Lampert F - Search Results

1

Double target in situ hybridization applied to the study of numerical aberrations in childhood acute lymphoblastic leukemia.

Tosi S, Ritterbach J, Maglia O, Harbott J, Riehm H, Masera G, Biondi A, Lampert F. Tosi S, et al. Among authors: lampert f. Cancer Genet Cytogenet. 1994 Apr;73(2):103-8. doi: 10.1016/0165-4608(94)90193-7. Cancer Genet Cytogenet. 1994. PMID: 8174084

2

12q13, a new recurrent breakpoint in acute non-lymphoblastic leukemia.

Seyger MM, Ritterbach J, Creutzig U, Gnekow AK, Göbel U, Graf N, Reiter A, Lampert F, Harbott J. Seyger MM, et al. Among authors: lampert f. Cancer Genet Cytogenet. 1995 Mar;80(1):23-8. doi: 10.1016/0165-4608(94)00157-7. Cancer Genet Cytogenet. 1995. PMID: 7697629

3

Characterization of chromosome 8 abnormalities by fluorescence in situ hybridization in childhood B-acute lymphoblastic leukemia/non-Hodgkin lymphoma.

Nishida K, Ritterbach J, Repp R, Harbott J, Lampert F. Nishida K, et al. Among authors: lampert f. Cancer Genet Cytogenet. 1995 Jan;79(1):8-14. doi: 10.1016/0165-4608(94)00096-t. Cancer Genet Cytogenet. 1995. PMID: 7850758

4

Evolution of tumor cytogenetic aberrations and N-myc oncogene amplification in a case of disseminated neuroblastoma.

Christiansen H, Franke F, Bartram CR, Adolph S, Rudolph B, Harbott J, Reiter A, Lampert F. Christiansen H, et al. Among authors: lampert f. Cancer Genet Cytogenet. 1987 Jun;26(2):235-44. doi: 10.1016/0165-4608(87)90057-4. Cancer Genet Cytogenet. 1987. PMID: 3567877

5

Blastic phase chronic myeloid leukemia with a four-break rearrangement: t(11;9)(9;22)(q23;p22q34;q11).

Li L, Ritterbach J, Harbott J, Schroyens W, Lohmeyer J, Pralle H, Lampert F. Li L, et al. Among authors: lampert f. Cancer Genet Cytogenet. 1993 Jul 15;68(2):131-4. doi: 10.1016/0165-4608(93)90009-b. Cancer Genet Cytogenet. 1993. PMID: 8353804

6

Incidence and clinical relevance of TEL/AML1 fusion genes in children with acute lymphoblastic leukemia enrolled in the German and Italian multicenter therapy trials. Associazione Italiana Ematologia Oncologia Pediatrica and the Berlin-Frankfurt-Münster Study Group.

Borkhardt A, Cazzaniga G, Viehmann S, Valsecchi MG, Ludwig WD, Burci L, Mangioni S, Schrappe M, Riehm H, Lampert F, Basso G, Masera G, Harbott J, Biondi A. Borkhardt A, et al. Among authors: lampert f. Blood. 1997 Jul 15;90(2):571-7. Blood. 1997. PMID: 9226156 Free article.

7

Detection of hyperdiploid karyotypes (>50 chromosomes) in childhood acute lymphoblastic leukemia (ALL) using fluorescence in situ hybridization (FISH).

Ritterbach J, Hiddemann W, Beck JD, Schrappe M, Janka-Schaub G, Ludwig WD, Harbott J, Lampert F. Ritterbach J, et al. Among authors: lampert f. Leukemia. 1998 Mar;12(3):427-33. doi: 10.1038/sj.leu.2400930. Leukemia. 1998. PMID: 9529139

8

Philadelphia chromosome-positive (Ph+) childhood acute lymphoblastic leukemia: good initial steroid response allows early prediction of a favorable treatment outcome.

Schrappe M, Aricò M, Harbott J, Biondi A, Zimmermann M, Conter V, Reiter A, Valsecchi MG, Gadner H, Basso G, Bartram CR, Lampert F, Riehm H, Masera G. Schrappe M, et al. Among authors: lampert f. Blood. 1998 Oct 15;92(8):2730-41. Blood. 1998. PMID: 9763557 Free article.

9

Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion.

Loncarevic IF, Roitzheim B, Ritterbach J, Viehmann S, Borkhardt A, Lampert F, Harbott J. Loncarevic IF, et al. Among authors: lampert f. Genes Chromosomes Cancer. 1999 Mar;24(3):272-7. Genes Chromosomes Cancer. 1999. PMID: 10451708

10

Clinical significance of cytogenetic studies in childhood acute lymphoblastic leukemia: experience of the BFM trials.

Harbott J, Ritterbach J, Ludwig WD, Bartram CR, Reiter A, Lampert F. Harbott J, et al. Among authors: lampert f. Recent Results Cancer Res. 1993;131:123-32. doi: 10.1007/978-3-642-84895-7_12. Recent Results Cancer Res. 1993. PMID: 8210633 Clinical Trial. No abstract available.

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