نتائج البحث - "Fano, Virginia"

1

دورية

International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia

المؤلفون: Savarirayan, Ravi, Ireland, Penny, Irving, Melita, Thompson, Dominic, Alves, Inês, Baratela, Wagner A. R., Betts, James, Bober, Michael B., Boero, Silvio, Briddell, Jenna, Campbell, Jeffrey, Campeau, Philippe M., Carl-Innig, Patricia, Cheung, Moira S., Cobourne, Martyn, Cormier-Daire, Valérie, Deladure-Molla, Muriel, del Pino, Mariana, Elphick, Heather, Fano, Virginia, Fauroux, Brigitte, Gibbins, Jonathan, Groves, Mari L., Hagenäs, Lars, Hannon, Therese, Hoover-Fong, Julie, Kaisermann, Morrys, Leiva-Gea, Antonio, Llerena, Juan, Mackenzie, William, Martin, Kenneth, Mazzoleni, Fabio, McDonnell, Sharon, Meazzini, Maria Costanza, Milerad, Josef, Mohnike, Klaus, Mortier, Geert R., Offiah, Amaka, Ozono, Keiichi, Phillips, John A., Powell, Steven, Prasad, Yosha, Raggio, Cathleen, Rosselli, Pablo, Rossiter, Judith, Selicorni, Angelo, Sessa, Marco, Theroux, Mary, Thomas, Matthew, Trespedi, Laura, Tunkel, David, Wallis, Colin, Wright, Michael, Yasui, Natsuo, Fredwall, Svein Otto

المصدر: Nature Reviews Endocrinology; March 2022, Vol. 18 Issue: 3 p173-189, 17p

2

دورية

Hereditary hypophosphatemic rickets and craniosynostosis

المؤلفون: Arenas, María Alejandra, Jaimovich, Sebastián, Perez Garrido, Natalia, del Pino, Mariana, Viterbo, Gisela, Marino, Roxana, Fano, Virginia

المصدر: Journal of Pediatric Endocrinology & Metabolism; September 2021, Vol. 34 Issue: 9 p1105-1113, 9p

3

دورية

Growth in achondroplasia, from birth to adulthood, analysed by the JPA-2 model

المؤلفون: del Pino, Mariana, Fano, Virginia, Adamo, Paula

المصدر: Journal of Pediatric Endocrinology & Metabolism; December 2020, Vol. 33 Issue: 12 p1589-1595, 7p

4

دورية

Skeletal dysplasias in Latin America

المؤلفون: Cavalcanti, Denise P., Fano, Virginia, Mellado, Cecilia, Lacarrubba‐Flores, Maria Dora J., Silveira, Cynthia, Silveira, Karina C., Pino, Mariana, Moresco, Angelica, Caino, Silvia, Ramos Mejía, Rosario, García, Cristián J., Lay‐Son, Guillermo, Ferreira, Carlos R.

المصدر: American Journal of Medical Genetics. Part C, Seminars in Medical Genetics; December 2020, Vol. 184 Issue: 4 p986-995, 10p

5

دورية

Clinical and Radiologic Evaluation of an Individual with Hypochondroplasia and a Novel FGFR3 Mutation

المؤلفون: Ramos Mejía, Rosario, Aza-Carmona, Miriam, del Pino, Mariana, Heath, Karen E., Fano, Virginia, Obregon, Maria Gabriela

المصدر: Journal of Pediatric Genetics; March 2020, Vol. 9 Issue: 1 p048-052, 5p

6

دورية

SHOX Deficiency in Argentinean Cohort: Long-Term Auxological Follow-Up and a Family's New Mutation

المؤلفون: del Pino, Mariana, Aza-Carmona, Miriam, Medino-Martín, David, Gomez, Abel, Heath, Karen E., Fano, Virginia, Obregon, María Gabriela

المصدر: Journal of Pediatric Genetics; September 2019, Vol. 8 Issue: 3 p123-132, 10p

7

دورية

FGFR3-related hypochondroplasia: longitudinal growth in 57 children with the p.Asn540Lys mutation

المؤلفون: Arenas, María Alejandra, del Pino, Mariana, Fano, Virginia

المصدر: Journal of Pediatric Endocrinology & Metabolism; November 2018, Vol. 31 Issue: 11 p1279-1284, 6p

8

دورية

Growth velocity and biological variables during puberty in achondroplasia

المؤلفون: del Pino, Mariana, Fano, Virginia, Adamo, Paula

المصدر: Journal of Pediatric Endocrinology & Metabolism; March 2018, Vol. 31 Issue: 4 p421-428, 8p

9

دورية

Acetabular Protrusion in a Cohort of Patients with Osteogenesis Imperfecta Evaluated in a Pediatric Hospital

المؤلفون: Ramos-Mejía, Rosario, Monterroza-Quintana, Francisco, Primomo, Claudio, Goyeneche, Rodolfo, Fano, Virginia

المصدر: Journal of Pediatric Genetics; 20220101, Issue: Preprints

10

دورية

Clinical‐etiologic correlation in children with Prader‐Willi syndrome (PWS): An interdisciplinary studyHow to cite this article: Torrado M, Araoz V, Baialardo E, Abraldes K, Mazza C, Krochik G, Ozuna B, Leske V, Caino S, Fano V, Chertkoff L. 2007. Clinical‐etiologic correlation in children with Prader‐Willi syndrome (PWS): An interdisciplinary study. Am J Med Genet Part A 143A:460–468.

المؤلفون: Torrado, Maria, Araoz, Veronica, Baialardo, Edgardo, Abraldes, Karina, Mazza, Carmen, Krochik, Gabriela, Ozuna, Blanca, Leske, Vivian, Caino, Silvia, Fano, Virginia, Chertkoff, Lilien

المصدر: American Journal of Medical Genetics. Part A; March 2007, Vol. 143 Issue: 5 p460-468, 9p

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