Girolami A - Search Results

1

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: girolami b. Acta Haematol. 2008;120(2):82-6. doi: 10.1159/000162281. Epub 2008 Oct 14. Acta Haematol. 2008. PMID: 18852482 No abstract available.

2

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. Acta Haematol. 2008;119(4):236-40. doi: 10.1159/000141782. Epub 2008 Jun 28. Acta Haematol. 2008. PMID: 18583905

3

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: girolami b. Acta Haematol. 2009;121(1):42-6. doi: 10.1159/000210063. Epub 2009 Mar 31. Acta Haematol. 2009. PMID: 19332986

4

Thrombotic events in patients with congenital prekallikrein deficiency: a critical evaluation of all reported cases.

Girolami A, Allemand E, Bertozzi I, Candeo N, Marun S, Girolami B. Girolami A, et al. Among authors: girolami b. Acta Haematol. 2010;123(4):210-4. doi: 10.1159/000313361. Epub 2010 Apr 27. Acta Haematol. 2010. PMID: 20424433

5

Pregnancy and oral contraceptives in congenital bleeding disorders of the vitamin K-dependent coagulation factors.

Girolami A, Randi ML, Ruzzon E, Lombardi AM, Girolami B, Fabris F. Girolami A, et al. Among authors: girolami b. Acta Haematol. 2006;115(1-2):58-63. doi: 10.1159/000089467. Acta Haematol. 2006. PMID: 16424651

6

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. Am J Hematol. 2008 Aug;83(8):668-71. doi: 10.1002/ajh.21207. Am J Hematol. 2008. PMID: 18506702 Free article. Review.

7

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: girolami a. Blood Coagul Fibrinolysis. 2008 Oct;19(7):639-43. doi: 10.1097/MBC.0b013e32830d8629. Blood Coagul Fibrinolysis. 2008. PMID: 18832903

8

The clinical significance of the lack of arterial or venous thrombosis in patients with congenital prothrombin or FX deficiency.

Girolami A, Candeo N, Vettore S, Lombardi AM, Girolami B. Girolami A, et al. Among authors: girolami b. J Thromb Thrombolysis. 2010 Apr;29(3):299-302. doi: 10.1007/s11239-009-0342-2. J Thromb Thrombolysis. 2010. PMID: 19412729 Review.

9

The clinical and laboratory significance of cases of congenital FX deficiency due to defects in the Gla-domain.

Girolami A, Allemand E, Scandellari R, Lombardi AM, Girolami B. Girolami A, et al. Among authors: girolami b. Hematology. 2009 Jun;14(3):177-81. doi: 10.1179/102453309X426173. Hematology. 2009. PMID: 19490765 Free article.

10

Congenital prekallikrein deficiency.

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

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