Michal Piechota
Overview
Explore the profile of Michal Piechota including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
7
Citations
26
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Matuszewska K, Bukowska-Olech E, Piechota M, Staniek-Lacna K, Drews K, Wieckowska B, et al.
J Matern Fetal Neonatal Med
. 2024 Jul;
37(1):2364249.
PMID: 39069503
Objective: To determine the frequency of chromosomal aberrations in chorions after a miscarriage. The second was to examine selected euploid chorions using a next-generation sequencing (NGS) panel designed to assess...
2.
Badura-Stronka M, Wolynska K, Winczewska-Wiktor A, Marcinkowska J, Karolewska D, Tomkowiak-Kedzia D, et al.
Front Neurol
. 2024 Feb;
14:1316933.
PMID: 38328757
Introduction: Targeted Next-Generation Sequencing Panels (TNGSP) have become a standard in global clinical practice. Instead of questioning the necessity of next-generation sequencing in epilepsy patients, contemporary large-scale research focuses on...
3.
Szczawinska-Poplonyk A, Bernat-Sitarz K, Schwartzmann E, Piechota M, Badura-Stronka M
Allergol Immunopathol (Madr)
. 2022 Jul;
50(4):1-9.
PMID: 35789397
Monoallelic loss-of-function (LOF) mutations in the phosphatidylinositol 3-kinase () gene affecting the inter-Src homology 2 domain of the p85α regulatory subunit of phosphoinositide--3-kinase δ (PI3Kδ) cause the activated PI3K δ...
4.
Bukowska-Olech E, Gawlinski P, Jakubiuk-Tomaszuk A, Jedrzejowska M, Obersztyn E, Piechota M, et al.
Orphanet J Rare Dis
. 2021 Jun;
16(1):286.
PMID: 34174922
Background: Craniofrontonasal syndrome (CFNS) is a rare X-linked disorder that results from pathogenic variants in the EFNB1 gene. The syndrome paradoxically presents with greater severity of the symptoms in heterozygous...
5.
Phenotypic description of two adult brothers presenting with mild form of Smith-Lemli-Opitz syndrome
Olech E, Matuszewska K, Piechota M, Latos-Bielenska A, Jamsheer A
Clin Dysmorphol
. 2019 Mar;
28(3):154-156.
PMID: 30925529
No abstract available.
6.
Piechota M, Banaszewska A, Dudziak J, Slomczynski M, Plewa R
Protein J
. 2012 Jul;
31(6):511-8.
PMID: 22763563
Acute Coronary Syndromes (ACS) are a group of disorders caused by the significant reduction of circulation in coronary arteries. The most common reason of the dysfunction is a blood clot...
7.
Banaszewska A, Piechota M, Plewa R
Cell Mol Biol Lett
. 2012 Feb;
17(2):228-39.
PMID: 22311433
Proprotein convertase subtilisin/kexin type 9 (PCSK9) has emerged as a novel target for controlling plasma levels of low-density lipoprotein cholesterol (LDL-C) and decreasing the risk of cardiovascular diseases. At present...