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2016
Rabach I, Salis S, Bruno I, Ventura A. Macrocephaly and palmoplantar pitting. Arch Dis Child 2016;
Zupin L, Polesello V, Segat L, Kuhn L, Crovella S. MBL2 genetic polymorphisms and HIV-1 mother-to-child transmission in Zambia. Immunol Res 2016;64(3):775-84.
Zupin L, Polesello V, Alberi G, Moratelli G, Crocè SL, Masutti F, Pozzato G, Crovella S, Segat L. MBL2 Genetic Variants in HCV Infection Susceptibility, Spontaneous Viral Clearance and Pegylated Interferon Plus Ribavirin Treatment Response. Scand J Immunol 2016;84(1):61-9.
Nicchia E, Giordano P, Greco C, De Rocco D, Savoia A. Molecular diagnosis of thrombocytopenia-absent radius syndrome using next-generation sequencing. Int J Lab Hematol 2016;38(4):412-8.
Lazzerini M, Seward N, Lufesi N, Banda R, Sinyeka S, Masache G, Nambiar B, Makwenda C, Costello A, McCollum ED, Colbourn T. Mortality and its risk factors in Malawian children admitted to hospital with clinical pneumonia, 2001-12: a retrospective observational study. Lancet Glob Health 2016;4(1):e57-68.
Lazzerini M, Seward N, Lufesi N, Banda R, Sinyeka S, Masache G, Nambiar B, Makwenda C, Costello A, McCollum ED, Colbourn T. Mortality and its risk factors in Malawian children admitted to hospital with clinical pneumonia, 2001-12: a retrospective observational study. Lancet Glob Health 2016;4(1):e57-68.
Russo S, Calzari L, Mussa A, Mainini E, Cassina M, Di Candia S, Clementi M, Guzzetti S, Tabano S, Miozzo M, Sirchia S, Finelli P, Prontera P, Maitz S, Sorge G, Calcagno A, Maghnie M, Divizia MTeresa, Melis D, Manfredini E, Ferrero GBattista, Pecile V, Larizza L. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes. Clin Epigenetics 2016;8:23.
Russo S, Calzari L, Mussa A, Mainini E, Cassina M, Di Candia S, Clementi M, Guzzetti S, Tabano S, Miozzo M, Sirchia S, Finelli P, Prontera P, Maitz S, Sorge G, Calcagno A, Maghnie M, Divizia MTeresa, Melis D, Manfredini E, Ferrero GBattista, Pecile V, Larizza L. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes. Clin Epigenetics 2016;8:23.
Verver EJJ, Topsakal V, Kunst HPM, Huygen PLM, Heller PG, Pujol-Moix N, Savoia A, Benazzo M, Fierro T, Grolman W, Gresele P, Pecci A. Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease. Ear Hear 2016;37(1):112-20.
Kostevsek N, Locatelli E, Garrovo C, Arena F, Monaco I, Nikolov IPetrov, Sturm S, Rozman KZuzek, Lorusso V, Giustetto P, Bardini P, Biffi S, Franchini MComes. The one-step synthesis and surface functionalization of dumbbell-like gold-iron oxide nanoparticles: a chitosan-based nanotheranostic system. Chem Commun (Camb) 2016;52(2):378-81.
Farruggia P, Puccio G, Sala A, Todesco A, Buffardi S, Garaventa A, Bottigliero G, Bianchi M, Zecca M, Locatelli F, Pession A, Pillon M, Favre C, D'Amico S, Provenzi M, Trizzino A, Zanazzo GAndrea, Sau A, Santoro N, Murgia G, Casini T, Mascarin M, Burnelli R. The prognostic value of biological markers in paediatric Hodgkin lymphoma. Eur J Cancer 2016;52:33-40.
Farruggia P, Puccio G, Sala A, Todesco A, Buffardi S, Garaventa A, Bottigliero G, Bianchi M, Zecca M, Locatelli F, Pession A, Pillon M, Favre C, D'Amico S, Provenzi M, Trizzino A, Zanazzo GAndrea, Sau A, Santoro N, Murgia G, Casini T, Mascarin M, Burnelli R. The prognostic value of biological markers in paediatric Hodgkin lymphoma. Eur J Cancer 2016;52:33-40.

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