Search Results - "Eldin, Karen"
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Sample-to-answer, extraction-free, real-time RT-LAMP test for SARS-CoV-2 in nasopharyngeal, nasal, and saliva samples: Implications and use for surveillance testing
Published in PloS one (25-02-2022)“…The global COVID-19 pandemic has highlighted the need for rapid, accurate and accessible nucleic acid tests to enable timely identification of infected…”
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Lupus Nephritis
Published in The Pediatric clinics of North America (01-02-2019)“…Childhood-onset systemic lupus erythematosus (SLE) is a subset of SLE with an onset before 18 years of age. Patients with early onset SLE tend to have a…”
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3
A Recurrent PDGFRB Mutation Causes Familial Infantile Myofibromatosis
Published in American journal of human genetics (06-06-2013)“…Infantile myofibromatosis (IM) is the most common benign fibrous tumor of soft tissues affecting young children. By using whole-exome sequencing, RNA…”
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4
Recurrent internal tandem duplications of BCOR in clear cell sarcoma of the kidney
Published in Nature communications (17-11-2015)“…The X-linked BCL-6 co-repressor ( BCOR ) gene encodes a key constituent of a variant polycomb repressive complex (PRC) that is mutated or translocated in human…”
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Efficacy and Safety of COVID-19 Convalescent Plasma in Hospitalized Patients: A Randomized Clinical Trial
Published in JAMA internal medicine (01-02-2022)“…There is clinical equipoise for COVID-19 convalescent plasma (CCP) use in patients hospitalized with COVID-19. To determine the safety and efficacy of CCP…”
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Twelve tips for the introduction of emotional intelligence in medical education
Published in Medical teacher (03-07-2019)“…Emotional intelligence (EI) is the ability to recognize, understand, and manage emotions in yourself and in others. EI has long been recognized as a critical…”
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Copa Syndrome: a Novel Autosomal Dominant Immune Dysregulatory Disease
Published in Journal of clinical immunology (01-05-2016)“…Inherently defective immunity typically results in either ineffective host defense, immune regulation, or both. As a category of primary immunodeficiency…”
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A Zebra at the Rodeo: Dyspnea, Hematuria, and a Family History of Arthritis
Published in Arthritis care & research (2010) (01-02-2022)Get full text
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Juvenile Granulosa Cell Tumor of the Ovary: A Clinicopathologic Study
Published in Journal of pediatric & adolescent gynecology (01-02-2017)“…Abstract Study Objective To report on the clinical characteristics and outcome of pediatric patients with juvenile granulosa cell tumor (JGCT) of the ovary…”
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10
Idiopathic membranous nephropathy in children treated with rituximab: report of two cases
Published in Pediatric nephrology (Berlin, West) (01-06-2018)“…Background Idiopathic membranous nephropathy is an uncommon cause of nephrotic syndrome in children and can present treatment challenges. The current treatment…”
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Clinico-radiologic features of pleuroparenchymal fibroelastosis in children
Published in Pediatric radiology (01-08-2019)“…Background Pleuroparenchymal fibroelastosis (PPFE) may be underdiagnosed clinically and radiographically in children with a remote history of cancer, leading…”
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Evaluation of the International Society on Thrombosis and Haemostasis and institutional diagnostic criteria of disseminated intravascular coagulation in pediatric patients
Published in American journal of clinical pathology (01-06-2013)“…Globally, adult intensive care units routinely use the International Society on Thrombosis and Haemostasis (ISTH) scoring system for identifying overt…”
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Correlating surgical and pathological diagnoses in pediatric appendicitis
Published in Journal of pediatric surgery (01-04-2015)“…Abstract Background The stratification of appendicitis into simple and complex variants has far-reaching implications. While the operative diagnosis made by…”
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Clinical presentation and outcomes of childhood-onset membranous lupus nephritis
Published in Pediatric nephrology (Berlin, West) (01-12-2017)“…Background Best practices for managing childhood-onset membranous lupus nephritis (MLN) are not yet established. Most studies involve primarily or exclusively…”
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Smad1-Smad5 Ovarian Conditional Knockout Mice Develop a Disease Profile Similar to the Juvenile Form of Human Granulosa Cell Tumors
Published in Endocrinology (Philadelphia) (01-12-2009)“…Granulosa cell tumors (GCTs) of the ovary are rare sex cord stromal tumors. Although generally indolent, GCTs recur, and if not diagnosed and treated in early…”
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Human Herpesvirus 6 Infection in Pediatric Liver Transplantation: Single-Center Study of Incidence, Outcomes, and Management
Published in Journal of the Pediatric Infectious Diseases Society (28-05-2021)“…Abstract Background Distinctions between HHV-6 primary infection in seronegative patients and HHV-6 reactivation in seropositive patients remains largely…”
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Persistent cat scratch disease requiring surgical excision in a patient with MPGN
Published in Pediatrics (Evanston) (01-06-2015)“…We present the case of a 13-year-old immunosuppressed patient with unrelenting cat scratch disease despite 9 months of antibiotic therapy. The patient was…”
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Identification of Chromatin Remodeling Genes Arid4a and Arid4b as Leukemia Suppressor Genes
Published in JNCI : Journal of the National Cancer Institute (03-09-2008)“…Background Leukemia evolves through a multistep process from premalignancy to malignancy. Epigenetic alterations, including histone modifications, have been…”
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Reverse transcription loop-mediated isothermal amplification (RT-LAMP) for point-of-care detection of SARS-CoV-2: a clinical study to evaluate agreement with RT-qPCR
Published in The Lancet global health (01-03-2021)“…The global COVID-19 pandemic caused by the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has highlighted the need for rapid, accurate, and…”
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Screen for abnormal mitochondrial phenotypes in mouse embryonic stem cells identifies a model for succinyl-CoA ligase deficiency and mtDNA depletion
Published in Disease models & mechanisms (01-02-2014)“…Mutations in subunits of succinyl-CoA synthetase/ligase (SCS), a component of the citric acid cycle, are associated with mitochondrial encephalomyopathy,…”
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