M Lak
Overview
Explore the profile of M Lak including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
178
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Recent Articles
1.
Ghadam P, Sharifian R, Farsangi Z, Kianmehr Z, Lak M
Pak J Biol Sci
. 2009 Nov;
12(16):1160-3.
PMID: 19899329
For the first time in this study, the pharmacogenetic effects of CYP2C9 polymorphism on warfarin sensitivity in some Iranian patients who are on warfarin treatment were shown. The study group...
2.
Lak M, Scharling B, Blemings A, Sharifian R, Maleki Z, Daraee A, et al.
Haemophilia
. 2007 Dec;
14(1):103-10.
PMID: 18070065
Glanzmann thrombasthenia (GT) is a rare platelet function disorder characterized by a defect in fibrinogen binding to platelet membrane glycoprotein (GP) IIb/IIIa. Recombinant FVIIa (rFVIIa) is a haemostatic agent approved...
3.
Nourbala M, Hollisaaz M, Nasiri M, Bahaeloo-Horeh S, Najafi M, Araghizadeh H, et al.
Transplant Proc
. 2007 May;
39(4):1126-9.
PMID: 17524910
Background: Chronic pain is prevalent in end-stage renal disease patients undergoing chronic hemodialysis. We do not fully know the intensity of chronic pain experienced by kidney recipients in comparison to...
4.
Mortazavi S, Asadollahi S, Farzan M, Shahriaran S, Aghili M, Izadyar S, et al.
Haemophilia
. 2007 Feb;
13(2):182-8.
PMID: 17286772
Repeated intra-articular bleeding with subsequent development of chronic synovitis and cartilage changes, leading to haemophilic arthropathy, is one the most debilitating problems in haemophilic patients. Radiosynovectomy is a familiar therapeutic...
5.
Toogeh G, Sharifian R, Lak M, Safaee R, Artoni A, Peyvandi F
Am J Hematol
. 2004 Sep;
77(2):198-9.
PMID: 15389911
Glanzmann thrombasthenia (GT) is a rare autosomal recessive disease characterized by prolonged bleeding time with normal platelet count and morphology. It is caused by the quantitative or qualitative deficiency of...
6.
Lak M, Peyvandi F, Ali Sharifian A, Karimi K, Mannucci P
J Thromb Haemost
. 2003 Aug;
1(8):1852-3.
PMID: 12911609
No abstract available.
7.
Karimipoor M, Zeinali S, Lak M, Safaee R
Haemophilia
. 2003 Feb;
9(1):116-8.
PMID: 12558788
Haemophilia B is an X-linked recessive bleeding disorder caused by multiple molecular defects in factor IX gene. During our genotyping programme of haemophilia B patients, a family from the west...
8.
Lak M, Peyvandi F, Mannucci P
Br J Haematol
. 2001 Feb;
111(4):1236-9.
PMID: 11167767
Type 3 is the most severe form of von Willebrand disease (VWD) transmitted as an autosomal recessive trait. We collected data on the clinical manifestations of type 3 VWD by...
9.
Akhavan S, Mannucci P, Lak M, Mancuso G, Mazzucconi M, Rocino A, et al.
Thromb Haemost
. 2001 Jan;
84(6):989-97.
PMID: 11154146
Prothrombin deficiency is an autosomal recessive disorder associated with a moderately severe bleeding tendency. In this study, 13 patients with prothrombin deficiency were screened for the presence of alterations in...
10.
Lak M, Keihani M, Elahi F, Peyvandi F, Mannucci P
Br J Haematol
. 1999 Oct;
107(1):204-6.
PMID: 10520042
Knowledge of the spectrum of symptoms in patients with inherited afibrinogenaemia is limited by the rarity of this coagulation defect. We compared a large series of 55 afibrinogenaemic patients from...