https://doi.org/10.4081/pmc.2013.33
Turner-like Syndrome: a case report
Submitted: 17 November 2014
Accepted: 17 November 2014
Published: 31 October 2013
Accepted: 17 November 2014
Abstract Views: 1164
PDF: 1128
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Authors
How to Cite
Velletri, M., Valenzise, M., Wasniewska, M., Arasi, S., Santisi, A., Romeo, M., … Zirilli, G. (2013). Turner-like Syndrome: a case report. La Pediatria Medica E Chirurgica, 35(5). https://doi.org/10.4081/pmc.2013.33
PAGEPress has chosen to apply the Creative Commons Attribution NonCommercial 4.0 International License (CC BY-NC 4.0) to all manuscripts to be published.
Similar Articles
- Ivan Ivanovski, Livia Garavelli, Olivera Djurić, Aleksandar Ćirović, Dejan Škorić, Petar I. Ivanovski, Mitotic crossover promotes leukemogenesis in children born with TEL-AML1 via the generation of loss of heterozygosity at 12p , La Pediatria Medica e Chirurgica: Vol. 37 No. 2 (2015)
- Agostino Berio, Attilia Piazzi, Carlo Enrico Traverso, Kearns-Sayre syndrome with facial and white matter extensive involvement: a (mitochondrial and nuclear gene related?) neurocristopathy? , La Pediatria Medica e Chirurgica: Vol. 39 No. 4 (2017)
- Agostino Berio, Giacomo Garlaschi, Giuseppe Mangiante, Attilia Piazzi, Oculo-auriculo-vertebral spectrum with craniosynostosis and osteo-cartilagineous multiple defects: a diffuse chondro-membranous-osteo-dysplasia , La Pediatria Medica e Chirurgica: Vol. 37 No. 3 (2015)
- Savina Mannarino, Eitan Keizman, Michele Pasotti, Alessia Claudia Codazzi, Elisabetta De Sando, Alessandro Giamberti, A rare case of discrete aortic coarctation in Williams-Beuren syndrome. Diagnostic and therapeutic considerations , La Pediatria Medica e Chirurgica: Vol. 37 No. 2 (2015)
- Massimo Agosti, Francesco Tandoi, Laura Morlacchi, Angela Bossi, Nutritional and metabolic programming during the first thousand days of life , La Pediatria Medica e Chirurgica: Vol. 39 No. 2 (2017)
- F. Porcaro, M. Valenzise, G. Candela, F. Chiera, D. Corica, E. Pitrolo, S. Santucci, M. Romeo, S. Nigro, G. Zirilli, Evans Syndrome: A case report , La Pediatria Medica e Chirurgica: Vol. 36 No. 4 (2014)
- A.A. Zuppa, G. Alighieri, A. Fracchiolla, P. Catenazzi, A. D’Antuono, R. Riccardi, M. Cavani, C. Romagnoli, Comparison between two treatment protocols with recombinant Human Erythropoietin (rHuEpo) in the treatment of late anemia in neonates with Rh-Isoimmunization , La Pediatria Medica e Chirurgica: Vol. 34 No. 4 (2012)
- Giovanni Murialdo, Attilia Piazzi, Giuseppe Badolati, Enrico Calcagno, Agostino Berio, Oculo-auriculo-vertebral spectrum with myopathy and velopharyngeal insufficiency. A case report with a non-branchiomeric muscle biopsy , La Pediatria Medica e Chirurgica: Vol. 38 No. 2 (2016)
- Muhammad Faizi, Nur Rochmah, Soetjipto Soetjipto, Anang Endaryanto, Sukmawati Basuki, Yuni Hisbiyah, Rayi Kurnia Perwitasari, Protein tyrosine phosphatase non-receptor type 22 C1858T gene polymorphism in children with Down syndrome and autoimmune thyroid diseases , La Pediatria Medica e Chirurgica: Vol. 45 No. 1 (2023)
- E. Ruffini, A.M. Bianchi, L. De Petris, M.K. Fares, G. Zorzi, A. Carlucci, Chronic Massive Fetomaternal Hemorrhage in a newborn from immigrants. Clinical and organizational implications , La Pediatria Medica e Chirurgica: Vol. 34 No. 5 (2012)
You may also start an advanced similarity search for this article.