Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Małgorzata Lisik"'
Autor:
Mateusz Lejawa, Marcin Goławski, Martyna Fronczek, Tadeusz Osadnik, Francesco Paneni, Massimiliano Ruscica, Natalia Pawlas, Małgorzata Lisik, Maciej Banach
Publikováno v:
Cardiovascular Diabetology, Vol 23, Iss 1, Pp 1-12 (2024)
Abstract Background Numerous observational studies have demonstrated that circulating lipoprotein(a) [Lp(a)] might be inversely related to the risk of type 2 diabetes (T2D). However, recent Mendelian randomization (MR) studies do not consistently sup
Externí odkaz:
https://doaj.org/article/ce5d74e3f982490e8133abdf26e5bf10
Autor:
Joanna Huszno, Zofia Kolosza, Marta Nycz-Bochenek, Małgorzata Lisik, Magdalena Mazur, Jolanta Pamuła-Piłat, Ewa Grzybowska
Publikováno v:
Contemporary Oncology, Vol 24, Iss 2, Pp 79-86 (2020)
Externí odkaz:
https://doaj.org/article/8ebd083b7a294037923a5991effe4fd7
Autor:
Marta Nycz-Bochenek, Magdalena Mazur, Ewa Grzybowska, Zofia Kołosza, Małgorzata Lisik, Jolanta Pamula-Pilat, Joanna Huszno
Publikováno v:
Contemporary Oncology, Vol 24, Iss 2, Pp 79-86 (2020)
Introduction The purpose of the present study was to characterise patients with breast cancer (BC) and NOD2-mutation (age ≥ 50 years) according to their clinicopathological factors or family history. Patients aged ≥ 50 years were compared with th
Autor:
Małgorzata Lisik
Publikováno v:
Psychiatria Polska. 51:899-907
Nosicielstwo premutacji w genie FMR1 dotyczy 1 na 130-260 kobiet oraz 1 na 250-810 mężczyzn. Obecnie wiadomo, że nosiciele premutacji są w grupie ryzyka rozwinięcia spektrum zaburzeń neurologicznych, psychiatrycznych oraz immunologicznych w wie
Autor:
Mateusz Lejawa, Martyna Fronczek, Kamil Bujak, Kamila Osadnik, Tadeusz Osadnik, Natalia Pawlas, Małgorzata Lisik, Mariusz Gąsior
Publikováno v:
Nutrition, metabolism, and cardiovascular diseases : NMCD. 30(6)
Background and aims Elevated homocysteine concentration is associated with a higher risk of cardiovascular disease. The aim of our study was to determine the environmental and genetic factors associated with serum homocysteine concentration in health
Publikováno v:
Lipids
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 expansion of the CGG repeats in the promoter region of the FMR1 gene resulting
Publikováno v:
Neuroimmunomodulation. 23(4)
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 expansion of the CGG repeats in the promoter region of the FMR1 gene, resulting
Autor:
Aleksander Sieroń, Małgorzata Lisik
Publikováno v:
Neurologia i Neurochirurgia Polska. 44:504-510
The fragile X syndrome (FRAX) is the most common familial form of mental retardation. The incidence is estimated at 1 in 4000 males. The leading symptom of the syndrome is mental retardation, with accompanying behavioural problems. About 25-35% of af
Autor:
Hanna Czekaj, Ewa Gutmajster, Aleksandra Auguściak-Duma, Anna Szydło, Małgorzata Lisik, Tomasz M Czekaj, Maciej Tarnowski, Joanna Witecka, Paweł Stańczak, Aleksander Sieroń
Publikováno v:
European Journal of Human Genetics. 17:344-351
Atrial septal defect (ASD) is an incomplete septation of atria in human heart causing circulatory problems. Its frequency is estimated at one per 10 000. Actions of numerous genes have been linked to heart development. However, no single gene defect
Publikováno v:
Neuro-degenerative diseases. 15(1)
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 association with autism. Objectives: