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Case report: coeliac disease as a cause of secondary failure of glibenclamide therapy in a patient with permanent neonatal diabetes due to KCNJ11/R201C mutation
| Autores principales: | , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer Berlin Heidelberg
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187167/ https://www.ncbi.nlm.nih.gov/pubmed/33987715 http://dx.doi.org/10.1007/s00125-021-05454-y |
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| author | Iafusco, Dario Zanfardino, Angela Piscopo, Alessia Casaburo, Francesca De Nigris, Angelica Alfiero, Salvatore Russo, Giuseppina Arenella, Mattia Russo, Maria Cecilia Barbetti, Fabrizio |
| author_facet | Iafusco, Dario Zanfardino, Angela Piscopo, Alessia Casaburo, Francesca De Nigris, Angelica Alfiero, Salvatore Russo, Giuseppina Arenella, Mattia Russo, Maria Cecilia Barbetti, Fabrizio |
| author_sort | Iafusco, Dario |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-8187167 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2021 |
| publisher | Springer Berlin Heidelberg |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-81871672021-06-11 Case report: coeliac disease as a cause of secondary failure of glibenclamide therapy in a patient with permanent neonatal diabetes due to KCNJ11/R201C mutation Iafusco, Dario Zanfardino, Angela Piscopo, Alessia Casaburo, Francesca De Nigris, Angelica Alfiero, Salvatore Russo, Giuseppina Arenella, Mattia Russo, Maria Cecilia Barbetti, Fabrizio Diabetologia Research Letter Springer Berlin Heidelberg 2021-05-14 2021 /pmc/articles/PMC8187167/ /pubmed/33987715 http://dx.doi.org/10.1007/s00125-021-05454-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
| spellingShingle | Research Letter Iafusco, Dario Zanfardino, Angela Piscopo, Alessia Casaburo, Francesca De Nigris, Angelica Alfiero, Salvatore Russo, Giuseppina Arenella, Mattia Russo, Maria Cecilia Barbetti, Fabrizio Case report: coeliac disease as a cause of secondary failure of glibenclamide therapy in a patient with permanent neonatal diabetes due to KCNJ11/R201C mutation |
| title | Case report: coeliac disease as a cause of secondary failure of glibenclamide therapy in a patient with permanent neonatal diabetes due to KCNJ11/R201C mutation |
| title_full | Case report: coeliac disease as a cause of secondary failure of glibenclamide therapy in a patient with permanent neonatal diabetes due to KCNJ11/R201C mutation |
| title_fullStr | Case report: coeliac disease as a cause of secondary failure of glibenclamide therapy in a patient with permanent neonatal diabetes due to KCNJ11/R201C mutation |
| title_full_unstemmed | Case report: coeliac disease as a cause of secondary failure of glibenclamide therapy in a patient with permanent neonatal diabetes due to KCNJ11/R201C mutation |
| title_short | Case report: coeliac disease as a cause of secondary failure of glibenclamide therapy in a patient with permanent neonatal diabetes due to KCNJ11/R201C mutation |
| title_sort | case report: coeliac disease as a cause of secondary failure of glibenclamide therapy in a patient with permanent neonatal diabetes due to kcnj11/r201c mutation |
| topic | Research Letter |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187167/ https://www.ncbi.nlm.nih.gov/pubmed/33987715 http://dx.doi.org/10.1007/s00125-021-05454-y |
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