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Patrick Wong

Researcher at University of British Columbia

Publications -  11
Citations -  133

Patrick Wong is an academic researcher from University of British Columbia. The author has contributed to research in topics: Hyperviscosity syndrome & Cancer. The author has an hindex of 6, co-authored 10 publications receiving 117 citations. Previous affiliations of Patrick Wong include St. Paul's Hospital & Richmond Hospital.

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IgG4-related disease and lymphocyte-variant hypereosinophilic syndrome: A comparative case series.

TL;DR: To compare the clinical and laboratory features of IgG4‐related disease (IgG 4‐RD) and lymphocyte‐variant hypereosinophilic syndrome (L‐HES), two rare diseases that often present with lymphadenopathy, gastrointestinal symptoms, eOSinophilia, and elevated immunoglobulins/IgE are compared.
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TDP1 and PARP1 Deficiency Are Cytotoxic to Rhabdomyosarcoma Cells

TL;DR: The results of these studies suggest a compensatory role for TDP1 in rhabdomyosarcoma after topoisomerase-I based therapy and further demonstrate that TDP 1 knockdown, PARP-1 inhibition, and dietary restriction have therapeutic validity.
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PRL-3: a metastasis-associated phosphatase in search of a function.

TL;DR: The discovery that the expression of a protein tyrosine phosphatase, protein of regenerating liver-3 (PRL-3), is upregulated in colon cancer metastases provided an exciting indication that the altered regulation of specific protein tyosine phosphorylation events and signaling pathways might characterize these metastatic cells and/or be key in promoting the tumor-to-metastasis transition in this, and perhaps other, cancers of epithelial origin.
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IgG4‐related disease with hypergammaglobulinemic hyperviscosity and retinopathy

TL;DR: A novel case of IgG4‐RD with hypergammaglobulinemic hyperviscosity responsive to fludarabine and rituximab is described, which can be considered in patients with severe refractory disease.
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Polyclonal hyperviscosity syndrome in IgG4-related disease and associated conditions

TL;DR: A review of seven cases establishes IgG4‐RD as an important cause of polyclonal HVS and establishes it as an emerging disorder often associated with exuberant hypergammaglobulinemia.