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Works (8)

Imaging in osteogenesis imperfecta: Where we are and where we are going

European Journal of Medical Genetics
2024 | Journal article
EID:

2-s2.0-85186426483

Part of ISSN: 18780849 17697212
Contributors: Gazzotti, S.; Sassi, R.; Aparisi Gómez, M.P.; Moroni, A.; Brizola, E.; Miceli, M.; Bazzocchi, A.
Source: Self-asserted source
Alice Moroni via Scopus - Elsevier

Multiple Osteochondritis Dissecans as Main Manifestation of Multiple Epiphyseal Dysplasia Caused by a Novel Cartilage Oligomeric Matrix Protein Pathogenic Variant: A Clinical Report

Genes
2024-11-20 | Journal article
Contributors: Antonio Mazzotti; Elena Artioli; Evelise Brizola; Alice Moroni; Morena Tremosini; Alessia Di Cecco; Salvatore Gallone; Cesare Faldini; Luca Sangiorgi; Maria Gnoli
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A Novel Pathogenic Large Duplication in EXT1 Identified in a Family with Multiple Osteochondromas

Genes
2024-09-05 | Journal article
Contributors: Isabella Bartolotti; Klaudia Sobul; Serena Corsini; Davide Scognamiglio; Alice Moroni; Maria Gnoli; Luca Sangiorgi; Elena Pedrini
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The Role of the European Reference Network for Rare Bone Diseases (ERN BOND) and European Registries for Rare Bone and Mineral Conditions (EuRR-Bone) in the Governance of the Management of Rare Bone and Mineral Diseases

Calcified Tissue International
2024-07-26 | Journal article
Contributors: Ana Luisa Priego Zurita; Manila Boarini; Lorena Casareto; Mariya Cherenko; Marina Mordenti; Alice Moroni; S. Faisal Ahmed; Natasha M. Appelman-Dijkstra; Luca Sangiorgi
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Pathological mandibular fracture complicated by osteonecrosis in an adult patient with pycnodysostosis: clinical report and review of the literature

European Journal of Medical Genetics
2024-02 | Journal article
Contributors: Alice Moroni; Evelise Brizola; Alessia Di Cecco; Morena Tremosini; Marta Sergiampietri; Alberto Bianchi; Barbara Tappino; Maria Piana; Maria Gnoli
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Rock around DYRK1A: Ethnic diversity, clinical challenges

American Journal of Medical Genetics Part A
2023-05 | Journal article
Contributors: Alice Moroni; Lidia Pezzani; Enrico Alfei; Agnese Scatigno; Anna Cereda; Michela Marzaroli; Claudia Guuva; Sara Gabbiadini; Laura Pezzoli; Daniela Marchetti et al.
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Atypical microdeletion 22q11.2 in a patient with tetralogy of Fallot

Journal of Genetics
2021 | Journal article
EID:

2-s2.0-85100963559

Part of ISSN: 09737731 00221333
Contributors: Carli, D.; Moroni, A.; Eleonora, D.G.; Zonta, A.; Montin, D.; Licciardi, F.; Aidala, E.; Bordese, R.; Carlo, P.N.; Brusco, A. et al.
Source: Self-asserted source
Alice Moroni via Scopus - Elsevier

Nutrients intake is associated with DNA methylation of candidate inflammatory genes in a population of obese subjects

Nutrients
2014 | Journal article
EID:

2-s2.0-84908177730

Part of ISSN: 20726643
Contributors: Bollati, V.; Favero, C.; Albetti, B.; Tarantini, L.; Moroni, A.; Byun, H.-M.; Motta, V.; Conti, D.M.; Tirelli, A.S.; Vigna, L. et al.
Source: Self-asserted source
Alice Moroni via Scopus - Elsevier

Peer review (1 review for 1 publication/grant)

Review activity for Journal of bone oncology. (1)