A. Alhaq

发表

Disruption of a binding site for hepatocyte nuclear factor 1 in the protein C gene promoter is associated with hereditary thrombophilia.

D. Cooper, V. Kakkar, L. Berg, 1994, Human molecular genetics.

Identification of an intronic regulatory element in the human protein C (PROC) gene

D. Cooper, N. Chuzhanova, D. Millar, 2000, Human Genetics.

Pathways to complement activation during cardiopulmonary bypass.

D. Vergani, B. Collett, J. Ponte, 1984 .

Immune Tolerance Therapy for Haemophilia A Patients with Acquired Factor VIII Alloantibodies: Comprehensive Analysis of Experience at a Single Institution

M. Mitchell, S. Brown, G. Savidge, 1999, Thrombosis and Haemostasis.

Spectrum of factor XI (F11) mutations in the UK population – 116 index cases and 140 mutations

R. Mountford, M. Mitchell, P. Bolton-Maggs, 2006, Human mutation.

The profibrinolytic effect of plasma thrombomodulin in factor XI deficiency and its implications in hemostasis

M. Mitchell, G. Savidge, A. Alhaq, 2004, Journal of thrombosis and haemostasis : JTH.

Evaluation of an automated screening assay for von Willebrand disease type 2N.

S. Taylor, G. Savidge, A. Alhaq, 2002, Clinical and laboratory haematology.

Validation of a quantitative SPR assay for recombinant FVIII.

G. Savidge, A N McCormick, M E Leach, 2004, Clinical and laboratory haematology.

Clinical application of new technique that measures C4d for assessment of activation of classical complement pathway.

D. Vergani, G. Senaldi, A. Alhaq, 1988, Journal of clinical pathology.

Activation of the alternative complement pathway: clinical application of a new technique to measure fragment Ba.

D. Vergani, M. Peakman, G. Senaldi, 1987, Journal of clinical pathology.

Characterisation of five factor XI mutations

M. Mitchell, P. Bolton-Maggs, G. Savidge, 2007, Thrombosis and Haemostasis.

An Alu-mediated 31.5-kb deletion as the cause of factor XI deficiency in 2 unrelated patients.

M. Mitchell, G. Savidge, A. Alhaq, 2004, Blood.

Heterozygous factor XI deficiency associated with three novel mutations

M. Mitchell, G. Moore, G. Savidge, 1999, British journal of haematology.

Identification of a novel mutation in a non‐Jewish factor XI deficient kindred

M. Mitchell, G. Flynn, G. Savidge, 1999, British journal of haematology.

Real‐Time quantitative PCR analysis of factor XI mRNA variants in human platelets

M Smith, G. Savidge, G Savidge, 2004, Journal of thrombosis and haemostasis : JTH.

Severe factor XI deficiency caused by compound heterozygosity

M. Mitchell, G. Savidge, A. Alhaq, 2004, British journal of haematology.

Eighteen unrelated patients with factor XI deficiency, four novel mutations and a 100% detection rate by denaturing high‐performance liquid chromatography

S. Rangarajan, M. Mitchell, G. Savidge, 2003, British journal of haematology.

Novel mutations in heterozygous factor XI deficiency and hemorrhagic tendency

G. Savidge, D. Pepper, A. Alhaq, 2000 .

Muslimness Discourse, Religious Authority, and Cyber-Media Activism in Contemporary Indonesia

A. Alhaq, A. Kurniawan, 2020 .