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Julia J. Scarisbrick

Skin Tumour Unit

St John's Institute of Dermatology

St Thomas' Hospital

London

UK

[email]@doctors.org.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Skin Tumour Unit, St John's Institute of Dermatology, St Thomas' Hospital, London, UK. 1999 - 2009

References

  1. Extracorporeal photopheresis: what is it and when should it be used? Scarisbrick, J. Clin. Exp. Dermatol. (2009) [Pubmed]
  2. Microsatellite instability is associated with hypermethylation of the hMLH1 gene and reduced gene expression in mycosis fungoides. Scarisbrick, J.J., Mitchell, T.J., Calonje, E., Orchard, G., Russell-Jones, R., Whittaker, S.J. J. Invest. Dermatol. (2003) [Pubmed]
  3. Frequent abnormalities of the p15 and p16 genes in mycosis fungoides and sezary syndrome. Scarisbrick, J.J., Woolford, A.J., Calonje, E., Photiou, A., Ferreira, S., Orchard, G., Russell-Jones, R., Whittaker, S.J. J. Invest. Dermatol. (2002) [Pubmed]
  4. Pseudocarcinomatous change in lymphomatoid papulosis and primary cutaneous CD30+ lymphoma: a clinicopathologic and immunohistochemical study of 6 patients. Scarisbrick, J.J., Calonje, E., Orchard, G., Child, F.J., Russell-Jones, R. J. Am. Acad. Dermatol. (2001) [Pubmed]
  5. A trial of fludarabine and cyclophosphamide combination chemotherapy in the treatment of advanced refractory primary cutaneous T-cell lymphoma. Scarisbrick, J.J., Child, F.J., Clift, A., Sabroe, R., Whittaker, S.J., Spittle, M., Russell-Jones, R. Br. J. Dermatol. (2001) [Pubmed]
  6. Allelotyping in mycosis fungoides and Sézary syndrome: common regions of allelic loss identified on 9p, 10q, and 17p. Scarisbrick, J.J., Woolford, A.J., Russell-Jones, R., Whittaker, S.J. J. Invest. Dermatol. (2001) [Pubmed]
  7. Loss of heterozygosity on 10q and microsatellite instability in advanced stages of primary cutaneous T-cell lymphoma and possible association with homozygous deletion of PTEN. Scarisbrick, J.J., Woolford, A.J., Russell-Jones, R., Whittaker, S.J. Blood (2000) [Pubmed]
  8. Secondary malignant neoplasms in 71 patients with Sézary syndrome. Scarisbrick, J.J., Child, F.J., Evans, A.V., Fraser-Andrews, E.A., Spittle, M., Russell-Jones, R. Arch. Dermatol (1999) [Pubmed]
 
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