Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Marissa J. Kilberg"'
Autor:
Saba Sheikh, Darko Stefanovski, Marissa J. Kilberg, Denis Hadjiliadis, Ronald C. Rubenstein, Michael R. Rickels, Andrea Kelly
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
Insulin secretion within 30 minutes of nutrient ingestion is reduced in people with cystic fibrosis (PwCF) and pancreatic insufficiency and declines with worsening glucose tolerance. The glucose potentiated arginine (GPA) test is validated for quanti
Externí odkaz:
https://doaj.org/article/9eeb2aa56d794eaba42d9d8a793761d6
Autor:
Wang Shin Lei, Marissa J. Kilberg, Babette S. Zemel, Ronald C. Rubenstein, Clea Harris, Saba Sheikh, Andrea Kelly, Joseph M. Kindler
Publikováno v:
Journal of Clinical & Translational Endocrinology, Vol 30, Iss , Pp 100304- (2022)
Background: Gut-derived incretin hormones, including glucose-dependent insulinotropic peptide (GIP) and glucagon-like peptide 1 (GLP-1), regulate post-prandial glucose metabolism by promoting insulin production. GIP, GLP-1, and insulin contribute to
Externí odkaz:
https://doaj.org/article/6860a54c0e744a5f9d9902a3fb6fd026
Autor:
Marissa J Kilberg, Maria G Vogiatzi
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism.
Central precocious puberty (CPP) classically refers to premature activation of the hypothalamic–pituitary–gonadal axis with onset of sexual development before the age of 8 years in girls and 9 years in boys. A decrease in the age of thelarche has
Autor:
Clea D Harris, Christina Kubrak, Andrea Kelly, Denis Hadjiliadis, Marina Cuchel, Saba Sheikh, Marissa J. Kilberg, Darko Stefanovski, Michael R. Rickels, Ronald C. Rubenstein
Publikováno v:
J Clin Endocrinol Metab
Context Oral glucose tolerance test (OGTT)-related hypoglycemia is common in pancreatic-insufficient cystic fibrosis (PI-CF), but its mechanistic underpinnings are yet to be established. Objective To delineate the mechanism(s) underlying OGTT-related
Autor:
Andrea Kelly, Victor S. Harrison, Jonathan A. Mitchell, Zofia N. Zysman-Colman, Saba Sheikh, Alessandra Chesi, Struan F.A. Grant, Michael R. Rickels, Ronald C. Rubenstein, Denis Hadjiliadis, Marissa J. Kilberg
Publikováno v:
Pediatric research
BACKGROUND Despite improved health, shorter stature is common in cystic fibrosis (CF). We aimed to describe height velocity (HV) and contribution of height-related genetic variants to height (HT) in CF. METHODS HV cohort: standard deviation scores (-
Autor:
Andrea Kelly, Diva D. De León, Saba Sheikh, Marissa J. Kilberg, Christina Kubrak, Denis Hadjiliadis, Darko Stefanovski, Ronald C. Rubenstein, Michael R. Rickels
Publikováno v:
J Cyst Fibros
BACKGROUND: Post-prandial and oral glucose tolerance test-related hypoglycemia is common in cystic fibrosis (CF); however, the underlying mechanisms are unclear. METHODS: To understand the relationship of hypoglycemia with meal-related glucose excurs
Autor:
E. Aliaj, Dara Riva, Jessica Hudson, C. Roman, Andrea Kelly, Brynn E. Marks, Kelsey Fredkin, Melissa S. Putman, Marissa J Kilberg
Publikováno v:
Diabetes Technology & Therapeutics.
Background: Diabetes technologies are associated with improvements in glycemic control and health-related quality of life among people with type 1 diabetes (T1D). Use and perceptions of continuous ...
Publikováno v:
Endocrinol Metab Clin North Am
Although type 1 diabetes mellitus and, to a lesser extent, type 2 diabetes mellitus, are the prevailing forms of diabetes in youth, atypical forms of diabetes are not uncommon and may require etiology-specific therapies. By some estimates, up to 6.5%
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91818ba32e6ad6905fc6f58cdda6240e
https://europepmc.org/articles/PMC8221417/
https://europepmc.org/articles/PMC8221417/
Autor:
Ronald C. Rubenstein, Clea D Harris, Denis Hadjiliadis, Marina Cuchel, Andrea Kelly, Christina Kubrak, Darko Stefanovski, Saba Sheikh, Michael R. Rickels, Marissa J. Kilberg
Publikováno v:
Journal of the Endocrine Society
Glucose homeostasis is often abnormal in people with pancreatic insufficient cystic fibrosis (PI-CF). This dysfunction is viewed on a continuum from “normal” glucose tolerance to cystic fibrosis-related diabetes (CFRD), and may also include postp
Publikováno v:
Pediatr Endocrinol Rev
Ovotesticular Differences in Sexual Development (OT-DSD) is a rare subset of DSD with great phenotypic variability characterized by the presence of both testicular and ovarian tissue in the same individual. Here, we describe the case of 46,XX, SRY-ne