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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

  1405

  PDF: 1338
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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

  1602

  PDF: 323

  HTML: 33
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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

  9575

  PDF: 5413

  Appendix: 474

  HTML: 1462
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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

  703

  PDF: 287

  HTML: 4

• 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

  1888

  PDF: 1568
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  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

  941

  PDF: 448

  HTML: 19
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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

  1914

  PDF: 1007

  HTML: 301
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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

  1897

  PDF: 1083

  HTML: 263
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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

  1894

  PDF: 944

  HTML: 603
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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

  2739

  PDF: 1342

  HTML: 237