tallózása szerző szerint "Molnar, Mária Judit"

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  • Broadening the phenotype of the TWNK gene associated Perrault syndrome 
    Fekete, Bálint András; Pentelényi, Klára; Rudas, Gábor; Gál, Anikó; Grosz, Zoltán; Illés, Anett; Jimoh, Idris János; Csukly, Gábor; Domonkos, Andor; Molnar, Mária Judit (2019)
    Perrault syndrome is a genetically heterogenous, very rare disease, characterized clinically by sensorineural hearing loss, ovarian dysfunction and neurological symptoms. We present the case of a 33 years old female patient ...
  • Systematic review on the evaluation criteria of orphan medicines in Central and Eastern European countries. 
    Zelei, Tamás; Molnar, Mária Judit; Szegedi, Márta; Kálo, Zoltán (2016)
    BACKGROUND: In case of orphan drugs applicability of the standard health technology assessment (HTA) process is limited due to scarcity of good clinical and health economic evidence. Financing these premium priced drugs ...