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European Journal of Haematology|January 12, 2010
Co-inheritance of Hb Hershey [beta70(E14) Ala-->Gly] and Hb La Pommeraie [beta133(H11)Val-->Met] in a Sicilian subjectAntonino Giambona, Margherita Vinciguerra, Cristina Passarello, et al.
International Archives of Allergy and Immunology|June 9, 2012
Serum IL-23 strongly and inversely correlates with FEV1 in asthmatic childrenGiorgio Ciprandi, Caterina Cuppari, Anna Maria Salpietro, et al.
The American Journal of Cardiology|July 23, 2013
Early identification of cardiovascular involvement in patients with β-thalassemia majorMaurizio Cusmà Piccione, Basilia Piraino, Concetta Zito, et al.
European Journal of Endocrinology|September 10, 2013
Thyroid dysfunction in thalassaemic patients: ferritin as a prognostic marker and combined iron chelators as an ideal therapyValeria Chirico, Chirico Valeria, Antonio Lacquaniti, et al.
World Journal of Gastroenterology|August 6, 2008
Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel diseaseLuciana Rigoli, Claudio Romano, Rosario Alberto Caruso, et al.
Human Mutation|December 6, 2008
MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvementFrancesco Brancati, Miriam Iannicelli, Lorena Travaglini, et al.
American Journal of Human Genetics|June 15, 2007
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disordersFrancesco Brancati, Giuseppe Barrano, Jennifer L Silhavy, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Expanding CEP290 mutational spectrum in ciliopathiesLorena Travaglini, Francesco Brancati, Tania Attie-Bitach, et al.
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