Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Vlatka Mejaski Bosnjak"'
Autor:
Ivana Đaković, Ivica Kostović, Katarina Vulin, Iva Prvčić, Goran Tešović, Goran Krakar, Tomislav Gojmerac, Jadranka Sekelj Fureš, Vlatka Mejaški Bošnjak
Publikováno v:
Journal of International Medical Research, Vol 52 (2024)
Objective Congenital cytomegalovirus infection (cCMV) is a common, frequently unrecognized cause of childhood disability. The aim of the present study was to determine the symptoms that raise the suspicion of cCMV, define the neurodevelopmental outco
Externí odkaz:
https://doaj.org/article/7422bbcab720407fb8a1ea26ae10e46e
Autor:
Sunčica Martinec, Gordana Cesarec, Ana Marija Tomečak Krilić, Tomislav Radošević, Žarko Bakran, Vlatka Mejaški Bošnjak
Publikováno v:
Acta Clinica Croatica, Vol 60., Iss 2., Pp 282-289 (2021)
The aim was to study functional abilities and to create functional classification of children with cerebral palsy (CP) in Krapina-Zagorje County, based on the classification of gross and fine motor skills and associated impairments. Classification
Externí odkaz:
https://doaj.org/article/f7694c03e326479e865b01eadc591bae
Autor:
Sanja Delin, Katarina Bošnjak Nađ, Sunčica Martinec, Dunja Čokolić Petrović, Andrea Šimić Klarić, Vlatka Mejaški Bošnjak
Publikováno v:
Acta Clinica Croatica, Vol 59., Iss 2., Pp 260-269 (2020)
The aim of this population-based study was to evaluate the characteristics of cerebral palsy (CP) in relation to the predominant pattern of the Magnetic Resonance Imaging Classification System (MRI CS) that was analogously applied to the neonatal/ear
Externí odkaz:
https://doaj.org/article/00f181209eab4963a2395718c5fb284f
Autor:
Elisa Frullanti, Filomena T. Papa, Elisa Grillo, Angus Clarke, Bruria Ben-Zeev, Mercedes Pineda, Nadia Bahi-Buisson, Thierry Bienvenu, Judith Armstrong, Ana Roche Martinez, Francesca Mari, Andreea Nissenkorn, Caterina Lo Rizzo, Edvige Veneselli, Silvia Russo, Aglaia Vignoli, Giorgio Pini, Milena Djuric, Anne-Marie Bisgaard, Kirstine Ravn, Vlatka Mejaski Bosnjak, Joussef Hayek, Rajni Khajuria, Barbara Montomoli, Francesca Cogliati, Maria Pintaudi, Kinga Hadzsiev, Dana Craiu, Victoria Voinova, Aleksandra Djukic, Laurent Villard, Alessandra Renieri
Publikováno v:
International Journal of Genomics, Vol 2019 (2019)
Rett spectrum disorder is a progressive neurological disease and the most common genetic cause of intellectual disability in females. MECP2 is the major causative gene. In addition, CDKL5 and FOXG1 mutations have been reported in Rett patients, espec
Externí odkaz:
https://doaj.org/article/5503a980b8c64cb1aa57eb1f3caf31c0
Autor:
Kate, Himmelmann, Veronka, Horber, Javier, De La Cruz, Karen, Horridge, Vlatka, Mejaski-Bosnjak, Katalin, Hollody, Ingeborg, Krägeloh-Mann, K, Rostasy
Publikováno v:
Developmental medicine and child neurology. 59(1)
Aim To develop and evaluate a classification system for magnetic resonance imaging (MRI) findings of children with cerebral palsy (CP) that can be used in CP registers. Method The classification system was based on pathogenic patterns occurring in di
Autor:
Ana, Katusić, Vlatka, Mejaski-Bosnjak
Publikováno v:
Collegium antropologicum
Volume 35 supplement 1
Issue 1
Volume 35 supplement 1
Issue 1
Afferent signals from the muscle's proprioceptors play important role in the control of muscle tone and in the facilitation of movements. Peripheral afferent pathway enables the restoration of connections with supraspinal structures and so includes m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::acf6e8c0b97720d60662508bce3681cd
https://www.bib.irb.hr/510314
https://www.bib.irb.hr/510314
Publikováno v:
Acta medica Croatica : casopis Hravatske akademije medicinskih znanosti. 62(2)
The "gold standard" in the diagnosis of pediatric migraine includes personal history, clinical and neurological examination. Many important data on previous morbidity, psychosocial status and recent sickness (today's headache) can be found by using a