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Browsing by Author Milic-Rasic, Vedrana M
Showing results 1 to 11 of 11
| Issue Date | Title | Author(s) | Type | М-cat. |
|---|---|---|---|---|
| 2012 | A founder R32G mutation in GJB1 gene of Serbian CMT patients | Keckarevic-Markovic, Milica; Kecmanovic, Miljana; Keckarevic, Dusan P; Mladenovic, Jelena M; Milic-Rasic, Vedrana M; Romac, Stanka P | Conference Paper | Mp. category will be shown later |
| 2021 | Biallelic ADPRHL2 mutations in complex neuropathy affect ADP ribosylation and DNA damage response | Beijer, Danique; Agnew, Thomas; Rack, Johannes Gregor Matthias; Prokhorova, Evgeniia; Deconinck, Tine; Ceulemans, Berten; Peric, Stojan Z  ; Milic-Rasic, Vedrana M; De, Jonghe Peter; Ahel, Ivan;
Baets, Jonathan;
| Article | 21M21 |
| 2010 | Childhood Cerebral X-Linked Adrenoleukodystrophy More Than 5 Years After Hematopoietic Cell Transplantation: The First Case From Serbia and Southeastern Europe | Potic, Ana D; Rovelli, Attilio M; Uziel, Graziella; Kozic, Dusko B; Mladenovic, Jelena M; Milic-Rasic, Vedrana M | Article | 22M22 |
| 2013 | Cognitive impairment of males with Duchenne muscular dystrophy | Vojinovic, Dina; Milic-Rasic, Vedrana M | Conference Paper | Mp. category will be shown later |
| 2016 | Compound Heterozygous Mutation in SGPL1 Causes Autosomal Recessive Charcot-Marie-Tooth Disease Type 2 in a Serbian Family | Atkinson, Derek; Asselbergs, B; De, Vriendt Els; Ooms, T; Estrada-Cuzcano, A; Nikodinovic, Jelena; Milic-Rasic, Vedrana M; Jordanova, Albena | Conference Paper | Mp. category will be shown later |
| 2009 | Heterozygous missense mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy or silver syndrome | Rakocevic-Stojanovic, Vidosava M; Milic-Rasic, Vedrana M; Van, Broeckhoven C; De, Jonghe Peter; Nelis, Eva; Nikolic, Ana V; Tasic, Z; Marjanovic, Ivan V; Lavrnic, Dragana V | Conference Paper | Mp. category will be shown later |
| 2004 | Problems in prenatal diagnosis of Charcot Marie Tooth type 1 | Milic-Rasic, Vedrana M; Todorovic, Slobodanka; Brankovic-Sreckovic, Vesna | Conference Paper | Mp. category will be shown later |
| 2022 | Serum leptin levels in children and adolescents with spinal muscular atrophy types 2 and 3 | Djordjevic, Stefan A; Milic-Rasic, Vedrana M; Brankovic, Vesna; Kosac, Ana P ; Dejanovic-Djordjevic, Ivana; Bijelic, Maja; Dimkic-Tomic, Tijana J; Markovic-Denic, Ljiljana N ; Kovacevic, Smiljka; Petrovic, Hristina;
Vitorovic, S; Dobric, Z; Zdravkovic, Vera M;
| Article | 23M23 |
| 2017 | Sphingosine 1-phosphate lyase deficiency causes Charcot-Marie-Tooth neuropathy | Atkinson, Derek; Nikodinovic-Glumac, Jelena; Asselbergh, Bob; Ermanoska, Biljana; Blocquel, David; Steiner, Regula; Estrada-Cuzcano, Alejandro; Peeters, Kristien; Ooms, Tinne; De, Vriendt Els;
Yang, Xiang-Lei; Hornemann, Thorsten; Milic-Rasic, Vedrana M; Jordanova, Albena;
| Article | 21aM21a |
| 2003 | Telemedicine as a new multimedia services: Concepts and advances | Samcovic, Andreja  ; Bojkovic, Zoran S; Milic-Rasic, Vedrana M | Conference Paper | Mp. category will be shown later |
| 2004 | The recurrence risk of ischemic stroke in childhood | Brankovic-Sreckovic, Vesna; Milic-Rasic, Vedrana M; Jovic, Nebojsa J; Milic, Natasa M; Todorovic, Slobodanka | Article | 23M23 |