Mitochondrial myopathy associated with a novel 5522G>A mutation in the mitochondrial tRNA(Trp) gene
Barić, Ivo, Fumić, Ksenija, Petković Ramadža, Danijela, Sperl, Wolfgang, Zimmermann, Franz A, Muačević-Katanec, Diana, Mitrović, Zoran, Pažanin, Leo, Cvitanović Šojat, Ljerka, Kekez, Tihomir, Reiner, Zeljko, Mayr, Johannes A
Published in European journal of human genetics : EJHG (01.08.2013)
Published in European journal of human genetics : EJHG (01.08.2013)
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Mitochondrial myopathy associated with a novel 5522G>A mutation in the mitochondrial tRNATrp gene
Barić, Ivo, Fumić, Ksenija, Petković Ramadža, Danijela, Sperl, Wolfgang, Zimmermann, Franz A, Muačević-Katanec, Diana, Mitrović, Zoran, Pažanin, Leo, Cvitanović Šojat, Ljerka, Kekez, Tihomir, Reiner, Željko, Mayr, Johannes A
Published in European journal of human genetics : EJHG (12.12.2012)
Published in European journal of human genetics : EJHG (12.12.2012)
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Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency
Cederbaum, Stephen D, Koo-McCoy, Samantha, Tein, Ingrid, Hsu, Betty Y.L, Ganguly, Arupa, Vilain, Eric, Dipple, Katrina, Cvitanovic-Sojat, Ljerka, Stanley, Charles
Published in Molecular genetics and metabolism (01.11.2002)
Published in Molecular genetics and metabolism (01.11.2002)
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Novel OCTN2 mutations: no genotype-phenotype correlations: early carnitine therapy prevents cardiomyopathy
Lamhonwah, Anne-Marie, Olpin, Simon E, Pollitt, Rodney J, Vianey-Saban, Christine, Divry, Priscille, Guffon, Nathalie, Besley, Guy T N, Onizuka, Russell, De Meirleir, Linda J, Cvitanovic-Sojat, Ljerka, Baric, Ivo, Dionisi-Vici, Carlo, Fumic, Ksenija, Maradin, Miljenka, Tein, Ingrid
Published in American journal of medical genetics (15.08.2002)
Published in American journal of medical genetics (15.08.2002)
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Prospective surveillance of Croatian pregnant women on lamotrigine monotherapy--aspects of pre-pregnancy counseling and drug monitoring
Miskov, Snjezana, Gjergja-Juraski, Romana, Cvitanović-Sojat, Ljerka, Bakulić, Tomislav Ivicević, Fucić, Aleksandra, Bosnjak-Pasić, Marija, Mikula, Ivan, Demarin, Vida
Published in Acta clinica Croatica (Tisak) (01.09.2009)
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Published in Acta clinica Croatica (Tisak) (01.09.2009)
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Subacute sclerosing panencephalitis in Croatia (1994-2004)
Cavlek, Tatjana Vilibic, Sternak, Suncanica Ljubin, Kaic, Bernard, Zarkovic, Kamelija, Marina, Branka Marusic Della, Sojat, Ljerka Cvitanovic, Basnec, Anica, Galinovic, Gordana Mlinaric
Published in Acta microbiologica et immunologica Hungarica (01.03.2007)
Published in Acta microbiologica et immunologica Hungarica (01.03.2007)
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Subacute sclerosing panencephalitis--the continuing threat
Cavlek, Tatjana Vilibić, Sternak, Suncanica Ljubin, Zarković, Kamelija, Marina, Branka Marusić Della, Sojat, Ljerka Cvitanović, Basnec, Anica, Kaić, Bernard, Turković, Branko, Galinović, Gordana Mlinarić
Published in Collegium antropologicum (01.12.2006)
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Published in Collegium antropologicum (01.12.2006)
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The expertise for social rights for children and the unique expertise system for children with handicaps, developmental disabilities, rare and chronic diseases in croatia
Cvitanovic-Sojat, Ljerka, Dosen, Dubravka, Dulic, Ruzica, Gavric, Danjela, Naglic, Nada, Kosanovic, Blanka, Dominikovic Safranic, Suncica, Nevistic, Renata, Bulic, Dragica, Jelas, Zlata, Turcic, Nada, Martinac, Eos
Published in European journal of paediatric neurology (01.06.2017)
Published in European journal of paediatric neurology (01.06.2017)
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Mitochondrial myopathy associated with a novel 5522G>A mutation in the mitochondrial tRNA super(Trp) gene
Baric, Ivo, Fumic, Ksenija, Petkovic Ramadza, Danijela, Sperl, Wolfgang, Zimmermann, Franz A, Muacevic-Katanec, Diana, Mitrovic, Zoran, Pazanin, Leo, Cvitanovic Sojat, Ljerka, Kekez, Tihomir, Reiner, Zeljko, Mayr, Johannes A
Published in European journal of human genetics : EJHG (01.08.2013)
Published in European journal of human genetics : EJHG (01.08.2013)
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Age-related pattern of the antiepileptic drug utilization in active epilepsy: a population-based survey
Bielen, Ivan, Sruk, Ana, Planjar-Prvan, Miljenka, Cvitanović-Sojat, Ljerka, Kosicek, Miljenko, Bergman-Marković, Biserka, Baraba, Ranka, Butković-Soldo, Silva
Published in Collegium antropologicum (01.06.2009)
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Published in Collegium antropologicum (01.06.2009)
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Detection and characterization of measles virus strains in cases of subacute sclerosing panencephalitis in Croatia
Forčić, Dubravko, Baričević, Marijana, Zgorelec, Renata, Kružić, Vjekoslava, Kaić, Bernard, Marina, Branka Marušić Della, Šojat, Ljerka Cvitanović, Tešović, Goran, Mažuran, Renata
Published in Virus research (2004)
Published in Virus research (2004)
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14 Surveillance of Croatian pregnant women with epilepsy and effects of antiepileptic drugs exposure in their offspring
Miškov, Snježana, Juraški, Romana Gjergja, Fučić, Aleksandra, Bakuli, Tomislav Ivičević, Sojat, Ljerka Cvitanović, Vuković, Vlasta, Kes, Vanja Basic, Demarin, Vida
Published in Acta neuropsychiatrica (01.06.2009)
Published in Acta neuropsychiatrica (01.06.2009)
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The ethical framework for performing research with rare inherited neurometabolic disease patients
Giannuzzi, Viviana, Devlieger, Hugo, Margari, Lucia, Odlind, Viveca Lena, Ragab, Lamis, Bellettato, Cinzia Maria, D’Avanzo, Francesca, Lampe, Christina, Cassis, Linda, Cortès-Saladelafont, Elisenda, Cazorla, Ángels Garcia, Barić, Ivo, Cvitanović-Šojat, Ljerka, Fumić, Ksenija, Dali, Christine I, Bartoloni, Franco, Bonifazi, Fedele, Scarpa, Maurizio, Ceci, Adriana
Published in European journal of pediatrics (01.03.2017)
Published in European journal of pediatrics (01.03.2017)
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Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disorders
Cassis, Linda, Cortès-Saladelafont, Elisenda, Molero-Luis, Marta, Yubero, Delia, González, Maria Julieta, Ormazábal, Aida, Fons, Carme, Jou, Cristina, Sierra, Cristina, Castejon Ponce, Esperanza, Ramos, Federico, Armstrong, Judith, O'Callaghan, M Mar, Casado, Mercedes, Montero, Raquel, Meavilla-Olivas, Silvia, Artuch, Rafael, Barić, Ivo, Bartoloni, Franco, Bellettato, Cinzia Maria, Bonifazi, Fedele, Ceci, Adriana, Cvitanović-Šojat, Ljerka, Dali, Christine I, D'Avanzo, Francesca, Fumic, Ksenija, Giannuzzi, Viviana, Lampe, Christina, Scarpa, Maurizio, Garcia-Cazorla, Ángels
Published in Orphanet journal of rare diseases (30.12.2015)
Published in Orphanet journal of rare diseases (30.12.2015)
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Social and medical care of preschool children with epilepsy in Croatia: Population-based survey
Cvitanovic-Sojat, Ljerka, Bielen, Ivan, Sruk, Ana, Kosicek, Miljenko, Planjar-Prvan, Miljenka, Baraba, Ranka, Bergman-Markovic, Biserka, Butković-Soldo, Silva
Published in European journal of paediatric neurology (01.01.2010)
Published in European journal of paediatric neurology (01.01.2010)
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Erratum to: Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disorders
Cassis, Linda, Cortès-Saladelafont, Elisenda, Molero-Luis, Marta, Yubero, Delia, González, Maria Julieta, Ormazábal, Aida, Fons, Carme, Jou, Cristina, Sierra, Cristina, Ponce, Esperanza Castejon, Ramos, Federico, Armstrong, Judith, O'Callaghan, M Mar, Casado, Mercedes, Montero, Raquel, Meavilla-Olivas, Silvia, Artuch, Rafael, Barić, Ivo, Bartoloni, Franco, Bellettato, Cinzia Maria, Bonifazi, Fedele, Ceci, Adriana, Cvitanović-Šojat, Ljerka, Dali, Christine I, D'Avanzo, Francesca, Fumic, Ksenija, Giannuzzi, Viviana, Lampe, Christina, Scarpa, Maurizio, Garcia-Cazorla, Ángels
Published in Orphanet journal of rare diseases (03.11.2016)
Published in Orphanet journal of rare diseases (03.11.2016)
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Distinctive phenotype in a girl with Rett syndrome and a novel 25 bp deletion mutation in exon 4 (c.881_905del25, nm_004992.3) of the MECP2 gene
Katavić, Matej, Kukuruzović, Monika, Malenica, Maša, Seneca, Saša, Cvitanović Šojat, Ljerka
Published in Paediatria Croatica (30.12.2014)
Published in Paediatria Croatica (30.12.2014)
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Niemann-Pick disease type C: mutations of NPC1 gene and the course of disease
Cvitanović Šojat, Ljerka, Malenica, Maša, Kukuruzović, Monika, Žigman, Tamara, Kužnik, Kristina, Bielen, Ana
Published in Paediatria Croatica (30.12.2014)
Published in Paediatria Croatica (30.12.2014)
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Addendum to “Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency” [Mol. Genet. Metab. 77 (2002) 195–201]
Cederbaum, Stephen D., Koo-McCoy, Samantha, Tein, Ingrid, Hsu, Betty Y.L., Ganguly, Arupa, Vilain, Eric, Dipple, Katrina, Cvitanovic-Sojat, Ljerka, Stanley, Charles
Published in Molecular genetics and metabolism (01.01.2003)
Published in Molecular genetics and metabolism (01.01.2003)
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