Virginia Fano (V Fano)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 16

Top Topics

Particulate Matter

Neuropathic Pain

Ejection Fraction

Top Venues

American journal of medical genetics. Part A

Journal of pediatric genetics

Archivos argentinos de pediatria

Journal of endocrinological investigation

This page only lists publications with an associated author ORCID identifier.

Publications

Rosario Ramos Mejía, G Isoldi, Penelope J Ireland, Mercedes Rodriguez Celin, Virginia Fano
Evaluation of functionality-mobility in patients with skeletal dysplasias. Application of the STEMS tool ("everyday symptoms and mobility screening tool for skeletal dysplasias"). American journal of medical genetics. Part A 194 (5) (2024)
Rosario Ramos Mejía, G Isoldi, Penelope J Ireland, Mercedes Rodriguez Celin, Virginia Fano
Evaluation of functionality-mobility in patients with skeletal dysplasias. Application of the STEMS tool ("everyday symptoms and mobility screening tool for skeletal dysplasias"). American journal of medical genetics. Part A (2024)
Rosario Ramos Mejía, G Isoldi, Penelope J Ireland, Mercedes Rodriguez Celin, Virginia Fano
Evaluation of functionality-mobility in patients with skeletal dysplasias. Application of the STEMS tool ("everyday symptoms and mobility screening tool for skeletal dysplasias"). American journal of medical genetics. Part A 194 (5) (2024)
Rosario Ramos Mejía, G Isoldi, Penelope J Ireland, Mercedes Rodriguez Celin, Virginia Fano
Evaluation of functionality-mobility in patients with skeletal dysplasias. Application of the STEMS tool ("everyday symptoms and mobility screening tool for skeletal dysplasias"). American journal of medical genetics. Part A 194 (5) (2024)
María V Wolf, Angélica A Moresco, Virginia Fano, Silvia Caino
Clinical and auxological characteristics and quality of life of 50 children and adolescents with segmental overgrowth syndromes at a single center. Archivos argentinos de pediatria (2023)
Rosario Ramos Mejía, Karen E Heath, Silvia Modamio-HØybjØr, Victoria Huckstadt, Calcagni Julián, Rodrigo G Remondino, Virginia Fano
Unexpected findings in cervical spine in spondylometaphyseal dysplasia Sutcliff type FN1-related. American journal of medical genetics. Part A (2023)
Silvia Caino, Romina Alba, Silvina Bevilacqua, Mariana Roizen, María Gabriela Obregon, Virginia Fano
Osteochondromatosis: clinical variability and factors related to quality of life in children and adults. Archivos argentinos de pediatria 120 (3) (2022)
Mariana Del Pino, Gisela L Viterbo, María Alejandra Arenas, Natalia Perez Garrido, Pablo Ramirez, Roxana Marino, Alicia Belgorosky, Virginia Fano
Growth in height and body proportion from birth to adulthood in hereditary hypophosphatemic rickets: a retrospective cohort study. Journal of endocrinological investigation 45 (7) (2022)
Rosario Ramos Mejía, Mariana Del Pino, M Aza-Carmona, Silvina Abbate, María Gabriela Obregon, Karen E Heath, Virginia Fano
Novel FLNB Variants in Seven Argentinian Cases with Spondylocarpotarsal Synostosis Syndrome. Journal of pediatric genetics 13 (3) (2022)
Silvia Caino, Marisa Angelica Cubilla, Romina Alba, María Gabriela Obregón, Virginia Fano, Abel Gómez, Lorena Zecchini, Pablo Lapunzina, Miriam Aza-Carmona, Karen Elise Heath, Carla Gabriela Asteggiano
Clinical and Genetic Analysis of Multiple Osteochondromas in A Cohort of Argentine Patients. Genes 13 (11) (2022)
Rosario Ramos Mejía, Mariana Del Pino, M Aza-Carmona, Silvina Abbate, María Gabriela Obregon, Karen E Heath, Virginia Fano
Novel FLNB Variants in Seven Argentinian Cases with Spondylocarpotarsal Synostosis Syndrome. Journal of pediatric genetics 13 (3) (2022)
María J Romaris, Silvia Caino, Paula Adamo, Virginia Fano
Isolated lateralized overgrowth: clinical, radiological, and auxological characteristics of a single-site cohort of 76 cases. Archivos argentinos de pediatria 120 (6) (2022)
Rosario Ramos Mejía, Francisco Monterroza-Quintana, Claudio Primomo, Rodolfo Goyeneche, Virginia Fano
Acetabular Protrusion in a Cohort of Patients with Osteogenesis Imperfecta Evaluated in a Pediatric Hospital. Journal of pediatric genetics 12 (1) (2021)
Ravi Savarirayan, Penny Ireland, Melita Irving, Dominic Thompson, Inês Alves, Wagner A R Baratela, James Betts, Michael B Bober, Silvio Boero, Jenna Briddell, Jeffrey Campbell, Philippe M Campeau, Patricia Carl-Innig, Moira Shang-Mei Cheung, Martyn Cobourne, Valérie Cormier-Daire, Muriel Deladure-Molla, Mariana Del Pino, Heather Elphick, Virginia Fano, Brigitte Fauroux, Jonathan Gibbins, Mari L Groves, Lars Hagenäs, Therese Hannon, Julie Elizabeth Hoover-Fong, Morrys Kaisermann, Antonio Leiva-Gea, Juan Llerena, William G Mackenzie, Kenneth Martin, Fabio Mazzoleni, Sharon McDonnell, Maria Costanza Meazzini, Josef Milerad, Klaus Mohnike, Geert R Mortier, Amaka C Offiah, Keiichi Ozono, John A Phillips, Steven Powell, Yosha Prasad, Cathleen Raggio, Pablo Rosselli, Judith Rossiter, Angelo Selicorni, Marco Sessa, Mary Theroux, Matthew Thomas, Laura Trespedi, David Tunkel, Colin Wallis, Michael Wright, Natsuo Yasui, Svein Otto Fredwall
International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia. Nature reviews. Endocrinology (2021)
Rosario Ramos Mejía, Francisco Monterroza-Quintana, Claudio Primomo, Rodolfo Goyeneche, Virginia Fano
Acetabular Protrusion in a Cohort of Patients with Osteogenesis Imperfecta Evaluated in a Pediatric Hospital. Journal of pediatric genetics 12 (1) (2021)
María Alejandra Arenas, Sebastián Jaimovich, Natalia Perez Garrido, Mariana Del Pino, Gisela L Viterbo, Roxana Marino, Virginia Fano
Hereditary hypophosphatemic rickets and craniosynostosis. Journal of pediatric endocrinology & metabolism : JPEM 34 (9) (2021)