Main features and disease outcome of congenital myotonic dystrophy - experience from a single tertiary center

Authors: Ostojić, Slavica, Kovačević, Gordana, Meola, Giovanni, Pešović, Jovan, Savić-Pavićević, Dušanka, Brkušanin, Miloš, Kravljanac, Ružica, Perić, Marina, Martić, Jelena, Pejić, Katarina, Ristić, Snežana, Perić, Stojan

Source: In Neuromuscular Disorders July 2024 40:16-23

The genomic and clinical landscape of fetal akinesia

Authors: Pergande, Matthias, Motameny, Susanne, Özdemir, Özkan, Kreutzer, Mona, Wang, Haicui, Daimagüler, Hülya-Sevcan, Becker, Kerstin, Karakaya, Mert, Ehrhardt, Harald, Elcioglu, Nursel, Ostojic, Slavica, Chao, Cho-Ming, Kawalia, Amit, Duman, Özgür, Koy, Anne, Hahn, Andreas, Reimann, Jens, Schoner, Katharina, Schänzer, Anne, Westhoff, Jens H., Schwaibold, Eva Maria Christina, Cossee, Mireille, Imbert-Bouteille, Marion, von Pein, Harald, Haliloglu, Göknur, Topaloglu, Haluk, Altmüller, Janine, Nürnberg, Peter, Thiele, Holger, Heller, Raoul, Cirak, Sebahattin ^*

Source: In Genetics in Medicine March 2020 22(3):511-523

Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability—An Exception or a Necessity?

Authors: Ilic, Nikola, Maric, Nina, Maver, Ales, Armengol, Lluis, Kravljanac, Ruzica, Cirkovic, Jana, Krstic, Jovana, Radivojevic, Danijela, Cirkovic, Sanja, Ostojic, Slavica, Krasic, Stasa, Paripovic, Aleksandra, Vukomanovic, Vladislav, Peterlin, Borut, Maric, Gorica, Sarajlija, Adrijan

Source: Genes; Jun2024, Vol. 15 Issue 6, p789, 13p

Subject Terms: INTELLECTUAL disabilities, DEVELOPMENTAL delay, CHILDREN with developmental disabilities, CHILDREN with intellectual disabilities, ARTIFICIAL neural networks, CHILD patients, AGENESIS of corpus callosum, GENETIC counseling

Quality of life and its correlates in adolescent multiple sclerosis patients

Authors: Ostojic, Slavica, Stevanovic, Dejan, Jancic, Jasna

Source: In Multiple Sclerosis and Related Disorders November 2016 10:57-62

Ten years of experience in molecular prenatal diagnosis and carrier testing for spinal muscular atrophy among families from Serbia

Authors: Miskovic, Marijana, Lalic, Tanja, Radivojevic, Danijela, Cirkovic, Sanja, Ostojic, Slavica, Guc-Scekic, Marija

Source: In International Journal of Gynecology and Obstetrics January 2014 124(1):55-58

Chronic kidney disease in TARS2-related mitochondrial disease – A case report

Authors: Paripović, Aleksandra, Stajić, Nataša, Putnik, Jovana, Ostojić, Slavica, Alimpić, Biljana, Sarajlija, Adrijan

Source: In Global Pediatrics June 2024 8

Schinzel-Giedion syndrome: a rare cause of psychomotor delay and refractory seizures

Authors: Kovačević, Gordana, Kravljanac, Ružica, Tadić, Biljana Vučetić, Ostojić, Slavica, Ryu, Seung Woo

Source: In Global Pediatrics March 2024 7

Correction: The genomic and clinical landscape of fetal akinesia

Authors: Pergande, Matthias, Motameny, Susanne, Özdemir, Özkan, Kreutzer, Mona, Wang, Haicui, Daimagüler, Hülya-Sevcan, Becker, Kerstin, Karakaya, Mert, Ehrhardt, Harald, Elcioglu, Nursel, Ostojic, Slavica, Chao, Cho-Ming, Kawalia, Amit, Duman, Özgür, Koy, Anne, Hahn, Andreas, Reimann, Jens, Schoner, Katharina, Schänzer, Anne, Westhoff, Jens H., Schwaibold, Eva Maria Christina, Cossee, Mireille, Imbert-Bouteille, Marion, von Pein, Harald, Haliloglu, Göknur, Topaloglu, Haluk, Altmüller, Janine, Nürnberg, Peter, Thiele, Holger, Heller, Raoul, Cirak, Sebahattin

Source: In Genetics in Medicine August 2020 22(8):1426-1428

LTBP4 , SPP1 , and CD40 Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian Patients.

Authors: Kosac, Ana, Pesovic, Jovan, Radenkovic, Lana, Brkusanin, Milos, Radovanovic, Nemanja, Djurisic, Marina, Radivojevic, Danijela, Mladenovic, Jelena, Ostojic, Slavica, Kovacevic, Gordana, Kravljanac, Ruzica, Savic Pavicevic, Dusanka, Milic Rasic, Vedrana

Source: Genes; Aug2022, Vol. 13 Issue 8, p1385-N.PAG, 15p

Subject Terms: DUCHENNE muscular dystrophy, GENETIC variation, SERBS, HAPLOTYPES, CLUSTER analysis (Statistics), GENETIC mutation

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