Get started
Author

Claudia Cantarini

Observed names: C. Cantarini, Cantarini, Claudia
ORCID: 0000-0002-8960-2678
Observed ORCID: 0000-0002-8960-2678
OpenAlex ID: A5084070914
Hereditary Hemorrhagic Telangiectasia in Pediatric Age: Focus on Genetics and Diagnosis
2023 · Cesare Danesino, Claudia Cantarini, et al. · Pediatric Reports · 22
PDF
Endoglin and Systemic Sclerosis: A PRISMA-driven systematic review
2022 · Silvia Grignaschi, Anna Sbalchiero, et al. · Frontiers in Medicine · 9
PDF
Specifications of the ACMG/AMP Variant Curation Guidelines for Hereditary Hemorrhagic Telangiectasia Genes—ENG and ACVRL1
2024 · Desiree DeMille, Jamie McDonald, et al. · Human Mutation · 7
PDF
Generation of ALK1 p.Gly48Glu mutant LUMCi029-A-3 for modeling Hereditary hemorrhagic telangiectasia type 2
2026 · E. Koutala, C. Cantarini, et al. · Stem Cell Research
Generation of ENG p.Met1Val mutant LUMCi029-A-2 for modeling Hereditary Hemorrhagic Telangiectasia type 1
2026 · C. Cantarini, V. Lorrain, et al. · Stem Cell Research
Specifications of the ACMG/AMP Variant Curation Guidelines for Hereditary Hemorrhagic Telangiectasia Genes—ENG and ACVRL1
2024 · Tusseau, Maud, Shovlin, Claire L., et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
PDF
Ab0140 Role of Endoglin in the Pathogenesis of Systemic Sclerosis: a Prisma-driven Systematic Review
2022 · S. Grignaschi, B.L. Palermo, et al. · Annals of the Rheumatic Diseases
PDF
Works count: 8
Citation count: 38
H-index: 3
I10-index: 1
Year
Topic
Type