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Results by year

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

Year Number of Results
1962 1
1965 2
1967 1
1968 3
1969 1
1970 6
1971 2
1972 2
1973 1
1974 2
1975 1
1976 6
1977 3
1978 4
1980 8
1981 2
1982 9
1983 1
1984 5
1985 6
1986 8
1987 5
1988 5
1989 5
1990 6
1991 4
1992 3
1993 2
1994 1
1995 5
1996 8
1997 5
1998 7
1999 6
2000 6
2001 2
2002 4
2003 1
2004 6
2005 4
2006 5
2007 1
2008 3
2009 7
2010 6
2011 5
2012 2
2013 3
2014 2
2015 2
2016 3
2017 4
2020 1
2021 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

195 results

Results by year

Filters applied: . Clear all
Page 1
Niemann-Pick disease.
Kolodny EH. Kolodny EH. Curr Opin Hematol. 2000 Jan;7(1):48-52. doi: 10.1097/00062752-200001000-00009. Curr Opin Hematol. 2000. PMID: 10608504 Review.
Inborn errors of metabolism.
Kolodny EH, Cable WJ. Kolodny EH, et al. Ann Neurol. 1982 Mar;11(3):221-32. doi: 10.1002/ana.410110302. Ann Neurol. 1982. PMID: 6807191 Review.
Prenatal genetic diagnosis. I.
Milunsky A, Littlefield JW, Kanfer JN, Kolodny EH, Shih VE, Atkins L. Milunsky A, et al. Among authors: kolodny eh. N Engl J Med. 1970 Dec 17;283(25):1370-81. doi: 10.1056/NEJM197012172832505. N Engl J Med. 1970. PMID: 4921307 Review. No abstract available.
Prenatal genetic diagnosis. 3.
Milunsky A, Littlefield JW, Kanvfer JN, Kolodny EH, Shih VE, Atkins L. Milunsky A, et al. Among authors: kolodny eh. N Engl J Med. 1970 Dec 31;283(27):1498-504. doi: 10.1056/NEJM197012312832705. N Engl J Med. 1970. PMID: 4992307 Review. No abstract available.
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.
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.
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.
Molecular aspects of Gaucher disease.
Levy H, Or A, Eyal N, Wilder S, Widgerson M, Kolodny EH, Zimran A, Horowitz M. Levy H, et al. Among authors: kolodny eh. Dev Neurosci. 1991;13(4-5):352-62. doi: 10.1159/000112185. Dev Neurosci. 1991. PMID: 1817042 Review.
195 results