D J Perry|F Peyvandi - JoVE Visualize

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Thrombosis and Haemostasis|March 11, 1998

Antithrombin cambridge II (Ala384Ser): clinical, functional and haplotype analysis of 18 familiesD J Perry, M E Daly, R C Tait, et al.

Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 1, 1996

Type I antithrombin deficiency: five novel mutations associated with thrombosisM Daly, D J Perry, D B Bruce, et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia|May 11, 2006

Genetic diagnosis of haemophilia and other inherited bleeding disordersF Peyvandi, G Jayandharan, M Chandy, et al.

Journal of Thrombosis and Haemostasis : JTH|May 8, 2013

Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosisL A Lotta, G Tuana, J Yu, et al.

The European Respiratory Journal|June 12, 1998

Alpha1-antitrypsin deficiency alleles and the Taq-I G-->A allele in cystic fibrosis lung diseaseR Mahadeva, R C Westerbeek, D J Perry, et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia|September 11, 2004

The rare coagulation disorders--review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' OrganisationP H B Bolton-Maggs, D J Perry, E A Chalmers, et al.

Journal of Cellular and Molecular Medicine|October 6, 2009

Familial and racial determinants of tumour suppressor genes promoter hypermethylation in breast tissues from healthy womenR G Dumitrescu, C Marian, S S Krishnan, et al.

Journal of Thrombosis and Haemostasis : JTH|July 30, 2008

Second international collaborative study evaluating performance characteristics of methods measuring the von Willebrand factor cleaving protease (ADAMTS-13)A Tripodi, F Peyvandi, V Chantarangkul, et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia|April 7, 2005

A framework for genetic service provision for haemophilia and other inherited bleeding disordersC A Ludlam, K J Pasi, P Bolton-Maggs, et al.

Journal of Thrombosis and Haemostasis : JTH|February 11, 2012

Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding DisordersF Peyvandi, R Palla, M Menegatti, et al.

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Showing results (221-230 of 232) with videos related to

Sort By:

Pageof 24

Thrombosis and Haemostasis|March 11, 1998

Antithrombin cambridge II (Ala384Ser): clinical, functional and haplotype analysis of 18 familiesD J Perry, M E Daly, R C Tait, et al.

Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 1, 1996

Type I antithrombin deficiency: five novel mutations associated with thrombosisM Daly, D J Perry, D B Bruce, et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia|May 11, 2006

Genetic diagnosis of haemophilia and other inherited bleeding disordersF Peyvandi, G Jayandharan, M Chandy, et al.

Journal of Thrombosis and Haemostasis : JTH|May 8, 2013

Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosisL A Lotta, G Tuana, J Yu, et al.

The European Respiratory Journal|June 12, 1998

Alpha1-antitrypsin deficiency alleles and the Taq-I G-->A allele in cystic fibrosis lung diseaseR Mahadeva, R C Westerbeek, D J Perry, et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia|September 11, 2004

The rare coagulation disorders--review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' OrganisationP H B Bolton-Maggs, D J Perry, E A Chalmers, et al.

Journal of Cellular and Molecular Medicine|October 6, 2009

Familial and racial determinants of tumour suppressor genes promoter hypermethylation in breast tissues from healthy womenR G Dumitrescu, C Marian, S S Krishnan, et al.

Journal of Thrombosis and Haemostasis : JTH|July 30, 2008

Second international collaborative study evaluating performance characteristics of methods measuring the von Willebrand factor cleaving protease (ADAMTS-13)A Tripodi, F Peyvandi, V Chantarangkul, et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia|April 7, 2005

A framework for genetic service provision for haemophilia and other inherited bleeding disordersC A Ludlam, K J Pasi, P Bolton-Maggs, et al.

Journal of Thrombosis and Haemostasis : JTH|February 11, 2012

Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding DisordersF Peyvandi, R Palla, M Menegatti, et al.

Pageof 24