Search Results - "Karkoska, Kristine"
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Molecular and environmental contributors to neurological complications in sickle cell disease
Published in Experimental Biology and Medicine (01-08-2023)“…Sickle cell disease (SCD) is an inherited hemoglobinopathy in which affected hemoglobin polymerizes under hypoxic conditions resulting in red cell distortion…”
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Inherited disorders of hemoglobin: A review of old and new diagnostic methods
Published in Blood cells, molecules, & diseases (01-01-2024)“…The genetic regulation of hemoglobin is complex and there are a number of genetic abnormalities that result in clinically important hemoglobin disorders. Here,…”
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Academic Challenges and School Service Utilization in Children with Sickle Cell Disease
Published in The Journal of pediatrics (01-03-2021)“…To describe the academic concerns and risk strata of children with sickle cell disease (SCD) as identified through a parent-directed screening tool and to…”
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Quantifying dilated perivascular spaces in children with sickle cell disease
Published in Pediatric blood & cancer (01-09-2024)“…Sickle cell disease (SCD)-related neurological effects are particularly devastating. Dilated perivascular spaces (dPVS) are a well-described component of…”
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Uncovering an undisclosed diagnosis: a glucose‐6‐phosphate dehydrogenase deficiency diagnosis in a critically ill adult
Published in EJHaem (01-02-2024)“…Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency affects over 400 million people worldwide. The most common variant of G6PD deficiency in the United States…”
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A bone to pick-cellular and molecular mechanisms of bone pain in sickle cell disease
Published in Frontiers in pain research (Lausanne, Switzerland) (04-01-2024)“…The bone is one of the most commonly affected organs in sickle cell disease (SCD). Repeated ischemia, oxidative stress and inflammation within the bone is…”
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Effect of Blood Transfusion on Cerebral Hemodynamics and Vascular Topology Described by Computational Fluid Dynamics in Sickle Cell Disease Patients
Published in Brain sciences (18-10-2022)“…The main objective of this study was to demonstrate that computational fluid dynamics (CFD) modeling can be used to study the contribution of covert and overt…”
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Neuroprotection: further evidence for the early and universal use of hydroxyurea in children with sickle cell disease
Published in British journal of haematology (01-10-2021)Get full text
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Characterization of a genomic divergence island between black-and-yellow and gopher Sebastes rockfishes
Published in Molecular ecology (01-06-2011)“…Islands of high genomic divergence that contain genes of evolutionary significance may form between diverging species. The gopher rockfish, Sebastes carnatus,…”
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Changing Trends in Sickle Cell Disease-Related Mortality in the United States over Four Decades
Published in Blood (02-11-2023)“…Introduction: Sickle cell disease (SCD) causes significant morbidity and early mortality. The Cooperative Study of Sickle Cell Disease estimated median life…”
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Trends in Sickle Cell Disease Mortality: 1979–2020
Published in Pediatrics (Evanston) (18-11-2024)“…BACKGROUND AND OBJECTIVES: Although sickle cell disease (SCD)-related childhood mortality in the United States significantly improved in the 1990s, unclear is…”
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Abstract 718: Cerebral Small Vessel Disease In Children With Sickle Cell Disease
Published in Arteriosclerosis, thrombosis, and vascular biology (01-05-2023)“…Abstract only Introduction: The neurological complications of sickle cell disease (SCD) are particularly devastating and range from “overt stroke” to cerebral…”
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Quantifying Dilated Perivascular Spaces in Children with Sickle Cell Disease
Published in Blood (15-11-2022)Get full text
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Early Hydroxyurea Use May be Neuroprotective in Children with Sickle Cell Anemia
Published in Blood (23-11-2021)“…Introduction: The neurologic changes of sickle cell anemia (SCA) are particularly devastating and include acute stroke, silent infarctions, and cerebral…”
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How I approach disease‐modifying therapy in children with sickle cell disease in an era of novel therapies
Published in Pediatric blood & cancer (01-12-2021)“…Finally,after decades of stagnation, the therapeutic landscape for sickle cell disease (SCD) is changing with an increasing number of novel therapeutics…”
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Academic Challenges and Concerns for Children with Sickle Cell Disease: Analysis of a Hospital-Based School Intervention Program
Published in Blood (13-11-2019)“…Introduction: Neurocognitive deficits are a well-known complication in patients with sickle cell disease (SCD) and are often associated with overt stroke and…”
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Severe infusion‐related reaction to crizanlizumab in an adolescent with sickle cell disease
Published in American journal of hematology (01-12-2020)Get full text
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Improving Transition of Emerging Adults with Sickle Cell Disease to Adult Care through a Multidisciplinary Process: The Development of a Transition Clinic to Support Transition Success
Published in Blood (02-11-2023)“…The transition period from pediatric to adult care is challenging for people with sickle cell disease (SCD). Emerging adults with SCD who do not successfully…”
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Early hydroxyurea use is neuroprotective in children with sickle cell anemia
Published in American journal of hematology (01-10-2022)“…Children with sickle cell disease (SCD) who began hydroyxurea before age five years scored no differently on a measure of cognitive funciton than age, sex, and…”
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Academic Challenges and School Service Utilization in Children With Sickle Cell Disease
Published 01-01-2021“…Objectives: To describe the academic concerns and risk strata of a pediatric sickle cell population as identified through a parent-directed screening tool and…”
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Dissertation