UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Chromosome abnormalities clustering and its implications for pathogenesis and prognosis in myeloma

Leukemia, 2003-02, Vol.17 (2), p.427-436

2003

Volltextzugriff (PDF)

JAK2 V617F is a rare finding in de novo acute myeloid leukemia, but STAT3 activation is common and remains unexplained

Leukemia, 2006-06, Vol.20 (6), p.971-978

2006

Volltextzugriff (PDF)

Recurrent episodes of skin angioedema and severe attacks of abdominal pain induced by oral contraceptives or hormone replacement therapy

The American journal of medicine, 2003-03, Vol.114 (4), p.294-298

2003

Volltextzugriff (PDF)

Hereditary angio‐oedema with normal C1 inhibitor in a family with affected women and men

British journal of dermatology (1951), 2006-03, Vol.154 (3), p.542-545

2006

Volltextzugriff (PDF)

Primary pulmonary MALT lymphomas show frequent and heterogeneous cytogenetic abnormalities, including aneuploidy and translocations involving API2 and MALT1 and IGH and MALT1

Leukemia, 2004-01, Vol.18 (1), p.156-160

2004

Volltextzugriff (PDF)

B-CLL cells are capable of synthesis and secretion of both pro- and anti-angiogenic molecules

Leukemia, 2002-05, Vol.16 (5), p.911-919

2002

Volltextzugriff (PDF)

WHO-defined chronic neutrophilic leukemia: a long-term analysis of 12 cases and a critical review of the literature

Leukemia, 2005-02, Vol.19 (2), p.313-317

2005

Volltextzugriff (PDF)

Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor

Biochemical and biophysical research communications, 2006-05, Vol.343 (4), p.1286-1289

2006

Volltextzugriff (PDF)

Interphase fluorescence in situ hybridization with an IGH probe is important in the evaluation of patients with a clinical diagnosis of chronic lymphocytic leukaemia

British journal of haematology, 2005-07, Vol.130 (1), p.36-42

2005

Volltextzugriff (PDF)

Diagnostic utility of fluorescence in situ hybridization in mantle‐cell lymphoma

British journal of haematology, 2000-09, Vol.110 (4), p.856-862

2000

Volltextzugriff (PDF)

Deletions of chromosome 13 in multiple myeloma identified by interphase FISH usually denote large deletions of the q arm or monosomy

Leukemia, 2001-06, Vol.15 (6), p.981-986

2001

Volltextzugriff (PDF)

FIP1L1-PDGFRA in eosinophilic disorders: Prevalence in routine clinical practice, long-term experience with imatinib therapy, and a critical review of the literature

Leukemia research, 2006-08, Vol.30 (8), p.965-970

2006

Volltextzugriff (PDF)

Advanced tubular solid oxide fuel cells with high efficiency for internal reforming of hydrocarbon fuels

Journal of power sources, 2009-03, Vol.188 (2), p.521-526

2009

Volltextzugriff (PDF)

A retrospective study of 69 patients with t(6;9)(p23;q34) AML emphasizes the need for a prospective, multicenter initiative for rare 'poor prognosis' myeloid malignancies

Leukemia, 2006-07, Vol.20 (7), p.1295-1297

2006

Volltextzugriff (PDF)

Pregnancies in Women with Hereditary Angioedema due to Mutations in the F12 gene

Journal of allergy and clinical immunology, 2012-02, Vol.129 (2), p.AB80-AB80

2012

Volltextzugriff (PDF)

Secondary myelodysplastic syndrome and acute myelogenous leukemia are significant complications following autologous stem cell transplantation for lymphoma

Bone marrow transplantation (Basingstoke), 2003-08, Vol.32 (3), p.317-324

2003

Volltextzugriff (PDF)

Cytogenetic findings and their clinical relevance in myelofibrosis with myeloid metaplasia

British journal of haematology, 2001-06, Vol.113 (3), p.763-771

2001

Volltextzugriff (PDF)

Idiopathic Angioedema and Coagulation Factor XII Mutation

Journal of allergy and clinical immunology, 2011-02, Vol.127 (2), p.AB99-AB99

2011

Volltextzugriff (PDF)

Abnormal Function of the Bone Marrow Microenvironment in Chronic Myelogenous Leukemia: Role of Malignant Stromal Macrophages

Blood, 1995-06, Vol.85 (12), p.3636-3645

1995

Volltextzugriff (PDF)

Dysgranulopoiesis is an independent adverse prognostic factor in chronic myeloid disorders with an isolated interstitial deletion of chromosome 5q

Leukemia, 2009-04, Vol.23 (4), p.796-800

2009

Volltextzugriff (PDF)

Analysis of clonal B‐cell CD38 and immunoglobulin variable region sequence status in relation to clinical outcome for B‐chronic lymphocytic leukaemia

British journal of haematology, 2001-12, Vol.115 (4), p.854-861

2001

Volltextzugriff (PDF)

Chronic neutrophilic leukemia (CNL): a clinical, pathologic and cytogenetic study

Leukemia, 2001, Vol.15 (1), p.35-40

2001

Volltextzugriff (PDF)

The (11;14)(q13;q32) translocation in multiple myeloma. A morphologic and immunohistochemical study

American journal of clinical pathology, 2000-06, Vol.113 (6), p.831-837

2000

Volltextzugriff (PDF)

Hereditary Angioedema due to Missense Mutations Thr309Lys and Thr309Arg in the Factor 12 Gene

Journal of allergy and clinical immunology, 2010-02, Vol.125 (2), p.AB164-AB164

2010

Volltextzugriff (PDF)

Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical course

British journal of haematology, 1999-08, Vol.106 (2), p.445-454

1999

Volltextzugriff (PDF)

1 – 25 von 1.236

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(976)
Mit Volltextzugriff
(1.029)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

Englisch
(1.208)
Japanisch
(101)
Deutsch
(23)
Norwegisch
(4)
Französisch
(2)
Russisch
(1)

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(606)
Life Sciences & Biomedicine
(344)
Humans
(317)
Physics
(262)
Physical Sciences
(240)
Biological And Medical Sciences
(205)
Female
(176)
Medical Sciences
(176)
Male
(173)
Middle Aged
(125)
Adult
(119)
Aged
(109)
Hematologic And Hematopoietic Diseases
(90)
Hematology
(88)
Physics, Nuclear
(87)
Leukemias. Malignant Lymphomas. Malignant Reticulosis. Myelofibrosis
(85)
Chromosome Aberrations
(81)
Oncology
(81)
Technology
(72)
Karyotyping
(69)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Chromosome abnormalities clustering and its implications for pathogenesis and prognosis in myeloma

JAK2 V617F is a rare finding in de novo acute myeloid leukemia, but STAT3 activation is common and remains unexplained

Recurrent episodes of skin angioedema and severe attacks of abdominal pain induced by oral contraceptives or hormone replacement therapy

Hereditary angio‐oedema with normal C1 inhibitor in a family with affected women and men

Primary pulmonary MALT lymphomas show frequent and heterogeneous cytogenetic abnormalities, including aneuploidy and translocations involving API2 and MALT1 and IGH and MALT1

B-CLL cells are capable of synthesis and secretion of both pro- and anti-angiogenic molecules

WHO-defined chronic neutrophilic leukemia: a long-term analysis of 12 cases and a critical review of the literature

Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor

Interphase fluorescence in situ hybridization with an IGH probe is important in the evaluation of patients with a clinical diagnosis of chronic lymphocytic leukaemia

Diagnostic utility of fluorescence in situ hybridization in mantle‐cell lymphoma

Deletions of chromosome 13 in multiple myeloma identified by interphase FISH usually denote large deletions of the q arm or monosomy

FIP1L1-PDGFRA in eosinophilic disorders: Prevalence in routine clinical practice, long-term experience with imatinib therapy, and a critical review of the literature

Advanced tubular solid oxide fuel cells with high efficiency for internal reforming of hydrocarbon fuels

A retrospective study of 69 patients with t(6;9)(p23;q34) AML emphasizes the need for a prospective, multicenter initiative for rare 'poor prognosis' myeloid malignancies

Pregnancies in Women with Hereditary Angioedema due to Mutations in the F12 gene

Secondary myelodysplastic syndrome and acute myelogenous leukemia are significant complications following autologous stem cell transplantation for lymphoma

Cytogenetic findings and their clinical relevance in myelofibrosis with myeloid metaplasia

Idiopathic Angioedema and Coagulation Factor XII Mutation

Abnormal Function of the Bone Marrow Microenvironment in Chronic Myelogenous Leukemia: Role of Malignant Stromal Macrophages

Dysgranulopoiesis is an independent adverse prognostic factor in chronic myeloid disorders with an isolated interstitial deletion of chromosome 5q

Analysis of clonal B‐cell CD38 and immunoglobulin variable region sequence status in relation to clinical outcome for B‐chronic lymphocytic leukaemia

Chronic neutrophilic leukemia (CNL): a clinical, pathologic and cytogenetic study

The (11;14)(q13;q32) translocation in multiple myeloma. A morphologic and immunohistochemical study

Hereditary Angioedema due to Missense Mutations Thr309Lys and Thr309Arg in the Factor 12 Gene

Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical course

Suchergebnisse filtern