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pro vyhledávání: '"MODY 1"'
Akademický článek
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Autor:
Liping Du, John Virostko, Alvin C. Powers, Hakmook Kang, William E. Russell, Jonathan M. Williams, Siri Atma W. Greeley, Daniel J. Moore, Jordan J. Wright, Melissa A. Hilmes
Publikováno v:
Diabetes. 69
Individuals with new-onset type 1 diabetes (T1D) have a smaller pancreas volume, which declines further during the first years after diagnosis. Whether this reflects the insulin deficiency associated with T1D or the underlying process leading to T1D
Publikováno v:
Journal of the Endocrine Society
Monogenic Diabetes (MODY) results from mutations or changes in a single gene, and currently account for about 1 to 4% of all cases of diabetes (1). Our group has previously published on the successful use of glucagon-like peptide-1 receptor agonist (
Autor:
Guillermo Di Girolamo, Gustavo Daniel Frechtel, Claudio Gonzalez, Agustina Alves de Lima, Rocio Fogar, Victoria Insussarry Perkins
Publikováno v:
Current reviews in clinical and experimental pharmacology. 16(3)
Background: Monogenic Diabetes (MFD) represents close to 2% of all the cases of diabetes diagnosed in people younger than 45 years old. Maturity-Onset Diabetes of the Young (MODY), neonatal diabetes, and several syndromic forms of diabetes are includ
Autor:
Catarina I Gonçalves, Leonor Gomes, Joana T Almeida, Carla Baptista, Daniela Guelho, Miguel Melo, Isabel Dinis, Maria Manuela Estima Gomes, Joana Saraiva, Manuel C. Lemos, Maria Inês Alvelos, Sofia Martins, Luísa Barros, Diana Martins, Alice Mirante, Margarida Bastos, Carolina Moreno, Eduarda Coutinho, Mara Ventura, Maria L Sampaio, Bernardo Dias Pereira, Susana Gama-de-Sousa
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 1, p 288 (2020)
Journal of Clinical Medicine
Volume 9
Issue 1
Journal of Clinical Medicine
Volume 9
Issue 1
Maturity-onset diabetes of the young (MODY) is a frequently misdiagnosed type of diabetes, which is characterized by early onset, autosomal dominant inheritance, and absence of insulin dependence. The most frequent subtypes are due to mutations of th
Publikováno v:
Orvosi Hetilap. 157:469-473
The classification of diabetes mellitus in adolescents and young adults is often difficult. The diagnosis of the monogenic form of diabetes may have substantial influence on quality of life, prognosis and the choice of the appropriate treatment of af
Publikováno v:
Diabetes. 67
Current practice guidelines recommend considering a diagnosis of MODY in patients with a strong family history but without typical features of type 2 diabetes (T2D) (i.e., obesity, insulin resistance, high-risk ethnicity) or type 1 diabetes (T1D) (i.
BACKGROUND: MODY diabetes includes rare familiar forms due to genetic mutations resulting in β-cell dysfunction. MODY 3 is due to mutations in the gene transcription factor HNF-1α, with diabetes diagnosis in adolescence or early adult life. Few dat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79ff2da8194d208191410790dbcd7747
http://hdl.handle.net/11588/644814
http://hdl.handle.net/11588/644814
Autor:
Basudev Bhattacharya, Suman Kalyan Paine, Chaitry Ghosal, Shuvodip Chowdhury, Aditi Sen, S. R. Banerjee, Subhankar Chowdhury, Kaushik Pandit
Publikováno v:
Open Journal of Preventive Medicine. :116-122
The disorder, Maturity Onset of Diabetes of the young (MODY) is a monogenic form of Non-Insulin dependent Diabetes Mellitus (NIDDM), characterized by autosomal dominant mode of inheritance and onset is usually before 25 years of age. Clinical studies
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 136:1111-1115
Background Monogenic forms of diabetes are often diagnosed by chance, due to the variety of clinical presentation and limited experience of the diabetologists with this kind of diabetes. Aim of this study was to evaluate clinical parameters for an ef