Search Results - "Pussegoda, K"

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    Replication of TPMT and ABCC3 Genetic Variants Highly Associated With Cisplatin-Induced Hearing Loss in Children by Pussegoda, K, Ross, C J, Visscher, H, Yazdanpanah, M, Brooks, B, Rassekh, S R, Zada, Y F, Dubé, M-P, Carleton, B C, Hayden, M R

    Published in Clinical pharmacology and therapeutics (01-08-2013)
    “…Cisplatin is a widely used chemotherapeutic agent for the treatment of solid tumors. A serious complication of cisplatin treatment is permanent hearing loss…”
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    Journal Article
  3. 3

    Exome sequencing: locating causative genes in rare disorders by Pussegoda, KA

    Published in Clinical genetics (01-07-2010)
    “…Exome sequencing identifies the cause of a mendelian disorder Ng et al. (2009) Nature Genetics. Advanced online publication…”
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    Genetic variants associated with cisplatin-induced hearing loss by Pussegoda, KA

    Published in Clinical genetics (01-07-2010)
    “…Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy Ross et al. (2009) Nature Genetics 41:1345–1349…”
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    Journal Article
  5. 5

    Down's syndrome patients are less likely to develop cancer by Pussegoda, KA

    Published in Clinical genetics (01-07-2010)
    “…Down's syndrome suppression of tumour growth and the role of the calcineurin inhibitor DSCR1 Baek et al. (2009) Nature 459:1126–1130…”
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    Genetic Markers of Cisplatin-Induced Hearing Loss in Children by Carleton, B C, Ross, C J, Pussegoda, K, Bhavsar, A P, Visscher, H, Lee, J W, Brooks, B, Rassekh, S R, Dubé, M-P P, Hayden, M R

    Published in Clinical pharmacology and therapeutics (01-09-2014)
    “…This journal recently published a Commentary by Ratain and colleagues at the University of Chicago that criticizes our work on cisplatin‐induced hearing loss…”
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    Journal Article
  8. 8

    Exome sequencing: locating causative genes in rare disorders by Pussegoda, KA

    Published in Clinical genetics (01-07-2010)
    “…Exome sequencing identifies the cause of a mendelian disorder…”
    Get full text
    Journal Article