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More Than an Itch: An Unusual Cause of Severe Anemia in a 5-Year-Old

Clinical pediatrics, 2022-12, Vol.61 (12), p.879-882

2022

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Switching patients in the age of long-acting recombinant products?

Expert review of hematology, 2019-01, Vol.12 (sup1), p.1-13

2019

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Legg-Calve-Perthes disease and thrombophilia

Journal of bone and joint surgery. American volume, 2004-12, Vol.86 (12), p.2642

2004

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The relationship of mutations in the MTHFR, prothrombin, and PAI-1 genes to plasma levels of homocysteine, prothrombin, and PAI-1 in children and adults

Thrombosis and haemostasis, 1999-05, Vol.81 (5), p.739

1999

Volltextzugriff (PDF)

Case 1: raccoon eyes in an 8-month-old infant. Case 2: jaundice in a teenage girl. Case 3: extreme muscle weakness in a 10-year-old boy

Pediatrics in review, 2014-04, Vol.35 (4), p.169

2014

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New anticoagulants: A pediatric perspective

Pediatric Blood & Cancer, 2005-11, Vol.45 (6), p.741-752

Balasa, Vinod V.

2005

Volltextzugriff (PDF)

Characterization of Inborn Errors of Immunity in Recurrent Autoimmune Cytopenias in Children: A Report from Central California Cohort

Blood, 2022-11, Vol.140 (Supplement 1), p.8356-8357

2022

Volltextzugriff (PDF)

SARS-CoV-2 Infection Presenting as Acute Chest Syndrome in a Child With Hemoglobin SD-Los Angeles Disease: A Case Report and Review of Literature

Journal of pediatric hematology/oncology, 2023-03, Vol.45 (2), p.82

2023

Volltextzugriff (PDF)

Real-world study of rurioctocog alfa pegol and emicizumab in US clinical practice among patients with hemophilia A

Expert review of hematology, 2022-10, Vol.15 (10), p.943-950

2022

Volltextzugriff (PDF)

Effects of PK‐guided prophylaxis on clinical outcomes and FVIII consumption for patients with moderate to severe Haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2023-09, Vol.29 (5), p.1234-1242

2023

Volltextzugriff (PDF)

A systematic review evaluating the efficacy and factor consumption of long-acting recombinant factor VIII products for the prophylactic treatment of hemophilia A

Journal of medical economics, 2020-12, Vol.23 (12), p.1493-1498

2020

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Unusually High Prevalence of Silent Stroke and Cerebral Vasculopathy in Hemoglobin SC Disease

Blood, 2019-11, Vol.134 (Supplement_1), p.2276-2276

2019

Volltextzugriff (PDF)

Treatment of Congenital Afibrinogenemia in a Neonate With Critical Pulmonary Stenosis

The journal of pediatric pharmacology and therapeutics, 2023, Vol.28 (3), p.268-271

2023

Volltextzugriff (PDF)

Development and Validation of a Population-Pharmacokinetic Model for Rurioctacog Alfa Pegol (Adynovate®): A Report on Behalf of the WAPPS-Hemo Investigators Ad Hoc Subgroup

Clinical pharmacokinetics, 2020-02, Vol.59 (2), p.245-256

2020

Volltextzugriff (PDF)

Unusually High Prevalence of Stroke and Cerebral Vasculopathy in Hemoglobin SC Disease: A Retrospective Single Institution Study

Acta haematologica, 2022-01, Vol.145 (2), p.160-169

2022

Volltextzugriff (PDF)

Hyperhomocysteinemia is associated with low plasma pyridoxine levels in children with sickle cell disease

Journal of pediatric hematology/oncology, 2002-06, Vol.24 (5), p.374-379

2002

Volltextzugriff (PDF)

Two rare presentations and treatments of Ewing's sarcoma: A need for a standard treatment approach

Journal of clinical oncology, 2013-05, Vol.31 (15_suppl), p.e21000-e21000

2013

Volltextzugriff (PDF)

Morbidity and mortality in chronically transfused subjects with thalassemia and sickle cell disease: A report from the multi‐center study of iron overload

American journal of hematology, 2007-04, Vol.82 (4), p.255-265

2007

Volltextzugriff (PDF)

Low-dose tissue plasminogen activator thrombolysis in children

Journal of pediatric hematology/oncology, 2003-05, Vol.25 (5), p.379-386

2003

Volltextzugriff (PDF)

Disparity in the management of iron overload between patients with sickle cell disease and thalassemia who received transfusions

Transfusion (Philadelphia, Pa.), 2008-09, Vol.48 (9), p.1971-1980

2008

Volltextzugriff (PDF)

Protein C deficiency related to valproic acid therapy: A possible association with childhood stroke

The Journal of pediatrics, 2000-11, Vol.137 (5), p.714-718

2000

Volltextzugriff (PDF)

Correlation of the C677T MTHFR genotype with homocysteine levels in children with sickle cell disease

Journal of pediatric hematology/oncology, 1999-09, Vol.21 (5), p.397-400

1999

Volltextzugriff (PDF)

Emergencies in Patients With Inherited Hemoglobin Disorders—An Emergency Department Perspective

Clinical pediatric emergency medicine, 2005-09, Vol.6 (3), p.138-148

2005

Volltextzugriff (PDF)

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More Than an Itch: An Unusual Cause of Severe Anemia in a 5-Year-Old

Switching patients in the age of long-acting recombinant products?

Legg-Calve-Perthes disease and thrombophilia

The relationship of mutations in the MTHFR, prothrombin, and PAI-1 genes to plasma levels of homocysteine, prothrombin, and PAI-1 in children and adults

Case 1: raccoon eyes in an 8-month-old infant. Case 2: jaundice in a teenage girl. Case 3: extreme muscle weakness in a 10-year-old boy

New anticoagulants: A pediatric perspective

Characterization of Inborn Errors of Immunity in Recurrent Autoimmune Cytopenias in Children: A Report from Central California Cohort

SARS-CoV-2 Infection Presenting as Acute Chest Syndrome in a Child With Hemoglobin SD-Los Angeles Disease: A Case Report and Review of Literature

Real-world study of rurioctocog alfa pegol and emicizumab in US clinical practice among patients with hemophilia A

Effects of PK‐guided prophylaxis on clinical outcomes and FVIII consumption for patients with moderate to severe Haemophilia A

A systematic review evaluating the efficacy and factor consumption of long-acting recombinant factor VIII products for the prophylactic treatment of hemophilia A

Unusually High Prevalence of Silent Stroke and Cerebral Vasculopathy in Hemoglobin SC Disease

Treatment of Congenital Afibrinogenemia in a Neonate With Critical Pulmonary Stenosis

Development and Validation of a Population-Pharmacokinetic Model for Rurioctacog Alfa Pegol (Adynovate®): A Report on Behalf of the WAPPS-Hemo Investigators Ad Hoc Subgroup

Unusually High Prevalence of Stroke and Cerebral Vasculopathy in Hemoglobin SC Disease: A Retrospective Single Institution Study

Hyperhomocysteinemia is associated with low plasma pyridoxine levels in children with sickle cell disease

Two rare presentations and treatments of Ewing's sarcoma: A need for a standard treatment approach

Morbidity and mortality in chronically transfused subjects with thalassemia and sickle cell disease: A report from the multi‐center study of iron overload

Low-dose tissue plasminogen activator thrombolysis in children

Disparity in the management of iron overload between patients with sickle cell disease and thalassemia who received transfusions

Protein C deficiency related to valproic acid therapy: A possible association with childhood stroke

Correlation of the C677T MTHFR genotype with homocysteine levels in children with sickle cell disease

Emergencies in Patients With Inherited Hemoglobin Disorders—An Emergency Department Perspective

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