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Congenital dyserythropoietic anemia type IV with KLF1 E325K mutation: A new case with dysmorphic male genitalia

Pediatric blood & cancer, 2024-06, Vol.71 (6), p.e30955-n/a

2024

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Natural history of transient myeloproliferative disorder clinically diagnosed in Down syndrome neonates: a report from the Children's Oncology Group Study A2971

Blood, 2011-12, Vol.118 (26), p.6752-6759

2011

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A prospective study of the natural history of transient leukemia (TL) in neonates with Down syndrome (DS): Children's Oncology Group (COG) study POG-9481

Blood, 2006-06, Vol.107 (12), p.4606-4613

2006

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Medich Giant Platelet Syndrome: An Evolving Qualitative and Quantitative Platelet Disorder

Hematology reports, 2022-12, Vol.14 (4), p.349-357

2022

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Opiod Induced Pruritus: The Need for Palliative Care for a Palliative Medicine (S707)

Journal of pain and symptom management, 2015-02, Vol.49 (2), p.410-410

2015

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Cardiomyopathy in Children With Down Syndrome Treated for Acute Myeloid Leukemia: A Report From the Children's Oncology Group Study POG 9421

Journal of clinical oncology, 2008-01, Vol.26 (3), p.414-420

2008

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Transient leukemia in newborns with Down syndrome

Pediatric Blood & Cancer, 2005-01, Vol.44 (1), p.29-32

Massey, Gita V.

2005

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Pediatric Paroxysmal Nocturnal Hemoglobinuria Presenting as Acute Kidney Injury

Journal of pediatric hematology/oncology, 2021-05, Vol.43 (4), p.e543

2021

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Real‐world use of emicizumab in patients with haemophilia A: Bleeding outcomes and surgical procedures

Haemophilia : the official journal of the World Federation of Hemophilia, 2020-07, Vol.26 (4), p.631-636

2020

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Incidence and treatment of potentially lethal diseases in Transient leukemia of down syndrome: Pediatric Oncology Group study

Journal of pediatric hematology/oncology, 2002, Vol.24 (1), p.9-13

2002

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Peri-Procedural Management and Outcomes of Patients with Hemophilia on Emicizumab Prophylaxis

Blood, 2019-11, Vol.134 (Supplement_1), p.2396-2396

2019

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Pulmonary Alveolar Proteinosis in Association with Congenital Dyserythropoietic Anemia: A Case Report

Case reports in pediatrics, 2012-01, Vol.2012, p.624740-3

2012

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Translocation positive acute myeloid leukemia associated with valproic acid therapy

Pediatric Blood & Cancer, 2008-03, Vol.50 (3), p.641-643

2008

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Real-World Use of Emicizumab in Patients with Hemophilia with and without Inhibitors

Blood, 2019-11, Vol.134 (Supplement_1), p.1137-1137

2019

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Real‐world cost estimates of initiating emicizumab in US patients with haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2021-07, Vol.27 (4), p.591-598

2021

Volltextzugriff (PDF)

Synonymous mutation in TP53 results in a cryptic splice site affecting its DNA‐binding site in an adolescent with two primary sarcomas

Pediatric blood & cancer, 2017-11, Vol.64 (11), p.n/a

2017

Volltextzugriff (PDF)

Change Theory Contributes to Choosing Wisely for Immune Thrombocytopenia

Hospital pediatrics, 2019-03, Vol.9 (3), p.156

2019

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F8 and F9 mutations in US haemophilia patients: correlation with history of inhibitor and race/ethnicity

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-05, Vol.18 (3), p.375-382

2012

Volltextzugriff (PDF)

Comparison of clot‐based, chromogenic and fluorescence assays for measurement of factor VIII inhibitors in the US Hemophilia Inhibitor Research Study

Journal of thrombosis and haemostasis, 2013-07, Vol.11 (7), p.1300-1309

2013

Volltextzugriff (PDF)

Continuous lidocaine infusion for the relief of refractory malignant pain in a terminally ill pediatric cancer patient

Journal of pediatric hematology/oncology, 2002-10, Vol.24 (7), p.566-568

2002

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Vitamin d deficiency in children with cancer

Journal of pediatric hematology/oncology, 2014-04, Vol.36 (3), p.212-217

2014

Volltextzugriff (PDF)

Dietary Determinants Of The White Blood Cell Count

Blood, 2013-11, Vol.122 (21), p.1705-1705

2013

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A study of prospective surveillance for inhibitors among persons with haemophilia in the United States

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-03, Vol.20 (2), p.230-237

2014

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Clinical Features and Risk Factors Associated With Multisystem Inflammatory Syndrome in Children With Cancer and COVID-19

JAMA oncology, 2023-08, Vol.9 (8), p.1108

2023

Volltextzugriff (PDF)

Evaluation of von Willebrand factor phenotypes and genotypes in Hemophilia A patients with and without identified F8 mutations

Journal of thrombosis and haemostasis, 2015-06, Vol.13 (6), p.1036-1042

2015

Volltextzugriff (PDF)

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Congenital dyserythropoietic anemia type IV with KLF1 E325K mutation: A new case with dysmorphic male genitalia

Natural history of transient myeloproliferative disorder clinically diagnosed in Down syndrome neonates: a report from the Children's Oncology Group Study A2971

A prospective study of the natural history of transient leukemia (TL) in neonates with Down syndrome (DS): Children's Oncology Group (COG) study POG-9481

Medich Giant Platelet Syndrome: An Evolving Qualitative and Quantitative Platelet Disorder

Opiod Induced Pruritus: The Need for Palliative Care for a Palliative Medicine (S707)

Cardiomyopathy in Children With Down Syndrome Treated for Acute Myeloid Leukemia: A Report From the Children's Oncology Group Study POG 9421

Transient leukemia in newborns with Down syndrome

Pediatric Paroxysmal Nocturnal Hemoglobinuria Presenting as Acute Kidney Injury

Real‐world use of emicizumab in patients with haemophilia A: Bleeding outcomes and surgical procedures

Incidence and treatment of potentially lethal diseases in Transient leukemia of down syndrome: Pediatric Oncology Group study

Peri-Procedural Management and Outcomes of Patients with Hemophilia on Emicizumab Prophylaxis

Pulmonary Alveolar Proteinosis in Association with Congenital Dyserythropoietic Anemia: A Case Report

Translocation positive acute myeloid leukemia associated with valproic acid therapy

Real-World Use of Emicizumab in Patients with Hemophilia with and without Inhibitors

Real‐world cost estimates of initiating emicizumab in US patients with haemophilia A

Synonymous mutation in TP53 results in a cryptic splice site affecting its DNA‐binding site in an adolescent with two primary sarcomas

Change Theory Contributes to Choosing Wisely for Immune Thrombocytopenia

F8 and F9 mutations in US haemophilia patients: correlation with history of inhibitor and race/ethnicity

Comparison of clot‐based, chromogenic and fluorescence assays for measurement of factor VIII inhibitors in the US Hemophilia Inhibitor Research Study

Continuous lidocaine infusion for the relief of refractory malignant pain in a terminally ill pediatric cancer patient

Vitamin d deficiency in children with cancer

Dietary Determinants Of The White Blood Cell Count

A study of prospective surveillance for inhibitors among persons with haemophilia in the United States

Clinical Features and Risk Factors Associated With Multisystem Inflammatory Syndrome in Children With Cancer and COVID-19

Evaluation of von Willebrand factor phenotypes and genotypes in Hemophilia A patients with and without identified F8 mutations

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