R Peake - JoVE Visualize

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Haematologica|May 10, 2007

Mutational analysis of the von Willebrand factor gene in type 1 von Willebrand disease using conformation sensitive gel electrophoresis: a comparison of fluorescent and manual techniquesMohammad Hashemi Soteh, Ian R Peake, Luke Marsden, et al.

Nucleic Acids Research|September 25, 1991

Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII geneE G Tuddenham, D N Cooper, J Gitschier, et al.

Bulletin of the World Health Organization|January 1, 1993

Haemophilia: strategies for carrier detection and prenatal diagnosisI R Peake, D P Lillicrap, V Boulyjenkov, et al.

Thrombosis and Haemostasis|January 10, 1998

Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophiliaM Makris, F E Preston, N J Beauchamp, et al.

Thrombosis and Haemostasis|February 1, 1997

HLA class II profile: a weak determinant of factor VIII inhibitor development in severe haemophilia A. UKHCDO Inhibitor Working PartyC R Hay, W Ollier, L Pepper, et al.

Blood|March 9, 2000

Two novel type 2N von Willebrand disease-causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factorS Allen, A M Abuzenadah, J L Blagg, et al.

Blood|March 9, 2000

Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein SM Makris, M Leach, N J Beauchamp, et al.

Blood|February 1, 1990

Severe type III von Willebrand's disease caused by deletion of exon 42 of the von Willebrand factor gene: family studies that identify carriers of the condition and a compound heterozygous individualI R Peake, M B Liddell, P Moodie, et al.

British Journal of Haematology|November 25, 2000

FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk groupF M Abu-Duhier, A C Goodeve, G A Wilson, et al.

Blood|October 9, 1998

Antithrombins Wibble and Wobble (T85M/K): archetypal conformational diseases with in vivo latent-transition, thrombosis, and heparin activationN J Beauchamp, R N Pike, M Daly, et al.

Pageof 10

Showing results (71-80 of 94) with videos related to

Sort By:

Pageof 10

Haematologica|May 10, 2007

Mutational analysis of the von Willebrand factor gene in type 1 von Willebrand disease using conformation sensitive gel electrophoresis: a comparison of fluorescent and manual techniquesMohammad Hashemi Soteh, Ian R Peake, Luke Marsden, et al.

Nucleic Acids Research|September 25, 1991

Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII geneE G Tuddenham, D N Cooper, J Gitschier, et al.

Bulletin of the World Health Organization|January 1, 1993

Haemophilia: strategies for carrier detection and prenatal diagnosisI R Peake, D P Lillicrap, V Boulyjenkov, et al.

Thrombosis and Haemostasis|January 10, 1998

Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophiliaM Makris, F E Preston, N J Beauchamp, et al.

Thrombosis and Haemostasis|February 1, 1997

HLA class II profile: a weak determinant of factor VIII inhibitor development in severe haemophilia A. UKHCDO Inhibitor Working PartyC R Hay, W Ollier, L Pepper, et al.

Blood|March 9, 2000

Two novel type 2N von Willebrand disease-causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factorS Allen, A M Abuzenadah, J L Blagg, et al.

Blood|March 9, 2000

Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein SM Makris, M Leach, N J Beauchamp, et al.

Blood|February 1, 1990

Severe type III von Willebrand's disease caused by deletion of exon 42 of the von Willebrand factor gene: family studies that identify carriers of the condition and a compound heterozygous individualI R Peake, M B Liddell, P Moodie, et al.

British Journal of Haematology|November 25, 2000

FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk groupF M Abu-Duhier, A C Goodeve, G A Wilson, et al.

Blood|October 9, 1998

Antithrombins Wibble and Wobble (T85M/K): archetypal conformational diseases with in vivo latent-transition, thrombosis, and heparin activationN J Beauchamp, R N Pike, M Daly, et al.

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