Assessment of disease activity in systemic vasculitis.

Por Tse, W. Y., Cockwell, P., Savage, C. O.
Publicado em 1998

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

Por Becker, P S, Tse, W T, Lux, S E, Forget, B G
Publicado em 1993

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

Por Tse, W Y, Abadeh, S, Jefferis, R, Savage, C O S, Adu, D
Publicado em 2000

Arthroscopic Resection of Wrist Ganglion Arising from the Lunotriquetral Joint

Por Mak, Michael C. K., Ho, Pak-cheong, Tse, W. L., Wong, Clara W. Y.
Publicado em 2013

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

Por Chin, G K, Adams, C L, Carey, B S, Shaw, S, Tse, W-Y, Kaminski, E R
Publicado em 2008

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

Por Wilson, H, Wong, A, Shaw, S, Tse, W, Stapleton, G, Phelan, M, Hu, S, Marshall, J, McDermid, H
Publicado em 2003

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

Por Gallagher, P G, Weed, S A, Tse, W T, Benoit, L, Morrow, J S, Marchesi, S L, Mohandas, N, Forget, B G
Publicado em 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...

Por Garbarz, M, Tse, W T, Gallagher, P G, Picat, C, Lecomte, M C, Galibert, F, Dhermy, D, Forget, B G
Publicado em 1991

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

Por Tse, W T, Lecomte, M C, Costa, F F, Garbarz, M, Feo, C, Boivin, P, Dhermy, D, Forget, B G
Publicado em 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...

Por 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
Publicado em 1992

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

Por 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
Publicado em 2005

Efficacy of adalimumab in sarcoidosis

Por 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
Publicado em 2010

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

Por 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.
Publicado em 2007