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Browsing by Author Neocleous, Vassos
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| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2021 | Audiological features in Serbian patients with hearing impairment identified with c.35delG in the GJB2 gene | Dobric, Bojana; Radivojevic, Danijela; Jecmenica, Jovana R; Neocleous, Vassos; Fanis, Pavlos; Phylactou, Leonidas A; Djurisic, Marina | Article | 23M23 |
| 2017 | Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism | Badiu, Corin; Bonomi, Marco; Borshchevsky, Ivan; Cools, Martine; Craen, Margarita; Ghervan, Cristina; Hauschild, Michael; Hershkovitz, Eli; Hrabovszky, Erik; Juul, Anders;
Kim, Soo-Hyun; Kumanov, Phillip; Lecumberri, Beatriz; Lemos, Manuel C.; Neocleous, Vassos; Niedziela, Marek; Djurdjevic, Sandra Pekic; Persani, Luca; Phan-Hug, Franziska; Pignatelli, Duarte; Pitteloud, Nelly; Popović, Vera
 ; Quinton, Richard; Skordis, Nicos; Smith, Neil; Stefanija, Magdalena Avbelj; Xu, Cheng; Young, Jacques; Dwyer, Andrew A.; | Article | 21M21 |
| 2022 | Prevalence of Variants in DFNB1 Locus in Serbian Patients with Autosomal Recessive Non-Syndromic Hearing Loss | Dobric, Bojana; Radivojevic, Danijela; Jecmenica, Jovana R; Fanis, Pavlos; Neocleous, Vassos; Phylactou, Leonidas A; Djurisic, Marina | Article | 22M22 |