The clinical phenotype and genetic diagnosis of a rare cutis laxa syndrome in a newborn with multiple anomalies von Lenhartová, Nina, Kršiaková, Jana, Maťašová, Katarína, Zibolen, Mirko

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Gastrointestinal symptomatology of familial Mediterranean fever – is this a problem also in Central Europe? von Havlíčeková, Zuzana, Jeseňák, Miloš, Mišovicová, Nadežda, Kršiaková, Jana, Jakušová, Ľubica, Bánovčin, Peter

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To the 10th year of the Student (intermedia) conference von Jana Kršiaková

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K 10 ročníku Studentské intermediální konference von Kršiaková, Jana

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Pulmonary artery sling – A novel cardiovascular finding in a patient with distal 18q deletion von Jurko, Tomas, Jurko, Alexander, Jurko, Alexander, Krsiakova, Jana, Minarik, Milan, Mestanik, Michal, Tonhajzerova, Ingrid

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Prenatal diagnosis of cardiac rhabdomyoma associated with tuberous sclerosis: report of 3 cases von Jurko, Tomas, Jurko, Jr, Alexander, Krsiakova, Jana, Jurko, Alexander, Minarik, Milan, Matasova, Katarina, Zibolen, Mirko

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Congenital contractural arachnodactyly (Beals-Hecht syndrome): a rare connective tissue disorder von Jurko, Alexander, Krsiakova, Jana, Minarik, Milan, Tonhajzerova, Ingrid

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