Zobrazeno 1 - 10
of 45
pro vyhledávání: '"L. S. Lashford"'
Autor:
M. E. M. Jenney, E. Hesketh, L. S. Lashford, O. B. Eden, H. R. Gattamaneni, R. H. A. Campbell
Publikováno v:
Acta Paediatrica. 87:452-454
Four children with spinal cord compression due to malignant tumours are presented. The severity of the condition was not initially recognized by parents, or the nature of the likely cause by the initial physicians. Lower limb asymmetrical weakness, c
Publikováno v:
Archives of Disease in Childhood. 74:219-223
Standard treatment for the majority of malignant brain tumours consists of surgery and radiotherapy. This treatment has late morbidity which is accentuated in the very young child. As part of a strategy to improve quality of life and overall survival
Publikováno v:
International Journal of Cancer. 47:105-109
Whilst many human neuroblastoma cell lines have been studied to see if they are capable of taking up mIBG, few appear to have this ability. This contrasts markedly to the situation in vivo, where uptake has been demonstrated in the majority of tumour
Autor:
R B Richardson, Hugh B. Coakham, P. C. Jackson, G.E. Staddon, L. S. Lashford, A. G. Davies, John T. Kemshead
Publikováno v:
European Journal of Nuclear Medicine. 17:42-48
Radioiodinated monoclonal antibodies (MCA) were administered by the lumbar route into the cerebrospinal fluid (CSF) of four patients with malignant leptomeningeal disease. Evidence suggesting uptake of 131I-MCA by tumour sites was seen in scintigrams
Autor:
G W, Makin, O B, Eden, L S, Lashford, J, Moppett, M P, Gerrard, H A, Davies, C V, Powell, A N, Campbell, H, Frances
Publikováno v:
Cancer. 86(5)
Malignant melanoma (MM) is one of the least common types of childhood cancer, accounting for less than 1% of all pediatric malignancies. Neurocutaneous melanosis (NCM) is a rare phakomatosis consisting of congenital abnormal pigmentation of the skin
Autor:
L. J. Fairbairn, L. S. Lashford
Publikováno v:
Blood Cell Biochemistry ISBN: 9781461372189
The lysosomal storage disorders (LSDs) represent a wide group of clinically diverse types of disorders that include the mucopolysaccharidoses, sphingolipidoses, and defects in glycoprotein catabolism (Neufeld, 1991). All are characterized by the inab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06f874c87380fe118859b2491facb2d0
https://doi.org/10.1007/978-1-4615-4889-8_7
https://doi.org/10.1007/978-1-4615-4889-8_7
Autor:
A. Djeha, L. S. Lashford
Publikováno v:
Blood Cell Biochemistry ISBN: 9781461372189
Nucleic acids have acquired considerable significance as clinical reagents in genetic diseases. In genetic approaches to human disease, genes are introduced into cells to synthesize therapeutically active products which may in turn influence the clin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5486c31656f59c9e65b2a74bc401558f
https://doi.org/10.1007/978-1-4615-4889-8_5
https://doi.org/10.1007/978-1-4615-4889-8_5
Publikováno v:
Medical and pediatric oncology. 28(5)
Conventional treatment of medulloblastoma has involved surgery to the primary tumour and radiotherapy to the primary site and craniospinal axis. However CNS irradiation in a young child may result in significant side effects. Thus new treatment strat
Autor:
L. S. Lashford, O. B. Eden, E. Jones, J. Bruce, R. F. Stevens, R. H. A. Campbell, Anna Kelsey, H. R.G. Gattamaneni, M. E. M. Jenney, Jillian M Birch, A M Will
Publikováno v:
Pediatric hematology and oncology. 14(3)
The Manchester pediatric oncology unit is the third largest unit in the United Kingdom, with approximately 120 new referred cases per annum (10% of the U.K. total). Research activities include a gene therapy program, peripheral blood stem cell studie