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Profil bibliographique

Frances Burke

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

54Publications signalées
4874Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Immune Cell Function and InteractionCytokine Signaling Pathways and InteractionsMonoclonal and Polyclonal Antibodies ResearchDiet and metabolism studiesImmune cells in cancer

Les publications récentes

Accès ouvert 2023 article OpenAlex

Translating Evidence-based Approaches into optimal Care for individuals at High-risk of ASCVD: Pilot testing of case-based e-learning modules and design of the TEACH-ASCVD study

Katarina Clegg, Tyler J. Schubert, Robert Block, Frances Burke et autres

BACKGROUND: Atherosclerotic cardiovascular disease (ASCVD) remains the leading cause of death in the United States. Case-based learning using electronic delivery of the modules can educate clinicians and improve translation of evidence-based guidelines into practice for high-risk ASCVD patients. OBJECTIVE: To develop and …

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9 citations Journal of clinical lipidology
Accès ouvert 2022 article OpenAlex

Development of the Penn Healthy Diet screener with reference to adult dietary intake data from the National Health and Nutrition Examination Survey

Charlene Compher, R. P. Quinn, Frances Burke, Doris Piccinin et autres

BACKGROUND: There is a need for a feasible, user-friendly tool that can be employed to assess the overall quality of the diet in U.S. CLINICAL SETTINGS: Our objectives were to develop the Penn Healthy Diet (PHD) screener, evaluate screener item correlations with …

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7 citations Nutrition Journal
Accès ouvert 2021 article OpenAlex

Successful Nutritional Intervention for an Infant with Abetalipoproteinemia

Masako Ueda, Michelle Maeda, Frances Burke, Robert A. Hegele et autres

INTRODUCTION Medical nutrition therapy is the only therapeutic alternative for several rare lipoprotein disorders. Abetalipoproteinemia (ABL; OMIM 200100), “homozygous” hypobetalipoproteinemia (OMIM 615558), and chylomicron retention disease (OMIM 246700), due to biallelic mutations in microsomal triglyceride transfer protein (MTTP), apolipoprotein B (APOB), and …

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0 citations JPGN Reports
Accès ouvert 2020 article OpenAlex

SAT-578 A Rare Case of Laboratory Hypertriglyceridemia: Glycerol Kinase Deficiency

Masako Ueda, Anna Wolska, Maureen Sampson, Frances Burke et autres

Abstract Background: Hypertriglyceridemia (HTG) is common; however, pseudo-HTG due to high glycerol in glycerol kinase deficiency (GKD, MIM: 307030) is a rare cause of HTG that need to be delineated for appropriate management. GKD is an X-linked recessive disorder characterized by hyperglycerolemia …

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1 citation Journal of the Endocrine Society
Accès ouvert 2020 article OpenAlex

Experimental Therapeutics for Challenging Clinical Care of a Patient with an Extremely Rare Homozygous APOC2 Mutation

Masako Ueda, Anna Wolska, Frances Burke, Maria Escobar et autres

BACKGROUND: only account for <2% of cases. Medical nutrition therapy is critical for FCS because usual triglyceride- (TG-) lowering medications are ineffective. Therapeutic plasma exchange (TPE) with fresh frozen plasma (FFP) is an option to urgently reduce TG and pancreatitis episodes. Several …

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6 citations Case Reports in Endocrinology
2019 article OpenAlex

Familial Chylomicronemia Syndrome With a Novel Homozygous LPL Mutation Identified in Three Siblings in Their 50s

Masako Ueda, Frances Burke, Alan T. Remaley, Robert A. Hegele et autres

Letters7 April 2020Familial Chylomicronemia Syndrome With a Novel Homozygous LPL Mutation Identified in Three Siblings in Their 50sMasako Ueda, MD, Frances M. Burke, MS, RD, Alan T. Remaley, MD, PhD, Robert A. Hegele, MD, Daniel J. Rader, MD, and Richard L. Dunbar, …

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6 citations Annals of Internal Medicine
Accès ouvert 2019 article OpenAlex

OR21-3 Familial Chylomicronemia Syndrome: Distinguishing the Rare Among the Common in Adults for Appropriate Management

Masako Ueda, Frances Burke, Denis Sviridov, Maria Escobar et autres

Background: Hypertriglyceridemia (HTG) is common, but familial chylomicronemia syndrome (FCS) is a very rare cause of severe HTG, associated with pancreatitis, which can be fatal. It is due to impaired lipoprotein lipase (LPL) function, typically caused by bi-allelic LPL loss-of-function mutations. Although …

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0 citations Journal of the Endocrine Society

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