Researchers
Čuturilo, Goran
Results 21-40 of 45
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2017 | Structural, Functional, and Clinical Characterization of a Novel PTPN11 Mutation Cluster Underlying Noonan Syndrome | Pannone, Luca; Bocchinfuso, Gianfranco; Flex, Elisabetta; Rossi, Cesare; Baldassarre, Giuseppina; Lissewski, Christina; Pantaleoni, Francesca; Consoli, Federica; Lepri, Francesca; Magliozzi, Monia;
Anselmi, Massimiliano; Delle, Vigne Silvia; Sorge, Giovanni; Karaer, Kadri; Čuturilo, Goran
  ; Sartorio, Alessandro; Tinschert, Sigrid; Accadia, Maria; Digilio, Maria C.; Zampino, Giuseppe; De Luca, Alessandro; Cavé, Hélène; Zenker, Martin; Gelb, Bruce D.; Dallapiccola, Bruno; Stella, Lorenzo; Ferrero, Giovanni B.; Martinelli, Simone; Tartaglia, Marco; | Article | 21aM21a |
| 2017 | Genetic study of Achondroplasia in Serbian population | Radunović, Sara; Dobričić, Valerija ; Marjanović, Ana ; Branković, Marija ; Joksić, Ivana ; Kontić, Olivera ; Čuturilo, Goran ; Novaković, Ivana ; Kostić, Vladimir | Conference Paper | Mp. category will be shown later |
| 2017 | Articulation skills, oral praxis and cognitive maturity of children with 22q11.2 deletion syndrome and children with phenotype resembling 22q11.2 deletion sindrome but without microdeletions | Rakonjac, Marijana S. ; Čuturilo, Goran M. ; Stevanović, Milena J. ; Drakulić, Danijela D. | Conference Paper | Mp. category will be shown later |
| 2016 | Differences in speech and language abilities between children with 22q11.2 deletion syndrome and children with phenotypic features of 22q11.2 deletion syndrome but without microdeletion | Rakonjac, Marijana ; Čuturilo, Goran ; Stevanović, Milena ; Jeličić, Ljiljana ; Subotić, Miško ; Jovanović, Ida ; Drakulić, Danijela | Article | 21M21 |
| 2016 | Clients' Perception of Outcome of Team-Based Prenatal and Reproductive Genetic Counseling in Serbian Service Using the Perceived Personal Control (PPC) Questionnaire | Čuturilo, Goran ; Kontić-Vučinić, Olivera ; Novaković, Ivana ; Ignjatović, Svetlana ; Mijović, Marija; Šulović, Nenad ; Vukolić, Dušan; Komnenić, Milica ; Tadić, Jasmina; Ćetković, Aleksandar;
Belić, Aleksandra; Ljubić, Aleksandar
; | Article | 22M22 |
| 2016 | Improving the Diagnosis of Children with 22q11.2 Deletion Syndrome: A Single-center Experience from Serbia | Čuturilo, Goran ; Drakulić, Danijela ; Jovanović, Ida ; Krstić, Aleksandar ; Đukić, Milan ; Škorić, Dejan ; Mijović, Marija; Stefanović, Igor; Milivojević, Milena ; Stevanović, Milena | Article | 22M22 |
| 2016 | Phenotype analysis impacts testing strategy in patients with Currarino syndrome | Čuturilo, Goran ; Hodge, JC; Runke, CK; Thorland, EC; Al-Owain, MA; Ellison, JW; Babović-Vuksanović, D. | Article | 21M21 |
| 2016 | Speech and language abilities of children with the familial form of 22q11.2 deletion syndrome | Rakonjac, Marijana ; Čuturilo, Goran ; Stevanović, Milena ; Jovanović, Ida ; Jeličić Dobrijević, Ljiljana ; Mijović, Marija; Drakulić, Danijela | Article | 23M23 |
| 2015 | The importance of early stimulation of speech and language for children with microdeletion on chromosome 22 | Rakonjac, Marijana ; Vujović, Marina; Jeličić, Ljiljana ; Drakulić, Danijela ; Čuturilo, Goran ; Jovanović, Ida ; Stevanović, Milena | Conference Paper | Mp. category will be shown later |
| 2015 | Subtelomeric screening in Serbian children with dysmorphic features and unexplained developmental delay/intellectual disabilities | Damnjanović, Tatjana ; Čuturilo, Goran ; Maksimović, Nela ; Dimitrijević, Nikola; Jekić, Biljana ; Luković, Ljiljana ; Bunjevački, Vera ; Varljen, Tatjana; Dobričić, Valerija ; Jovanović, Ida ;
Kostić, Vladimir
; Novaković, Ivana ; | Article | 23M23 |
| 2015 | Early communication in Serbian speaking children with 22q11.2 deletion syndrome | Rakonjac, Marijana S. ; Jeličić, Ljiljana N. ; Drakulić, Danijela D. ; Čuturilo, Goran M. ; Jovanović, Ida V. ; Stevanović, Milena J. ; Vujović, M. | Conference Paper | Mp. category will be shown later |
| 2014 | Variability of speech and language problems in the children with 22q11.2 deletion syndrome | Rakonjac, Marijana ; Jeličić-Dobrijević, Ljiljana ; Drakulić, Danijela ; Čuturilo, Goran ; Jovanović, Ida ; Stevanović, Milena | Conference Paper | Mp. category will be shown later |
| 2014 | The Effect Of The Deletion 22q11.2 On Early Communication In Serbian Speaking Children: Children At Risk | Rakonjac, Marijana ; Jeličić-Dobrijević, Ljiljana ; Drakulić, Danijela D. ; Čuturilo, Goran M. ; Jovanović, Ida V. ; Stevanović, Milena J. | Conference Paper | Mp. category will be shown later |
| 2014 | Ectodermal defects and anal atresia in a child with a TP63 mutation-expanding the phenotypic spectrum | Ruml, Jelena ; Čuturilo, Goran ; Lukač, Marija ; Peters, Hartmut | Article | 22M22 |
| 2013 | Characterization of 22q11.2 region in patients with congenital heart malformations | Drakulić, Danijela ; Čuturilo, Goran ; Jovanović, Ida ; Milivojević, Milena ; Kalanj Jasna; Međo, Biljana ; Popović, Jelena ; Stanisavljević, Danijela ; Vuković, Vladanka ; Stevanović, Milena | Conference Paper | Mp. category will be shown later |
| 2013 | Potential mechanisms of speech and language problems in the 22Q11.2 deletion syndrome | Daničić, Marijana ; Čuturilo, Goran | Book parts | Mp. category will be shown later |
| 2012 | Inhaled nitric oxide therapy for acute respiratory distress syndrome in children | Medjo, Biljana; Atanasković-Marković, Marina ; Nikolić, Dimitrije ; Čuturilo, Goran ; Đukić, Slobodanka | Article | 22M22 |
| 2011 | 4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome | Čuturilo, Goran ; Menten, Björn; Krstic, Aleksandar; Drakulić, Danijela ; Jovanović, Ida ; Parezanović, Vojislav ; Stevanović, Milena | Article | 21M21 |
| 2011 | Epilepsy in a child with Wolf-Hirschhorn syndrome | Mitić, Vesna; Čuturilo, Goran ; Novaković, Ivana ; Dimitrijević, Nikola; Damnjanović, Tatjana ; Dimitrijević, Aleksandar ; Dobričić, Valerija; Kostić, Vladimir ; Radlović, Nedeljko | Article | 23M23 |
| 2011 | Subtelomeric study of the patients with developmental delay, dysmorphy and/or congenital anomalies of unexplained etiology | Maksimović, Nela S. ; Damnjanović, Tatjana M. ; Čuturilo, Goran M. ; Kostić, Vladimir S. ; V. Dobričić; T. Varljen; Jekić, Biljana B. ; Luković, Ljiljana F. ; Novaković, Ivana V. | Conference Paper | Mp. category will be shown later |