Pregled bibliografske jedinice broj: 352887
Acute lymphoblastic leukemia Ph+ (T9 ; 22)following Langerhans cell histiocytosis in child with heteromorphysm on chromosom #9
Acute lymphoblastic leukemia Ph+ (T9 ; 22)following Langerhans cell histiocytosis in child with heteromorphysm on chromosom #9 // The 3rd European-American school in forensic genetics and Mayo clinic course in advanced molecular and cellular medicine
Zagreb, Hrvatska, 2003. (poster, nije recenziran, sažetak, ostalo)
CROSBI ID: 352887 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Acute lymphoblastic leukemia Ph+ (T9 ; 22)following Langerhans cell histiocytosis in child with heteromorphysm on chromosom #9
Autori
Čulić, Srđana ; Čulić, Vida ; Kuzmić-Prusac, Ivana ; Šćukanec-Špoljar, Mira
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo
Skup
The 3rd European-American school in forensic genetics and Mayo clinic course in advanced molecular and cellular medicine
Mjesto i datum
Zagreb, Hrvatska, 01.09.2003. - 05.09.2003
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
Acute lymphoblastic leukemia; Langerhans cell histiocytosis
Sažetak
Malignancy occurs with more frequency that is expected in patians with Langerhans cell histiocytosis (LCH). Histiocyte Society in 1991 established a registry to collect information on these accidents. Haupt refereed that 92 patiens were registered: 71 were children with 27 solid tumors, 21 AnLL, 17 ALL and 6 with lymphoma.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Split
Profili:
Vida Čulić
(autor)
Mira Škrinjarić-Špoljar
(autor)
Ivana Kuzmić-Prusac
(autor)
Srđana Čulić
(autor)
