Autori: Cuturilo Goran
Naslov | The novel RAF1 mutation p.(Gly361Ala) located outside the kinase domain of the CR3 region in two patients with Noonan syndrome, including one with a rare brain tumor (Article) |
Autori | Harms Frederike L Alawi Malik Amor David J Tan Tiong Y Cuturilo Goran Lissewski Christina Brinkmann Julia Schanze Denny Kutsche Kerstin Zenker Martin |
Info | AMERICAN JOURNAL OF MEDICAL GENETICS PART A, (2018), vol. 176 br. 2, str. 470-476 |
Projekat | BMBF [01GM1519A, 01GM1519E]; Deutsche Forschungsgemeinschaft [KU 1240/9-1, ZE 524/10-1] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | The Impact of 22q11.2 Microdeletion on Cardiac Surgery Postoperative Outcome (Article) |
Autori | Cuturilo Goran Drakulic Danijela D Jovanovic Ida V Ilic Slobodan G Kalanj Jasna Vulicevic Irena Raus Misela V Skoric Dejan Mijovic Marija Medjo Biljana P Rsovac Snezana Stevanovic Milena J |
Info | PEDIATRIC CARDIOLOGY, (2017), vol. 38 br. 8, str. 1680-1685 |
Projekat | Ministry of Education, Science and Technological Development, Republic of Serbia [173051] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients (Article) |
Autori | Garavelli Livia ... Cuturilo Goran ... (broj koautora 58) |
Info | GENETICS IN MEDICINE, (2017), vol. 19 br. 6, str. 691-700 |
Projekat | Telethon Italy [GEP 14131, GTB12001]; National Institute of Neurological Disorders and Stroke [K08NS078054]; Associazione Italiana Mowat Wilson ONLUS (AIMW) |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Structural, Functional, and Clinical Characterization of a Novel PTPN11 Mutation Cluster Underlying Noonan Syndrome (Article) |
Autori | Pannone Luca ... Cuturilo Goran ... (broj koautora 29) |
Info | HUMAN MUTATION, (2017), vol. 38 br. 4, str. 451-459 |
Projekat | Telethon-Italy [GGP13107]; Associazione Italiana per la Ricerca sul Cancro [IG 17583]; Italian Ministry of Health [RF-2011-02349938, RC-2016]; ERA-Net for Research Programmes on Rare Diseases (NSEuroNet); Ministero dell'Istruzione, dell'Universita e della |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Improving the Diagnosis of Children with 22q11.2 Deletion Syndrome: A Single-center Experience from Serbia (Article) |
Autori | Cuturilo Goran Drakulic Danijela D Jovanovic Ida V Krstic Aleksandar Djukic Milan M Skoric Dejan Mijovic Marija Stefanovic Igor D Milivojevic Milena C Stevanovic Milena J |
Info | INDIAN PEDIATRICS, (2016), vol. 53 br. 9, str. 786-789 |
Projekat | Ministry of Education, Science and Technological Development, Republic of Serbia [173051] |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | 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 (Article) |
Autori | Rakonjac Marijana Cuturilo Goran Stevanovic Milena J Jelicic Ljiljana Subotic Misko Z Jovanovic Ida V Drakulic Danijela D |
Info | RESEARCH IN DEVELOPMENTAL DISABILITIES, (2016), vol. 55 br. , str. 322-329 |
Projekat | Ministry of Education, Science and Technological Development, Republic of Serbia [173051, 178027] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Speech and Language Abilities of Children with the Familial Form of 22q11.2 Deletion Syndrome (Article) |
Autori | Rakonjac Marijana Cuturilo Goran Stevanovic Milena J Jovanovic Ida V Jelicic-Dobrijevic Ljiljana Mijovic Marija Drakulic Danijela D |
Info | GENETIKA-BELGRADE, (2016), vol. 48 br. 1, str. 57-72 |
Projekat | Ministry of Education, Science and Technological Development, Republic of Serbia [173051, 178027] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Clients' Perception of Outcome of Team-Based Prenatal and Reproductive Genetic Counseling in Serbian Service Using the Perceived Personal Control (PPC) Questionnaire (Article) |
Autori | Cuturilo Goran Kontic-Vucinic Olivera Novakovic Ivana V Ignjatovic Svetlana D Mijovic Marija Sulovic Nenad Vukolic D Komnenic Milica Tadic Jasmina Cetkovic Aleksandar Belic Aleksandra Ljubic Aleksandar D |
Info | JOURNAL OF GENETIC COUNSELING, (2016), vol. 25 br. 1, str. 189-197 |
Projekat | Ministry of Education, Science and Technological Development, Republic of Serbia [175091] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Phenotype analysis impacts testing strategy in patients with Currarino syndrome (Article) |
Autori | Cuturilo Goran Hodge JC Runke CK Thorland EC Al-Owain MA Ellison JW Babovic-Vuksanovic D |
Info | CLINICAL GENETICS, (2016), vol. 89 br. 1, str. 109-114 |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Early communication in Serbian speaking children with 22q11.2 deletion syndrome (Meeting Abstract) |
Autori | Rakonjac Marijana Jelicic-Dobrijevic Ljiljana Drakulic Danijela D Cuturilo Goran Jovanovic Ida V Stevanovic Milena J Vujovic Marina |
Info | EUROPEAN CHILD & ADOLESCENT PSYCHIATRY, (2015), vol. 24 br. , Suppl. 1, str. S245-S246 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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