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Autori: Sarajlija Adrijan

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Naslov Acute disseminated encephalomyelitis in children and adolescents-20-year single-center experience in Serbia (Article)
Autori Ostojic Slavica B  Kravljanac Ruzica M  Kovacevic Gordana S  Vucetic-Tadic Biljana  Gazikalovic Slobodan  Sarajlija Adrijan 
Info SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, (2022), vol. 150 br. 9-10, str. 544-550
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Acute disseminated encephalomyelitis in children and adolescents-20-year single-center experience in Serbia (Article)
Autori Ostojic Slavica B  Kravljanac Ruzica M  Kovacevic Gordana S  Vucetic-Tadic Biljana  Gazikalovic Slobodan  Sarajlija Adrijan 
Info SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, (2022), vol. 150 br. 9-10, str. 544-550
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov A Novel Variant in the LIPA Gene Associated with Distinct Phenotype (Article)
Autori Sarajlija Adrijan  Armengol L  Maver Ales  Kitic Ivana  Prokic Dragan  Cehic Maja  Djuricic MS  Peterlin Borut 
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2022), vol. 25 br. 1, str. 93-99
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Ambiguous Genitalia and Lissencephaly in a 46,xy Neonate with a Novel Variant of Aristaless Gene (Article)
Autori Basa Mihail I  Vukovic Rade M  Sarajlija Adrijan  Milenkovic Tatjana  Djordjevic M  Vucetic Biljana  Martic Jelena M 
Info ACTA ENDOCRINOLOGICA-BUCHAREST, (2021), vol. 17 br. 3, str. -
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Clinical and genetic characteristics of patients with congenital hyperinsulinism in 21 non-consanguineous families from Serbia (Article)
Autori Raicevic Maja  Milenkovic Tatjana  Hussain Khalid  Djordjevic Maja S  Martic Jelena M  Todorovic Sladjana  Mitrovic Katarina  Sarajlija Adrijan  Vukovic Rade M 
Info EUROPEAN JOURNAL OF PEDIATRICS, (2021), vol. 180 br. 9, str. 2815-2821
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 G  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 Commission Joint Research Centre [EU-FP7-REGPOT-316088]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 Maja S  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 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   Citati: ISI/Web of Science   Scopus  
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 Maja S  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   Scopus  
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   Scopus  
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