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Barbi E, Berti I, Minute M, Zennaro F. Successful treatment of acne with isotretinoin in chronic granulomatous disease. Eur J Dermatol 2011;21(1):111-2.
Barbiero C, Lonciari I, Montico M, Monasta L, Penge R, Vio C, Tressoldi PEmanuele, Ferluga V, Bigoni A, Tullio A, Carrozzi M, Ronfani L. The submerged dyslexia iceberg: how many school children are not diagnosed? Results from an Italian study. PLoS One 2012;7(10):e48082.
Barbiero C, Lonciari I, Montico M, Monasta L, Penge R, Vio C, Tressoldi PEmanuele, Ferluga V, Bigoni A, Tullio A, Carrozzi M, Ronfani L. The submerged dyslexia iceberg: how many school children are not diagnosed? Results from an Italian study. PLoS One 2012;7(10):e48082.
Chow YW, Pietranico R, Mukerji A. Studies of oxygen binding energy to hemoglobin molecule. Biochem Biophys Res Commun 1975;66(4):1424-31.
Carrozzi M, Amaddeo A, Biondi A, Zanus C, Monti F, Alessandro V. Stem cells in severe infantile spinal muscular atrophy (SMA1). Neuromuscul Disord 2012;22(11):1032-4.
Fulle S, Centurione L, Mancinelli R, Sancilio S, Manzoli FAntonio, Di Pietro R. Stem cell ageing and apoptosis. Curr Pharm Des 2012;18(13):1694-717.
Fulle S, Centurione L, Mancinelli R, Sancilio S, Manzoli FAntonio, Di Pietro R. Stem cell ageing and apoptosis. Curr Pharm Des 2012;18(13):1694-717.
Nyqvist KH, Anderson GC, Bergman N, Cattaneo A, Charpak N, Davanzo R, Ewald U, Ludington-Hoe S, Mendoza S, Pallás-Allonso C, Peláez JG, Sizun J, Wiström AM. State of the art and recommendations. Kangaroo mother care: application in a high-tech environment. Breastfeed Rev 2010;18(3):21-8.
Nyqvist KH, Anderson GC, Bergman N, Cattaneo A, Charpak N, Davanzo R, Ewald U, Ludington-Hoe S, Mendoza S, Pallás-Allonso C, Peláez JG, Sizun J, Widström A-M. State of the art and recommendations. Kangaroo mother care: application in a high-tech environment. Acta Paediatr 2010;99(6):812-9.
Zampieri S, Buratti E, Dominissini S, Montalvo ALisa, Pittis MGabriela, Bembi B, Dardis A. Splicing mutations in glycogen-storage disease type II: evaluation of the full spectrum of mutations and their relation to patients' phenotypes. Eur J Hum Genet 2011;19(4):422-31.
Maschio M, Cozzi G, Sanabor D, Zennaro F, Gloria P, Barbi E. Splenomegaly as presentation of a wandering spleen. J Pediatr 2010;157(5):859.e1.
Savoia A, Kunishima S, De Rocco D, Zieger B, Rand ML, Pujol-Moix N, Caliskan U, Tokgoz H, Pecci A, Noris P, Srivastava A, Ward C, Morel-Kopp M-C, Alessi M-C, Bellucci S, Beurrier P, de Maistre E, Favier R, Hézard N, Hurtaud-Roux M-F, Latger-Cannard V, Lavenu-Bombled C, Proulle V, Meunier S, Négrier C, Nurden A, Randrianaivo H, Fabris F, Platokouki H, Rosenberg N, HadjKacem B, Heller PG, Karimi M, Balduini CL, Pastore A, Lanza F. Spectrum of the mutations in Bernard-Soulier syndrome. Hum Mutat 2014;35(9):1033-45.

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