MAGRIN, STEFANO

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MAGRIN, STEFANO

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DIPARTIMENTO DI TECNOLOGIE PER LA SALUTE (attivo dal 01/01/2008 al 27/04/2012)

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Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIb alpha (Bolzano mutation)

2012 P. Noris, S. Perrotta, R. Bottega, A. Pecci, F. Melazzini, E. Civaschi, S. Russo, S. Magrin, G. Loffredo, V. Di Salvo, G. Russo, M. Casale, D. De Rocco, C. Grignani, M. Cattaneo, C. Baronci, A. Dragani, V. Albano, M. Jankovic, S. Scianguetta, A. Savoia, C.L. Balduini

Titolo	Data di pubblicazione	Autori	Tipo	File	Abstract
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIb alpha (Bolzano mutation)	2012	P. NorisS. PerrottaR. BottegaA. PecciF. MelazziniE. CivaschiS. RussoMAGRIN, STEFANOG. LoffredoV. Di SalvoG. RussoM. CasaleD. De RoccoC. GrignaniM. CattaneoC. BaronciA. DraganiV. AlbanoM. JankovicS. ScianguettaA. SavoiaC. L. Balduini + -	Article (author)		-

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MAGRIN, STEFANO

Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIb alpha (Bolzano mutation)