Cargando…

Lipoprotein particles in patients with pediatric Cushing disease and possible cardiovascular risks

BACKGROUND: Cardiovascular (CV) complications are the most significant cause of mortality in adults with Cushing disease (CD); little is known about CV risk factors in children with CD. Measurement of lipoprotein particles by nuclear magnetic resonance (NMR) spectroscopy is a novel technology to ass...

Descripción completa

Detalles Bibliográficos
Autores principales:	Makri, Angeliki, Cheung, Anita, Sinaii, Ninet, Remaley, Alan T., Sampson, Maureen, Keil, Meg, Belyavskaya, Elena, Lyssikatos, Charalampos, De La Luz Sierra, Maria, Stratakis, Constantine A., Lodish, Maya
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	2019
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6702083/ https://www.ncbi.nlm.nih.gov/pubmed/31112990 http://dx.doi.org/10.1038/s41390-019-0438-0

Ejemplares similares

Decreased Lymphocytes and Increased Risk for Infection are Common in Endogenous Pediatric Cushing Syndrome
por: Tatsi, Christina, et al.
Publicado: (2017)

Aortic pulse wave velocity in children with Cushing syndrome: A window into a marker of early cardiovascular disease
por: Blain, Hailey, et al.
Publicado: (2019)

Pediatric Cushing Disease: Disparities in Disease Severity and Outcomes in the Hispanic and African American Populations
por: Gkourogianni, Alexandra, et al.
Publicado: (2017)

MON-433 The Spectrum Of Growth Hormone Excess In Carney Complex: Characterizing A Common Finding In A Rare Syndrome
por: Tatsi, Christina, et al.
Publicado: (2019)

MON-190 Telomere Length as a Novel Prognostic Marker of Cushing Complications
por: Tatsi, Christina, et al.
Publicado: (2020)

Pseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene
por: Nobel, Yael R, et al.
Publicado: (2016)

SUN-356 The Effects of Selective Serotonin Reuptake Inhibitors on Urinary Free Cortisol in Patients with Carney Complex and Primary Pigmented Nodular Adrenocortical Disease
por: Kamilaris, Crystal, et al.
Publicado: (2019)

SUN-058 Concurrent Hypercortisolism in Primary Aldosteronism Patients at a Tertiary Care Center: 2007-2017
por: Suzuki, Mari, et al.
Publicado: (2019)

Residual manifestations of hypercortisolemia following surgical treatment in a patient with Cushing syndrome
por: Bartz, Sara K., et al.
Publicado: (2015)

FRI099 Advanced Lipoprotein Analysis In Patients With Cushing’s Syndrome
por: Varghese, Ron T, et al.
Publicado: (2023)

Bone Mineral Density in Patients with Inherited Bone Marrow Failure Syndromes
por: Shankar, Roopa Kanakatti, et al.
Publicado: (2017)

Patterns of thyroid hormone levels in pediatric medullary thyroid carcinoma patients on vandetanib therapy
por: Lodish, Maya, et al.
Publicado: (2015)

Selective Serotonin Reuptake Inhibitors Increase Urinary Free Cortisol in Patients with Carney Complex and Primary Pigmented Nodular Adrenocortical Disease
por: Chrysavgi Kamilaris, Crystal Dawn, et al.
Publicado: (2021)

Somatic PRKAR1A Gene Mutation in a Nonsyndromic Metastatic Large Cell Calcifying Sertoli Cell Tumor
por: Tatsi, Christina, et al.
Publicado: (2019)

Harvey Cushing Treated the First Known Patient With Carney Complex
por: Tsay, Cynthia J., et al.
Publicado: (2017)

Health-Related Quality of Life in Cushing Disease: Discrepancy Between Parent and Child Reports
por: Keil, Margaret F, et al.
Publicado: (2021)

OR24-6 Non-syndromic Cushing's Disease Due To CDKN1B Mutations: Novel Mutations And Phenotypic Features In A Large Pediatric Cohort
por: Hernández-Ramírez, Laura, et al.
Publicado: (2019)

SAT-261 Prospective Study of the Association between Early Adrenarche and Cognitive Function in Children with Cushing Disease
por: Keil, Margaret, et al.
Publicado: (2019)

SUN-713 Prevalence of Renal Cysts in Patients with Carney Complex
por: Kamilaris, Crystal Dawn Chrysavgi, et al.
Publicado: (2020)

SAT-543 Human Hair Aldosterone Measurements for Evaluation of Primary Aldosteronism
por: Demidowich, Andrew Paul, et al.
Publicado: (2020)

OR22-07 Novel Variants in Protein Kinase a Signaling-Related Genes Identified in Obese Children with and Without NAFLD
por: Bloyd, Michelle, et al.
Publicado: (2020)

Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two Neonates
por: Korkut, Sabriye, et al.
Publicado: (2016)

High-frequency variants in PKA signaling-related genes within a large pediatric cohort with obesity or metabolic abnormalities
por: Bloyd, Michelle, et al.
Publicado: (2023)

Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease
por: Faucz, Fabio R., et al.
Publicado: (2017)

Molecular Genetic and Genomic Alterations in Cushing’s Syndrome and Primary Aldosteronism
por: Kamilaris, Crystal D. C., et al.
Publicado: (2021)

Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?
por: Martínez de LaPiscina, Idoia, et al.
Publicado: (2020)

Identification of Dysbetalipoproteinemia by an Enhanced Sampson-NIH Equation for Very Low-Density Lipoprotein-Cholesterol
por: Sampson, Maureen, et al.
Publicado: (2022)

SUN-366 Neonatal Severe Hyperparathyroidism: Extreme Hypercalcemia as a Robust Marker for Homozygous Dosage of Pathogenic CASR Variants
por: Marx, Stephen J, et al.
Publicado: (2020)

Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing’s disease
por: Hernández-Ramírez, Laura C, et al.
Publicado: (2017)

OR23-01 Intrapatient ACTH Variability in Cushing’s Disease: Prognostic Significance
por: Alvarez, Reinier, et al.
Publicado: (2020)

A Simple Fluorescent Cholesterol Labeling Method to Cryoprotect and Detect Plasma Lipoprotein-X
por: Neufeld, Edward B., et al.
Publicado: (2022)

OR06-01 The Role of Germline Defects in Cushing’s Disease
por: Hernández-Ramírez, Laura C, et al.
Publicado: (2020)

SAT-304 Pituitary Stem Cells May Drive Adenomas Causing Cushing’s Disease
por: Asuzu, David, et al.
Publicado: (2020)

Too Much Glucagon, Too Little Insulin: Time course of pancreatic islet dysfunction in new-onset type 1 diabetes
por: Brown, Rebecca J., et al.
Publicado: (2008)

SUN-917 Aggressive De Novo MEN1 Variant in a Child with Metastatic Pancreatic Acth and Crh Co-Secreting Neuroendocrine Tumor: Diagnosis and 10-Year Follow Up
por: Bompou, Maria Eleni, et al.
Publicado: (2020)

SAT-300 Evading Death: Noxa in Cushing’s Disease Pituitary Adenomas
por: Alvarez, Reinier, et al.
Publicado: (2020)

The NIH Lipo-COVID Study: A Pilot NMR Investigation of Lipoprotein Subfractions and Other Metabolites in Patients with Severe COVID-19
por: Ballout, Rami A., et al.
Publicado: (2021)

OR24-06 USP8 Genetic Variants May Contribute to the Development of Bilateral Adrenal Hyperplasia and ACTH-Independent Cushing Syndrome
por: Settas, Nikolaos, et al.
Publicado: (2020)

Abnormal Pituitary Imaging and Associated Endocrine Dysfunctions in Erdheim-Chester Disease
por: Shekhar, Skand, et al.
Publicado: (2021)

Accuracy and Clinical Impact of Estimating Low-Density Lipoprotein-Cholesterol at High and Low Levels by Different Equations
por: Sampson, Maureen, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_jq9htb0dlmcpmjo216sivc9fpe