UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 1.011

Sortiert nach

Trisomy 8-positive Polycythemia Vera Complicated with Intestinal Behçet's-like Disease: A New Perspective for a Clinical Approach

Internal Medicine, 2022, pp.8395-21

2022

Volltextzugriff (PDF)

Prenatal diagnosis of mosaic trisomy 8: Clinical report and literature review

Taiwanese journal of obstetrics & gynecology, 2011-09, Vol.50 (3), p.331-338

2011

Volltextzugriff (PDF)

MDS-472 STAG2 and SRSF2 Mutations Might Define Prognosis of MDS Patients With Isolated Trisomy 8

Clinical lymphoma, myeloma and leukemia, 2022-10, Vol.22, p.S316-S317

2022

Volltextzugriff (PDF)

RAD21 is a driver of chromosome 8 gain in Ewing sarcoma to mitigate replication stress

Genes & development, 2021-04, Vol.35 (7-8), p.556-572

2021

Volltextzugriff (PDF)

An unusual case of trisomy 8 mosaicism complicated by coexistence of phenylketonuria

Clinica chimica acta, 2024-03, Vol.555, p.117794, Article 117794

2024

Volltextzugriff (PDF)

Clinical Features of Clonal Cytogenetic Abnormalities in Philadelphia-negative Cells Developed During Tyrosine Kinase Inhibitor Treatment: A Case Series

Internal Medicine, 2023, pp.2182-23

2023

Volltextzugriff (PDF)

Cytogenetics in the management of clonal chromosomal abnormalities of undetermined significance and persistent polyclonal B-cell lymphocytosis: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH)

Current research in translational medicine, 2023-10, Vol.71 (4), p.103426-103426, Article 103426

2023

Volltextzugriff (PDF)

The acquisition of trisomy 8 associated with Behçet's-like disease in myelodysplastic syndrome

Leukemia research reports, 2020-01, Vol.13, p.100196-100196, Article 100196

2020

Volltextzugriff (PDF)

UBTF‐internal tandem duplication as a novel poor prognostic factor in pediatric acute myeloid leukemia

Genes chromosomes & cancer, 2023-04, Vol.62 (4), p.202-209

2023

Volltextzugriff (PDF)

Autoimmune and inflammatory manifestations associated with acute myeloid leukemia with Trisomy 8—Case series and review of the literature

European journal of haematology, 2022-03, Vol.108 (3), p.199-203

2022

Volltextzugriff (PDF)

Molecular genetic and clinical characterization of acute myeloid leukemia with trisomy 8 as the sole chromosome abnormality

Hematology (Luxembourg), 2022-12, Vol.27 (1), p.565-574

2022

Volltextzugriff (PDF)

Trisomy 8-positive Polycythemia Vera Complicated with Intestinal Behçet's-like Disease: A New Perspective for a Clinical Approach

Internal Medicine, 2022/06/01, Vol.61(11), pp.1713-1719

2022

Volltextzugriff (PDF)

Bilateral severe microphthalmia in a neonate with trisomy 8 mosaicism: A new finding

American journal of medical genetics. Part A, 2021-02, Vol.185 (2), p.534-538

2021

Volltextzugriff (PDF)

Behçet disease (BD) and BD‐like clinical phenotypes: NF‐κB pathway in mucosal ulcerating diseases

Scandinavian journal of immunology, 2020-11, Vol.92 (5), p.e12973-n/a

2020

Volltextzugriff (PDF)

A child with complementary mosaic trisomy 8 and mosaic trisomy 21; clinical description of Warkany-Down syndrome and mechanism of origin

European journal of medical genetics, 2020-06, Vol.63 (6), p.103922-103922, Article 103922

2020

Volltextzugriff (PDF)

Optimal Treatment Approaches to Intestinal Behçet's Disease Complicated by Myelodysplastic Syndrome: The KASID and KSBD Multicenter Study

Yonsei Medical Journal, 2024, 65(5), , pp.265-275

2024

Volltextzugriff (PDF)

Cytogenetic risk stratification of 417 patients with chronic myelomonocytic leukemia from a single institution

American journal of hematology, 2014-08, Vol.89 (8), p.813-818

2014

Volltextzugriff (PDF)

Issues arising from the prenatal diagnosis of some rare trisomy mosaics-the importance of cryptic fetal mosaicism

Prenatal diagnosis, 2004-07, Vol.24 (7), p.524-536

2004

Volltextzugriff (PDF)

How to treat myelodysplastic syndrome with clinical features resembling Behçet syndrome: a case-based systematic review

Annals of hematology, 2020-06, Vol.99 (6), p.1193-1203

2020

Volltextzugriff (PDF)

Cytogenetics in the management of myelodysplastic neoplasms (myelodysplastic syndromes, MDS): Guidelines from the groupe francophone de cytogénétique hématologique (GFCH)

Current research in translational medicine, 2023-10, Vol.71 (4), p.103409-103409, Article 103409

2023

Volltextzugriff (PDF)

Establishment and validation of prognostic nomogram in acute leukemia with trisomy 8

Hematology (Luxembourg), 2023-12, Vol.28 (1), p.2240131-2240131

2023

Volltextzugriff (PDF)

Prenatal detection of trisomy 8 mosaicism: Pregnancy outcome and follow up of a series of 17 consecutive cases

European journal of obstetrics & gynecology and reproductive biology, 2018-02, Vol.221, p.23-27

2018

Volltextzugriff (PDF)

Congenital Corneal Opacities Associated With Trisomy 8 Mosaicism Syndrome

Cornea, 2018-12, Vol.37 (12), p.1596

2018

Volltextzugriff (PDF)

Asian Population Is More Prone to Develop High-Risk Myelodysplastic Syndrome, Concordantly with Their Propensity to Exhibit High-Risk Cytogenetic Aberrations

Cancers, 2021-01, Vol.13 (3), p.481

2021

Volltextzugriff (PDF)

1 – 25 von 1.011

Suche als RSS-Feed

Aktive Filter

SpracheSpanisch

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(739)
Mit Volltextzugriff
(810)

Publikationsform

Sprache

11 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Humans
(887)
Science & Technology
(772)
Life Sciences & Biomedicine
(766)
Trisomy
(669)
Chromosomes, Human, Pair 8
(556)
Male
(532)
Female
(524)
Biological And Medical Sciences
(371)
Adult
(361)
Medical Sciences
(361)
Genetics & Heredity
(294)
Karyotyping
(290)
Oncology
(276)
Middle Aged
(272)
Trisomy 8
(260)
Chromosome Aberrations
(246)
Hematology
(244)
Chromosomes, Human, Pair 8 - Genetics
(242)
Aged
(237)
In Situ Hybridization, Fluorescence
(210)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Cancer Genetics And Cytogenetics
(120)
Leukemia
(41)
British Journal Of Haematology
(40)
American Journal Of Medical Genetics
(35)
Leukemia Research
(27)
Prenatal Diagnosis
(26)
American Journal Of Medical Genetics. Part A
(23)
Blood
(23)
Clinical Genetics
(23)
Genes Chromosomes & Cancer
(22)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Trisomy 8-positive Polycythemia Vera Complicated with Intestinal Behçet's-like Disease: A New Perspective for a Clinical Approach

Prenatal diagnosis of mosaic trisomy 8: Clinical report and literature review

MDS-472 STAG2 and SRSF2 Mutations Might Define Prognosis of MDS Patients With Isolated Trisomy 8

RAD21 is a driver of chromosome 8 gain in Ewing sarcoma to mitigate replication stress

An unusual case of trisomy 8 mosaicism complicated by coexistence of phenylketonuria

Clinical Features of Clonal Cytogenetic Abnormalities in Philadelphia-negative Cells Developed During Tyrosine Kinase Inhibitor Treatment: A Case Series

Cytogenetics in the management of clonal chromosomal abnormalities of undetermined significance and persistent polyclonal B-cell lymphocytosis: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH)

The acquisition of trisomy 8 associated with Behçet's-like disease in myelodysplastic syndrome

UBTF‐internal tandem duplication as a novel poor prognostic factor in pediatric acute myeloid leukemia

Autoimmune and inflammatory manifestations associated with acute myeloid leukemia with Trisomy 8—Case series and review of the literature

Molecular genetic and clinical characterization of acute myeloid leukemia with trisomy 8 as the sole chromosome abnormality

Trisomy 8-positive Polycythemia Vera Complicated with Intestinal Behçet's-like Disease: A New Perspective for a Clinical Approach

Bilateral severe microphthalmia in a neonate with trisomy 8 mosaicism: A new finding

Behçet disease (BD) and BD‐like clinical phenotypes: NF‐κB pathway in mucosal ulcerating diseases

A child with complementary mosaic trisomy 8 and mosaic trisomy 21; clinical description of Warkany-Down syndrome and mechanism of origin

Optimal Treatment Approaches to Intestinal Behçet's Disease Complicated by Myelodysplastic Syndrome: The KASID and KSBD Multicenter Study

Cytogenetic risk stratification of 417 patients with chronic myelomonocytic leukemia from a single institution

Issues arising from the prenatal diagnosis of some rare trisomy mosaics-the importance of cryptic fetal mosaicism

How to treat myelodysplastic syndrome with clinical features resembling Behçet syndrome: a case-based systematic review

Myelodysplastic syndrome (MDS) with isolated trisomy 8: a type of MDS frequently associated with myeloproliferative features? A report by the Groupe Francophone des Myélodysplasies

Cytogenetics in the management of myelodysplastic neoplasms (myelodysplastic syndromes, MDS): Guidelines from the groupe francophone de cytogénétique hématologique (GFCH)

Establishment and validation of prognostic nomogram in acute leukemia with trisomy 8

Prenatal detection of trisomy 8 mosaicism: Pregnancy outcome and follow up of a series of 17 consecutive cases

Congenital Corneal Opacities Associated With Trisomy 8 Mosaicism Syndrome

Asian Population Is More Prone to Develop High-Risk Myelodysplastic Syndrome, Concordantly with Their Propensity to Exhibit High-Risk Cytogenetic Aberrations

Aktive Filter

Suchergebnisse filtern