Pregled po CROSBI profilu: Giorgie Petković (CROSBI Profil: 23294, MBZ: 274155)
Pronađeno 57 radova
-
51.Barišić, Ingeborg; Huzjak, Nevenka; Petković, Giorgie; Tokić, Višnja; Fumić, Ksenija; Mrsić, MirandoEnzyme replacement therapy in two patients with mucopolysaccharidosis type I. // Book of Abstracts of the SSIEM 41st Annual Symposium ; u: Journal of Inherited Metabolic Disease. Supplement 27 (2004) (S1)
Amsterdam, Nizozemska, 2004. str. 177-177 (poster, međunarodna recenzija, sažetak, stručni) -
52.Barišić, Ingeborg; Tokić, Višnja; Petković, Giorgie; Fumić, KsenijaA child with generalised hypotonia: and unusual variant of GM1 gangliosidosis // Abstracts. 8th International Symposium on Mucopolysaccharide and Related Diseases. New therapeutic strategies - what can we hopefully expect?
Mainz, 2004. str. 32-33 (poster, sažetak, stručni) -
53.Nakić, Melita; Konja, Josip; Petković, GiorgieCytogenetic characteristics of childhood lymphoma // Journal of Pediatric Hematology/Oncology
Sjedinjene Američke Države, 2003. (poster, međunarodna recenzija, sažetak, znanstveni) -
54.Nakić, Melita; Konja, Josip; Petković, GiorgieClonal chromosomal aberrations in different age group of children with acute leukemia // Medical & Pediatric Oncology
Kairo, Egipat, 2003. (poster, međunarodna recenzija, sažetak, znanstveni) -
55.Barišić, Ingeborg; Petković, GiorgieSensorineural deafness, dysmorphic face, omphalocele, hypoplasia of the corpus callosum, seizures and developmental delay: a new syndrome? // The Third European-American School in Forensic Genetics and Mayo Clinic Course in Advanced Molecular and Cellular Medicine / Primorac D. ur. (ur.).
Zagreb: -, 2003. (poster, međunarodna recenzija, sažetak, stručni) -
56.Barišić, Ingeborg; Petković, Giorgie; Petković, IskraParcijalna 8p duplikacija - korelacija kliničkog očitovanja i rezultata analize molekulske citogenetike // Paediatria Croatica, 47 (2003), Suppl 2. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
-
57.Petković, Giorgie; Barišić, IngeborgAn apparently new syndrome of sensorineural deafness, distinctive facial features, exomphalos, hypoplasia of the corpus callosum, seizures and mental retardation // Book of Abstracts of the European Human Genetics Conference ; u: European Journal of Human Genetics. Supplement 11 (2003) (S1)
Birmingham, Ujedinjeno Kraljevstvo, 2003. str. 93-93 (poster, međunarodna recenzija, sažetak, znanstveni)
