Karimi M - Search Results

1

Von Willebrand factor propeptide and pathophysiological mechanisms in European and Iranian patients with type 3 von Willebrand disease enrolled in the 3WINTERS-IPS study.

Pagliari MT, Rosendaal FR, Ahmadinejad M, Badiee Z, Baghaipour MR, Baronciani L, Benítez Hidalgo O, Bodó I, Budde U, Castaman G, Eshghi P, Goudemand J, Karimi M, Keikhaei B, Lassila R, Leebeek FWG, Lopez Fernandez MF, Mannucci PM, Marino R, Oldenburg J, Peake I, Santoro C, Schneppenheim R, Tiede A, Toogeh G, Tosetto A, Trossaert M, Yadegari H, Zetterberg EMK, Peyvandi F, Federici AB, Eikenboom J. Pagliari MT, et al. Among authors: karimi m. J Thromb Haemost. 2022 May;20(5):1106-1114. doi: 10.1111/jth.15658. Epub 2022 Feb 22. J Thromb Haemost. 2022. PMID: 35092343 Free PMC article.

2

Allele frequency of CYP2C9 gene polymorphisms in Iran.

Peyvandi F, Spreafico M, Karimi M, Zeinali S, Mannucci PM, Bianchi Bonomi A. Peyvandi F, et al. Among authors: karimi m. Thromb Haemost. 2002 Nov;88(5):874-5. Thromb Haemost. 2002. PMID: 12428110 No abstract available.

3

Patients with localized and disseminated tumors have reduced but measurable levels of ADAMTS-13 (von Willebrand factor cleaving protease).

Mannucci PM, Karimi M, Mosalaei A, Canciani MT, Peyvandi F. Mannucci PM, et al. Among authors: karimi m. Haematologica. 2003 Apr;88(4):454-8. Haematologica. 2003. PMID: 12681973

4

Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiency.

Peyvandi F, Tagliabue L, Menegatti M, Karimi M, Komáromi I, Katona E, Muszbek L, Mannucci PM. Peyvandi F, et al. Among authors: karimi m. Hum Mutat. 2004 Jan;23(1):98. doi: 10.1002/humu.9206. Hum Mutat. 2004. PMID: 14695539

5

Comparison of attitudes towards prenatal diagnosis and termination of pregnancy for haemophilia in Iran and Italy.

Karimi M, Peyvandi F, Siboni S, Ardeshiri R, Gringeri A, Mannucci PM. Karimi M, et al. Haemophilia. 2004 Jul;10(4):367-9. doi: 10.1111/j.1365-2516.2004.00927.x. Haemophilia. 2004. PMID: 15230951

6

A rare inherited coagulation disorder: combined homozygous factor VII and factor X deficiency.

Menegatti M, Karimi M, Garagiola I, Mannucci P, Peyvandi F. Menegatti M, et al. Among authors: karimi m. Am J Hematol. 2004 Sep;77(1):90-1. doi: 10.1002/ajh.20132. Am J Hematol. 2004. PMID: 15307115 Free article.

7

Glanzmann thrombasthenia and Bernard-Soulier syndrome in south Iran.

Afrasiabi A, Artoni A, Karimi M, Peyvandi F, Ashouri E, Mannucci PM. Afrasiabi A, et al. Among authors: karimi m. Clin Lab Haematol. 2005 Oct;27(5):324-7. doi: 10.1111/j.1365-2257.2005.00725.x. Clin Lab Haematol. 2005. PMID: 16178914

8

Changing epidemiology of the hemolytic uremic syndrome and thrombotic thrombocytopenic purpura in southern Iran.

Karimi M, Sabzi A, Peyvandi F, Mannucci PM. Karimi M, et al. J Thromb Haemost. 2006 Mar;4(3):701-2. doi: 10.1111/j.1538-7836.2006.01807.x. J Thromb Haemost. 2006. PMID: 16460465 Free article. No abstract available.

9

Clinical and laboratory patterns of the haemolytic uraemic syndrome and thrombotic thrombocytopenic purpura in southern Iran.

Karimi M, Sabzi A, Peyvandi F, Mannucci PM. Karimi M, et al. Intern Emerg Med. 2006;1(1):35-9. doi: 10.1007/BF02934718. Intern Emerg Med. 2006. PMID: 16941811

10

Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defects.

Monaldini L, Asselta R, Duga S, Peyvandi F, Karimi M, Malcovati M, Tenchini ML. Monaldini L, et al. Among authors: karimi m. Thromb Haemost. 2007 Apr;97(4):546-51. Thromb Haemost. 2007. PMID: 17393016

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