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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2005 1
2006 1
2008 4
2009 2
2010 3
2011 2
2012 7
2013 5
2014 2
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2026 0

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Page 1
Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.
Parikh S, Goldstein A, Karaa A, Koenig MK, Anselm I, Brunel-Guitton C, Christodoulou J, Cohen BH, Dimmock D, Enns GM, Falk MJ, Feigenbaum A, Frye RE, Ganesh J, Griesemer D, Haas R, Horvath R, Korson M, Kruer MC, Mancuso M, McCormack S, Raboisson MJ, Reimschisel T, Salvarinova R, Saneto RP, Scaglia F, Shoffner J, Stacpoole PW, Sue CM, Tarnopolsky M, Van Karnebeek C, Wolfe LA, Cunningham ZZ, Rahman S, Chinnery PF. Parikh S, et al. Among authors: reimschisel t. Genet Med. 2017 Dec;19(12):10.1038/gim.2017.107. doi: 10.1038/gim.2017.107. Epub 2017 Jul 27. Genet Med. 2017. PMID: 28749475 Free PMC article. Review.
Response to Newman et al.
Parikh S, Goldstein A, Karaa A, Koenig MK, Anselm I, Brunel-Guitton C, Christodoulou J, Cohen BH, Dimmock D, Enns GM, Falk MJ, Feigenbaum A, Frye RE, Ganesh J, Griesemer D, Haas R, Horvath R, Korson M, Kruer MC, Mancuso M, McCormack S, Josee Raboisson M, Reimschisel T, Salvarinova R, Saneto RP, Scaglia F, Shoffner J, Stacpoole PW, Sue CM, Tarnopolsky M, Van Karnebeek C, Wolfe LA, Zolkipli Cunningham Z, Rahman S, Chinnery PF. Parikh S, et al. Among authors: reimschisel t. Genet Med. 2017 Dec;19(12):10.1038/gim.2017.164. doi: 10.1038/gim.2017.164. Epub 2017 Oct 26. Genet Med. 2017. PMID: 29215644 Free PMC article. 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.
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.
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.
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.
American Academy of Neurology qualifications and guidelines for the physician expert witness.
Williams MA, Mackin GA, Beresford HR, Gordon J, Jacobson PL, McQuillen MP, Reimschisel TE, Taylor RM, Bernat JL, Rizzo M, Snyder RD, Sagsveen MG, Amery M, Brannon WL Jr; American Academy of Neurology. Williams MA, et al. Among authors: reimschisel te. Neurology. 2006 Jan 10;66(1):13-4. doi: 10.1212/01.wnl.0000190568.69950.11. Neurology. 2006. PMID: 16401838 No abstract available.
CNS involvement in OFD1 syndrome: a clinical, molecular, and neuroimaging study.
Del Giudice E, Macca M, Imperati F, D'Amico A, Parent P, Pasquier L, Layet V, Lyonnet S, Stamboul-Darmency V, Thauvin-Robinet C, Franco B; Oral-Facial-Digital Type I (OFD1) Collaborative Group. Del Giudice E, et al. Orphanet J Rare Dis. 2014 May 10;9:74. doi: 10.1186/1750-1172-9-74. Orphanet J Rare Dis. 2014. PMID: 24884629 Free PMC article.
30 results