Scarparo P - Search Results

1

Hemospermia in patients with congenital coagulation disorders: a study of three cases.

Girolami A, Scarparo P, Candeo N, Sartori R, Scandellari R, Girolami B. Girolami A, et al. Among authors: scarparo p. Acta Haematol. 2009;121(1):42-6. doi: 10.1159/000210063. Epub 2009 Mar 31. Acta Haematol. 2009. PMID: 19332986

2

Congenital prekallikrein deficiency.

Girolami A, Scarparo P, Candeo N, Lombardi AM. Girolami A, et al. Among authors: scarparo p. Expert Rev Hematol. 2010 Dec;3(6):685-95. doi: 10.1586/ehm.10.69. Expert Rev Hematol. 2010. PMID: 21091145 Review.

3

Control of ovulation-induced hemoperitoneum by oral contraceptives in a patient with congenital hypoprothrombinemia and in another with congenital factor V deficiency.

Girolami A, Lombardi AM, Candeo N, Scarparo P, Paternoster A. Girolami A, et al. Among authors: scarparo p. Acta Haematol. 2008;119(4):236-40. doi: 10.1159/000141782. Epub 2008 Jun 28. Acta Haematol. 2008. PMID: 18583905

4

True congenital prothrombin deficiency due to a 'new' mutation in the pre-propeptide (ARG-39 GLN).

Girolami A, Santarossa L, Scarparo P, Candeo N, Girolami B. Girolami A, et al. Among authors: scarparo p. Acta Haematol. 2008;120(2):82-6. doi: 10.1159/000162281. Epub 2008 Oct 14. Acta Haematol. 2008. PMID: 18852482 No abstract available.

5

Congenital factor X deficiencies with a defect only or predominantly in the extrinsic or in the intrinsic system: a critical evaluation.

Girolami A, Scarparo P, Scandellari R, Allemand E. Girolami A, et al. Among authors: scarparo p. Am J Hematol. 2008 Aug;83(8):668-71. doi: 10.1002/ajh.21207. Am J Hematol. 2008. PMID: 18506702 Free article. Review.

6

Heparin-induced thrombocytopenia in patients with Philadelphia-negative myeloproliferative disorders and unusual splanchnic or cerebral vein thrombosis.

Randi ML, Tezza F, Scapin M, Duner E, Scarparo P, Scandellari R, Fabris F. Randi ML, et al. Among authors: scarparo p. Acta Haematol. 2010;123(3):140-5. doi: 10.1159/000280466. Epub 2010 Feb 4. Acta Haematol. 2010. PMID: 20134155

7

Congenital FX deficiency combined with other clotting defects or with other abnormalities: a critical evaluation of the literature.

Girolami A, Ruzzon E, Tezza F, Scandellari R, Scapin M, Scarparo P. Girolami A, et al. Among authors: scarparo p. Haemophilia. 2008 Mar;14(2):323-8. doi: 10.1111/j.1365-2516.2007.01612.x. Epub 2007 Dec 10. Haemophilia. 2008. PMID: 18081833 Review.

8

Unexplained discrepancies in the activity--antigen ratio in congenital FX deficiencies with defects in the catalytic domain.

Girolami A, Scarparo P, Vettore S, Candeo N, Scandellari R, Lombardi AM. Girolami A, et al. Among authors: scarparo p. Clin Appl Thromb Hemost. 2009 Dec;15(6):621-7. doi: 10.1177/1076029609343447. Epub 2009 Aug 9. Clin Appl Thromb Hemost. 2009. PMID: 19666942 Free article. Review.

9

Persistent validity of a classification of congenital factor X defects based on clotting, chromogenic and immunological assays even in the molecular biology era.

Girolami A, Vettore S, Scarparo P, Lombardi AM. Girolami A, et al. Among authors: scarparo p. Haemophilia. 2011 Jan;17(1):17-20. doi: 10.1111/j.1365-2516.2010.02328.x. Haemophilia. 2011. PMID: 20546029

10

Genetic study in patients with factor XII deficiency: a report of three new mutations exon 13 (Q501STOP), exon 14 (P547L) and -13C>T promoter region in three compound heterozygotes.

Lombardi AM, Bortoletto E, Scarparo P, Scapin M, Santarossa L, Girolami A. Lombardi AM, et al. Among authors: scarparo p. Blood Coagul Fibrinolysis. 2008 Oct;19(7):639-43. doi: 10.1097/MBC.0b013e32830d8629. Blood Coagul Fibrinolysis. 2008. PMID: 18832903

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