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Page 1
Adjuvant Treatment for Phenylketonuria (PKU) [Internet].
Lindegren ML, Krishnaswami S, Fonnesbeck C, Reimschisel T, Fisher J, Jackson K, Shields T, Sathe NA, McPheeters ML. Lindegren ML, et al. Among authors: reimschisel t. Rockville (MD): Agency for Healthcare Research and Quality (US); 2012 Feb. Report No.: 12-EHC035-EF. Rockville (MD): Agency for Healthcare Research and Quality (US); 2012 Feb. Report No.: 12-EHC035-EF. PMID: 22457884 Free Books & Documents. Review.
Adjuvant Treatment for Phenylketonuria: Future Research Needs: Identification of Future Research Needs From Comparative Effectiveness Review No. 56 [Internet].
McPheeters ML, Lindegren ML, Sathe N, Reimschisel T. McPheeters ML, et al. Among authors: reimschisel t. Rockville (MD): Agency for Healthcare Research and Quality (US); 2012 Sep. Report No.: 12-EHC130-EF. Rockville (MD): Agency for Healthcare Research and Quality (US); 2012 Sep. Report No.: 12-EHC130-EF. PMID: 23678512 Free Books & Documents. Review.
You too can teach clinical reasoning!
Fleming A, Cutrer W, Reimschisel T, Gigante J. Fleming A, et al. Among authors: reimschisel t. Pediatrics. 2012 Nov;130(5):795-7. doi: 10.1542/peds.2012-2410. Epub 2012 Oct 22. Pediatrics. 2012. PMID: 23090337 No abstract available.
Heart Transplantation in Children with Mitochondrial Disease.
Weiner JG, Lambert AN, Thurm C, Hall M, Soslow JH, Reimschisel TE, Bearl DW, Dodd DA, Feingold B, Godown J. Weiner JG, et al. Among authors: reimschisel te. J Pediatr. 2020 Feb;217:46-51.e4. doi: 10.1016/j.jpeds.2019.10.016. Epub 2019 Nov 8. J Pediatr. 2020. PMID: 31711761 Free PMC article.
Clinical heterogeneity of mitochondrial NAD kinase deficiency caused by a NADK2 start loss variant.
Pomerantz DJ, Ferdinandusse S, Cogan J, Cooper DN, Reimschisel T, Robertson A, Bican A, McGregor T, Gauthier J, Millington DS, Andrae JLW, Tschannen MR, Helbling DC, Demos WM, Denis S, Wanders RJA, Newman JN, Hamid R, Phillips JA 3rd; Collaborators of UDN. Pomerantz DJ, et al. Among authors: reimschisel t. Am J Med Genet A. 2018 Mar;176(3):692-698. doi: 10.1002/ajmg.a.38602. Epub 2018 Feb 1. Am J Med Genet A. 2018. PMID: 29388319 Free PMC article. Review.
Inside the 8p23.1 duplication syndrome; eight microduplications of likely or uncertain clinical significance.
Barber JC, Rosenfeld JA, Graham JM, Kramer N, Lachlan KL, Bateman MS, Collinson MN, Stadheim BF, Turner CL, Gauthier JN, Reimschisel TE, Qureshi AM, Dabir TA, Humphreys MW, Marble M, Huang T, Beal SJ, Massiah J, Taylor EJ, Wynn SL. Barber JC, et al. Among authors: reimschisel te. Am J Med Genet A. 2015 Sep;167A(9):2052-64. doi: 10.1002/ajmg.a.37120. Epub 2015 Jun 11. Am J Med Genet A. 2015. PMID: 26097203
30 results