日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Fabry disease - a genetically conditioned extremely rare disease with a very unusual course

法布里病——一种由遗传因素引起的极其罕见的疾病,其病程非常特殊。

Śnit, Mirosław; Przyłudzka, Marcela; Grzeszczak, Władysław

A rare case of peritoneal dialysis-associated peritonitis caused by Comamonas testosteroni

一例由睾丸酮假单胞菌引起的罕见腹膜透析相关性腹膜炎

Kuźniewicz, Roman; Śnit, Mirosław; Szczyra, Dariusz

Association between Selected Polymorphisms rs12086634, rs846910, rs4844880, rs3753519 of 11β-Hydroxysteroid Dehydrogenase Type 1 (HSD11B1) and the Presence of Insulin Resistance in the Polish Population of People Living in Upper Silesia

11β-羟类固醇脱氢酶1型(HSD11B1)的特定多态性rs12086634、rs846910、rs4844880、rs3753519与波兰上西里西亚地区居民胰岛素抵抗的关联

Szweda-Gandor, Nikola; Śnit, Mirosław; Grzeszczak, Władysław

DIAPH2, PTPRD and HIC1 Gene Polymorphisms and Laryngeal Cancer Risk

DIAPH2、PTPRD 和 HIC1 基因多态性与喉癌风险

Śnit, Mirosław; Misiołek, Maciej; Ścierski, Wojciech; Koniewska, Anna; Stryjewska-Makuch, Grażyna; Okła, Sławomir; Grzeszczak, Władysław

Association of CX3CR1 Gene Polymorphisms with Fractalkine, Fractalkine Receptor, and C-Reactive Protein Levels in Patients with Kidney Failure

CX3CR1基因多态性与肾衰竭患者分形素、分形素受体和C反应蛋白水平的相关性

Woźny, Łukasz; Żywiec, Joanna; Gosek, Katarzyna; Kuźniewicz, Roman; Górczyńska-Kosiorz, Sylwia; Trautsolt, Wanda; Śnit, Mirosław; Grzeszczak, Władysław

Whether Prolyl Hydroxylase Blocker-Roxadustat-In the Treatment of Anemia in Patients with Chronic Kidney Disease Is the Future?

脯氨酰羟化酶阻滞剂罗沙司他能否成为治疗慢性肾病患者贫血的未来?

Grzeszczak, Władysław; Szczyra, Dariusz; Śnit, Mirosław