La Pediatria Medica e Chirurgica Vol. 37 No. 2 (2015)

Articles

Prevalence of child sexual abuse: a comparison among 4 Italian epidemiological studies

Beatrice Castelli, Fiorella Festa, Maria Angela Di Sanzo, Andrea Guala, Alberto Pellai

https://doi.org/10.4081/pmc.2015.114

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Laparoscopic herniorrhaphy in children

Mirko Bertozzi, Laura Marchesini, Simonetta Tesoro, Antonino Appignani

https://doi.org/10.4081/pmc.2015.109

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Obstructive sleep apnea in Prader-Willi syndrome: risks and advantages of adenotonsillectomy

Leone Giordano, Salvatore Toma, Francesca Palonta, Roberto Teggi, Marco Zucconi, Stefania Di Candia, Mario Bussi

https://doi.org/10.4081/pmc.2015.107

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Case Reports

Ureteral rupture after blunt abdominal trauma in a child with unknown horseshoe kidney

Arianna Mariotto, Nicola Zampieri, Mariangela Cecchetto, Francesco Saverio Camoglio

https://doi.org/10.4081/pmc.2015.110

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A rare case of discrete aortic coarctation in Williams-Beuren syndrome. Diagnostic and therapeutic considerations

Savina Mannarino, Eitan Keizman, Michele Pasotti, Alessia Claudia Codazzi, Elisabetta De Sando, Alessandro Giamberti

https://doi.org/10.4081/pmc.2015.120

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Short Communications

Mitotic crossover promotes leukemogenesis in children born with TEL-AML1 via the generation of loss of heterozygosity at 12p

Ivan Ivanovski, Livia Garavelli, Olivera DjuriÄ‡, Aleksandar Ä†iroviÄ‡, Dejan Å koriÄ‡, Petar I. Ivanovski

https://doi.org/10.4081/pmc.2015.112

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Vol. 37 No. 2 (2015)

Articles

Prevalence of child sexual abuse: a comparison among 4 Italian epidemiological studies

Laparoscopic herniorrhaphy in children

Obstructive sleep apnea in Prader-Willi syndrome: risks and advantages of adenotonsillectomy

Case Reports

Ureteral rupture after blunt abdominal trauma in a child with unknown horseshoe kidney

A rare case of discrete aortic coarctation in Williams-Beuren syndrome. Diagnostic and therapeutic considerations

Short Communications

Mitotic crossover promotes leukemogenesis in children born with TEL-AML1 via the generation of loss of heterozygosity at 12p

authors

reviewers

indexing

Keywords