G. Chiaffoni

Molecular genetic diagnosis of autosomal dominant polycystic kidney disease in a newborn with bilateral cystic kidneys detected prenatally and multiple skeletal malformations.

P. Pignatti, G. Maschio, S. Rossetti, 1993, Journal of medical genetics.

Routine coagulation tests in newborn and young infants

G. Lippi, M. Franchini, G. Salvagno, 2007, Journal of Thrombosis and Thrombolysis.

Skeletal malformations and polycystic kidney disease.

P. Pignatti, S. Rossetti, B. Peissel, 1994, Journal of medical genetics.

Intrauterine anemia due to parvovirus B19: successful treatment with intravenous immunoglobulins.

Smith Dw, C. Borgna-Pignatti, E. Grau, 1999, Haematologica.

malformations . detected prenatally and multiple skeletal newborn with bilateral cystic kidneys dominant polycystic kidney disease in a Molecular genetic diagnosis of autosomal

P. Pignatti, G. Maschio, S. Rossetti, 2022 .

Essential newborn care training activities: 8 years of experience in Eastern European, Caucasian and Central Asian countries.

V. Mangiaterra, F. Uxa, G. Chiaffoni, 2006, Seminars in fetal & neonatal medicine.

Staphylococcus epidermidis isolation and antibiotic resistance in a neonatal intensive care unit.

V. Fanos, E. Padovani, A. Dal Moro, 1995, Journal of chemotherapy.

Trends in perinatal care in developing countries.

G. Chiaffoni, A. Bacci, 2006, Seminars in fetal & neonatal medicine.