Assessment of disease activity in systemic vasculitis.

Yazar: Tse, W. Y., Cockwell, P., Savage, C. O.
Baskı/Yayın Bilgisi 1998

Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1.

Yazar: Becker, P S, Tse, W T, Lux, S E, Forget, B G
Baskı/Yayın Bilgisi 1993

Neutrophil FcγRIIIb allelic polymorphism in anti-neutrophil cytoplasmic antibody (ANCA)-positive systemic vasculitis

Yazar: Tse, W Y, Abadeh, S, Jefferis, R, Savage, C O S, Adu, D
Baskı/Yayın Bilgisi 2000

Arthroscopic Resection of Wrist Ganglion Arising from the Lunotriquetral Joint

Yazar: Mak, Michael C. K., Ho, Pak-cheong, Tse, W. L., Wong, Clara W. Y.
Baskı/Yayın Bilgisi 2013

The value of serum neopterin, interferon-gamma levels and interleukin-12B polymorphisms in predicting acute renal allograft rejection

Yazar: Chin, G K, Adams, C L, Carey, B S, Shaw, S, Tse, W-Y, Kaminski, E R
Baskı/Yayın Bilgisi 2008

Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms

Yazar: Wilson, H, Wong, A, Shaw, S, Tse, W, Stapleton, G, Phelan, M, Hu, S, Marshall, J, McDermid, H
Baskı/Yayın Bilgisi 2003

Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene.

Yazar: Gallagher, P G, Weed, S A, Tse, W T, Benoit, L, Morrow, J S, Marchesi, S L, Mohandas, N, Forget, B G
Baskı/Yayın Bilgisi 1995

Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a...

Yazar: Garbarz, M, Tse, W T, Gallagher, P G, Picat, C, Lecomte, M C, Galibert, F, Dhermy, D, Forget, B G
Baskı/Yayın Bilgisi 1991

Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.

Yazar: Tse, W T, Lecomte, M C, Costa, F F, Garbarz, M, Feo, C, Boivin, P, Dhermy, D, Forget, B G
Baskı/Yayın Bilgisi 1990

A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic c...

Yazar: Gallagher, P G, Tse, W T, Coetzer, T, Lecomte, M C, Garbarz, M, Zarkowsky, H S, Baruchel, A, Ballas, S K, Dhermy, D, Palek, J
Baskı/Yayın Bilgisi 1992

An increased MRP8/14 expression and adhesion, but a decreased migration towards proinflammatory chemokines of type 1 diabetes monocytes

Yazar: Bouma, G, Coppens, J M C, Lam-Tse, W-K, Luini, W, Sintnicolaas, K, Levering, W H, Sozzani, S, Drexhage, H A, Versnel, M A
Baskı/Yayın Bilgisi 2005

Functional Outcome for Arthroscopic Treatment of Septic Arthritis of the Wrist

Yazar: Chow, Esther M. W., Lau, Jimmy K. Y., Liyeung, Lucci L. C., Chau, W. W., Mak, Michael C. K., Tse, W. L., Ho, P. C.
Yayımlandı J Wrist Surg (2020)

Efficacy of adalimumab in sarcoidosis

Yazar: Kamphuis, LSJ, Lam-Tse, W K, Dik, W A, Bastiaans, J, van Biezen, P, van Daele, PLA, Kwekkeboom, D J, Kuijpers, RWAM, Baarsma, G S, van Hagen, P M, Hooijkaas, H, van Laar, JAM
Baskı/Yayın Bilgisi 2010

Molecular Characterization of Clinical Isolates of Mycobacterium tuberculosis and Their Association with Phenotypic Virulence in Human Macrophages

Yazar: Wong, K. C., Leong, W. M., Law, H. K. W., Ip, K. F., Lam, J. T. H., Yuen, K. Y., Ho, P. L., Tse, W. S., Weng, X. H., Zhang, W. H., Chen, S., Yam, W. C.
Baskı/Yayın Bilgisi 2007