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Page 1
Metabolic follow-up of a Croatian patient with gyrate atrophy and a new mutation in the OAT gene: a case report.
Biochem Med (Zagreb). 2018 Oct 15;28(3):030801. doi: 10.11613/BM.2018.030801.
Biochem Med (Zagreb). 2018.
PMID: 30429681
Free PMC article.
Diagnosis and the importance of early treatment of tyrosinemia type 1: A case report.
Škaričić A, Zekušić M, Fumić K, Rogić D, Uroić V, Petković Ramadža D, Žigman T, Barić I.
Škaričić A, et al.
Clin Mass Spectrom. 2019 Feb 2;12:1-6. doi: 10.1016/j.clinms.2019.01.005. eCollection 2019 Apr.
Clin Mass Spectrom. 2019.
PMID: 34841073
Free PMC article.
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Global impact of COVID-19 on newborn screening programmes.
Koracin V, Loeber JG, Mlinaric M, Battelino T, Bonham JR, Groselj U; COVID-NBS ISNS global network.
Koracin V, et al.
BMJ Glob Health. 2022 Mar;7(3):e007780. doi: 10.1136/bmjgh-2021-007780.
BMJ Glob Health. 2022.
PMID: 35236661
Free PMC article.
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Early initiation of ambroxol treatment diminishes neurological manifestations of type 3 Gaucher disease: A long-term outcome of two siblings.
Ramadža DP, Zekušić M, Žigman T, Škaričić A, Bogdanić A, Mustać G, Bošnjak-Nađ K, Ozretić D, Ohno K, Fumić K, Barić I.
Ramadža DP, et al. Among authors: skaricic a.
Eur J Paediatr Neurol. 2021 May;32:66-72. doi: 10.1016/j.ejpn.2021.03.013. Epub 2021 Mar 31.
Eur J Paediatr Neurol. 2021.
PMID: 33836415
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