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Page 1
Glycogen Storage Disease Type Ia: Current Management Options, Burden and Unmet Needs.
Nutrients. 2021 Oct 27;13(11):3828. doi: 10.3390/nu13113828.
Nutrients. 2021.
PMID: 34836082
Free PMC article.
Review.
Use of pegvaliase in the management of phenylketonuria: Case series of early experience in US clinics.
Adams D, Andersson HC, Bausell H, Crivelly K, Eggerding C, Lah M, Lilienstein J, Lindstrom K, McNutt M, Ray JW, Saavedra H, Sacharow S, Starin D, Tiffany-Amaro J, Thomas J, Vucko E, Wessenberg LB, Whitehall K.
Adams D, et al. Among authors: saavedra h.
Mol Genet Metab Rep. 2021 Aug 14;28:100790. doi: 10.1016/j.ymgmr.2021.100790. eCollection 2021 Sep.
Mol Genet Metab Rep. 2021.
PMID: 34430209
Free PMC article.
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A Quality Improvement Initiative to Decrease Time to Analgesia in Patients With Sickle Cell and Vaso-Occlusive Crisis: A Population With Disparities in Treatment.
Arnold T, Coffee RL Jr, Rosenberg L, Jacob SA, Thompson S, Saavedra H, Cico SJ, Wagers B.
Arnold T, et al. Among authors: saavedra h.
Cureus. 2022 Sep 25;14(9):e29569. doi: 10.7759/cureus.29569. eCollection 2022 Sep.
Cureus. 2022.
PMID: 36312605
Free PMC article.
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The youngest pair of siblings with Mucopolysaccharidosis type IVA to receive enzyme replacement therapy to date: A case report.
Frigeni M, Rodriguez-Buritica DF, Saavedra H, Gunther KA, Hillman PR, Balaguru D, Northrup H.
Frigeni M, et al. Among authors: saavedra h.
Am J Med Genet A. 2021 Nov;185(11):3510-3516. doi: 10.1002/ajmg.a.62469. Epub 2021 Sep 2.
Am J Med Genet A. 2021.
PMID: 34472180
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Use of Simulation to Improve the Comfort of Pediatric Residents Managing Critically Ill Emergency Department Patients.
Saavedra HR, Turner JS, Cooper DD.
Saavedra HR, et al.
Pediatr Emerg Care. 2018 Sep;34(9):633-635. doi: 10.1097/PEC.0000000000001596.
Pediatr Emerg Care. 2018.
PMID: 30180098
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Gastrostomy tube-related complaints in the pediatric emergency department: identifying opportunities for improvement.
Saavedra H, Losek JD, Shanley L, Titus MO.
Saavedra H, et al.
Pediatr Emerg Care. 2009 Nov;25(11):728-32. doi: 10.1097/PEC.0b013e3181bec847.
Pediatr Emerg Care. 2009.
PMID: 19864965
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Identification of HIBCH gene mutations causing autosomal recessive Leigh syndrome: a gene involved in valine metabolism.
Soler-Alfonso C, Enns GM, Koenig MK, Saavedra H, Bonfante-Mejia E, Northrup H.
Soler-Alfonso C, et al. Among authors: saavedra h.
Pediatr Neurol. 2015 Mar;52(3):361-5. doi: 10.1016/j.pediatrneurol.2014.10.023. Epub 2014 Nov 7.
Pediatr Neurol. 2015.
PMID: 25591832
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