Emotional dysfunction associated with diabetes in Mexican adolescents and young adults with type-1 diabetes

Autor: Lerman-Garber Israel, Barrón-Uribe Consuelo, Calzada-León Raúl, Mercado-Atri Moisés, Vidal-Tamayo Rafael, Quintana Silvia, Hernández María Elena, Ruiz-Reyes María de la Luz, Tamez-Gutiérrez Laura Elena, Nishimura-Meguro Elisa, Villa Antonio R

Publikováno v: Salud Pública de México, Vol 45, Iss 1, Pp 13-18 (2003)

OBJECTIVE: To assess the emotional dysfunction associated with diabetes in Mexican young individuals with type-1 diabetes. MATERIAL AND METHODS: A cross-sectional survey was conducted to perform a complete clinical and psychosocial evaluation of 93 c

Externí odkaz: https://doaj.org/article/52dc383261d3440e81ab64e9c5f6c97b

Relationship Between Serum Leptin Levels and Weight Gain in Girls with Central Precocious Puberty at 1-Year Follow-Up

Autor: Zurita-Cruz, Jessie N. ^*, Villasís-Keever, Miguel A., Damasio-Santana, Leticia, Manuel-Apolinar, Leticia, Nishimura-Meguro, Elisa, Rivera-Hernández, Aleidade J., Garrido-Magaña, Eulalia, Gutierrez-Gonzalez, Alejandro, Poblano-Alcalá, Adriana

Publikováno v: In Endocrine Practice May 2017 23(5):519-525

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, 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 identifie

Externí odkaz: https://doaj.org/article/1b5c701182f845c8b3edd1dee56b3fc0

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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