Rosario Ramos Mejía (Rosario Ramos-Mejía, Rosario Ramos-Mejia, R Ramos-Mejía)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 10

Top Topics

Particulate Matter

Palliative Care

Top Venues

American journal of medical genetics. Part A

Journal of pediatric genetics

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)
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)
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)
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)
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)
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)
Rosario Ramos Mejía, Miriam Aza-Carmona, Mariana Del Pino, Karen E Heath, Virginia Fano, Maria Gabriela Obregon
Clinical and Radiologic Evaluation of an Individual with Hypochondroplasia and a Novel FGFR3 Mutation. Journal of pediatric genetics 9 (1) (2019)