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Neonatology – Italian Society of Neonatology (SIN)

This section covers all aspects of neonatal and fetal health, disease, treatment, and outcomes.

Page 6 of 6

  1. Persistent pulmonary hypertension of the newborn (PPHN) is a severe condition that determines a profound brain hypoxia. Inhaled nitric oxide was approved for the treatment of PPHN since the end of the 1990s. T...

    Authors: Anna Berti, Augusta Janes, Riccardo Furlan and Francesco Macagno
    Citation: Italian Journal of Pediatrics 2010 36:45
  2. Liver failure in neonates is a rare but often fatal disease. Trisomy 21 is not usually associated with significant infantile liver disease. If present, hepatic dysfunction in an infant with Trisomy 21 is likel...

    Authors: Erin Neil, Josef Cortez, Aparna Joshi, Erawati V Bawle, Janet Poulik, Mark Zilberman, Mohammad F El-Baba and Beena G Sood
    Citation: Italian Journal of Pediatrics 2010 36:38
  3. Two premature twins (33 weeks gestation) were born to a woman who had used paroxetine during pregnancy for an anxiety-depression disorder. They were admitted to the NICU, where they showed prolonged RDS, cardi...

    Authors: Maria Marsella, Elisabetta Ubaldini, Agostina Solinas and Pietro Guerrini
    Citation: Italian Journal of Pediatrics 2010 36:27
  4. Classical Poland Syndrome (PS) is characterized by unilateral, partial or complete absence of the sternocostal head of the major pectoral muscle and brachysyndactyly of fingers on the same side.

    Authors: Doriana Lacorte, Maria Marsella and Pietro Guerrini
    Citation: Italian Journal of Pediatrics 2010 36:21
  5. The perfusion index, derived from the pulse oximeter signal, seems to be an accurate predictor for high illness severity in newborns. The aim of this study was to determine the perfusion index values of clinic...

    Authors: Francesco Cresi, Emanuela Pelle, Roberto Calabrese, Luciana Costa, Daniela Farinasso and Leandra Silvestro
    Citation: Italian Journal of Pediatrics 2010 36:6
  6. Pyloric atresia (PA) is a very rare condition. Its incidence is approximately 1 in 100,000 newborns and constitutes about 1% of all intestinal atresias. We describe the neonatal course of a peculiar case of ty...

    Authors: Enrico Zecca, Mirta Corsello, Claudio Pintus, Lorenzo Nanni and Susanna Zecca
    Citation: Italian Journal of Pediatrics 2010 36:3
  7. Congenital afibrinogenemia is a very rare inherited coagulation disorder, characterized by virtual absence of plasma fibrinogen (factor I). There are only about 250 cases reported in the world literature [1]. We ...

    Authors: Gopakumar Hariharan, Sivji Ramachandran and Rajiv Parapurath
    Citation: Italian Journal of Pediatrics 2010 36:1

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