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Comprehensive Iranian guidelines for the diagnosis and management of maple syrup urine disease: an evidence- and consensus- based approach.
Orphanet J Rare Dis. 2025 Jan 7;20(1):8. doi: 10.1186/s13023-025-03533-6.
Orphanet J Rare Dis. 2025.
PMID: 39773751
Free PMC article.
Review.
Meglitinide (repaglinide) therapy in permanent neonatal diabetes mellitus: two case reports.
Razzaghy-Azar M, Nourbakhsh M, Talea A, Mohammad Amoli M, Nourbakhsh M, Larijani B.
Razzaghy-Azar M, et al. Among authors: talea a.
J Med Case Rep. 2021 Oct 25;15(1):535. doi: 10.1186/s13256-021-03052-5.
J Med Case Rep. 2021.
PMID: 34696808
Free PMC article.
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Identification of a novel nonsense mutation and a missense substitution in the AGPAT2 gene causing congenital generalized lipodystrophy type 1.
Haghighi A, Razzaghy-Azar M, Talea A, Sadeghian M, Ellard S, Haghighi A.
Haghighi A, et al. Among authors: talea a.
Eur J Med Genet. 2012 Nov;55(11):620-4. doi: 10.1016/j.ejmg.2012.07.011. Epub 2012 Aug 1.
Eur J Med Genet. 2012.
PMID: 22902344
Free PMC article.
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