Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Silvija Pušeljić"'
Publikováno v:
Southeastern European Medical Journal, Vol 7, Iss 2, Pp 36-48 (2024)
The incidence of primary hypertension is on the rise in the pediatric population, with an approximate prevalence ranging from 3% to 5%. The most significant risk factors for the onset and development of primary hypertension are well-known, and some o
Externí odkaz:
https://doaj.org/article/c982d1fa6ac44d91822f2306b4dfb6c6
Autor:
Ivana Jurić, Silvija Pušeljić
Publikováno v:
Southeastern European Medical Journal, Vol 7, Iss 2 (2024)
Aim: To examine the incidence and etiology of neurodevelopmental outcomes in very low birth weight preterm infants, maternal and perinatal risk factors, comorbidities, and clinical presentation and compare with newborns of the same gestational age wh
Externí odkaz:
https://doaj.org/article/57a5854b34b748a5aeb640e590a6e702
Autor:
Ana Šmaguc, Danijela Petković Ramadža, Vladimir Sarnavka, Vjekoslav Krželj, Bernarda Lozić, Silvija Pušeljić, Valentina Rahelić, Nikola Mesarić, Marina Grubić, Ana Bogdanić, Anita Špehar Uroić, Tamara Žigman, Ruža Grizelj, Jurica Vuković, Duško Mardešić, Ildiko Szatmari, Isabel Rivera, Ksenija Fumić, Ivo Barić
Publikováno v:
Liječnički vjesnik, Vol 145, Iss 1-2, Pp 1-11 (2023)
The aim of our study was to describe the characteristics of patients with classical galactosemia in Croatia, with the description of patients with galactokinase deficiency and a patient who was a double heterozygote for mutations of the galactose-1-p
Externí odkaz:
https://doaj.org/article/172aeb75c94342c59411f163b00e629a
Autor:
Mateja Batnožić Varga, Mario Šestan, Jasenka Wagner, Kristina Crkvenac Gornik, Nastasia Kifer, Marijan Frković, Laura Stefinovec, Valentina Vučemilović Jurić, Danica Grgurić, Silvija Pušeljić, Marija Jelušić
Publikováno v:
Acta Clinica Croatica, Vol 62., Iss 1, Pp 25-35 (2023)
Immunoglobulin A vasculitis (IgAV) or Henoch-Schönlein purpura is the most prevalent systemic small vessel vasculitis in childhood. High mobility group box 1 protein (HMBG1) is a pleiotropic cytokine that functions as a pro-inflammatory signal, im
Externí odkaz:
https://doaj.org/article/aae97e3125aa413db66ee268c96930bd
Autor:
Nenad Koruga, Silvija Pušeljić, Marko Babić, Mario Ćuk, Andrea Cvitković Roić, Vjenceslav Vrtarić, Anamarija Soldo Koruga, Alen Rončević, Višnja Tomac, Tatjana Rotim, Tajana Turk, Domagoj Kretić, Nora Pušeljić, Rebeka Nađ, Ivana Serdarušić
Publikováno v:
Children, Vol 10, Iss 4, p 623 (2023)
Gabriele-de Vries syndrome is a rare autosomal dominant genetic disease caused by de novo pathogenic variants in the Yin Yang 1 (YY1) gene. Individuals with this syndrome present with multiple congenital anomalies, as well as a delay in development a
Externí odkaz:
https://doaj.org/article/16f492541cda4a989f88f97b2dabf2cb
Publikováno v:
Southeastern European Medical Journal, Vol 4, Iss 2, Pp 69-76 (2020)
Aim: The objectives of this study are to evaluate the incidence of headache considering the type of headache, to define the types of headaches, to determine the difference in the status of diagnostic scanning in children with headaches, to establish
Externí odkaz:
https://doaj.org/article/6fb88d7f4f4f496fa20b68fdc9909b05
Publikováno v:
Southeastern European Medical Journal, Vol 4, Iss 2, Pp 88-96 (2020)
Aim: In this case-control study we wanted to compare the perinatal outcome of naturally conceived newborns to those born after in vitro fertilization (IVF). Methods: At the University Hospital Centre Osijek, in the period from January 2014 to Dece
Externí odkaz:
https://doaj.org/article/bcccd13534ee45ef87e23f6d78e19c6f
Publikováno v:
Southeastern European Medical Journal, Vol 4, Iss 1, Pp 87-95 (2020)
Introduction: Numerical and structural chromosomal aberrations are some of the most common causes of intellectual disability/mental retardation (ID/MR), especially syndromic, and they represent about 10% of ID/MR that can be detected using cytogeneti
Externí odkaz:
https://doaj.org/article/be1e57cfcb8c4747aff170a2e1fb2f2a
Autor:
Nenad Koruga, Silvija Pušeljić, Višnja Tomac, Anamarija Soldo Koruga, Igor Marjanac, Borna Biljan, Krešimir Šantić, Ivana Lenz, Nora Pušeljić
Publikováno v:
Children, Vol 9, Iss 4, p 532 (2022)
Introduction: Saul Wilson syndrome (SWS) is a rare congenital syndrome characterized by a variety of symptoms, mostly skeletal changes. Saul and Wilson were the first to describe children with extremely short stature and craniofacial dysmorphism. Cas
Externí odkaz:
https://doaj.org/article/3b284ad419e44438a654848f3850f4ae
Publikováno v:
Southeastern European Medical Journal, Vol 1, Iss 1, Pp 144-153 (2017)
Intellectual disability/mental retardation (ID/MR) is defined as incomplete mental and cognitive development present from childhood. There are number of pre-natal and post-natal risk factors that can cause ID/MR, but about 50% of all causes are genet
Externí odkaz:
https://doaj.org/article/b5d09dc2bf94463db51b30c330869c0a