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Autori: Badnjarevic Ivana

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Naslov Consensus Guideline for the Diagnosis and Treatment of Tyrosine Hydroxylase (TH) Deficiency (Article)
Autori Sigatullina-Bondarenko Mariya  ...  Badnjarevic Ivana  ...  Stevanovic Galina B  ...  (broj koautora 19) 
Info JOURNAL OF INHERITED METABOLIC DISEASE, (2025), vol. 48 br. 6, str. -
Projekat Fondo Europeo de Desarrollo Regional; Instituto de Salud Carlos III [PI21/00073, PI24/00469]; Lil' Brave One (Hrabrisa) [109840069, 28218303]; La Fundaci La Marat de TV3 [1026(NIFG61209706)]; SSIEM Guidelines Development Support; Chan Zuckerberg Initiative Foundation [2024-347839]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Navigating the rare neurotransmitter disease diagnosis: Insights from patients and health care professionals (Letter)
Autori Badnjarevic Ivana  Moyer Kelly  Bertoldi Mariarita  Opladen Thomas  Flint Lisa 
Info JOURNAL OF INHERITED METABOLIC DISEASE, (2024), vol. 47 br. 3, str. 413-416
Projekat We would like to express our heartfelt gratitude to all rare inherited neurotransmitter HCP and families of diagnosed individuals from around the world who contributed to this study. Participating HCP expressed a keen interest in collaborating with patient
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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