Freund M - Search Results

1

17p anomalies in lymphoid malignancies: diagnostic and prognostic implications.

Schoch C, Rieder H, Stollmann-Gibbels B, Freund M, Tischler HJ, Silling-Engelhardt G, Fonatsch C. Schoch C, et al. Among authors: freund m. Leuk Lymphoma. 1995 Apr;17(3-4):271-9. doi: 10.3109/10428199509056832. Leuk Lymphoma. 1995. PMID: 8580796

2

Twenty-three cases of acute lymphoblastic leukemia with translocation t(4;11)(q21;q23): the implication of additional chromosomal aberrations.

Schoch C, Rieder H, Freund M, Hoelzer D, Riehm H, Fonatsch C. Schoch C, et al. Among authors: freund m. Ann Hematol. 1995 Apr;70(4):195-201. doi: 10.1007/BF01700375. Ann Hematol. 1995. PMID: 7748964

3

Correlation of cytogenetic findings with clinical features in 18 patients with inv(3)(q21q26) or t(3;3)(q21;q26).

Fonatsch C, Gudat H, Lengfelder E, Wandt H, Silling-Engelhardt G, Ludwig WD, Thiel E, Freund M, Bodenstein H, Schwieder G, et al. Fonatsch C, et al. Among authors: freund m. Leukemia. 1994 Aug;8(8):1318-26. Leukemia. 1994. PMID: 8057667

4

Fifty-one patients with acute myeloid leukemia and translocation t(8;21)(q22;q22): an additional deletion in 9q is an adverse prognostic factor.

Schoch C, Haase D, Haferlach T, Gudat H, Büchner T, Freund M, Link H, Lengfelder E, Wandt H, Sauerland MC, Löffler H, Fonatsch C. Schoch C, et al. Among authors: freund m. Leukemia. 1996 Aug;10(8):1288-95. Leukemia. 1996. PMID: 8709633

5

Karyotype instability in myelodysplastic syndromes--a specific step in pathogenesis preceding clonal chromosome anomalies.

Haase D, Fonatsch C, Freund M. Haase D, et al. Among authors: freund m. Leuk Lymphoma. 1992 Oct;8(3):221-8. doi: 10.3109/10428199209054908. Leuk Lymphoma. 1992. PMID: 1490148

6

Cytogenetic findings in 179 patients with myelodysplastic syndromes.

Haase D, Fonatsch C, Freund M, Wörmann B, Bodenstein H, Bartels H, Stollmann-Gibbels B, Lengfelder E. Haase D, et al. Among authors: freund m. Ann Hematol. 1995 Apr;70(4):171-87. doi: 10.1007/BF01700373. Ann Hematol. 1995. PMID: 7748962

7

Incidence and implication of additional chromosome aberrations in acute promyelocytic leukaemia with translocation t(15;17)(q22;q21): a report on 50 patients.

Schoch C, Haase D, Haferlach T, Freund M, Link H, Lengfelder E, Löffler H, Büchner T, Fonatsch C. Schoch C, et al. Among authors: freund m. Br J Haematol. 1996 Sep;94(3):493-500. doi: 10.1046/j.1365-2141.1996.d01-1829.x. Br J Haematol. 1996. PMID: 8790148

8

Partial trisomy 1q. A nonrandom primary chromosomal abnormality in myelodysplastic syndromes?

Fonatsch C, Haase D, Freund M, Bartels H, Tesch H. Fonatsch C, et al. Among authors: freund m. Cancer Genet Cytogenet. 1991 Oct 15;56(2):243-53. doi: 10.1016/0165-4608(91)90177-v. Cancer Genet Cytogenet. 1991. PMID: 1756470

9

Abnormalities of the short arm of chromosome 9. A nonrandom secondary aberration in Philadelphia chromosome-positive acute lymphoblastic leukemia (ALL).

Rieder H, Fonatsch C, Freund M. Rieder H, et al. Among authors: freund m. Cancer Genet Cytogenet. 1991 May;53(1):139-42. doi: 10.1016/0165-4608(91)90126-f. Cancer Genet Cytogenet. 1991. PMID: 2036635 No abstract available.

10

Correlation of cytogenetic, molecular cytogenetic, and clinical findings in 59 patients with ANLL or MDS and abnormalities of the short arm of chromosome 12.

Streubel B, Sauerland C, Heil G, Freund M, Bartels H, Lengfelder E, Wandt H, Ludwig WD, Nowotny H, Baldus M, Grothaus-Pinke B, Büchner T, Fonatsch C. Streubel B, et al. Among authors: freund m. Br J Haematol. 1998 Mar;100(3):521-33. doi: 10.1046/j.1365-2141.1998.00591.x. Br J Haematol. 1998. PMID: 9504635 Free article.

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