Anna Sulek
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Explore the profile of Anna Sulek including associated specialties, affiliations and a list of published articles.
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54
Citations
561
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Recent Articles
1.
Sulek A
Postep Psychiatr Neurol
. 2024 Dec;
33(3):147-162.
PMID: 39678458
Purpose: Extracellular vesicles are the subject of many studies in various medical specialties. Their role in neurodegenerative diseases is increasing and they worth introducing in more detail. Methods: This review...
2.
Hoffman-Zacharska D, Sulek A
Int J Mol Sci
. 2024 Aug;
25(15).
PMID: 39125760
Since 1991, several genetic disorders caused by unstable trinucleotide repeats (TNRs) have been identified, collectively referred to as triplet repeat diseases (TREDs). They share a common mutation mechanism: the expansion...
3.
Radziwonik-Fraczyk W, Elert-Dobkowska E, Kubalska J, Stepniak I, Lipowska M, Potulska-Chromik A, et al.
Postep Psychiatr Neurol
. 2024 Aug;
33(2):109-114.
PMID: 39119544
Purpose: Muscular dystrophy is a group of heterogeneous diseases causing progressive muscle weakness and atrophy. Many types have been defined, including Duchenne/Becker, myotonic, limb-girdle, congenital, and facioscapulohumeral muscular dystrophies. This...
4.
Radziwonik-Fraczyk W, Elert-Dobkowska E, Karpinski M, Pilch J, Ziora-Jakutowicz K, Kubalska J, et al.
Neurogenetics
. 2024 May;
25(3):233-247.
PMID: 38758368
Neuromuscular disorders (NMDs) include a wide range of diseases affecting the peripheral nervous system. The genetic diagnoses are increasingly obtained with using the next generation sequencing (NGS). We applied the...
5.
Elert-Dobkowska E, Stepniak I, Radziwonik-Fraczyk W, Jahic A, Beetz C, Sulek A
Int J Mol Sci
. 2024 May;
25(9).
PMID: 38732227
The most common form of hereditary spastic paraplegia (HSP), SPG4 is caused by single nucleotide variants and microrearrangements in the gene. The high percentage of multi-exonic deletions or duplications observed...
6.
Sobanska A, Czerwosz L, Sulek A, Rola R, Stepniak I, Rakowicz M
Cerebellum
. 2024 Mar;
23(5):1882-1891.
PMID: 38492164
The aim of this study was to determine the time between the first detection of postural control impairments and the evident manifestation of ataxia in preclinical SCA1 individuals. Twenty five...
7.
Dulski J, Al-Shaikh R, Prudencio M, Petrucelli L, Sulek A, Bernatowicz K, et al.
Neurol Neurochir Pol
. 2023 Jun;
57(3):310-313.
PMID: 37283503
Introduction: We present the first two Polish families diagnosed with spinocerebellar ataxia type 7 (SCA7) and draw attention to cardiac involvement as a new potential manifestation of this disease. Material...
8.
Wislowska-Stanek A, Lehner M, Tomczuk F, Gawryluk A, Kolosowska K, Sulek A, et al.
Pharmacol Rep
. 2022 Nov;
75(1):119-127.
PMID: 36385611
Background: The present study assessed the influence of recurrent social isolation stress on the aversive memory extinction and dopamine D receptors (DR) expression in the amygdala and the hippocampus subnuclei....
9.
Dulski J, Al-Shaikh R, Sulek A, Kasprzak J, Slawek J, Wszolek Z
Parkinsonism Relat Disord
. 2022 Nov;
105:39-42.
PMID: 36334556
Spinocerebellar ataxia type 3 (SCA3; Machado-Joseph disease, MJD) is the most common autosomal-dominant form of genetic ataxia worldwide. However, it has never been reported in Eastern Europe. This letter presents...
10.
Malczynska-Sims P, Chalimoniuk M, Wronski Z, Marusiak J, Sulek A
Aging Clin Exp Res
. 2022 Aug;
34(9):2243.
PMID: 36018480
No abstract available.