UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 40

Sortiert nach

MDS with Isolated Trisomy 8: A type of MDS Frequently Associated with Myeloproliferative Features? A Report by the GFM

Leukemia research, 2017-04, Vol.55, p.S21-S22

2017

Volltextzugriff (PDF)

Acute myeloid leukaemia with 8p11 ( ) rearrangement: an integrated cytologic, cytogenetic and molecular study by the groupe francophone de cytogénétique hématologique

Leukemia, 2008-08, Vol.22 (8), p.1567-1575

2008

Volltextzugriff (PDF)

Defective blood dendritic cells in chronic myeloid leukemia correlate with high plasmatic VEGF and are not normalized by imatinib mesylate

Leukemia, 2004-10, Vol.18 (10), p.1656-1661

2004

Volltextzugriff (PDF)

Sustained major molecular response in the absence of any antileukaemic therapy after dasatinib treatment and autologous peripheral blood stem cell transplantation in a patient with imatinib-resistant myeloblastic-phase chronic myeloid leukaemia

Leukemia, 2009-06, Vol.23 (6), p.1158-1159

2009

Volltextzugriff (PDF)

Isochromosome 7q and trisomy 8 are consistent primary, non-random chromosomal abnormalities associated with hepatosplenic T γ/δ lymphoma

Leukemia, 1996-09, Vol.10 (9), p.1453-1455

1996

Volltextzugriff (PDF)

Fluorescence in situ hybridization analysis of chromosome 1 abnormalities in hematopoietic disorders : rearrangements of DNA satellite II and new recurrent translocations

Leukemia, 1999-12, Vol.13 (12), p.1975-1981

1999

Volltextzugriff (PDF)

A clinical, molecular and cytogenetic study of 12 cases of human herpesvirus 8 associated primary effusion lymphoma in HIV-infected patients

The hematology journal : the official journal of the European Haematology Association, 2001, Vol.2 (3), p.172

2001

Volltextzugriff (PDF)

Faconi anemia and bone marrow clonal chromosome abnormalities

Leukemia, 1996-11, Vol.10 (11), p.1700-1704

1996

Volltextzugriff (PDF)

Overexpression of CEBPA resulting from the translocation t(14;19)(q32;q13) of human precursor B acute lymphoblastic leukemia

Blood, 2006-11, Vol.108 (10), p.3560-3563

2006

Volltextzugriff (PDF)

Interstitial telomere repeats in translocations of hematopoietic disorders

Leukemia, 2000-09, Vol.14 (9), p.1630-1633

2000

Volltextzugriff (PDF)

33 - MDS with Isolated Trisomy 8: A type of MDS Frequently Associated with Myeloproliferative Features? A Report by the GFM

Leukemia research, 2017-04, Vol.55, p.S21-S22

2017

Volltextzugriff (PDF)

PF257 GEMTUZUMAB OZOGAMICIN COMBINED WITH CYTARABINE FOR ACUTE MYELOID LEUKEMIA PATIENTS IN FIRST RELAPSE

HemaSphere, 2019-06, Vol.3 (S1), p.80-n/a

2019

Volltextzugriff (PDF)

Transplantation for Fanconi's anaemia: long‐term follow‐up of fifty patients transplanted from a sibling donor after low‐dose cyclophosphamide and thoraco‐abdominal irradiation for conditioning

British journal of haematology, 1998-10, Vol.103 (1), p.249-255

1998

Volltextzugriff (PDF)

Abnormal telomere metabolism in Fanconi's anaemia correlates with genomic instability and the probability of developing severe aplastic anaemia

British journal of haematology, 2003-03, Vol.120 (5), p.836-845

2003

Volltextzugriff (PDF)

Long‐term complete haematological and molecular remission after allogeneic bone marrow transplantation in a patient with a stem cell myeloproliferative disorder associated with t(8;13)(p12;q12)

British journal of haematology, 2003-04, Vol.121 (2), p.312-314

2003

Volltextzugriff (PDF)

Leukemia : Official Journal of the Leukemia Society of America, Leukemia Research Fund, U.K

Leukemia, 2008, p.1567-1575

2008

Volltextzugriff (PDF)

Aplastic anaemia in a case of hereditary neutrophil Fcgamma receptor IIIb deficiency

British journal of haematology, 1997-11, Vol.99 (2), p.422-425

1997

Volltextzugriff (PDF)

Aplastic anaemia in a case of hereditary neutrophil Fcγ receptor IIIb deficiency

British journal of haematology, 1997-11, Vol.99 (2), p.422-425

1997

Volltextzugriff (PDF)

Sustained major molecular response in the absence of any antileukaemic therapy after dasatinib treatment and autologous peripheral blood stem cell transplantation in a patient with imatinib-resistant myeloblastic-phase chronic myeloid leukaemia

Leukemia, 2009, Vol.23 (6), p.1158-1159

2009

Volltextzugriff (PDF)

Importance of the DIRVISH technique for detecting microdeletions

Annales de génétique, 1996, Vol.39 (3), p.173

1996

Volltextzugriff (PDF)

A novel translocation, t(9;21)(q13;q22) rearranging the RUNX1 gene in acute myelomonocytic leukemia

Annales de génétique, 2002-04, Vol.45 (2), p.67-69

2002

Volltextzugriff (PDF)

Chromosome 16 Inversion-Associated Translocation: Two New Cases

Cancer genetics and cytogenetics, 1999-10, Vol.114 (2), p.126-129

1999

Volltextzugriff (PDF)

1 – 25 von 40

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(33)
Mit Volltextzugriff
(38)

Publikationsform

Artikel
(38)
Berichte
(2)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(26)
Life Sciences & Biomedicine
(25)
Male
(23)
Humans
(22)
Biological And Medical Sciences
(21)
Medical Sciences
(19)
Adult
(17)
Hematology
(17)
Female
(15)
Hematologic And Hematopoietic Diseases
(15)
Middle Aged
(13)
Leukemias. Malignant Lymphomas. Malignant Reticulosis. Myelofibrosis
(12)
Aged
(11)
Karyotyping
(8)
Oncology
(8)
Adolescent
(7)
Leukemia
(7)
Aged, 80 And Over
(5)
Animals
(5)
Child
(5)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

MDS with Isolated Trisomy 8: A type of MDS Frequently Associated with Myeloproliferative Features? A Report by the GFM

Acute myeloid leukaemia with 8p11 ( ) rearrangement: an integrated cytologic, cytogenetic and molecular study by the groupe francophone de cytogénétique hématologique

Report of 34 patients with clonal chromosomal abnormalities in Philadelphia-negative cells during imatinib treatment of Philadelphia-positive chronic myeloid leukemia

Defective blood dendritic cells in chronic myeloid leukemia correlate with high plasmatic VEGF and are not normalized by imatinib mesylate

Sustained major molecular response in the absence of any antileukaemic therapy after dasatinib treatment and autologous peripheral blood stem cell transplantation in a patient with imatinib-resistant myeloblastic-phase chronic myeloid leukaemia

Effect of gemtuzumab ozogamicin on survival of adult patients with de-novo acute myeloid leukaemia (ALFA-0701): a randomised, open-label, phase 3 study

Isochromosome 7q and trisomy 8 are consistent primary, non-random chromosomal abnormalities associated with hepatosplenic T γ/δ lymphoma

Fluorescence in situ hybridization analysis of chromosome 1 abnormalities in hematopoietic disorders : rearrangements of DNA satellite II and new recurrent translocations

A clinical, molecular and cytogenetic study of 12 cases of human herpesvirus 8 associated primary effusion lymphoma in HIV-infected patients

Faconi anemia and bone marrow clonal chromosome abnormalities

Overexpression of CEBPA resulting from the translocation t(14;19)(q32;q13) of human precursor B acute lymphoblastic leukemia

Interstitial telomere repeats in translocations of hematopoietic disorders

33 - MDS with Isolated Trisomy 8: A type of MDS Frequently Associated with Myeloproliferative Features? A Report by the GFM

PF257 GEMTUZUMAB OZOGAMICIN COMBINED WITH CYTARABINE FOR ACUTE MYELOID LEUKEMIA PATIENTS IN FIRST RELAPSE

A report from the LALA-94 and LALA-SA groups on hypodiploidy with 30 to 39 chromosomes and near-triploidy: 2 possible expressions of a sole entity conferring poor prognosis in adult acute lymphoblastic leukemia (ALL)

Transplantation for Fanconi's anaemia: long‐term follow‐up of fifty patients transplanted from a sibling donor after low‐dose cyclophosphamide and thoraco‐abdominal irradiation for conditioning

Abnormal telomere metabolism in Fanconi's anaemia correlates with genomic instability and the probability of developing severe aplastic anaemia

Long‐term complete haematological and molecular remission after allogeneic bone marrow transplantation in a patient with a stem cell myeloproliferative disorder associated with t(8;13)(p12;q12)

Leukemia : Official Journal of the Leukemia Society of America, Leukemia Research Fund, U.K

Aplastic anaemia in a case of hereditary neutrophil Fcgamma receptor IIIb deficiency

Aplastic anaemia in a case of hereditary neutrophil Fcγ receptor IIIb deficiency

Sustained major molecular response in the absence of any antileukaemic therapy after dasatinib treatment and autologous peripheral blood stem cell transplantation in a patient with imatinib-resistant myeloblastic-phase chronic myeloid leukaemia

Importance of the DIRVISH technique for detecting microdeletions

A novel translocation, t(9;21)(q13;q22) rearranging the RUNX1 gene in acute myelomonocytic leukemia

Chromosome 16 Inversion-Associated Translocation: Two New Cases

Suchergebnisse filtern