Mijelodisplastični sindrom – nove spoznaje i „stara“ morfologija (CROSBI ID 273817)
Prilog u časopisu | prethodno priopćenje | domaća recenzija
Podaci o odgovornosti
Kaić, Gordana ; Jelić Puškarić, Biljana ; Pažur, Marina ; Šunjić Stakor, Mia ; Ostojić Kolonić, Slobodanka ; Radić Krišto, Delfa ; Martinović, Marko ; Kardum-Skelin, Ika.
hrvatski
Mijelodisplastični sindrom – nove spoznaje i „stara“ morfologija
Myelodysplastic syndromes (MDS) are a heterogenous group of diseases sharing some clinical and morphological features. Their cause is unknown. Since the rapid development of molecular genetics allows an insight into underlying genetic aberrations, today it is possible to determine some pathogenetic mechanisms in MDS. In this presentation we would like to explain some of the discoveries in this area and their connection to the myelodysplastic phenotype as seen in everyday cytomorphology work
Mijelodisplastični sindrom – genetika, patologija ; eritropoeza – gnetika ; mutacije ; kromosomske aberacije ; kromosomi, humani, PAIR 5 – genetics ; kromosomske delecije ; ribosomalni proteini – genetika ; ribonukleoproteini – genetika ; RNA
nije evidentirano
engleski
Myelodysplastic syndromes – new discoveries and an “old” morphology
nije evidentirano
Myelodysplastic syndromes – genetics, pathology ; erythropoiesis – genetics ; mutation ; chromosome aberratios ; chromosomes, human, pair 5 – genetics ; chromosome deletion ; ribosomal proteins – genetics ; ribonucleoproteins – genetics ; RNA splicing factors – genetics ; phenotype
nije evidentirano
Podaci o izdanju
141 (7-8)
2019.
209-213
objavljeno
0024-3477
1849-2177
10.26800/LV-141-7-8-26
Povezanost rada
Kliničke medicinske znanosti