Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Ivona Sansović"'
Autor:
Marko Bašković, Davor Ježek, Ivona Sansovic, Luca Zaninović, Ana Maria Meašić, Ana Katušić Bojanac
Publikováno v:
World Journal of Pediatric Surgery, Vol 5, Iss 4 (2022)
Objective Undescended testes (UDT) is the most common anomaly of the male genitourinary tract. The guidelines suggest that orchidopexy in congenitally UDT should be performed between 6 months and 18 months of age, while in acquired UDT, orchidopexy s
Externí odkaz:
https://doaj.org/article/a9afb19ad552409e87db1a473f1cca87
Autor:
Ljubica Boban, Ivona Sansović, Adriana Bobinec, Ana-Maria Meašić, Ingeborg Barišić, Mijana Kero
Publikováno v:
Abstracts.
Autor:
Ljubica Boban, Silvija Pušeljić, Ana-Maria Meašić, Adriana Bobinec, Ana Močić Pavić, Ivona Sansović, Ingeborg Barišić
Publikováno v:
Abstracts.
Autor:
Mirko Tomić, Adriana Bobinec, Ljubica Odak, Ana-Marija Meašić, Ingeborg Barišić, Katarina Vulin, Mijana Kero, Ivona Sansović
Publikováno v:
Abstracts.
Autor:
Maša Davidović, Leona Morožin Pohovski, Ivan Malčić, Ingeborg Barišić, Mijana Kero, Ljubica Boban, Nikolina Vidan Rogulj, Adriana Bobinec, Ivona Sansović, Ana-Maria Meašić
Publikováno v:
Abstracts.
Publikováno v:
Abstracts.
Autor:
Robert C. Wilson, Maria I. New, Tony Yuen, Ingeborg Barišić, Katarina Stingl, Vesna Kušec, Katja Dumić, Veselin Škrabić, Ivona Sansović, Zorana Grubic, Miroslav Dumić
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 165:51-56
Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency is caused by mutation in the CYP21A2 gene. The frequency and spectrum of CYP21A2 mutations and genotype-phenotype correlations among different populations are variable. Aim of this stu
Publikováno v:
Paediatria Croatica
Volume 61
Issue 2
Volume 61
Issue 2
Iako kromosom 17 pokazuje vrlo veliku genetičku nestabilnost, intersticijske delecije unutar regije 17q24 vrlo su rijetke. Bolesnici s ovom promjenom pokazuju heterogen fenotip: mikrocefaliju, tipične dismorfi čne crte, srčane grješke, intelektu
Publikováno v:
Croatian Medical Journal
Volume 58
Issue 3
Volume 58
Issue 3
Aim: To determine the diagnostic yield and criteria that could help to classify and interpret the copy number variations (CNVs) detected by chromosomal microarray (CMA) technique in patients with congenital and developmental abnormalities including d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e193354ef2d5dae35d2e36389dfdc248
https://doi.org/10.3325/cmj.2017.58.231
https://doi.org/10.3325/cmj.2017.58.231
Publikováno v:
Paediatria Croatica
Volume 61
Issue 2
Volume 61
Issue 2
Složene kromosomske preraspodjele su rijetke strukturne kromosomske aberacije koje uključuju tri ili više mjesta lomova u jednom ili više kromosoma. Ako pokazuju lokalizaciju i nedostatak homologije na mjestima lomova, najvjerojatnije su nastale