Castaman G - Search Results

1

Major Orthopaedic Surgery in Persons with Haemophilia A with and without Inhibitors Treated by Emicizumab: A Mid-Term, Large, and Successful Series at a Single Center.

Carulli C, Daniele G, Linari S, Pieri L, Littera M, Mazzetti M, Tamburini C, Prisco D, Castaman G. Carulli C, et al. Among authors: castaman g. J Clin Med. 2024 Apr 30;13(9):2646. doi: 10.3390/jcm13092646. J Clin Med. 2024. PMID: 38731175 Free PMC article.

2

Total Hip Arthroplasty in Haemophilic Patients with Modern Cementless Implants.

Carulli C, Felici I, Martini C, Civinini R, Linari S, Castaman G, Innocenti M. Carulli C, et al. Among authors: castaman g. J Arthroplasty. 2015 Oct;30(10):1757-60. doi: 10.1016/j.arth.2015.04.035. Epub 2015 May 5. J Arthroplasty. 2015. PMID: 25998131

3

Acquired inhibitors of clotting factors: AICE recommendations for diagnosis and management.

Franchini M, Castaman G, Coppola A, Santoro C, Zanon E, Di Minno G, Morfini M, Santagostino E, Rocino A; AICE Working Group. Franchini M, et al. Among authors: castaman g. Blood Transfus. 2015 Jul;13(3):498-513. doi: 10.2450/2015.0141-15. Epub 2015 Jun 24. Blood Transfus. 2015. PMID: 26192778 Free PMC article. No abstract available.

4

Clinical, instrumental, serological and histological findings suggest that hemophilia B may be less severe than hemophilia A.

Melchiorre D, Linari S, Manetti M, Romano E, Sofi F, Matucci-Cerinic M, Carulli C, Innocenti M, Ibba-Manneschi L, Castaman G. Melchiorre D, et al. Among authors: castaman g. Haematologica. 2016 Feb;101(2):219-25. doi: 10.3324/haematol.2015.133462. Epub 2015 Oct 22. Haematologica. 2016. PMID: 26494839 Free PMC article.

5

Hematological manifestations and complications of Gaucher disease.

Linari S, Castaman G. Linari S, et al. Among authors: castaman g. Expert Rev Hematol. 2016 Jan;9(1):51-8. doi: 10.1586/17474086.2016.1112732. Epub 2015 Nov 13. Expert Rev Hematol. 2016. PMID: 26565753 Review.

6

Cancers in Patients with von Willebrand Disease: A Survey from the Italian Association of Haemophilia Centres.

Franchini M, Di Perna C, Santoro C, Castaman G, Siboni SM, Zanon E, Linari S, Gresele P, Pasca S, Coppola A, Santoro R, Napolitano M, Ranalli P, Tagliaferri A; Italian Association of Haemophilia Centres. Franchini M, et al. Among authors: castaman g. Semin Thromb Hemost. 2016 Feb;42(1):36-41. doi: 10.1055/s-0035-1564844. Epub 2015 Nov 23. Semin Thromb Hemost. 2016. PMID: 26595151 Clinical Trial.

7

Clinical manifestations and management of Gaucher disease.

Linari S, Castaman G. Linari S, et al. Among authors: castaman g. Clin Cases Miner Bone Metab. 2015 May-Aug;12(2):157-64. doi: 10.11138/ccmbm/2015.12.2.157. Epub 2015 Oct 26. Clin Cases Miner Bone Metab. 2015. PMID: 26604942 Free PMC article. Review.

8

Emerging Issues in Diagnosis, Biology, and Inhibitor Risk in Mild Hemophilia A.

Castaman G, Eckhardt C, van Velzen A, Linari S, Fijnvandraat K. Castaman G, et al. Semin Thromb Hemost. 2016 Jul;42(5):507-12. doi: 10.1055/s-0036-1571309. Epub 2016 May 5. Semin Thromb Hemost. 2016. PMID: 27148839 Review.

9

Human von Willebrand factor/factor VIII concentrates in the management of pediatric patients with von Willebrand disease/hemophilia A.

Castaman G, Linari S. Castaman G, et al. Ther Clin Risk Manag. 2016 Jun 30;12:1029-37. doi: 10.2147/TCRM.S87543. eCollection 2016. Ther Clin Risk Manag. 2016. PMID: 27445481 Free PMC article. Review.

10

The higher prevalence of missense mutations in hemophilia B compared to hemophilia A could be important in determining a milder clinical phenotype in patients with severe hemophilia B.

Melchiorre D, Linari S, Castaman G. Melchiorre D, et al. Among authors: castaman g. Haematologica. 2016 Oct;101(10):e429. doi: 10.3324/haematol.2016.150839. Haematologica. 2016. PMID: 27694504 Free PMC article. No abstract available.

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