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Autori: Cuturilo Goran

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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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