Cattaneo M - Search Results

1

Diagnosis of suspected inherited platelet function disorders: results of a worldwide survey.

Gresele P, Harrison P, Bury L, Falcinelli E, Gachet C, Hayward CP, Kenny D, Mezzano D, Mumford AD, Nugent D, Nurden AT, Orsini S, Cattaneo M. Gresele P, et al. Among authors: cattaneo m. J Thromb Haemost. 2014 Sep;12(9):1562-9. doi: 10.1111/jth.12650. Epub 2014 Jul 25. J Thromb Haemost. 2014. PMID: 24976115 Free article.

2

Evaluation of the abnormal platelet function in von Willebrand disease by the blood filtration test.

Pareti FI, Cattaneo M, Carpinelli L, Zighetti ML, Bressi C, Mannucci PM, Ruggeri ZM. Pareti FI, et al. Among authors: cattaneo m. Thromb Haemost. 1996 Sep;76(3):460-8. Thromb Haemost. 1996. PMID: 8883287

3

Deficiency of (33P)2MeS-ADP binding sites on platelets with secretion defect, normal granule stores and normal thromboxane A2 production. Evidence that ADP potentiates platelet secretion independently of the formation of large platelet aggregates and thromboxane A2 production.

Cattaneo M, Lombardi R, Zighetti ML, Gachet C, Ohlmann P, Cazenave JP, Mannucci PM. Cattaneo M, et al. Thromb Haemost. 1997 May;77(5):986-90. Thromb Haemost. 1997. PMID: 9184415

4

The P2Y1 receptor is normal in a patient presenting a severe deficiency of ADP-induced platelet aggregation.

Léon C, Vial C, Gachet C, Ohlmann P, Hechler B, Cazenave JP, Lecchi A, Cattaneo M. Léon C, et al. Among authors: cattaneo m. Thromb Haemost. 1999 May;81(5):775-81. Thromb Haemost. 1999. PMID: 10365753

5

Evaluation of the PFA-100 system in the diagnosis and therapeutic monitoring of patients with von Willebrand disease.

Cattaneo M, Federici AB, Lecchi A, Agati B, Lombardi R, Stabile F, Bucciarelli P. Cattaneo M, et al. Thromb Haemost. 1999 Jul;82(1):35-9. Thromb Haemost. 1999. PMID: 10456451

6

ADP receptors and clinical bleeding disorders.

Cattaneo M, Gachet C. Cattaneo M, et al. Arterioscler Thromb Vasc Biol. 1999 Oct;19(10):2281-5. doi: 10.1161/01.atv.19.10.2281. Arterioscler Thromb Vasc Biol. 1999. PMID: 10521355 Review.

7

Platelets from a patient heterozygous for the defect of P2CYC receptors for ADP have a secretion defect despite normal thromboxane A2 production and normal granule stores: further evidence that some cases of platelet 'primary secretion defect' are heterozygous for a defect of P2CYC receptors.

Cattaneo M, Lecchi A, Lombardi R, Gachet C, Zighetti ML. Cattaneo M, et al. Arterioscler Thromb Vasc Biol. 2000 Nov;20(11):E101-6. doi: 10.1161/01.atv.20.11.e101. Arterioscler Thromb Vasc Biol. 2000. PMID: 11073862

8

Multicenter study of homocysteine measurement--performance characteristics of different methods, influence of standards on interlaboratory agreement of results.

Tripodi A, Chantarangkul V, Lombardi R, Lecchi A, Mannucci PM, Cattaneo M. Tripodi A, et al. Among authors: cattaneo m. Thromb Haemost. 2001 Feb;85(2):291-5. Thromb Haemost. 2001. PMID: 11246550

9

The platelet ADP receptors.

Cattaneo M, Gachet C. Cattaneo M, et al. Haematologica. 2001 Apr;86(4):346-8. Haematologica. 2001. PMID: 11325637 Review. No abstract available.

10

Inherited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle Piastrine.

Balduini CL, Cattaneo M, Fabris F, Gresele P, Iolascon A, Pulcinelli FM, Savoia A; Italian Gruppo di Studio delle Piastrine. Balduini CL, et al. Among authors: cattaneo m. Haematologica. 2003 May;88(5):582-92. Haematologica. 2003. PMID: 12745278

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