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• Life Experiences and Coping Strategies in Adults with Congenital Heart Disease

  E. Callus, E. Quadri, A. Compare, A. Tovo, A. Giamberti, M. Chessa

  31-10-2013

  https://doi.org/10.4081/pmc.2013.34

  1865

  PDF: 1603
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  Outcomes of delayed chest closure after congenital heart surgery in neonates

  Meletios Kanakis, George Samanidis, Kyriaki Kolovou, Sotirios Katsaridis , Athina Maria Sait, Georgios Kourelis, Nicholas Giannopoulos, Dimitrios Bobos

  22-02-2024

  https://doi.org/10.4081/pmc.2024.328

  2282

  PDF: 734

  HTML: 211
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  Feeding dysfunctions and failure to thrive in neonates with congenital heart diseases

  Giovanna Mangili, Elena Garzoli, Youcef Sadou

  23-05-2018

  https://doi.org/10.4081/pmc.2018.196

  10590

  PDF: 6062

  Appendix: 563

  HTML: 1487
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  Follow-up study of three cases of congenital microgastria

  Sara Ugolini, Chiara Oreglio, Karl Christian Walsh, Antonino Morabito

  15-12-2023

  https://doi.org/10.4081/pmc.2023.326

  1791

  PDF: 562

  HTML: 15

• From outreach to ownership: building sustainable paediatric surgical capacity at a secondary hospital in rural Tanzania. A ten-year experience

  Boniphace Tresphory, Alessandro Calisti, Elide Ambrosetti, Grazia Andriani, Giovanna Maria Cangi, Giovanni Giuliani, Bahati Kamwezi, Agnes Mlawa, Andrea Joseph Mombo, Paola Presutti, Bruno Turchetta

  13-05-2026

  https://doi.org/10.4081/pmc.2026.377

  164

  PDF: 115

  Supplementary materials: 16

  HTML: 7

• Art therapy for hospitalised congenital heart disease patients: a method of psychological intervention at the IRCCS Policlinico San Donato Milanese Hopsital

  E. Quadri, C. Farè, E. Palmero, G. Campioni, M. Chessa, E. Callus

  31-12-2012

  https://doi.org/10.4081/pmc.2012.54

  2286

  PDF: 1771
• 

  Protein tyrosine phosphatase non-receptor type 22 C1858T gene polymorphism in children with Down syndrome and autoimmune thyroid diseases

  Muhammad Faizi, Nur Rochmah, Soetjipto Soetjipto, Anang Endaryanto, Sukmawati Basuki, Yuni Hisbiyah, Rayi Kurnia Perwitasari

  22-02-2023

  https://doi.org/10.4081/pmc.2023.283

  1360

  PDF: 732

  HTML: 31
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  Kearns-Sayre syndrome with facial and white matter extensive involvement: a (mitochondrial and nuclear gene related?) neurocristopathy?

  Agostino Berio, Attilia Piazzi, Carlo Enrico Traverso

  15-12-2017

  https://doi.org/10.4081/pmc.2017.169

  2248

  PDF: 1203

  HTML: 334
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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

  24-11-2015

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

  2314

  PDF: 1331

  HTML: 278
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  Oculo-auriculo-vertebral spectrum with craniosynostosis and osteo-cartilagineous multiple defects: a diffuse chondro-membranous-osteo-dysplasia

  Agostino Berio, Giacomo Garlaschi, Giuseppe Mangiante, Attilia Piazzi

  29-12-2015

  https://doi.org/10.4081/pmc.2015.123

  2219

  PDF: 1152

  HTML: 635
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  Mitotic crossover promotes leukemogenesis in children born with TEL-AML1 via the generation of loss of heterozygosity at 12p

  Ivan Ivanovski, Livia Garavelli, Olivera Djurić, Aleksandar Ćirović, Dejan Škorić, Petar I. Ivanovski

  24-11-2015

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

  3176

  PDF: 1498

  HTML: 244

• Advances in pediatrics: new technologies in clinical practice

  Gianvincenzo Zuccotti, Roberto Sassi, Maurizio Vertemati, Valeria Calcaterra

  26-02-2026

  https://doi.org/10.4081/pmc.2026.380

  685

  PDF: 391

  HTML: 19