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Scientific Publications

 

Publications and Presentation History

Gurcharan (Charan) Surdhar

Oral Presentations

Goodeve, A.C., Peake, I., Hashemi, M., Al-Buhairan, A., Castaman, G., Barronciani, L., Battle, J., Ribba, A-S., Oyen, F., Christianansen, K., Habart, D., Lethagen, S., Pasi, J., Guilliatt, A., Surdhar, G., Enayat, S., Lester, W. Mutations analysis in type 1 von Willebrand disease patients entered in the multicenter MCMDM-1VWD study. Supplement to the Journal of Thrombosis and Haemostasis July 2003. XIXth congress of the Internationals society on Thrombosis and Haemostasis, Birmingham, UK.

Guilliatt, A.M, Enayat, M.S., Surdhar, G.K., Jenkins, P.V., Pasi, J.K., Williams, M.D., Hill, F.G.H. Expression of type 2A (phenotype IID) von Willebrand Disease mutations in vitro. Supplement to Thrombosis and Haemostasis (2001). XVIIIth congress of the Internationals Society on Thrombosis and Haemostasis, Paris, France.

Publications

Surdhar GK, Enayat MS, Lawson S, Williams MD, Hill FGH. Homozygous gene conversion in von Willebrand Factor gene as a cause of type 3 von Willebrand disease and predisposition to inhibitor development. Blood 2001; 98: 248-250.

Enayat, M.S., Guilliatt, A.M., Surdhar, G.K., Jenkins, P.V., Pasi, K.P., Toh, C.H., Williams, M.D., Hill, F.G.H. Aberrant dimerization of von Willebrand Factor as the result of mutations in the carboxyl-terminal region: Identification of three mutations in members of three different families with type 2A (phenotype IID) von Willebrand Disease. Blood. (2001)98 (3) 674-680.

Enayat, M.S., Guilliatt, A.M., Surdhar, G.K., Theophilus, B.D.M., and Hill, F.G.H. A new candidate missense mutation (Leu 1657 Ile) in an apparently asymptomatic type 2A (phenotype IIA) von Willebrand disease family. Thrombosis and Haemostasis. (2000) 84: 369-373.

Conferences and Meetings Attended

International Society of Thrombosis and Haemostasis June 6-12 1997, Florence, Italy
European Society of Human Genetics. May 3-6 2003, Birmingham
International Society of Thrombosis and Haemostasis July 12-18, 2003 Birmingham, UK

Book Chapters

Use of Intron 40 VNTR I in vWD Gene Tracking
Author(s): Mohammed S. Enayat, Gurcharan K. Surdhar
Pub. Date: Aug-04-1999; DOI:10.1385/1-59259-248-1:179; Page Range: 179-186
Book: Hemostasis and Thrombosis Protocols
Editor(s): David J. Perry1, K. J. Pasi2
Affiliation(s): (1),Royal Free Hospital, London UK (2),Royal Free Hospital, London UK
Series: Methods in Molecular Medicine | Volume No.: 31

Print ISBN: 978-0-89603-419-8

Poster Presentations

Enayat, M.S., Guilliatt, A.M., Surdhar, G.K., Jones, N., Wilde, J.T., Keenan, R., Chalmers, E.A., Tait, R.C., Strevens, M.J., Williams, M.D., and Hill, F.G.H. Seven Novel Candidate Mutations in exon 27 and 28 of von Willebrand gene in patients with type 1, type 2M and Unclassified von Willebrand disease. Supplement to the Journal of Thrombosis and Haemostasis July 2005. XXth congress of the Internationals society on Thrombosis and Haemostasis, Sydney, Australia.

Enayat, M.S., Guilliatt, A.M., Surdhar, G.K., Williams, C.E., Williams, M.D., Hill, F.G.H. Two candidate type 2M von Willebrand disease mutations in two unrelated families with unusual phenotypes. Supplement to the Journal of Thrombosis and Haemostasis July 2003. XIXth congress of the Internationals society on Thrombosis and Haemostasis, Birmingham, UK.

Lester, W.A., Surdhar, G.K., Guilliatt, A.M., Enayat, M.S., Hill, F.G.H. Evaluation of a protein truncation test (PTT) for mutation detection in von Willebrand disease. Supplement to the Journal of Thrombosis and Haemostasis July 2003. XIXth congress of the Internationals society on Thrombosis and Haemostasis, Birmingham, UK.

Lester, W.A., Guilliatt, A.M., Surdhar, G.K., Enayat, M.S., Hill, F.G.H. Inherited and de novo von Willebrand disease “Vicenza” in UK families with the R1205H mutation. Supplement to the Journal of Thrombosis and Haemostasis July 2003. XIXth congress of the Internationals society on Thrombosis and Haemostasis, Birmingham, UK.

Lester, W.A., Jones, N.L., Guilliatt, A.M., Surdhar, G.K., Enayat, M.S., Hill, F.G.H. A common mutation 4247T>A (I1416N) causing type 2M von Willebrand disease in patients from 3 unrelated families previously diagnosed as severe type 1 VWD. Supplement to the Journal of Thrombosis and Haemostasis July 2003. XIXth congress of the Internationals society on Thrombosis and Haemostasis, Birmingham, UK.

Surdhar G., Kinning E., Enayat M.S., Williams M.D..Compound heterozygous Protein C deficiency resulting in neonatal purpura fulminans: identification of a novel mutation and its functional consequences. Supplement to the Journal of Thrombosis and Haemostasis July 2003. XIXth congress of the Internationals society on Thrombosis and Haemostasis, Birmingham, UK.

Enayat, M.S., Guilliatt, A.M, Surdhar, G.K., Jones, N.L., Bolton-Maggs, P., Wilde, J.T., Hill, F.G.H. Identification of five novel mutations in families with type 3 von Willebrand disease. Supplement to Thrombosis and Haemostasis (2001). XVIIIth congress of the Internationals society on Thrombosis and Haemostasis, Paris, France.

Guilliatt AM., Enayat MS., Surdhar GK., Jenkins PV, Pasi JK, Williams MD., Hill FGH. Expression of type 2A (phenotype IID) von Willebrand disease mutation in vitro. XVIIIth Congress of the International Society on Thrombosis and Haemostasis, 2001, Paris, France.

Enayat MS., Guilliatt AM., Surdhar GK., Jones NL., Williams MD., Bolton-Maggs P., Wilde JT., Hill FGH. Identification of five novel mutations in families with type 3 von Willebrand disease. XVIIIth Congress of the International Society on Thrombosis and Haemostasis, 2001, Paris, France.

ENAYAT MS, Surdhar GK, Theophilus BDM, Toh CH and Hill FGH. A novel 8 base deletion in exon 51 of VWF gene could be the cause of a IID phenotype of von Willebrand disease. 38th Annual Scientific Meeting of the British Society for Haematology, 1998, Glasgow, UK.

Enayat MS, Surdhar GK, Theophilus BDM, Williams MD, and Hill FGH. A new candidate mutation causing type IID von Willebrand disease in 3 patients in 3 generations of the same family. 39th Annual Scientific Meeting of the British Society for Haematology, 1997, Harrogate, UK. Also at XVI Congress of the International Society on Thrombosis and Haemostasis, 1997, Florence, Italy.

Surdhar GK, Enayat MS, Theophilus BDM, Williams MD, and Hill FGH. Usefulness of intro 40 variable tandem repeats (VNTR) in gene tracking 14 families with type 1 and 3 von Willebrand disease. 39th Annual Scientific Meeting of the British Society for Haematology, 1997, Harrogate, UK. Also at XVI Congress of the International Society on Thrombosis and Haemostasis, 1997, Florence, Italy.