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Clinical Genetics|July 9, 2013
Novel c.191C>G (p.Pro64Arg) MPV17 mutation identified in two pairs of unrelated Polish siblings with mitochondrial hepatoencephalopathyD Piekutowska-Abramczuk, M Pronicki, K Strawa, et al.
Free Radical Biology & Medicine|March 22, 2015
Cholesterol under oxidative stress-How lipid membranes sense oxidation as cholesterol is being replaced by oxysterolsWaldemar Kulig, Agnieszka Olżyńska, Piotr Jurkiewicz, et al.
Bone|March 27, 2025
A novel NEK1 variant disturbs the interaction between the C-terminal fragment of NEK1 and the VDAC1 channel, causing lethal short-rib polydactyly syndromeKarolina Gruca-Stryjak, Karolina Maciak, Maria Winiewska-Szajewska, et al.
American Heart Journal|May 27, 2003
Outcomes of primary coronary angioplasty and angioplasty after initial thrombolysis in the treatment of 374 consecutive patients with acute myocardial infarctionLech Poloński, Mariusz Gasior, Jarosław Wasilewski, et al.
Kardiologia Polska|October 14, 2003
Myocardial infarction in patients with diabetes. Results of primary coronary angioplastyMariusz Gasior, Jarosław Wasilewski, Marek Gierlotka, et al.
Materials (Basel, Switzerland)|June 13, 2025
Novel Research on Selected Mechanical and Environmental Properties of the Polyurethane-Based P3HB NanobiocompositesIwona Zarzyka, Beata Krzykowska, Karol Hęclik, et al.
Journal of Human Genetics|February 8, 2018
Clinical and molecular characteristics of newly reported mitochondrial disease entity caused by biallelic PARS2 mutationsElżbieta Ciara, Dariusz Rokicki, Michal Lazniewski, et al.
American Journal of Obstetrics and Gynecology|January 26, 2021
Severe acute respiratory syndrome coronavirus 2 serology levels in pregnant women and their neonatesJeffrey M Kubiak, Elisabeth A Murphy, Jim Yee, et al.
British Journal of Haematology|December 12, 2023
Cognitive decline in thrombotic thrombocytopenic purpura survivors: The role of white matter health as assessed by MRIF Hannan, J Hamilton, C J Patriquin, et al.
American Journal of Medical Genetics. Part A|April 2, 2010
Genomic alterations in biliary atresia suggest region of potential disease susceptibility in 2q37.3Melissa Leyva-Vega, Jennifer Gerfen, Brian D Thiel, et al.
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