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

Year Number of Results
1970 2
1974 1
1982 1
1986 1
1987 1
1988 4
1989 2
1990 1
1991 4
1992 1
1993 3
1994 2
1995 1
1996 1
1999 1
2000 2
2001 1
2002 1
2003 2
2004 6
2005 2
2006 3
2007 2
2008 1
2010 4
2011 5
2012 6
2013 4
2014 5
2015 4
2016 5
2017 6
2018 3
2019 2
2020 5
2021 6
2022 8
2023 0
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98 results
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Page 1
Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision.
Boy N, Mühlhausen C, Maier EM, Heringer J, Assmann B, Burgard P, Dixon M, Fleissner S, Greenberg CR, Harting I, Hoffmann GF, Karall D, Koeller DM, Krawinkel MB, Okun JG, Opladen T, Posset R, Sahm K, Zschocke J, Kölker S; Additional individual contributors. Boy N, et al. Among authors: koeller dm. J Inherit Metab Dis. 2017 Jan;40(1):75-101. doi: 10.1007/s10545-016-9999-9. Epub 2016 Nov 16. J Inherit Metab Dis. 2017. PMID: 27853989 Review.
Oral pharmacological chaperone migalastat compared with enzyme replacement therapy in Fabry disease: 18-month results from the randomised phase III ATTRACT study.
Hughes DA, Nicholls K, Shankar SP, Sunder-Plassmann G, Koeller D, Nedd K, Vockley G, Hamazaki T, Lachmann R, Ohashi T, Olivotto I, Sakai N, Deegan P, Dimmock D, Eyskens F, Germain DP, Goker-Alpan O, Hachulla E, Jovanovic A, Lourenco CM, Narita I, Thomas M, Wilcox WR, Bichet DG, Schiffmann R, Ludington E, Viereck C, Kirk J, Yu J, Johnson F, Boudes P, Benjamin ER, Lockhart DJ, Barlow C, Skuban N, Castelli JP, Barth J, Feldt-Rasmussen U. Hughes DA, et al. Among authors: koeller d. J Med Genet. 2017 Apr;54(4):288-296. doi: 10.1136/jmedgenet-2016-104178. Epub 2016 Nov 10. J Med Genet. 2017. PMID: 27834756 Free PMC article. Clinical Trial.
Reply: To PMID 23992672.
Gessner BD, Gillingham MB, Wood T, Koeller DM. Gessner BD, et al. Among authors: koeller dm. J Pediatr. 2014 Aug;165(2):420-2. doi: 10.1016/j.jpeds.2014.04.043. Epub 2014 Jun 11. J Pediatr. 2014. PMID: 24928700 No abstract available.
Reply: To PMID 23992672.
Gessner BD, Gillingham MB, Wood T, Koeller DM. Gessner BD, et al. Among authors: koeller dm. J Pediatr. 2014 Aug;165(2):419-20. doi: 10.1016/j.jpeds.2014.04.038. Epub 2014 May 23. J Pediatr. 2014. PMID: 24862382 No abstract available.
Call for action: expanding global access to hereditary cancer genetic testing.
Bychkovsky B, Rana HQ, Ademuyiwa F, Plichta J, Anderson K, Nogueira-Rodrigues A, Santa-Maria CA, Coffman LG, Marquez C, Das A, Taghian A, Koeller DR, Sandoval RL, Park BH, Dizon DS. Bychkovsky B, et al. Among authors: koeller dr. Lancet Oncol. 2022 Sep;23(9):1124-1126. doi: 10.1016/S1470-2045(22)00378-3. Lancet Oncol. 2022. PMID: 36055301 No abstract available.
Vulvar Melanoma in association with germline MITF p.E318K variant.
Koeller DR, Schwartz A, DeSimone MS, Rana HQ, Rojas-Rudilla V, Russell-Goldman E, Laga AC, Lindeman NI, Garber JE, Ghazani AA. Koeller DR, et al. Cancer Genet. 2022 Apr;262-263:102-106. doi: 10.1016/j.cancergen.2022.02.003. Epub 2022 Feb 15. Cancer Genet. 2022. PMID: 35220194
Diagnosis and management of glutaric aciduria type I--revised recommendations.
Kölker S, Christensen E, Leonard JV, Greenberg CR, Boneh A, Burlina AB, Burlina AP, Dixon M, Duran M, García Cazorla A, Goodman SI, Koeller DM, Kyllerman M, Mühlhausen C, Müller E, Okun JG, Wilcken B, Hoffmann GF, Burgard P. Kölker S, et al. Among authors: koeller dm. J Inherit Metab Dis. 2011 Jun;34(3):677-94. doi: 10.1007/s10545-011-9289-5. Epub 2011 Mar 23. J Inherit Metab Dis. 2011. PMID: 21431622 Free PMC article. Review.
98 results