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Constitutively active CaMKII Drives B lineage acute lymphoblastic leukemia/lymphoma in tp53 mutant zebrafish

PLoS genetics, 2023-12, Vol.19 (12), p.e1011102-e1011102

2023

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Contributions of side effects to contraceptive discontinuation and method switch among Kenyan women: a prospective cohort study

BJOG : an international journal of obstetrics and gynaecology, 2022-05, Vol.129 (6), p.926-937

2022

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Diagnostic d’un syndrome hémorragique de l’enfant

Journal de pédiatrie et de puériculture, 2019-02, Vol.32 (1), p.1-11

2019

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P.65 D-dimer as a tool for taking a decision about thromboprophylaxis in a patient with breast cancer

Thrombosis research, 2011, Vol.127, p.S144-S145

Rothschild, C

2011

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Definitions in hemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis

Thrombosis and haemostasis, 2001-03, Vol.85 (3), p.560

2001

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The activation of membrane targeted CaMK-II in the zebrafish Kupffer's vesicle is required for left-right asymmetry

Development (Cambridge), 2010-08, Vol.137 (16), p.2753-2762

2010

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CaMK-II activation is essential for zebrafish inner ear development and acts through Delta–Notch signaling

Developmental biology, 2013-09, Vol.381 (1), p.179-188

2013

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Myeloid Targeted Human MLL-ENL and MLL-AF9 Induces cdk9 and bcl2 Expression in Zebrafish Embryos

PLoS genetics, 2024-06, Vol.20 (6), p.e1011308

2024

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Le jeune hémophile, les inhibiteurs et la tolérance immune

Transfusion clinique et biologique : journal de la Société française de transfusion sanguine, 1999-06, Vol.6 (3), p.191-194

ROTHSCHILD, C

1999

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Specific CaMKIIs mediate convergent extension cell movements in early zebrafish development

Developmental dynamics, 2024-04, Vol.253 (4), p.390-403

2024

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Treatment of severe von Willebrand disease with a high‐purity von Willebrand factor concentrate (Wilfactin®): a prospective study of 50 patients

Journal of thrombosis and haemostasis, 2007-06, Vol.5 (6), p.1115-1124

2007

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PREVALENCE OF HEMATURIA IN PATIENTS WITH HEMOPHILIA A AND B AND ITS ASSOCIATION WITH COMORBIDITIES: EXPERIENCE FROM A BRAZILIAN CENTER

Hematology, Transfusion and Cell Therapy, 2021-10, Vol.43, p.S231-S231

2021

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Anti‐A2 and anti‐A1 domain antibodies are potential predictors of immune tolerance induction outcome in children with hemophilia A

Journal of thrombosis and haemostasis, 2015-04, Vol.13 (4), p.540-547

2015

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Open synovectomy of the ankle joint in young haemophiliacs: mid-term to long- term results of a single-centre series of 32 procedures

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-07, Vol.21 (4), p.e306-e311

2015

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Immune tolerance induction in haemophilia A patients with inhibitors by treatment with recombinant factor VIII: a retrospective non-interventional study

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-05, Vol.19 (3), p.449-455

2013

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PHARMACEUTICAL VIGILANCE AND EDUCATION: THE FIRST 6 MONTHS OF A NEW ANTICOAGULANT AT A BRAZILIAN PUBLIC CANCER INSTITUTE

Hematology, Transfusion and Cell Therapy, 2021-10, Vol.43, p.S466-S467

2021

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PLAQUETOPENIA INDUZIDA POR HEPARINA EM PACIENTE COM COVID-19: RELATO DE CASO

Hematology, Transfusion and Cell Therapy, 2020-11, Vol.42, p.547-548

2020

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ATENDIMENTO A PESSOAS COM COAGULOPATIAS HEREDITÁRIAS DURANTE A PANDEMIA DE COVID-19: EXPERIÊNCIA DA EQUIPE INTERDISCIPLINAR DO HC-FMUSP

Hematology, Transfusion and Cell Therapy, 2020-11, Vol.42, p.518-519

2020

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Molecular diagnosis of haemophilia A in patients from Senegal

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-05, Vol.23 (3), p.e225-e227

2017

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RECOMMENDATION ON THE TREATMENT OF VENOUS THROMBOEMBOLISM IN CANCER PATIENTS AT A BRAZILIAN PUBLIC ONCOLOGICAL INSTITUTION: EDUCATIONAL PLAN

Hematology, Transfusion and Cell Therapy, 2021-10, Vol.43, p.S457-S457

2021

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P.66 Hereditary hemorrhagic telangiectasia (HHT) in women: 6 case-reports and comments

Thrombosis research, 2011, Vol.127, p.S145-S145

2011

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SAFETY AND EFFECTIVENESS OF ANTICOAGULATION BASED ON AN INSTITUTIONAL RECOMMENDATION ON THE MANAGEMENT OF CANCER ASSOCIATED VENOUS THROMBOSIS

Hematology, Transfusion and Cell Therapy, 2021-10, Vol.43, p.S243-S244

2021

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Use of Haemate® P as immune tolerance induction in patients with severe haemophilia A who failed previous induction attempts: a multicentre observational study

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-03, Vol.19 (2), p.281-286

2013

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Genetic compensation of γ CaMKII, an evolutionarily conserved gene

Gene, 2020-06, Vol.742, p.144567, Article 144567

2020

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Pharmacokinetics and pharmacodynamics of a new highly secured fibrinogen concentrate

Journal of thrombosis and haemostasis, 2008-09, Vol.6 (9), p.1494-1499

2008

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Constitutively active CaMKII Drives B lineage acute lymphoblastic leukemia/lymphoma in tp53 mutant zebrafish

Contributions of side effects to contraceptive discontinuation and method switch among Kenyan women: a prospective cohort study

Diagnostic d’un syndrome hémorragique de l’enfant

P.65 D-dimer as a tool for taking a decision about thromboprophylaxis in a patient with breast cancer

Definitions in hemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis

The activation of membrane targeted CaMK-II in the zebrafish Kupffer's vesicle is required for left-right asymmetry

CaMK-II activation is essential for zebrafish inner ear development and acts through Delta–Notch signaling

Myeloid Targeted Human MLL-ENL and MLL-AF9 Induces cdk9 and bcl2 Expression in Zebrafish Embryos

Le jeune hémophile, les inhibiteurs et la tolérance immune

Specific CaMKIIs mediate convergent extension cell movements in early zebrafish development

Treatment of severe von Willebrand disease with a high‐purity von Willebrand factor concentrate (Wilfactin®): a prospective study of 50 patients

PREVALENCE OF HEMATURIA IN PATIENTS WITH HEMOPHILIA A AND B AND ITS ASSOCIATION WITH COMORBIDITIES: EXPERIENCE FROM A BRAZILIAN CENTER

Anti‐A2 and anti‐A1 domain antibodies are potential predictors of immune tolerance induction outcome in children with hemophilia A

Open synovectomy of the ankle joint in young haemophiliacs: mid-term to long- term results of a single-centre series of 32 procedures

Immune tolerance induction in haemophilia A patients with inhibitors by treatment with recombinant factor VIII: a retrospective non-interventional study

PHARMACEUTICAL VIGILANCE AND EDUCATION: THE FIRST 6 MONTHS OF A NEW ANTICOAGULANT AT A BRAZILIAN PUBLIC CANCER INSTITUTE

PLAQUETOPENIA INDUZIDA POR HEPARINA EM PACIENTE COM COVID-19: RELATO DE CASO

ATENDIMENTO A PESSOAS COM COAGULOPATIAS HEREDITÁRIAS DURANTE A PANDEMIA DE COVID-19: EXPERIÊNCIA DA EQUIPE INTERDISCIPLINAR DO HC-FMUSP

Molecular diagnosis of haemophilia A in patients from Senegal

RECOMMENDATION ON THE TREATMENT OF VENOUS THROMBOEMBOLISM IN CANCER PATIENTS AT A BRAZILIAN PUBLIC ONCOLOGICAL INSTITUTION: EDUCATIONAL PLAN

P.66 Hereditary hemorrhagic telangiectasia (HHT) in women: 6 case-reports and comments

SAFETY AND EFFECTIVENESS OF ANTICOAGULATION BASED ON AN INSTITUTIONAL RECOMMENDATION ON THE MANAGEMENT OF CANCER ASSOCIATED VENOUS THROMBOSIS

Use of Haemate® P as immune tolerance induction in patients with severe haemophilia A who failed previous induction attempts: a multicentre observational study

Genetic compensation of γ CaMKII, an evolutionarily conserved gene

Pharmacokinetics and pharmacodynamics of a new highly secured fibrinogen concentrate

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