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2012
Faletra F, Berti I, Tommasini A, Pecile V, Cleva L, Alberini E, Bruno I, Gasparini P. Phylloid pattern of hypomelanosis closely related to chromosomal abnormalities in the 13q detected by SNP array analysis. Dermatology 2012;225(4):294-7.
da Silva RCelerino, Segat L, Zanin V, Arraes LClaudio, Crovella S. Polymorphisms in DC-SIGN and L-SIGN genes are associated with HIV-1 vertical transmission in a Northeastern Brazilian population. Hum Immunol 2012;73(11):1159-65.
Monari F, Alberico S, Avagliano L, Cetin I, Cozzolino S, Gargano G, Marozio L, Mecacci F, Neri I, Tranquilli AL, Venturini P, Facchinetti F. Relation between maternal thrombophilia and stillbirth according to causes/associated conditions of death. Early Hum Dev 2012;88(4):251-4.
Monari F, Alberico S, Avagliano L, Cetin I, Cozzolino S, Gargano G, Marozio L, Mecacci F, Neri I, Tranquilli AL, Venturini P, Facchinetti F. Relation between maternal thrombophilia and stillbirth according to causes/associated conditions of death. Early Hum Dev 2012;88(4):251-4.
Abate MValentina, Davanzo R, Bibalo C, Zennaro F, Berti I. RICH (rapidly involuting congenital hemangioma): not only a definition of wealth. J Pediatr 2012;161(2):365-365.e1.
Amaddeo A, Ventura A, Marchetti F, Benettoni A, Londero M. Should cardiac involvement be included in the criteria for diagnosis of Churg Strauss syndrome?. J Pediatr 2012;160(4):707.
Mazzoni E, Rigolin GMatteo, Alaribe FNneka, Pancaldi C, Maniero S, Comar M, Martini F, Tognon M. Simian virus 40 efficiently infects human T lymphocytes and extends their lifespan. Exp Hematol 2012;40(6):466-76.
Agostinis C, Bulla R, Tisato V, De Seta F, Alberico S, Secchiero P, Zauli G. Soluble TRAIL is elevated in recurrent miscarriage and inhibits the in vitro adhesion and migration of HTR8 trophoblastic cells. Hum Reprod 2012;27(10):2941-7.
Agostinis C, Bulla R, Tisato V, De Seta F, Alberico S, Secchiero P, Zauli G. Soluble TRAIL is elevated in recurrent miscarriage and inhibits the in vitro adhesion and migration of HTR8 trophoblastic cells. Hum Reprod 2012;27(10):2941-7.
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.
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.
Athanasakis E, Fabretto A, Faletra F, Mocenigo M, Morgan A, Gasparini P. Two Novel COH1 Mutations in an Italian Patient with Cohen Syndrome. Mol Syndromol 2012;3(1):30-33.

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