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期刊名:Croatian medical journal

缩写:CROAT MED J

ISSN:0353-9504

e-ISSN:1332-8166

IF/分区:2.1/Q2

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共收录本刊相关文章索引1706
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Martin Medvid,Salome Glauser,Fabian Zürcher Martin Medvid
This report presents the case of a 61-year-old patient who experienced sporadically occurring episodes of chest pain lasting approximately 15 minutes. The initial electrocardiogram (ECG) showed unspecific repolarization disturbances but no ...
Iva Rukavina,Marijan Frković,Mario Sestan et al. Iva Rukavina et al.
Pachydermodactily is a rare digital fibromatosis of unknown origin, mainly affecting adolescent boys. It presents as symmetrical, painless thickening of the soft tissues, usually around the proximal interphalangeal joints (PIP). Patients of...
Ana Marušić,Igor Jerković,Petra Jelić et al. Ana Marušić et al.
Aim: To analyze the most influential publications from researchers in medicine at the University of Split in Croatia, as well as their participation in publicly registered clinical trials, to gain insight into medical res...
Ivana Jurin,Irzal Hadžibegović,Hrvoje Jurin et al. Ivana Jurin et al.
Aim: To assess the relative efficacy of dapagliflozin and empagliflozin in routinely treated chronic heart failure (CHF) patients. Methods: ...
Klara Dubravčić,Ružica Lasan Trčić,Ernest Bilić et al. Klara Dubravčić et al.
Aim: To assess the clinical-biological characteristics and outcomes of Croatian pediatric patients with acute lymphoblastic leukemia (ALL). A secondary aim was to evaluate the predictive value of pretreatment leukemia-ass...
Emine Göktaş,Ahmet Burak Arslan,Betül Turan et al. Emine Göktaş et al.
Aim: To determine the diagnostic yield of chromosomal microarray analysis (CMA) in different patient groups: intellectual disability and developmental delay (ID/DD), multiple congenital anomalies (MCA), epilepsy, autism s...