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

Year Number of Results
2002 4
2003 6
2004 2
2005 5
2006 7
2007 4
2008 4
2009 7
2010 4
2011 12
2012 10
2013 12
2014 10
2015 4
2016 9
2017 5
2018 4
2019 2
2020 5
2021 5
2022 11
2023 2
2024 2

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120 results

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Page 1
Inherited defects of cobalamin metabolism.
Watkins D, Rosenblatt DS. Watkins D, et al. Among authors: rosenblatt ds. Vitam Horm. 2022;119:355-376. doi: 10.1016/bs.vh.2022.01.010. Epub 2022 Feb 21. Vitam Horm. 2022. PMID: 35337626
Mutations in Hcfc1 and Ronin result in an inborn error of cobalamin metabolism and ribosomopathy.
Chern T, Achilleos A, Tong X, Hill MC, Saltzman AB, Reineke LC, Chaudhury A, Dasgupta SK, Redhead Y, Watkins D, Neilson JR, Thiagarajan P, Green JBA, Malovannaya A, Martin JF, Rosenblatt DS, Poché RA. Chern T, et al. Among authors: rosenblatt ds. Nat Commun. 2022 Jan 10;13(1):134. doi: 10.1038/s41467-021-27759-7. Nat Commun. 2022. PMID: 35013307 Free PMC article.
Vitamin B(12) and birth defects.
Li F, Watkins D, Rosenblatt DS. Li F, et al. Among authors: rosenblatt ds. Mol Genet Metab. 2009 Sep-Oct;98(1-2):166-72. doi: 10.1016/j.ymgme.2009.06.004. Epub 2009 Jun 11. Mol Genet Metab. 2009. PMID: 19586788 Review.
A RaDiCAL gene hunt.
Pupavac M, Zawati MH, Rosenblatt DS. Pupavac M, et al. Among authors: rosenblatt ds. J Taibah Univ Med Sci. 2017 Jan 19;12(3):194-198. doi: 10.1016/j.jtumed.2016.11.007. eCollection 2017 Jun. J Taibah Univ Med Sci. 2017. PMID: 31435239 Free PMC article. Review.
120 results