Search Results - "Mejaski Bosnjak, Vlatka"

Visual impairment in children with cerebral palsy: Croatian population-based study for birth years 2003-2008 by Striber, Neda, Vulin, Katarina, Đaković, Ivana, Prvčić, Iva, Đuranović, Vlasta, Cerovski, Branimir, Pejić Roško, Sanja, Čokolić Petrović, Dunja, Martinec, Sunčica, Dawidowsky, Barbara, Mejaški Bošnjak, Vlatka

“…To evaluate visual impairment (VI) in children with cerebral palsy (CP). This population-based study included 419 children from the Surveillance of Cerebral…”
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S-Adenosylhomocysteine Hydrolase Deficiency in a Human: A Genetic Disorder of Methionine Metabolism by Barić, Ivo, Fumić, Ksenija, Glenn, Byron, Ćuk, Mario, Schulze, Andreas, Finkelstein, James D., James, S. Jill, Mejas̆ki-Bos̆njak, Vlatka, Paz̆anin, Leo, Pogribny, Igor P., Rados̆, Marko, Sarnavka, Vladimir, Sćukanec-Spoljar, Mira, Allen, Robert H., Stabler, Sally, Uzelac, Lidija, Vugrek, Oliver, Wagner, Conrad, Zeisel, Steven, Mudd, S. Harvey, Cantoni, Giulio L.

“…We report studies of a Croatian boy, a proven case of human S-adenosylhomocysteine (AdoHcy) hydrolase deficiency. Psychomotor development was slow until his…”
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Rett networked database: An integrated clinical and genetic network of rett syndrome databases by Grillo, Elisa, Villard, Laurent, Clarke, Angus, Ben Zeev, Bruria, Pineda, Mercedes, Bahi-Buisson, Nadia, Hryniewiecka-Jaworska, Anna, Bienvenu, Thierry, Armstrong, Judith, Roche-Martínez, Ana, Mari, Francesca, Veneselli, Edvige, Russo, Silvia, Vignoli, Aglaia, Pini, Giorgio, Djuric, Milena, Bisgaard, Anne-Marie, Mejaški Bošnjak, Vlatka, Polgár, Noémi, Cogliati, Francesca, Ravn, Kirstine, Pintaudi, Maria, Melegh, Béla, Craiu, Dana, Djukic, Aleksandra, Renieri, Alessandra

“…Rett syndrome (RTT) is a neurodevelopmental disorder with one principal phenotype and several distinct, atypical variants (Zappella, early seizure onset and…”
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Language development in preschool children born after asymmetrical intrauterine growth retardation by Simic Klaric, Andrea, Kolundzic, Zdravko, Galic, Slavka, Mejaski Bosnjak, Vlatka

“…Abstract Background After intrauterine growth retardation, many minor neurodevelopmental disorders may occur, especially in the motor skills domain, language…”
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Multiple presence of prothrombotic risk factors in Croatian children with arterial ischemic stroke and transient ischemic attack by Leniček Krleža, Jasna, Ðuranović, Vlasta, Bronić, Ana, Coen Herak, Desiree, Mejaški-Bošnjak, Vlatka, Zadro, Renata

“…To determine the frequency of inherited and acquired prothrombotic risk factors in children with arterial ischemic stroke (AIS) and transient ischemic attacks…”
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MRI classification system (MRICS) for children with cerebral palsy: development, reliability, and recommendations by Himmelmann, Kate, Horber, Veronka, De La Cruz, Javier, Horridge, Karen, Mejaski‐Bosnjak, Vlatka, Hollody, Katalin, Krägeloh‐Mann, Ingeborg, Cans, C, Bakel, Van, Arnaud, C, Delobel, M, Chalmers, J, McManus, V, Lyons, A, Parkes, J, Dolk, H, Pahlman, M, Dowding, V, Colver, A, Pennington, L, Kurinczuk, J, Surman, G, Platt, MJ, Udall, P, Rackauskaite, G, Torrioli, MG, Marcelli, M, Andersen, G, Julsen Hollung, S, Bottos, M, Gaffney, G, Gaffney, G, Pallas, C, Jekovec‐Vrhovšek, M, Virella, D, Andrada, M, Greitane, A, Sigurdardottir, S, Einarsson, I, Honold, M, Rostasy, K

“…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…”
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Megalencephalic leukoencephalopathy with subcortical cysts: Characterization of disease variants by Hamilton, Eline M.C, Tekturk, Pinar, Cialdella, Fia, van Rappard, Diane F, Wolf, Nicole I, Yalcinkaya, Cengiz, Çetinçelik, Ümran, Rajaee, Ahmad, Kariminejad, Ariana, Paprocka, Justyna, Yapici, Zuhal, Bošnjak, Vlatka Mejaški, van der Knaap, Marjo S

“…OBJECTIVETo provide an overview of clinical and MRI characteristics of the different variants of the leukodystrophy megalencephalic leukoencephalopathy with…”
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L-2-Hydroxyglutaric aciduria: pattern of MR imaging abnormalities in 56 patients by Steenweg, Marjan E, Salomons, Gajja S, Yapici, Zuhal, Uziel, Graziella, Scalais, Emmanuel, Zafeiriou, Dimitrios I, Ruiz-Falco, Maria L, Mejaski-Bosnjak, Vlatka, Augoustides-Savvopoulou, Persephone, Wajner, Moacir, Walter, John, Verhoeven-Duif, Nanda M, Struys, Eduard A, Jakobs, Cornelis, van der Knaap, Marjo S

“…To describe the pattern of magnetic resonance (MR) imaging abnormalities in l-2-hydroxyglutaric aciduria (L2HGA) and to evaluate the correlation between…”
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The characteristics of transcranial color-coded duplex sonography in children with cerebral arteriovenous malformation presenting with headache by Duranovic, Vlasta, Vulin, Katarina, Dakovic, Ivana, Lenicek Krleza, Jasna, Delin, Sanja, Galinovic, Ivana, Marjanovic, Josip, Tripalo Batos, Ana, Plesa Premilovac, Zdenka, Mejaski Bosnjak, Vlatka

“…Purpose Cerebral arteriovenous malformations (AVM) are uncommon lesions. They are most often presented in childhood as intracranial hemorrhage. The aim of this…”
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Neuropsychological Development in Preschool Children Born With Asymmetrical Intrauterine Growth Restriction and Impact of Postnatal Head Growth by Klaric, Andrea Simić, Galić, Slavka, Kolundzić, Zdravko, Bosnjak, Vlatka Mejaski

“…Neuropsychological development and the impact of postnatal head growth were studied in preschool children with asymmetrical intrauterine growth restriction…”
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overview of L-2-hydroxyglutarate dehydrogenase gene (L2HGDH) variants: a genotype-phenotype study by Steenweg, Marjan E, Jakobs, Cornelis, Errami, Abdellatif, van Dooren, Silvy J.M, Adeva Bartolomé, Maria T, Aerssens, Peter, Augoustides-Savvapoulou, Persephone, Baric, Ivo, Baumann, Matthias, Bonafé, Luisa, Chabrol, Brigitte, Clarke, Joe T.R, Clayton, Peter, Coker, Mahmut, Cooper, Sarah, Falik-Zaccai, Tzipora, Gorman, Mark, Hahn, Andreas, Hasanoglu, Alev, King, Mary D, de Klerk, Hans B.C, Korman, Stanley H, Lee, Céline, Meldgaard Lund, Allan, Mejaški-Bošnjak, Vlatka, Pascual-Castroviejo, Ignacio, Raadhyaksha, Aparna, Rootwelt, Terje, Roubertie, Agathe, Ruiz-Falco, Maria L, Scalais, Emmanuel, Schimmel, Ulf, Seijo-Martinez, Manuel, Suri, Mohnish, Sykut-Cegielska, Jolanta, Trefz, Friedrich K, Uziel, Graziella, Valayannopoulos, Vassili, Vianey-Saban, Christine, Vlaho, Stefan, Vodopiutz, Julia, Wajner, Moacir, Walter, John, Walter-Derbort, Claudia, Yapici, Zuhal, Zafeiriou, Dimitrios I, Spreeuwenberg, Marieke D, Celli, Jacopo, den Dunnen, Johan T, van der Knaap, Marjo S, Salomons, Gajja S

“…L-2-Hydroxyglutaric aciduria (L2HGA) is a rare, neurometabolic disorder with an autosomal recessive mode of inheritance. Affected individuals only have…”
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Functional vision in children with perinatal brain damage by Alimovi, Sonja, Juri, Nikolina, Bošnjak, Vlatka Mejaški

“…Abstract Many authors have discussed the effects of visual stimulations on visual functions, but there is no research about the effects on using vision in…”
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Analysis of the Phenotypes in the Rett Networked Database by Frullanti, Elisa, Papa, Filomena T., Grillo, Elisa, Clarke, Angus, Ben-Zeev, Bruria, Pineda, Mercedes, Bahi-Buisson, Nadia, Bienvenu, Thierry, Armstrong, Judith, Roche Martinez, Ana, Mari, Francesca, Nissenkorn, Andreea, Lo Rizzo, Caterina, Veneselli, Edvige, Russo, Silvia, Vignoli, Aglaia, Pini, Giorgio, Djuric, Milena, Bisgaard, Anne-Marie, Ravn, Kirstine, Bosnjak, Vlatka Mejaski, Hayek, Joussef, Khajuria, Rajni, Montomoli, Barbara, Cogliati, Francesca, Pintaudi, Maria, Hadzsiev, Kinga, Craiu, Dana, Voinova, Victoria, Djukic, Aleksandra, Villard, Laurent, Renieri, Alessandra

“…Rett spectrum disorder is a progressive neurological disease and the most common genetic cause of intellectual disability in females. MECP2 is the major…”
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MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement by Brancati, Francesco, Iannicelli, Miriam, Travaglini, Lorena, Mazzotta, Annalisa, Bertini, Enrico, Boltshauser, Eugen, D'Arrigo, Stefano, Emma, Francesco, Fazzi, Elisa, Gallizzi, Romina, Gentile, Mattia, Loncarevic, Damir, Mejaski-Bosnjak, Vlatka, Pantaleoni, Chiara, Rigoli, Luciana, Salpietro, Carmelo D, Signorini, Sabrina, Stringini, Gilda Rita, Verloes, Alain, Zabloka, Dominika, Dallapiccola, Bruno, Gleeson, Joseph G, Valente, Enza Maria

“…The acronym COACH defines an autosomal recessive condition of Cerebellar vermis hypo/aplasia, Oligophrenia, congenital Ataxia, Coloboma and Hepatic fibrosis…”
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Visual stimulations' critical period in infants with perinatal brain damage by Alimović, Sonja, Katušić, Ana, Mejaški-Bošnjak, Vlatka

“…Children with perinatal brain damage have a high prevalence of visual impairment. Stimulation of vision at a critical period can encourage brain plasticity and…”
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Megalencephalic leukoencephalopathy with subcortical cysts: an update and extended mutation analysis of MLC1 by Ilja Boor, P. K., Groot, Koen de, Mejaski-Bosnjak, Vlatka, Brenner, Christiana, van der Knaap, Marjo S., Scheper, Gert C., Pronk, Jan C.

“…Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is an autosomal recessive cerebral white matter disorder in children. This disease is…”
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Are important predictors of adverse outcome in children with symptomatic congenital cytomegalovirus infection overlooked in clinical settings? by Đaković, Ivana, Kostović, Ivica, Vulin, Katarina, Prvčić, Iva, Tešović, Goran, Krakar, Goran, Gojmerac, Tomislav, Sekelj Fureš, Jadranka, Mejaški Bošnjak, Vlatka

“…Objective Congenital cytomegalovirus infection (cCMV) is a common, frequently unrecognized cause of childhood disability. The aim of the present study was to…”
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Functional Classification of Children with Cerebral Palsy in Krapina-Zagorje County by Martinec, Sunčica

“…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…”
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Prognostic value of cranial ultrasonography in comparison with magnetic resonance imaging in children with cerebral palsy: a population-based study by Delin, Sanja, Bošnjak Nađ, Katarina, Martinec, Sunčica, Čokolić Petrović, Dunja, Šimic Klarić, Andrea, Mejaški Bošnjak, Vlatka

“…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…”
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Evolutive Leukoencephalopathy in Congenital Cytomegalovirus Infection by Krakar, Goran, Đaković, Ivana, Delin, Sanja, Bošnjak, Vlatka Mejaški

“…Congenital cytomegalovirus infection is the most common infectious cause of congenital brain injury. Type and severity of congenital cytomegalovirus…”
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