Ewa Gutmajster
Overview
Explore the profile of Ewa Gutmajster including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
71
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0
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Recent Articles
1.
Fus-Kujawa A, Mendrek B, Bajdak-Rusinek K, Diak N, Strzelec K, Gutmajster E, et al.
Front Bioeng Biotechnol
. 2023 Jul;
11:1205122.
PMID: 37456734
The benefits of patient's specific cell/gene therapy have been reported in relation to numerous genetic related disorders including osteogenesis imperfecta (OI). In osteogenesis imperfecta particularly also a drug therapy based...
2.
Strzelec K, Dziedzic A, Lazarz-Bartyzel K, Grabiec A, Gutmajster E, Kaczmarzyk T, et al.
Orphanet J Rare Dis
. 2021 Nov;
16(1):492.
PMID: 34819125
Background: Hereditary gingival fibromatosis (HGF) is a rare condition characterized by slowly progressive overgrowth of the gingiva. The severity of overgrowth may differ from mild causing phonetic and masticatory issues,...
3.
Augusciak-Duma A, Lesiak M, Stepien K, Gutmajster E, Sieron A
Acta Biochim Pol
. 2021 Oct;
68(4):745-750.
PMID: 34669362
Abdominal aortic aneurysm is a process involving the disruption and reconstruction of the extracellular matrix and the apoptosis of smooth muscle cells under the strong influence of the immune system....
4.
Augusciak-Duma A, Stepien K, Lesiak M, Gutmajster E, Fus-Kujawa A, Botor M, et al.
J Appl Genet
. 2021 Jun;
62(3):499-506.
PMID: 34091862
Abdominal aortic aneurysm refers to abnormal, asymmetric distension of the infrarenal aortic wall due to pathological remodelling of the extracellular matrix. The distribution of enzymes remodelling the extracellular matrix and...
5.
Lesiak M, Sieron L, Gutmajster E, Kowalczuk A, Bochenek M, Utrata-Wesolek A, et al.
Eur J Dermatol
. 2019 Apr;
29(2):126-140.
PMID: 31010797
The treatment of difficult-to-treat wounds can be challenging. Although a number of approaches have been investigated, the healing process may be slow and unsatisfactory. An alternative approach is the use...
6.
Gutmajster E, Chudek J, Augusciak-Duma A, Szwed M, Szybalska A, Mossakowska M, et al.
J Appl Genet
. 2018 Jun;
59(3):291-299.
PMID: 29938393
One of the markers of aging is lymphocyte telomere length (LTL), which is affected by genetic constitution of the organism and environmental conditions, such as development and diseases, including diabetes....
7.
Lisik M, Gutmajster E, Sieron A
Neuroimmunomodulation
. 2016 Dec;
23(4):239-243.
PMID: 27902989
Material And Methods: Twenty-three male patients affected by FXS (full mutation in the FMR1 gene) and 24 controls were included in the study. Plasma leptin and adiponectin levels were measured...
8.
Lisik M, Gutmajster E, Sieron A
Lipids
. 2015 Dec;
51(2):189-92.
PMID: 26712713
Fragile X syndrome (FXS) is the most common form of familial mental retardation and one of the leading known causes of autism. The mutation responsible for FXS is a large...
9.
Lisik M, Gutmajster E, Sieron A
Neurodegener Dis
. 2014 Dec;
15(1):45-9.
PMID: 25500855
Background: Fragile X syndrome (FXS) is a single-gene disorder with a broad spectrum of involvement, including cognitive and behavioural impairments of varying degrees with specific physical features and a strong...
10.
Gutmajster E, Witecka J, Wyskida M, Koscinska-Marczewska J, Szwed M, Owczarz M, et al.
ScientificWorldJournal
. 2014 Jan;
2013:153608.
PMID: 24453794
Background: Age-related decrease in bone marrow erythropoietic capacity is often accompanied by the telomere length shortening in peripheral white blood cells. However, limited and conflicting data hamper the conclusive opinion...