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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

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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

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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

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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

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

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

2024

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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

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

2023

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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

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Congenital Corneal Opacities Associated With Trisomy 8 Mosaicism Syndrome

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

2018

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Mutational Profile Enables the Identification of a High-Risk Subgroup in Myelodysplastic Syndromes with Isolated Trisomy 8

Cancers, 2023-07, Vol.15 (15), p.3822

2023

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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

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

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

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

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

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

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

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

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

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

Mutational Profile Enables the Identification of a High-Risk Subgroup in Myelodysplastic Syndromes with Isolated Trisomy 8

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