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

Year Number of Results
2002 2
2004 5
2005 3
2006 4
2008 2
2009 7
2010 4
2011 4
2012 2
2013 3
2014 1
2015 3
2016 3
2017 4
2020 0
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41 results
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Page 1
Long-term hematological, visceral, and growth outcomes in children with Gaucher disease type 3 treated with imiglucerase in the International Collaborative Gaucher Group Gaucher Registry.
El-Beshlawy A, Tylki-Szymanska A, Vellodi A, Belmatoug N, Grabowski GA, Kolodny EH, Batista JL, Cox GF, Mistry PK. El-Beshlawy A, et al. Among authors: kolodny eh. Mol Genet Metab. 2017 Jan-Feb;120(1-2):47-56. doi: 10.1016/j.ymgme.2016.12.001. Epub 2016 Dec 6. Mol Genet Metab. 2017. PMID: 28040394 Free article. Clinical Trial.
The enigma of the E326K mutation in acid β-glucocerebrosidase.
Horowitz M, Pasmanik-Chor M, Ron I, Kolodny EH. Horowitz M, et al. Among authors: kolodny eh. Mol Genet Metab. 2011 Sep-Oct;104(1-2):35-8. doi: 10.1016/j.ymgme.2011.07.002. Epub 2011 Jul 12. Mol Genet Metab. 2011. PMID: 21831682 Review.
Anderson-Fabry disease: extrarenal, neurologic manifestations.
Kolodny EH, Pastores GM. Kolodny EH, et al. J Am Soc Nephrol. 2002 Jun;13 Suppl 2:S150-3. J Am Soc Nephrol. 2002. PMID: 12068029 Free article. Review. No abstract available.
Leukodystrophies: clinical and genetic aspects.
Lyon G, Fattal-Valevski A, Kolodny EH. Lyon G, et al. Among authors: kolodny eh. Top Magn Reson Imaging. 2006 Aug;17(4):219-42. doi: 10.1097/RMR.0b013e31804c99d4. Top Magn Reson Imaging. 2006. PMID: 17414998 Review.
Characterization of Strength and Function in Ambulatory Adults With GNE Myopathy.
Argov Z, Bronstein F, Esposito A, Feinsod-Meiri Y, Florence JM, Fowler E, Greenberg MB, Malkus EC, Rebibo O, Siener CS, Caraco Y, Kolodny EH, Lau HA, Pestronk A, Shieh P, Skrinar AM, Mayhew JE. Argov Z, et al. Among authors: kolodny eh. J Clin Neuromuscul Dis. 2017 Sep;19(1):19-26. doi: 10.1097/CND.0000000000000181. J Clin Neuromuscul Dis. 2017. PMID: 28827485 Free PMC article.
Enzyme replacement therapy and monitoring for children with type 1 Gaucher disease: consensus recommendations.
Charrow J, Andersson HC, Kaplan P, Kolodny EH, Mistry P, Pastores G, Prakash-Cheng A, Rosenbloom BE, Scott CR, Wappner RS, Weinreb NJ. Charrow J, et al. Among authors: kolodny eh. J Pediatr. 2004 Jan;144(1):112-20. doi: 10.1016/j.jpeds.2003.10.067. J Pediatr. 2004. PMID: 14722528 Review. No abstract available.
Roscoe Owen Brady, MD: Remembrances of co-investigators and colleagues.
Desnick RJ, Barton NW, Furbish S, Grabowski GA, Karlsson S, Kolodny EH, Medin JA, Murray GJ, Mistry PK, Patterson MC, Schiffmann R, Weinreb NJ. Desnick RJ, et al. Among authors: kolodny eh. Mol Genet Metab. 2017 Jan-Feb;120(1-2):1-7. doi: 10.1016/j.ymgme.2016.10.010. Epub 2016 Nov 12. Mol Genet Metab. 2017. PMID: 27866832
Late-onset Tay-Sachs disease.
Neudorfer O, Kolodny EH. Neudorfer O, et al. Among authors: kolodny eh. Isr Med Assoc J. 2004 Feb;6(2):107-11. Isr Med Assoc J. 2004. PMID: 14986470 Free article. No abstract available.
Transformation in pretreatment manifestations of Gaucher disease type 1 during two decades of alglucerase/imiglucerase enzyme replacement therapy in the International Collaborative Gaucher Group (ICGG) Gaucher Registry.
Mistry PK, Batista JL, Andersson HC, Balwani M, Burrow TA, Charrow J, Kaplan P, Khan A, Kishnani PS, Kolodny EH, Rosenbloom B, Scott CR, Weinreb N. Mistry PK, et al. Among authors: kolodny eh. Am J Hematol. 2017 Sep;92(9):929-939. doi: 10.1002/ajh.24801. Epub 2017 Jul 7. Am J Hematol. 2017. PMID: 28569047 Free PMC article. Clinical Trial.
Frequency of MELAS main mutation in a phenotype-targeted young ischemic stroke patient population.
Tatlisumak T, Putaala J, Innilä M, Enzinger C, Metso TM, Curtze S, von Sarnowski B, Amaral-Silva A, Jungehulsing GJ, Tanislav C, Thijs V, Rolfs A, Norrving B, Fazekas F, Suomalainen A, Kolodny EH. Tatlisumak T, et al. Among authors: kolodny eh. J Neurol. 2016 Feb;263(2):257-262. doi: 10.1007/s00415-015-7969-z. Epub 2015 Nov 14. J Neurol. 2016. PMID: 26566914
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