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Cigarette smoke-induced pulmonary inflammation, but not airway remodelling, is attenuated in chemokine receptor 5-deficient mice

Clinical and experimental allergy, 2007-10, Vol.37 (10), p.1467-1479

2007

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Murine models of COPD

Pulmonary pharmacology & therapeutics, 2006-01, Vol.19 (3), p.155-165

2006

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Short-Term Cigarette Smoke Exposure Enhances Allergic Airway Inflammation in Mice

American journal of respiratory and critical care medicine, 2005-07, Vol.172 (2), p.168-172

2005

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Cigarette smoke exposure facilitates allergic sensitization in mice

Respiratory research, 2006-03, Vol.7 (1), p.49-49, Article 49

2006

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Tisagenlecleucel in Children and Young Adults with B-Cell Lymphoblastic Leukemia

The New England journal of medicine, 2018-02, Vol.378 (5), p.439-448

2018

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IKZF1 deletion is an independent prognostic marker in childhood B-cell precursor acute lymphoblastic leukemia, and distinguishes patients benefiting from pulses during maintenance therapy: results of the EORTC Children's Leukemia Group study 58951

Leukemia, 2015-11, Vol.29 (11), p.2154-2161

2015

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The association between circulating antibodies against domain I of beta2‐glycoprotein I and thrombosis: an international multicenter study

Journal of thrombosis and haemostasis, 2009-11, Vol.7 (11), p.1767-1773

2009

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Characteristics and outcome of primary resistant disease in paediatric acute myeloid leukaemia

British journal of haematology, 2023-05, Vol.201 (4), p.757-765

2023

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Cigarette Smoke-Induced Pulmonary Inflammation and Emphysema Are Attenuated in CCR6-Deficient Mice

Journal of Immunology, 2006-10, Vol.177 (7), p.4350-4359

2006

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Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency

Leukemia, 2020-10, Vol.34 (10), p.2673-2687

2020

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2023 ACR/EULAR antiphospholipid syndrome classification criteria

Annals of the rheumatic diseases, 2023-10, Vol.82 (10), p.1258

2023

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Congenital combined deficiency of coagulation factors VII and X - different genetic mechanisms

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-05, Vol.21 (3), p.386-391

2015

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The genetic basis and cell of origin of mixed phenotype acute leukaemia

Nature (London), 2018-10, Vol.562 (7727), p.373-379

2018

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Classification of rare bleeding disorders (RBDs) based on the association between coagulant factor activity and clinical bleeding severity

Journal of thrombosis and haemostasis, 2012-09, Vol.10 (9), p.1938-1943

2012

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CNS-3 status remains an independent adverse prognosis factor in children with acute lymphoblastic leukemia (ALL) treated without cranial irradiation: Results of EORTC Children Leukemia Group study 58951

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2021-07, Vol.28 (5), p.411-416

2021

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SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity

Journal of bone and mineral research, 2013-05, Vol.28 (5), p.1041-1049

2013

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Complex and monosomal karyotype are distinct cytogenetic entities with an adverse prognostic impact in paediatric acute myeloid leukaemia. A NOPHO‐DBH‐AML study

British journal of haematology, 2018-11, Vol.183 (4), p.618-628

2018

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RUNX2 regulates leukemic cell metabolism and chemotaxis in high-risk T cell acute lymphoblastic leukemia

The Journal of clinical investigation, 2021-03, Vol.131 (6), p.1-19

2021

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Not all pediatric intestinal polyps are alike

Acta gastro-enterologica belgica, 2020-07, Vol.83 (3), p.393-397

2020

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Outcome measures in European patients with haemophilia: Survey of implementation in routine clinical practice, perception of relevance and recommendations by European treaters in the EHTSB

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-03, Vol.23 (2), p.222-229

2017

Volltextzugriff (PDF)

Topic: AS04-MDS Biology and Pathogenesis/AS04d-Somatic mutations: THE EVOLVING GENETIC LANDSCAPE OF PEDIATRIC MDS-EB

Leukemia research, 2023-05, Vol.128, p.107186, Article 107186

2023

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The use of propranolol in the treatment of periocular infantile haemangiomas: a review

British Journal of Ophthalmology, 2011-09, Vol.95 (9), p.1199-1202

2011

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Non-genetic risk factors and the development of inhibitors in haemophilia: a comprehensive review and consensus report

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-09, Vol.16 (5), p.747-766

2010

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Cigarette smoke-induced pulmonary inflammation, but not airway remodelling, is attenuated in chemokine receptor 5-deficient mice

Murine models of COPD

Short-Term Cigarette Smoke Exposure Enhances Allergic Airway Inflammation in Mice

Cigarette smoke exposure facilitates allergic sensitization in mice

Tisagenlecleucel in Children and Young Adults with B-Cell Lymphoblastic Leukemia

IKZF1 deletion is an independent prognostic marker in childhood B-cell precursor acute lymphoblastic leukemia, and distinguishes patients benefiting from pulses during maintenance therapy: results of the EORTC Children's Leukemia Group study 58951

The association between circulating antibodies against domain I of beta2‐glycoprotein I and thrombosis: an international multicenter study

Characteristics and outcome of primary resistant disease in paediatric acute myeloid leukaemia

Cigarette Smoke-Induced Pulmonary Inflammation and Emphysema Are Attenuated in CCR6-Deficient Mice

Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency

Dexamethasone (6 mg/m2/day) and prednisolone (60 mg/m2/day) were equally effective as induction therapy for childhood acute lymphoblastic leukemia in the EORTC CLG 58951 randomized trial

2023 ACR/EULAR antiphospholipid syndrome classification criteria

Congenital combined deficiency of coagulation factors VII and X - different genetic mechanisms

The genetic basis and cell of origin of mixed phenotype acute leukaemia

Classification of rare bleeding disorders (RBDs) based on the association between coagulant factor activity and clinical bleeding severity

CNS-3 status remains an independent adverse prognosis factor in children with acute lymphoblastic leukemia (ALL) treated without cranial irradiation: Results of EORTC Children Leukemia Group study 58951

SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity

Complex and monosomal karyotype are distinct cytogenetic entities with an adverse prognostic impact in paediatric acute myeloid leukaemia. A NOPHO‐DBH‐AML study

RUNX2 regulates leukemic cell metabolism and chemotaxis in high-risk T cell acute lymphoblastic leukemia

Not all pediatric intestinal polyps are alike

Outcome measures in European patients with haemophilia: Survey of implementation in routine clinical practice, perception of relevance and recommendations by European treaters in the EHTSB

Topic: AS04-MDS Biology and Pathogenesis/AS04d-Somatic mutations: THE EVOLVING GENETIC LANDSCAPE OF PEDIATRIC MDS-EB

The use of propranolol in the treatment of periocular infantile haemangiomas: a review

Non-genetic risk factors and the development of inhibitors in haemophilia: a comprehensive review and consensus report

O05 - Topic: AS04-MDS Biology and Pathogenesis/AS04b-Clonal diversity & evolution: SOMATIC GENETIC RESCUE IN SAMD9/SAMD9L MDS PREDISPOSITION SYNDROMES

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