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Case Report: Two Families With HPDL Related Neurodegeneration.
Front Genet. 2022 Feb 9;13:780764. doi: 10.3389/fgene.2022.780764. eCollection 2022.
Front Genet. 2022.
PMID: 35222531
Free PMC article.
New-Born Screening for Spinal Muscular Atrophy: Results of a Latvian Pilot Study.
Gailite L, Sterna O, Konika M, Isakovs A, Isakova J, Micule I, Setlere S, Diriks M, Auzenbaha M.
Gailite L, et al. Among authors: diriks m.
Int J Neonatal Screen. 2022 Feb 14;8(1):15. doi: 10.3390/ijns8010015.
Int J Neonatal Screen. 2022.
PMID: 35225937
Free PMC article.
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The Beneficial Outcome of Subsequent Treatment with Anakinra during the Chronic Phase of Febrile Infection-Related Epilepsy Syndrome (FIRES): A Case Report.
Cupane TL, Strautmanis J, Setlere S, Diriks M, Auzenbaha M.
Cupane TL, et al. Among authors: diriks m.
Neurol Int. 2023 Dec 11;15(4):1489-1496. doi: 10.3390/neurolint15040097.
Neurol Int. 2023.
PMID: 38132976
Free PMC article.
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The First Registered Type 0 Spinal Muscular Atrophy Patient in Latvia: Call for Change in Prenatal Diagnostic Procedures.
Čupāne TL, Dīriks M, Tauriņa G, Korņejeva L, Gailīte L, Mālniece I, Auzenbaha M.
Čupāne TL, et al. Among authors: diriks m.
Case Rep Med. 2023 Jun 1;2023:3480298. doi: 10.1155/2023/3480298. eCollection 2023.
Case Rep Med. 2023.
PMID: 37303748
Free PMC article.
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