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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 D  ; ...; (broj, koautora 27)

Navigating the rare neurotransmitter disease diagnosis: Insights from patients and health care professionals   [2023]

Badnjarevic, Ivana  ; Moyer, Kelly; Bertoldi, Mariarita; Opladen, Thomas; Flint, Lisa

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  ; (broj, koautora 27)

NOVEL MITOCHONDRIAL DNA DELETION IN PATIENT WITH DISTINCT PRESENTATION OF PEARSON SYNDROME   [2010]

Kecman, Bozica; Mayr, Johannes A; Djordjevic, Maja S; Sarajlija, Adrijan  ; Stajic, Natasa

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, Nikola ; ...; (broj, koautora 34)

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