A. Correra

发表

L. Terracciano, G. Marseglia, S. Modi, 2009, Biologics : targets & therapy.

Reduction of Inappropriate Hospital Admissions of Children With Influenza-Like Illness Through the Implementation of Specific Guidelines: A Case-Controlled Study

T. Jefferson, A. Guarino, A. Correra, 2005, Pediatrics.

Molecular Epidemiology of Phenylalanine Hydroxylase Deficiency in Southern Italy: a 96% Detection Rate with Ten Novel Mutations

G. Castaldo, F. Salvatore, G. Cardillo, 2007, Annals of human genetics.

Deficiency of the Fas apoptosis pathway without Fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation.

U. Dianzani, I. Dianzani, S. Bonissoni, 1997, Blood.

Lymphoproliferative Syndrome : A Molecular and Immunological Analysis Missense Mutations in the Fas Gene Resulting in Autoimmune

L. Notarangelo, E. Quiros-Roldan, A. Correra, 1997 .

Prevention of food and airway allergy: consensus of the Italian Society of Preventive and Social Paediatrics, the Italian Society of Paediatric Allergy and Immunology, and Italian Society of Pediatrics

L. Terracciano, G. Marseglia, G. D. de’ Angelis, 2016, The World Allergy Organization journal.

Five human phenylalanine hydroxylase proteins identified in mild hyperphenylalaninemia patients are disease-causing variants.

A. Zagari, L. Esposito, G. Castaldo, 2008, Biochimica et biophysica acta.

HHH syndrome (hyperornithinaemia, hyperammonaemia, homocitrullinuria), with fulminant hepatitis-like presentation

F. Santorelli, G. Andria, P. Vajro, 2006, Journal of Inherited Metabolic Disease.

Short duration of breastfeeding and early introduction of cow's milk as a result of mothers’low level of education

A. Guarino, A. Correra, D. Ummarino, 2003, Acta paediatrica (Oslo, Norway : 1992). Supplement.

Prediction of Intellectual Deficits in Children with Acute Lymphoblastic Leukemia

I. Schonfeld, A. Sitarz, D. Shaffer, 1988, Journal of developmental and behavioral pediatrics : JDBP.

Radiotherapy of a pseudotumor in a hemophiliac with Factor VIII inhibitor.

A. Correra, J. Buckley, A. Schreiber, 1984, The American journal of pediatric hematology/oncology.

Missense mutations in the Fas gene resulting in autoimmune lymphoproliferative syndrome: a molecular and immunological analysis.

L. Notarangelo, S. La Grutta, E. Quiros-Roldan, 1997, Blood.

Pediatric claims in Italy during a 8-years survey

L. Greco, E. d’Aloja, V. Fanos, 2014, Italian Journal of Pediatrics.

Neonatal malpractice claims in Italy: how big is the problem and which are the causes?

L. Greco, V. Fanos, P. Tagliabue, 2012, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Sensitivity and Specificity of Soluble Triggering Receptor Expressed on Myeloid Cells-1, Midregional Proatrial Natriuretic Peptide and Midregional Proadrenomedullin for Distinguishing Etiology and to Assess Severity in Community-Acquired Pneumonia

E. Baraldi, S. Esposito, N. Principi, 2016, PloS one.

[Italian Pediatrician's consensus statement on anti-Rotavirus vaccines].

A. Ugazio, F. Ansaldi, A. Guarino, 2008, Minerva pediatrica.

Peptichemio in children with neoplastic disease.

A. Correra, M. Pasino, L. Massimo, 1976, Anales espanoles de pediatria.