T. Eden

发表

Bone mineral density in childhood survivors of acute lymphoblastic leukemia treated without cranial irradiation.

S. Roberts, K. Ward, Judith E. Adams, 2005, The Journal of clinical endocrinology and metabolism.

Benefit of dexamethasone compared with prednisolone for childhood acute lymphoblastic leukaemia: results of the UK Medical Research Council ALL97 randomized trial

S. Richards, A. Vora, J. Lilleyman, 2005, British journal of haematology.

Parvovirus B19 as a cause of chronic anemia in rhabdomyosarcoma

B. Cohen, T. Eden, Peter J. Shaw, 1993, Cancer.

No evidence of significant silencing of Fanconi genes FANCF and FANCB or Nijmegen breakage syndrome gene NBS1 by DNA hyper‐methylation in sporadic childhood leukaemia

Robert Brown, S. Meyer, G. Strathdee, 2006, British Journal of Haematology.

Spectrum and significance of variants and mutations in the Fanconi anaemia group G gene in children with sporadic acute myeloid leukaemia

J. Birch, S. Meyer, H. Joenje, 2006, British journal of haematology.

Inherited FANCD1/BRCA2 exon 7 splice mutations associated with acute myeloid leukaemia in Fanconi anaemia D1 are not found in sporadic childhood leukaemia

S. Meyer, D. White, A. Will, 2005, British journal of haematology.

Inactivation of HOXA Genes by Hypermethylation in Myeloid and Lymphoid Malignancy is Frequent and Associated with Poor Prognosis

Robert Brown, J. Melo, T. Holyoake, 2007, Clinical Cancer Research.

Three distinct subgroups of hypodiploidy in acute lymphoblastic leukaemia

S. Richards, A. Vora, A. Moorman, 2004, British journal of haematology.

A dyad of lymphoblastic lysosomal cysteine proteases degrades the antileukemic drug L-asparaginase.

Marc N. Offman, P. Bates, H. Ariffin, 2009, The Journal of clinical investigation.

Intracerebral recurrence of primary intrathoracic rhabdomyosarcoma.

J. Steers, P. Micallef-Eynaud, T. Eden, 1993, Medical and pediatric oncology.

Is the locus for Costello syndrome on 11p?

N. Philip, B. Kerr, R. Elles, 2003, Journal of medical genetics.

Is growth hormone treatment beneficial or harmful in Costello syndrome?

N. Philip, B. Kerr, P. Clayton, 2003, Journal of medical genetics.

Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia‐derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruption

Reinhard Ullmann, Crispin Miller, Crispin J. Miller, 2007, Genes, chromosomes & cancer.

Dexamethasone protects against cisplatin-induced activation of the mitochondrial apoptotic pathway in human osteosarcoma cells

S. Meyer, H. Kalirai, T. Eden, 2006, Cancer biology & therapy.

Mutation studies in CD3+, CD19+ and CD34+ cell fractions in myeloproliferative disorders with homozygous JAK2V617F in granulocytes

G. M. Taylor, R. Mesa, A. Tefferi, 2005, British journal of haematology.

p53 germline mutations in Li-Fraumeni syndrome

A. Craft, J. Birch, M. Santibanez-Koref, 1991, The Lancet.

MDM2 mediated nuclear exclusion of p53 attenuates etoposide-induced apoptosis in neuroblastoma cells.

C. Chresta, J. Hickman, D. Xenaki, 2001, Molecular pharmacology.

Inactivation of HOXAGenes by Hypermethylation in Myeloid and LymphoidMalignancy is Frequent and Associated with Poor Prognosis

Robert Brown, J. Melo, T. Holyoake, 2007 .

Neuroblastoma with intracranial involvement: an ENSG Study.

P. Shaw, T. Eden, T. Eden, 1992, Medical and pediatric oncology.