Pretraga
Rezultati
The continuously evolving phenotype of succinic semialdehyde dehydrogenase deficiency [2024]
Julia-Palacios, Natalia Alexandra; ...; Stevanovic, Galina B; ...; (broj, koautora 22)TMEM70 deficiency: long-term outcome of 48 patients (vol 38, pg 417, 2015) [2015]
Magner, Martin; ...; Stojanovic, Vesna DNavigating the rare neurotransmitter disease diagnosis: Insights from patients and health care professionals
[2023]
Badnjarevic, Ivana Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea-cycle disorders: On the basis of information from a European multicenter registry
[2019]
Molema, Femke; ...; Đorđević, Maja S. Levodopa-refractory hyperprolactinemia and pituitary findings in inherited disorders of biogenic amine metabolism
[2023]
Yılmaz Yıldız; Oya Kuseyri Hübschmann; Ayça Akgöz Karaosmanoğlu; Filippo Manti; Meryem Karaca; Ida Vanessa; ... et al; Kavečan, Ivana NOVEL MITOCHONDRIAL DNA DELETION IN PATIENT WITH DISTINCT PRESENTATION OF PEARSON SYNDROME [2010]
Kecman, Bozica; Mayr, Johannes A; Djordjevic, Maja S; Sarajlija, AdrijanTransatlantic combined and comparative data analysis of 1095 patients with urea cycle disordersA successful strategy for clinical research of rare diseases
[2019]
Posset, Roland; ...; Sarajlija, Adrijan Diagnosis of inborn errors of metabolism in Serbian children a referral centre experience [2006]
Đorđević, Maja S.; Grković, Sanja; Đurić, Milena; Janković, Borisav; Šumarac, Zorica; Kecman, B.; Stojanov, Lj.2025 Consensus Clinical Management Guidelines for Niemann-Pick Disease Type C [2026]
Hiwot, Tarekegn; ...; Kresojevic, NikolaAssessment of intellectual impairment, health-related quality of life, and behavioral phenotype in patients with neurotransmitter related disorders: Data from the iNTD registry
[2021]
Keller, Mareike; ...; Kavecan, Ivana I Filteri
Po tipu
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