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Medical imaging utilization and associated radiation exposure in children with down syndrome

PloS one, 2023-09, Vol.18 (9), p.e0289957-e0289957

2023

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Modelling future usage and cost of factor and emicizumab to treat haemophilia A for the US Western States Region IX haemophilia treatment centres

Haemophilia : the official journal of the World Federation of Hemophilia, 2021-01, Vol.27 (1), p.e22-e29

2021

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Primary Renal Lymphoma Presenting as End-Stage Renal Disease

Case reports in medicine, 2017-01, Vol.2017 (2017), p.1-3

2017

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Parthenolide induces significant apoptosis and production of reactive oxygen species in high-risk pre-B leukemia cells

Cancer letters, 2007-08, Vol.254 (1), p.119-127

2007

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Children and adolescents with ALL are taller than expected at diagnosis

Journal of pediatric hematology/oncology, 2014-01, Vol.36 (1), p.16-21

2014

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Alprolix (recombinant Factor IX Fc fusion protein): extended half-life product for the prophylaxis and treatment of hemophilia B

Expert review of hematology, 2014-10, Vol.7 (5), p.559-571

2014

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Resveratrol given intraperitoneally does not inhibit the growth of high-risk t(4;11) acute lymphoblastic leukemia cells in a NOD/SCID mouse model

International journal of oncology, 2012-04, Vol.40 (4), p.1277-1284

2012

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Dietary resveratrol does not delay engraftment, sensitize to vincristine or inhibit growth of high-risk acute lymphoblastic leukemia cells in NOD/SCID mice

International journal of oncology, 2012-12, Vol.41 (6), p.2207-2212

2012

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Parthenolide treatment activates stress signaling proteins in high-risk acute lymphoblastic leukemia cells with chromosomal translocation t(4;11)

International journal of oncology, 2010-11, Vol.37 (5), p.1307-1313

2010

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Novel in vivo model of inducible multi-drug resistance in acute lymphoblastic leukemia with chromosomal translocation t(4;11)

Cancer letters, 2010-10, Vol.296 (1), p.49-54

2010

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Oral or parenteral administration of curcumin does not prevent the growth of high-risk t(4;11) acute lymphoblastic leukemia cells engrafted into a NOD/SCID mouse model

International journal of oncology, 2013-02, Vol.42 (2), p.741-748

2013

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Assessing Safe Discharge Criteria for Pediatric Oncology Patients Admitted for Febrile Neutropenia

Journal of pediatric hematology/oncology, 2021-08, Vol.43 (6), p.e880-e885

2021

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A Novel Approach to Immune Tolerance Induction in Hemophilia Α with Factor VIII Inhibitor

Blood, 2018-11, Vol.132 (Supplement 1), p.5042-5042

2018

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End-Stage Renal Disease From Cast Nephropathy in a Teenager With Neuroendocrine Carcinoma

Journal of pediatric hematology/oncology, 2016-07, Vol.38 (5), p.e177-e179

2016

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Assessing Safe Discharge Criteria for Pediatric Oncology Patients Admitted for Febrile Neutropenia

Blood, 2017-12, Vol.130, p.4699-4699

2017

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BAX 335 Hemophilia B Gene Therapy Phase 1/2 Clinical Trial: Long-Term Safety and Efficacy Follow-up

Blood, 2022-11, Vol.140 (Supplement 1), p.10656-10657

2022

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Diagnostic X-rays and risk of childhood leukaemia

International journal of epidemiology, 2010-12, Vol.39 (6), p.1628-1637

2010

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A novel approach to immune tolerance induction in haemophilia A with factor VIII inhibitor

Haemophilia : the official journal of the World Federation of Hemophilia, 2019-01, Vol.25 (1), p.e48-e50

2019

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Leukemia Risk in a Cohort of 3.9 Million Children with and without Down Syndrome

The Journal of pediatrics, 2021-07, Vol.234, p.172-180.e3

2021

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Characteristics of Bleed-Free Patients on Every-5-Day Dosing in the Protect VIII (BAY 94-9027) Study

Blood, 2018-11, Vol.132 (Supplement 1), p.2486-2486

2018

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Decrease in Overall and Joint Bleeding Rates with Extended-Interval Dosing: > 4 Years of Bay 94-9027 Prophylaxis in the Protect VIII Extension

Blood, 2018-11, Vol.132 (Supplement 1), p.1206-1206

2018

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Long-Term Efficacy and Safety of Damoctocog Alfa Pegol Prophylaxis in Patients with Haemophilia A Aged 12–<18 Years at Enrolment into PROTECT VIII

Acta haematologica, 2024-04, p.1-10

2024

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Improvement in Quality of Life Outcomes and Bleeding Rates among Patients Switching from On-demand FVIII to Prophylactic BAY 94-9027 in the PROTECT VIII Study

Blood, 2019-11, Vol.134 (Supplement_1), p.1129-1129

2019

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Single 225μg/Kg Dose Treatment with Eptacog Beta (Factor VIIa, Recombinant) Results in Rapid Hemostasis in Joint Bleeds for Persons with Hemophilia Α or Β with Inhibitors: A PERSEPT1 Subset Analysis

Blood, 2020-11, Vol.136 (Supplement 1), p.2-3

2020

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Surveillance Neuroimaging to Detect Relapse in Childhood Brain Tumors: A Pediatric Oncology Group Study

Journal of clinical oncology, 2001-11, Vol.19 (21), p.4135-4140

2001

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Medical imaging utilization and associated radiation exposure in children with down syndrome

Modelling future usage and cost of factor and emicizumab to treat haemophilia A for the US Western States Region IX haemophilia treatment centres

Primary Renal Lymphoma Presenting as End-Stage Renal Disease

Parthenolide induces significant apoptosis and production of reactive oxygen species in high-risk pre-B leukemia cells

Children and adolescents with ALL are taller than expected at diagnosis

Alprolix (recombinant Factor IX Fc fusion protein): extended half-life product for the prophylaxis and treatment of hemophilia B

Resveratrol given intraperitoneally does not inhibit the growth of high-risk t(4;11) acute lymphoblastic leukemia cells in a NOD/SCID mouse model

Dietary resveratrol does not delay engraftment, sensitize to vincristine or inhibit growth of high-risk acute lymphoblastic leukemia cells in NOD/SCID mice

Parthenolide treatment activates stress signaling proteins in high-risk acute lymphoblastic leukemia cells with chromosomal translocation t(4;11)

Novel in vivo model of inducible multi-drug resistance in acute lymphoblastic leukemia with chromosomal translocation t(4;11)

Oral or parenteral administration of curcumin does not prevent the growth of high-risk t(4;11) acute lymphoblastic leukemia cells engrafted into a NOD/SCID mouse model

Assessing Safe Discharge Criteria for Pediatric Oncology Patients Admitted for Febrile Neutropenia

A Novel Approach to Immune Tolerance Induction in Hemophilia Α with Factor VIII Inhibitor

End-Stage Renal Disease From Cast Nephropathy in a Teenager With Neuroendocrine Carcinoma

Assessing Safe Discharge Criteria for Pediatric Oncology Patients Admitted for Febrile Neutropenia

BAX 335 Hemophilia B Gene Therapy Phase 1/2 Clinical Trial: Long-Term Safety and Efficacy Follow-up

Diagnostic X-rays and risk of childhood leukaemia

A novel approach to immune tolerance induction in haemophilia A with factor VIII inhibitor

Leukemia Risk in a Cohort of 3.9 Million Children with and without Down Syndrome

Characteristics of Bleed-Free Patients on Every-5-Day Dosing in the Protect VIII (BAY 94-9027) Study

Decrease in Overall and Joint Bleeding Rates with Extended-Interval Dosing: > 4 Years of Bay 94-9027 Prophylaxis in the Protect VIII Extension

Long-Term Efficacy and Safety of Damoctocog Alfa Pegol Prophylaxis in Patients with Haemophilia A Aged 12–<18 Years at Enrolment into PROTECT VIII

Improvement in Quality of Life Outcomes and Bleeding Rates among Patients Switching from On-demand FVIII to Prophylactic BAY 94-9027 in the PROTECT VIII Study

Single 225μg/Kg Dose Treatment with Eptacog Beta (Factor VIIa, Recombinant) Results in Rapid Hemostasis in Joint Bleeds for Persons with Hemophilia Α or Β with Inhibitors: A PERSEPT1 Subset Analysis

Surveillance Neuroimaging to Detect Relapse in Childhood Brain Tumors: A Pediatric Oncology Group Study

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