Export 1687 results:
Autore Titolo Tipo [ Anno(Asc)]
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2016
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.
Pastore S, Contorno S, Caddeo G, Calligaris L, Taddio A. A minor trauma revealing linear morphoea in a 4-year-old female. Arch Dis Child 2016;
Pastore S, Contorno S, Caddeo G, Calligaris L, Taddio A. A minor trauma revealing linear morphoea in a 4-year-old female. Arch Dis Child 2016;
Pastore S, Contorno S, Caddeo G, Calligaris L, Taddio A. A minor trauma revealing linear morphoea in a 4-year-old female. Arch Dis Child 2016;
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.
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.
Benini F, Piga S, Zangardi T, Messi G, Tomasello C, Pirozzi N, Cuttini M. Nationwide study of headache pain in Italy shows that pain assessment is still inadequate in paediatric emergency care. Acta Paediatr 2016;105(5):e200-8.
Cocca M, Bedognetti D, La Bianca M, Gasparini P, Girotto G. Pharmacogenetics driving personalized medicine: analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations. J Transl Med 2016;14:22.

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