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Treatment of severe primary IGF-1 deficiency using rhIGF-1 preparation - first three years of Polish experience.
Petriczko E, Jackowski T, Horodnicka-Józwa A, Wikiera B, Noczyńska A, Korpal-Szczyrska M, Birkholz-Walerzak D, Małecka-Tendera E, Kalina-Fraska B, Kalina M, Barg E, Beń-Skowronek I, Szewczyk L, Hilczer M, Smyczyńska J, Stawerska R, Lewiński A, Ziora K, Bossowski A, Pietrewicz E, Pyrżak B, Kędzia A, Szalecki M, Kilian A, Walczak M. Petriczko E, et al. Endokrynol Pol. 2019;70(1):20-27. doi: 10.5603/EP.a2018.0074. Epub 2018 Oct 23. Endokrynol Pol. 2019. PMID: 30351442 Free article.
IPEX Syndrome: Genetics and Treatment Options.
Ben-Skowronek I. Ben-Skowronek I. Genes (Basel). 2021 Feb 24;12(3):323. doi: 10.3390/genes12030323. Genes (Basel). 2021. PMID: 33668198 Free PMC article. Review.
Von Hippel-Lindau Syndrome.
Ben-Skowronek I, Kozaczuk S. Ben-Skowronek I, et al. Horm Res Paediatr. 2015;84(3):145-52. doi: 10.1159/000431323. Epub 2015 Aug 5. Horm Res Paediatr. 2015. PMID: 26279462 Free article. Review.
54 results