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Autori: Sarajlija Adrijan

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Naslov Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib (Article)
Autori Sarajlija Adrijan Djordjevic Maja S Kecman Bozica Skakic Anita Pavlovic Sonja T Pasic Srdjan S Stojiljkovic Maja M 
Info EUROPEAN JOURNAL OF MEDICAL GENETICS, (2020), vol. 63 br. 3, str. -
Projekat Ministry of Education, Science and Technological Development, Republic of Serbia [III41004]; European CommissionEuropean Commission Joint Research Centre [EU-FP7-REGPOT-316088]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea-cycle disorders: On the basis of information from a European multicenter registry (Article; Proceedings Paper)
Autori Molema Femke ... Djordjevic M Sarajlija Adrijan ... (broj koautora 68) 
Info JOURNAL OF INHERITED METABOLIC DISEASE, (2019), vol. 42 br. 6, str. 1162-1175
Projekat Metakids; Erasmus University Medical Center; European UnionEuropean Union (EU) [2010 12 01]; Kindness-for-Kids Foundation (Munich, Germany); Dietmar Hopp Foundation (St. Leon-Rot, Germany)
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Decreased plasma L-arginine levels in organic acidurias (MMA and PA) and decreased plasma branched-chain amino acid levels in urea cycle disorders as a potential cause of growth retardation: Options for treatment (Article)
Autori Molema Femke ... Djordjevic M Sarajlija Adrijan ... (broj koautora 67) 
Info MOLECULAR GENETICS AND METABOLISM, (2019), vol. 126 br. 4, str. 397-405
Projekat Metakids and Erasmus University Medical Center; European Union within the framework of the Health Programme [2010 12 01]; Kindness-for-Kids Foundation (Munich, Germany); Dietmar Hopp Foundation (St. Leon-Rot, Germany); EU
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disordersA successful strategy for clinical research of rare diseases (Article)
Autori Posset Roland ... Sarajlija Adrijan ... (broj koautora 107) 
Info JOURNAL OF INHERITED METABOLIC DISEASE, (2019), vol. 42 br. 1, str. 93-106
Projekat University of Zurich; Kettering Foundation; Kettering Fund
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype (Editorial Material)
Autori Kulikovskaja Leonora Sarajlija Adrijan Savic-Pavicevic Dusanka Lj  Dobricic Valerija S Klein Christine Westenberger Ana 
Info NEUROLOGY-GENETICS, (2018), vol. 4 br. 2, str. -
Projekat Hermann and Lilly Schilling Foundation; Land Schleswig-Holstein within the funding programme Open Access Publikationsfonds
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants (Article)
Autori Skakic Anita Djordjevic Maja S Sarajlija Adrijan Klaassen Kristel M Tosic Natasa M Kecman Bozica Ugrin Milena Spasovski Vesna M Pavlovic Sonja T Stojiljkovic Maja M 
Info CLINICAL GENETICS, (2018), vol. 93 br. 2, str. 350-355
Projekat Ministry of Education, Science and Technological Development, Republic of Serbia [III41004]; European Commission [EU-FP7-REGPOT-316088]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Appendiceal involvement in a patient with Gaucher disease (Article)
Autori Kocic Marija Djuricic Slavisa M  Djordjevic Maja S Savic Djordje Kecman Bozica Sarajlija Adrijan 
Info BLOOD CELLS MOLECULES AND DISEASES, (2018), vol. 68 br. , str. 109-111
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Novel intragenic deletions within the UBE3A gene in two unrelated patients with Angelman syndrome: case report and review of the literature (Review)
Autori Aguilera Cinthia Vinas-Jornet Marina Baena Neus Gabau Elisabeth Fernandez Concepcion Capdevila Nuria Cirkovic Sanja S Sarajlija Adrijan Miskovic Marijana Radivojevic Danijela  Ruiz Anna Guitart Miriam 
Info BMC MEDICAL GENETICS, (2017), vol. 18 br. , str. -
Projekat Fundacio Parc Tauli- Institut d'Investigacio i Innovacio Parc Tauli I3PT [CIR2015/040]; Asociacion Espanola de Sindrome de Angelman; Instituto de Salud Carlos III [PI16/01411]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Postprandial hyperinsulinemic hypoglycemia in a child as a late complication of esophageal reconstruction (Article)
Autori Vukovic Rade M  Milenkovic Tatjana Djordjevic Maja S Mitrovic Katarina Todorovic Sladjana  Sarajlija Adrijan Hussain Khalid 
Info JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, (2017), vol. 30 br. 7, str. 791-795
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Late-presenting congenital diaphragmatic hernia in a child with TMEM70 deficiency (Letter)
Autori Sarajlija Adrijan Magner Martin Djordjevic Maja S Kecman Bozica Grujic Blagoje Tesarova Marketa Minic Predrag B 
Info CONGENITAL ANOMALIES, (2017), vol. 57 br. 2, str. 64-65
Projekat [RVO-VFN64165/2012]; [PRVOUK P24/LF1/3]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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