- → Fibrodysplasia Ossificans Progressiva: What Have We Achieved and Where Are We Now? Follow-up to the 2015 Lorentz Workshop(2021)26 cited
- → International physician survey on management of FOP: a modified Delphi study(2017)21 cited