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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
1969 3
1970 1
1971 2
1972 2
1973 2
1974 2
1975 1
1976 2
1978 4
1979 2
1980 3
1981 2
1982 4
1983 4
1984 6
1985 5
1986 12
1987 3
1988 7
1989 3
1990 7
1991 8
1992 4
1993 1
1994 1
1995 4
1996 7
1997 2
1998 1
1999 1
2000 2
2001 4
2002 2
2006 1
2007 1
2010 1
2014 1
2018 1
2019 2
2022 1
2023 0

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PubMed (OMIM) Links for id: 5009

123 results

Results by year

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Page 1
Prenatal treatment of ornithine transcarbamylase deficiency.
Wilnai Y, Blumenfeld YJ, Cusmano K, Hintz SR, Alcorn D, Benitz WE, Berquist WE, Bernstein JA, Castillo RO, Concepcion W, Cowan TM, Cox KL, Lyell DJ, Esquivel CO, Homeyer M, Hudgins L, Hurwitz M, Palma JP, Schelley S, Akula VP, Summar ML, Enns GM. Wilnai Y, et al. Mol Genet Metab. 2018 Mar;123(3):297-300. doi: 10.1016/j.ymgme.2018.01.004. Epub 2018 Jan 16. Mol Genet Metab. 2018. PMID: 29396029
A longitudinal study of urea cycle disorders.
Batshaw ML, Tuchman M, Summar M, Seminara J; Members of the Urea Cycle Disorders Consortium. Batshaw ML, et al. Mol Genet Metab. 2014 Sep-Oct;113(1-2):127-30. doi: 10.1016/j.ymgme.2014.08.001. Epub 2014 Aug 10. Mol Genet Metab. 2014. PMID: 25135652 Free PMC article. Review.
Hyperammonaemia due to ornithine transcarbamylase deficiency.
Hopkins IJ, Connelly JF, Dawson AG, Hird FJ, Maddison TG. Hopkins IJ, et al. Arch Dis Child. 1969 Apr;44(234):143-8. doi: 10.1136/adc.44.234.143. Arch Dis Child. 1969. PMID: 21032452 Free PMC article. No abstract available.
123 results