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Date Issued:  [2010 TO 2019]
Type:  Article
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Date Issued:  2010

Results 1-20 of 30 (Search time: 0.04 seconds).

PreviewTitleAuthor(s)Issue DateType
1ADHD as an executive dysfunctionZorcec, T ; Pop-Jordanova, N2010Article
2Anomalous origin of the vertebral arteryDodevski, Ace ; Lazareska, Menka ; Aliji, Vjolca; Zafirova, Biljana ; Trpkovska, Biljana 2010Article
3Autoimmune thyroiditis and diabetes mellitus type 1 after long-term gonadotropin-releasing hormone agonist treatment for central precocious puberty: evolution or coincidence?Marina Krstevska-Konstantinova ; Aleksandra Jancevska; Zoran Gucev Apr-2010Article
4Aнестезиолошки протокол при трансплантација на бубрег кај дете. Приказ на случајЏамбазовска Трајковска Вања ; Донев Љупчо; Шољакова Марија ; Николова Тодорова Зорка; Карталов Андријан ; Алексовски Елвис; Талеска Гордана; Толеска Марија; Andonovska, Biljana ; Трајковски Ѓорѓи 2010Article
5Brain oxygenation during laparoscopyKuzmanovska, Biljana ; Kartalov, Andrijan Dec-2010Article
6Chronic kidney disease bone and mineral disorder (CKD-MBD) in apolipoprotein E-deficient mice with chronic renal failureNikolov, Igor G ; Joki, Nobuhiko; Nguyen-Khoa, Thao; Ivanovski, Ognen ; Phan, Olivier; Lacour, Bernard; Drüeke, Tilman B; Massy, Ziad A; Dos Reis, Luciene Machado; Jorgetti, Vanda; Lafage-Proust, Marie-HélèneJul-2010Article
7Comparative analysis of executive functions in children with Attention Deficit Hyperactivity Disorder and Obsessive Compulsive DisorderZorcec, Tatjana 2010Article
8Detected heterozygotes during the molecular analysis of the common CYP21A2 point mutations in Macedonian patients with congenital adrenal hyperplasia and their relativesAnastasovska Violeta ; Kocova Mirjana 2010Article
9Disease progression and search for monogenic diabetes among children with new onset type 1 diabetes negative for ICA, GAD- and IA-2 AntibodiesPörksen, Sven; Laborie, Lene Bjerke; Nielsen, Lotte; Louise Max Andersen, Marie; Sandal, Tone; de Wet, Heidi; Schwarcz, Erik; Aman, Jan; Swift, Peter; Kocova, Mirjana ; Schönle, Eugen J; de Beaufort, Carine; Hougaard, Philip; Ashcroft, Frances; Molven, Anders; Knip, Mikael; Mortensen, Henrik B; Hansen, Lars; Njølstad, Pål R23-Sep-2010Article
10Distribution of killer cell immunoglobulinlike receptors in the Macedonian populationEli Djulejic; Aleksandar Petlichkovski ; Dejan Trajkov ; Slavica Hristomanova ; Derek Middleton; Mirko Spiroski Mar-2010Article
11Does hepatitis C increase the accumulation of advanced glycation end products in haemodialysis patients?Arsov, Stefan; Graaff, Reindert; Morariu, Aurora M; van Oeveren, Wim; Smit, Andries J; Bushletikj, Irena; Trajcheska, Lada ; Selim, Gjulshen ; Dzekova Vidimliski, Pavlina ; Stegmayr, Bernd; Shikole, Aleksandar ; Rakhorst, GerhardMar-2010Article
12Epidemiology of Disasters in the Republic of Macedonia and the Balkan Region: Improving Public Health PreparednessStikova, Elisaveta ; LaPorte, Ron; Linkov, FainaJun-2010Article
13Epilepsy presenting only with severe abdominal painNikolina Zdraveska ; Aco Kostovski Jul-2010Article
14Four generations in a family with neurofibromatosis 1: precocious puberty and optic nerve tumor (OPT)Gucev, Z ; Krstevska Konstantinova, M ; Tasic, V ; Jancevska, Aleksandra; Kirovski, I ; Pop Jordanova, Nada2010Article
15Genotype-phenotype correlation in CAH patients with severe CYP21A2 point mutations in the Republic of MacedoniaVioleta Anastasovska ; Mirjana Kocova Sep-2010Article
16Interagency Collaboration Topology for Counteracting Global ThreatsGalindo, Fernando; Gursky, Elin; LaPorte, Ron; Linkov, Faina; Rosddodivita, Alessandra; Shubnikov, Eugene; Stikova, Elisaveta ; Trufanov, Andrey; Vinograd, NatalyaFeb-2010Article
17Intron 2 Splice Mutation at CYP21 Gene in Patients with Congenital Adrenal Hyperplasia in the Republic of MacedoniaAnastasovska, V ; Kocova, M 1-Jan-2010Article
18Lesch-Nyhan syndrome: a novel complex mutation with severe phenotypeZ Guchev ; S Koceva; Marinaki, Anthony; Fairbanks, Lynette; I Kirovski ; V Tasic Sep-2010Article
19Neuropsychological profile of children with obsessive-compulsive disorderZorcec, T ; Pop-Jordanova N2010Article
20A p.P30L Mutation at the CYP21A2 Gene in Macedonian Patients with Nonclassical Congenital Adrenal HyperplasiaAnastasovska, V ; Kocova, E; Kocova, M 1-Jan-2010Article

Organization name
Faculty of Medicine
City
Skopje
Country
Macedonia, the Former Yugoslav Republic of