Search Results - "Day, Megan"
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Elevation of IL-17 Cytokines Distinguishes Kawasaki Disease From Other Pediatric Inflammatory Disorders
Published in Arthritis & rheumatology (Hoboken, N.J.) (01-02-2024)“…Kawasaki disease (KD) is a systemic vasculitis of young children that can lead to development of coronary artery aneurysms. We aimed to identify diagnostic…”
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Journal Article -
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Incidence and Risk Factors for Eosinophilia and Lung Disease in Biologic-Exposed Children With Systemic Juvenile Idiopathic Arthritis
Published in Arthritis care & research (2010) (01-10-2023)“…Although interleukin-1 (IL-1)/IL-6 inhibitors are effective therapies for systemic juvenile idiopathic arthritis (JIA), some patients develop eosinophilia and…”
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3
Gene therapy: perspectives from young adults with Leber’s congenital amaurosis
Published in Eye (London) (01-11-2022)“…Aims/purpose To investigate Leber congenital amaurosis (LCA) patients’ expectations, decision-making processes and gene therapy-related concerns. Methods Using…”
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Correction: Gene therapy: perspectives from young adults with Leber’s congenital amaurosis
Published in Eye (London) (25-02-2022)Get full text
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Distinct clinical and immunological features of SARS-CoV-2-induced multisystem inflammatory syndrome in children
Published in The Journal of clinical investigation (01-11-2020)“…BACKGROUNDPediatric SARS-CoV-2 infection can be complicated by a dangerous hyperinflammatory condition termed multisystem inflammatory syndrome in children…”
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Development of a Screening Algorithm for Lung Disease in Systemic Juvenile Idiopathic Arthritis
Published in ACR open rheumatology (01-10-2023)“…Lung disease (LD) is an increasingly recognized complication of systemic juvenile idiopathic arthritis (sJIA). As there are no currently available guidelines…”
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A novel p.Gly603Arg mutation in CACNA1F causes Åland island eye disease and incomplete congenital stationary night blindness phenotypes in a family
Published in Molecular vision (15-12-2011)“…To report, for the first time, that X-linked incomplete congenital stationary night blindness (CSNB2A) and Åland island eye disease (AIED) phenotypes coexist…”
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8
Type I interferon signature and cycling lymphocytes in macrophage activation syndrome
Published in The Journal of clinical investigation (15-11-2023)“…BACKGROUNDMacrophage activation syndrome (MAS) is a life-threatening complication of Still's disease (SD) characterized by overt immune cell activation and…”
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9
Genetic counseling and genetic testing in ophthalmology
Published in Current opinion in ophthalmology (01-09-2009)“…PURPOSE OF REVIEWTo introduce the issues specific to the genetic counseling profession for genetic eye diseases. RECENT FINDINGSTo discuss current issues in…”
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10
LMNA‐related muscular dystrophy presenting as an inflammatory myopathy
Published in Annals of the Child Neurology Society (01-09-2024)“…Abstract Introduction There are overlapping features between inflammatory myopathies and muscular dystrophies, particularly laminopathies. Key features that…”
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Intersections of disadvantaged communities and renewable energy potential: Data set and analysis to inform equitable investment prioritization in the United States
Published in Renewable energy focus (01-06-2022)“…•Renewable energy development potential in disadvantaged communities identified.•Compared renewable energy development potential across U.S. counties.•Analysis…”
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Intersections of Disadvantaged Communities and Renewable Energy Potential: Data Set and Analysis to Inform Equitable Investment Prioritization in the United States
Published 18-11-2022“…Renewable energy development can bolster local economies through job creation, local tax revenues, and reduced energy costs; however, communities most in need…”
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Conference Proceeding -
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Mating proximity blinds threat perception
Published in Nature (London) (17-10-2024)“…Romantic engagement can bias sensory perception. This ‘love blindness’ reflects a common behavioural principle across organisms: favouring pursuit of a coveted…”
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14
Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis
Published in Nature genetics (01-09-2012)“…Ming Qi and colleagues report that compound heterozygous mutations in NMNAT1 cause Leber congenital amaurosis, a childhood form of retinal dystrophy. NMNAT1…”
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15
Rogue Feminism: Reframing Digital Feminist Rhetorics in Academia
Published 01-01-2019“…Feminist rhetoric often looks back in history to find instances of women’s voices in writings, but for my thesis, I argue the importance of looking at modern…”
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Dissertation -
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Mechanisms underlying genetic susceptibility to multisystem inflammatory syndrome in children (MIS-C)
Published in Journal of allergy and clinical immunology (01-09-2021)“…Multisystem inflammatory syndrome in children (MIS-C) is a pediatric complication of severe acute respiratory syndrome coronavirus 2 infection that is…”
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Updated Case Definition of MIS-C and Implications for Clinical Care
Published in Pediatrics (Evanston) (01-01-2024)“…A broad, surveillance case definition was implemented when multisystem inflammatory syndrome in children (MIS-C) emerged in 2020. In 2023, a revised MIS-C case…”
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Validation of the scale: A measure of middle school students' transition experiences
Published 01-01-2015“…The SCALE, a measure of students' middle school transition experiences, was validated for use with diverse, sixth-grade students attending metropolitan middle…”
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Dissertation -
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Socioeconomic and Racial and/or Ethnic Disparities in Multisystem Inflammatory Syndrome
Published in Pediatrics (Evanston) (01-05-2021)“…To characterize the socioeconomic and racial and/or ethnic disparities impacting the diagnosis and outcomes of multisystem inflammatory syndrome in children…”
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MIS-C across three SARS-CoV-2 variants: Changes in COVID-19 testing and clinical characteristics in a cohort of U.S. children
Published in European journal of pediatrics (01-06-2023)“…As new variants of SARS-Co-V 2 have emerged over time and Omicron sub-variants have become dominant, the severity of illness from COVID-19 has declined despite…”
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Journal Article