Search Results - "Crary, Shelley E"
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Vascular complications after splenectomy for hematologic disorders
Published in Blood (01-10-2009)“…The most widely recognized long-term risk of splenectomy is overwhelming bacterial infection. More recently, thrombosis has become appreciated as another…”
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Comparative Effectiveness of Different Types of Splenectomy for Children with Congenital Hemolytic Anemias
Published in The Journal of pediatrics (01-04-2012)“…Objective To compare the effectiveness of different types of splenectomy in children with congenital hemolytic anemias. Study design We constructed key…”
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Prominent Forehead Hematomas (“Goose-Eggs”) as an Initial Manifestation of Hemophilia
Published in The Journal of pediatrics (01-12-2013)“…Prominent forehead hematomas, “goose-eggs,” may suggest an underlying disorder of coagulation. We reviewed records of 324 children with hemophilia and…”
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Traditional laboratory measures of cardiovascular risk in hereditary spherocytosis
Published in Pediatric blood & cancer (01-10-2010)“…Background Individuals who have undergone splenectomy may be at an increased risk of arterial and venous thrombosis. We sought to determine if splenectomy…”
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How we approach coagulopathy with vascular anomalies
Published in Pediatric blood & cancer (01-08-2022)“…Some vascular anomalies can present with challenging hematologic aberrations. Kaposiform hemangioendothelioma (KHE) may be complicated with Kasabach–Merritt…”
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Mental health in persons with von Willebrand disease in the United States – a large national database study
Published in Journal of thrombosis and haemostasis (01-06-2024)“…There are very few large population-based studies studying mental health in persons with von Willebrand disease (PwVWD). We aim to assess prevalence of…”
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Effect of sirolimus on coagulopathy of slow‐flow vascular malformations
Published in Pediatric blood & cancer (01-10-2019)“…Background/Objectives Stagnant blood flow present in slow‐flow vascular malformations can lead to localized intravascular coagulopathy (LIC), measured by…”
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Acquired Hemophilia: A Rare Complication of Pediatric Idiopathic Multicentric Castleman Disease
Published in Pediatrics (Evanston) (01-04-2024)“…Acquired hemophilia is caused by acquired autoantibodies to 1 of the factors of the coagulation cascade, usually factor VIII or IX, and is an exceedingly rare…”
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Invasive procedures and surgery following etranacogene dezaparvovec gene therapy in people with hemophilia B
Published in Journal of thrombosis and haemostasis (26-09-2024)“…Little information regarding the management of invasive procedures in people with hemophilia B (HB) after undergoing gene therapy is available. Here, we report…”
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Pupil Size and Reactivity in Pediatric Patients With Sickle Cell Disease
Published in Journal of pediatric hematology/oncology (01-01-2023)“…Pupil size and reactivity have been studied to objectively measure pain utilizing pupillometry measurements. Given the challenges associated with treating…”
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Anticoagulation and vascular anomalies
Published in Research and practice in thrombosis and haemostasis (01-03-2024)“…A State of the Art lecture titled “Anticoagulation and Vascular Anomalies” was presented at the International Society on Thrombosis and Haemostasis (ISTH)…”
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Pharmacokinetics of bleomycin sclerotherapy in patients with vascular malformations
Published in Pediatric blood & cancer (01-08-2022)“…Bleomycin, a chemotherapy agent that inhibits synthesis of DNA, has been increasingly utilized in sclerotherapy for patients with vascular malformations. A…”
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Multiple Autoimmune Disorders in Aicardi-Goutières Syndrome
Published in Pediatric neurology (01-07-2019)“…Aicardi-Goutières syndrome is an early-onset encephalopathy with presumed immune pathogenesis caused by inherited defects in nucleic acid metabolism. It is a…”
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Intravenous iron sucrose for children with iron deficiency failing to respond to oral iron therapy
Published in Pediatric blood & cancer (01-04-2011)“…Background For decades, parenteral iron has been used in patients with iron deficiency unresponsive to oral iron therapy and in hemodialysis‐dependent patients…”
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Treatment practices and response in kaposiform hemangioendothelioma: A multicenter cohort study
Published in Pediatric blood & cancer (01-03-2024)“…Background and objectives Kaposiform hemangioendothelioma (KHE) and tufted angioma (TA) are rare vascular tumors in children historically associated with…”
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Long‐term biological effects in sickle cell disease: insights from a post‐crizanlizumab study
Published in British journal of haematology (01-11-2021)Get full text
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Second‐line treatments in children with immune thrombocytopenia: Effect on platelet count and patient‐centered outcomes
Published in American journal of hematology (01-07-2019)“…Immune thrombocytopenia (ITP) is an autoimmune bleeding disorder with isolated thrombocytopenia and hemorrhagic risk. While many children with ITP can be…”
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Analyzing coagulation dynamics during treatment of vascular malformations with thromboelastography
Published in Pediatric blood & cancer (01-02-2021)“…Background/Objectives Slow‐flow vascular malformations are abnormal vessels that can lead to activation and consumption of coagulation factors and thrombosis,…”
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Short‐term side effects and patient‐reported outcomes of bleomycin sclerotherapy in vascular malformations
Published in Pediatric blood & cancer (01-06-2018)“…Background Vascular malformations (VM) are congenital lesions that can be debilitating and cause significant aesthetic and functional limitations. The…”
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