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Genotype-phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder.
D'Onofrio G, Accogli A, Severino M, Caliskan H, Kokotović T, Blazekovic A, Jercic KG, Markovic S, Zigman T, Goran K, Barišić N, Duranovic V, Ban A, Borovecki F, Ramadža DP, Barić I, Fazeli W, Herkenrath P, Marini C, Vittorini R, Gowda V, Bouman A, Rocca C, Alkhawaja IA, Murtaza BN, Rehman MMU, Al Alam C, Nader G, Mancardi MM, Giacomini T, Srivastava S, Alvi JR, Tomoum H, Matricardi S, Iacomino M, Riva A, Scala M, Madia F, Pistorio A, Salpietro V, Minetti C, Rivière JB, Srour M, Efthymiou S, Maroofian R, Houlden H, Vernes SC, Zara F, Striano P, Nagy V. D'Onofrio G, et al. Among authors: duranovic v. Hum Genet. 2023 Jul;142(7):909-925. doi: 10.1007/s00439-023-02552-2. Epub 2023 May 14. Hum Genet. 2023. PMID: 37183190 Free PMC article. Review.
Hemispherotomy in an infant with hemimegalencephaly and Ohtahara syndrome.
Pavičić Klancir K, Habek D, Đuranović V, Tripalo Batoš A, Pejić Roško S, Stanojević M. Pavičić Klancir K, et al. Among authors: duranovic v. Wien Med Wochenschr. 2024 Apr;174(5-6):107-110. doi: 10.1007/s10354-023-01009-5. Epub 2023 Apr 18. Wien Med Wochenschr. 2024. PMID: 37071300 English.
Genetics of Pediatric Epilepsy: Next-Generation Sequencing in Clinical Practice.
Blazekovic A, Gotovac Jercic K, Meglaj S, Duranovic V, Prpic I, Lozic B, Malenica M, Markovic S, Lujic L, Petelin Gadze Z, Juraski RG, Barišic N, Baric I, Borovecki F. Blazekovic A, et al. Among authors: duranovic v. Genes (Basel). 2022 Aug 17;13(8):1466. doi: 10.3390/genes13081466. Genes (Basel). 2022. PMID: 36011376 Free PMC article.
18 results