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Glycogen Storage Disease Type Ia: Current Management Options, Burden and Unmet Needs.
Derks TGJ, Rodriguez-Buritica DF, Ahmad A, de Boer F, Couce ML, Grünert SC, Labrune P, López Maldonado N, Fischinger Moura de Souza C, Riba-Wolman R, Rossi A, Saavedra H, Gupta RN, Valayannopoulos V, Mitchell J. Derks TGJ, et al. Among authors: ahmad a. Nutrients. 2021 Oct 27;13(11):3828. doi: 10.3390/nu13113828. Nutrients. 2021. PMID: 34836082 Free PMC article. Review.
Infantile onset Pompe disease presenting with non-immune hydrops fetalis.
Lee K, Fisher R, Quinonez SC, Ahmad A. Lee K, et al. Among authors: ahmad a. Mol Genet Metab Rep. 2019 Aug 21;21:100503. doi: 10.1016/j.ymgmr.2019.100503. eCollection 2019 Dec. Mol Genet Metab Rep. 2019. PMID: 31467850 Free PMC article. No abstract available.
Interstitial lung disease of infancy caused by a new NKX2-1 mutation.
Safi KH, Bernat JA, Keegan CE, Ahmad A, Hershenson MB, Arteta M. Safi KH, et al. Among authors: ahmad a. Clin Case Rep. 2017 Apr 4;5(6):739-743. doi: 10.1002/ccr3.901. eCollection 2017 Jun. Clin Case Rep. 2017. PMID: 28588801 Free PMC article.
6,412 results