Noris P - Search Results

1

Max(a), a new low-frequency platelet-specific antigen localized on glycoprotein IIb, is associated with neonatal alloimmune thrombocytopenia.

Noris P, Simsek S, de Bruijne-Admiraal LG, Porcelijn L, Huiskes E, van der Vlist GJ, van Leeuwen EF, van der Schoot CE, von dem Borne AE. Noris P, et al. Blood. 1995 Aug 1;86(3):1019-26. Blood. 1995. PMID: 7620155 Free article.

2

Defect of platelet aggregation and adhesion induced by autoantibodies against platelet glycoprotein IIIa.

Balduini CL, Bertolino G, Noris P, Piovella F, Sinigaglia F, Bellotti V, Samaden A, Torti M, Mazzini G. Balduini CL, et al. Among authors: noris p. Thromb Haemost. 1992 Aug 3;68(2):208-13. Thromb Haemost. 1992. PMID: 1412168

3

Cys209 Ser mutation in the platelet membrane glycoprotein Ib alpha gene is associated with Bernard-Soulier syndrome.

Simsek S, Noris P, Lozano M, Pico M, von dem Borne AE, Ribera A, Gallardo D. Simsek S, et al. Among authors: noris p. Br J Haematol. 1994 Dec;88(4):839-44. doi: 10.1111/j.1365-2141.1994.tb05125.x. Br J Haematol. 1994. PMID: 7819107

4

Acquired cyclic thrombocytopenia-thrombocytosis with periodic defect of platelet function.

Balduini CL, Stella CC, Rosti V, Bertolino G, Noris P, Ascari E. Balduini CL, et al. Among authors: noris p. Br J Haematol. 1993 Dec;85(4):718-22. doi: 10.1111/j.1365-2141.1993.tb03214.x. Br J Haematol. 1993. PMID: 7918035

5

A phenylalanine-55 to serine amino-acid substitution in the human glycoprotein IX leucine-rich repeat is associated with Bernard-Soulier syndrome.

Noris P, Simsek S, Stibbe J, von dem Borne AE. Noris P, et al. Br J Haematol. 1997 May;97(2):312-20. doi: 10.1046/j.1365-2141.1997.582706.x. Br J Haematol. 1997. PMID: 9163595 Free article.

6

Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome.

Savoia A, Balduini CL, Savino M, Noris P, Del Vecchio M, Perrotta S, Belletti S, Poggi, Iolascon A. Savoia A, et al. Among authors: noris p. Blood. 2001 Mar 1;97(5):1330-5. doi: 10.1182/blood.v97.5.1330. Blood. 2001. PMID: 11222377 Free article.

7

Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations.

Pecci A, Gresele P, Klersy C, Savoia A, Noris P, Fierro T, Bozzi V, Mezzasoma AM, Melazzini F, Balduini CL. Pecci A, et al. Among authors: noris p. Blood. 2010 Dec 23;116(26):5832-7. doi: 10.1182/blood-2010-08-304725. Epub 2010 Sep 15. Blood. 2010. PMID: 20844233 Free article. Clinical Trial.

8

Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families.

Noris P, Perrotta S, Seri M, Pecci A, Gnan C, Loffredo G, Pujol-Moix N, Zecca M, Scognamiglio F, De Rocco D, Punzo F, Melazzini F, Scianguetta S, Casale M, Marconi C, Pippucci T, Amendola G, Notarangelo LD, Klersy C, Civaschi E, Balduini CL, Savoia A. Noris P, et al. Blood. 2011 Jun 16;117(24):6673-80. doi: 10.1182/blood-2011-02-336537. Epub 2011 Apr 5. Blood. 2011. PMID: 21467542 Free article.

9

ANKRD26-related thrombocytopenia and myeloid malignancies.

Noris P, Favier R, Alessi MC, Geddis AE, Kunishima S, Heller PG, Giordano P, Niederhoffer KY, Bussel JB, Podda GM, Vianelli N, Kersseboom R, Pecci A, Gnan C, Marconi C, Auvrignon A, Cohen W, Yu JC, Iguchi A, Miller Imahiyerobo A, Boehlen F, Ghalloussi D, De Rocco D, Magini P, Civaschi E, Biino G, Seri M, Savoia A, Balduini CL. Noris P, et al. Blood. 2013 Sep 12;122(11):1987-9. doi: 10.1182/blood-2013-04-499319. Blood. 2013. PMID: 24030261 Free article. No abstract available.

10

ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization.

Bottega R, Marconi C, Faleschini M, Baj G, Cagioni C, Pecci A, Pippucci T, Ramenghi U, Pardini S, Ngu L, Baronci C, Kunishima S, Balduini CL, Seri M, Savoia A, Noris P. Bottega R, et al. Among authors: noris p. Blood. 2015 Jan 29;125(5):869-72. doi: 10.1182/blood-2014-08-594531. Epub 2014 Oct 31. Blood. 2015. PMID: 25361813 Free PMC article.

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