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» Authors » Iwona Solecka

Iwona Solecka

Explore the profile of Iwona Solecka including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 5
Citations 41
Followers 0
Related Specialties
Endocrinology
General Medicine
Top 10 Co-Authors
Maciej T Malecki
Jan Skupien
Magdalena Szopa
Jerzy Hohendorff
Wojciech Mlynarski
Tomasz Klupa
Agnieszka Gach
Damian Ucieklak
Sandra Mrozinska
Jacek Sieradzki
Published In
Endocrine
Diabetes Care
Minerva Med
Rev Diabet Stud
Affiliations
Soon will be listed here.
Recent Articles
1.
The utility of MODY Probability Calculator in probands of families with early-onset autosomal dominant diabetes from Poland
Hohendorff J, Zapala B, Ludwig-Slomczynska A, Solecka I, Ucieklak D, Matejko B, et al.
Minerva Med . 2019 Oct; 110(6):499-506. PMID: 31638358
Background: Maturity-onset diabetes of the young (MODY) accounts for 1-2% of all diabetes cases. Unfortunately, circa 90% of MODY cases are misdiagnosed as type 1 or type 2 diabetes. A...
2.
Quality of life assessment in patients with HNF1A-MODY and GCK-MODY
Szopa M, Matejko B, Ucieklak D, Uchman A, Hohendorff J, Mrozinska S, et al.
Endocrine . 2018 Nov; 64(2):246-253. PMID: 30421137
Aim: The impact of maturity onset diabetes of the young (MODY) on quality of life (QoL) has never been examined. We assessed disease impact on QoL among patients with HNF1A-MODY...
3.
Circulating ghrelin level is higher in HNF1A-MODY and GCK-MODY than in polygenic forms of diabetes mellitus
Nowak N, Hohendorff J, Solecka I, Szopa M, Skupien J, Kiec-Wilk B, et al.
Endocrine . 2015 May; 50(3):643-9. PMID: 25987348
Ghrelin is a hormone that regulates appetite. It is likely to be involved in the pathophysiology of varying forms of diabetes. In animal studies, the ghrelin expression was regulated by...
4.
Assessment of insulin sensitivity in adults with permanent neonatal diabetes mellitus due to mutations in the KCNJ11 gene encoding Kir6.2
Skupien J, Malecki M, Mlynarski W, Klupa T, Wanic K, Gach A, et al.
Rev Diabet Stud . 2007 May; 3(1):17-20. PMID: 17491708
Activating mutations in the KCNJ11 gene encoding the Kir6.2 subunit of ATP-sensitive potassium channel have been described in patients with permanent neonatal diabetes mellitus (PNDM). The main pathophysiological feature of...
5.
Transfer to sulphonylurea therapy in adult subjects with permanent neonatal diabetes due to KCNJ11-activating [corrected] mutations: evidence for improvement in insulin sensitivity
Malecki M, Skupien J, Klupa T, Wanic K, Mlynarski W, Gach A, et al.
Diabetes Care . 2006 Dec; 30(1):147-9. PMID: 17192350
No abstract available.