Burden in primary informal caregivers of children and adolescents with type 1 diabetes: Is it associated with depression, family dysfunction, and glycemic control?

Autor: Lourdes Balcázar-Hernández, Hebert Huerta-Martínez, Eulalia Garrido Magaña, Elisa Nishimura-Meguro, Abigail Jiménez Márquez, Aleida Rivera-Hernández

Publikováno v: Frontiers in Endocrinology, Vol 13 (2023)

ObjectiveThe requirement of a chronic treatment and the increase in life expectancy in children with type 1 diabetes (T1D) leads to the possibility of caregiver burden. The aim of our study was to evaluate the burden in primary informal caregivers (P

Externí odkaz: https://doaj.org/article/ba72c279f98d4026a29ee4a669e35ba8

Evolución histórica del tratamiento de la diabetes tipo 1 en México

Autor: Paloma Almeda-Valdés, Israel Lerman-Garber, Elisa Nishimura-Meguro

Publikováno v: Revista Mexicana de Endocrinología, Metabolismo y Nutrición, Vol 8, Iss 93 (2021)

Con el advenimiento de la insulina, la diabetes mellitus tipo 1 (DM1) dejó de ser una enfermedad fatal para convertirse en una enfermedad crónica, asociada a descompensaciones agudas e importantes complicaciones microvasculares y macrovasculares. A

Externí odkaz: https://doaj.org/article/04108c08b9f14f7b826f997ea3bb1421

Influence of the informal primary caretaker on glycemic control among prepubertal pediatric patients with type 1 diabetes mellitus

Autor: Jessie Nallely Zurita‐Cruz, Elisa Nishimura‐Meguro, Miguel Angel Villasís‐Keever, Maria Elena Hernández‐Méndez, Eulalia Garrido‐Magaña, Aleida De Jesús Rivera‐Hernández

Publikováno v: Jornal de Pediatria (Versão em Português), Vol 93, Iss 2, Pp 136-141 (2017)

Objectives: In prepubertal type 1 diabetic patients (DM1), the availability of an informal primary caregiver (ICP) is critical to making management decisions; in this study, the ICP‐related risk factors associated with glycemic control were identif

Externí odkaz: https://doaj.org/article/5ed3dfd1eab344bdb956ec0df678d8ea

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Update of variants identified in the pancreatic β‐cell K ATP channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes

Autor: Jayne A L Houghton, Elisa De Franco, Raúl Calzada‐León, Siri Atma W. Greeley, Daniela del Gaudio, Annette Rønholt Larsen, Klaus Brusgaard, Elisa Nishimura-Meguro, Christine Bellanné-Chantelot, Bradley Harman, Sarah E. Flanagan, Amy E. Knight Johnson, Jean-Baptiste Arnoux, Cécile Saint-Martin, Pamela Bowman, Thomas W Laver, May Sanyoura, Sian Ellard, Lydia Aguilar-Bryan, Henrik Thybo Christesen

Publikováno v: Human Mutation
De Franco, E, Saint-Martin, C, Brusgaard, K, Knight Johnson, A E, Aguilar-Bryan, L, Bowman, P, Arnoux, J B, Larsen, A R, May, S, Greeley, S A W, Calzada-León, R, Harman, B, Houghton, J A L, Nishimura-Meguro, E, Laver, T W, Ellard, S, del Gaudio, D, Christesen, H T, Bellanné-Chantelot, C & Flanagan, S E 2020, ' Update of variants identified in the pancreatic β-cell K ATP channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes ', Human Mutation, vol. 41, no. 5, pp. 884-905 . https://doi.org/10.1002/humu.23995

The most common genetic cause of neonatal diabetes and hyperinsulinism is pathogenic variants in ABCC8 and KCNJ11. These genes encode the subunits of the β‐cell ATP‐sensitive potassium channel, a key component of the glucose‐stimulated insulin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c66ea5e0f0a34b21f6c3f814547fb269
https://doi.org/10.1002/humu.23995