eNauka - pregled
Pregled prema Autor Ellard, Sian
Prikaz rezultata 1 do 4 od 4
| Godina | Naslov | Autor(i) | Tip rezultata | Mp-kat. |
|---|---|---|---|---|
| 2014 | A novel syndrome of early-onset type 1 diabetes and multi-organ autoimmunity caused by activating germline mutations in STAT3 | Flanagan, SE; Haapaniemi, E; Russell, MA; McDonald, TJ; Barton, J; Murphy, NP; Seppanen, M; Milenkovic, Tatjana; Heiskanen, K; Lernmark, A;
Otonkoski, T; Kere, J; Morgan, NG; Ellard, Sian; Hattersley, AT;
| Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2017 | A successful transition to sulfonylurea treatment in male infant with neonatal diabetes caused by the novel abcc8 gene mutation and three years follow-up![]() | Katanic, Dragan | Naučni članak | 22M22 - Međunarodni časopis kategorije M22 |
| 2010 | Characterization of aryl hydrocarbon receptor interacting protein (AIP) mutations in familial isolated pituitary adenoma families | Igreja, Susana; Chahal, Harvinder S.; King, Peter; Bolger, Graeme B.; Srirangalingam, Umasuthan; Guasti, Leonardo; Chapple, J. Paul; Trivellin, Giampaolo; Gueorguiev, Maria; Guegan, Katie;
Stals, Karen; Khoo, Bernard; Kumar, Ajith V.; Ellard, Sian; Grossman, Ashley B.; Korbonits, Márta;
| Naučni članak | 21aM21a - Vodeći međunarodni časopis kategorije M21a |
| 2009 | Emerijevi osnovi medicinske genetike - [prevod sa engleskog jezika trinaestog izdanja knjige] | Turnpenny, Peter D.; Ellard, Sian | Monografija | Mp kategorija će biti prikazana naknadno. |
