Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

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

Year Number of Results
1973 1
1977 2
1978 2
1979 2
1980 1
1981 2
1982 2
1983 4
1984 2
1985 5
1986 4
1987 6
1988 4
1989 4
1990 6
1991 6
1992 11
1993 3
1994 12
1995 3
1996 8
1997 10
1998 5
1999 8
2000 6
2001 4
2002 4
2003 6
2004 2
2005 5
2006 9
2007 5
2008 5
2009 7
2010 4
2011 13
2012 11
2013 13
2014 11
2015 5
2016 9
2017 5
2018 4
2019 2
2020 6
2021 5
2022 11
2023 2
2024 3
2025 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

251 results

Results by year

Filters applied: . Clear all
Page 1
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.
Lerner-Ellis JP, Tirone JC, Pawelek PD, Doré C, Atkinson JL, Watkins D, Morel CF, Fujiwara TM, Moras E, Hosack AR, Dunbar GV, Antonicka H, Forgetta V, Dobson CM, Leclerc D, Gravel RA, Shoubridge EA, Coulton JW, Lepage P, Rommens JM, Morgan K, Rosenblatt DS. Lerner-Ellis JP, et al. Among authors: rosenblatt ds. Nat Genet. 2006 Jan;38(1):93-100. doi: 10.1038/ng1683. Epub 2005 Nov 27. Nat Genet. 2006. PMID: 16311595
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.
Methylenetetrahydrofolate reductase.
Rosenblatt DS. Rosenblatt DS. Clin Invest Med. 2001 Feb;24(1):56-9. Clin Invest Med. 2001. PMID: 11266034 Review. No abstract available.
Vitamin B12 (Cbl)-responsive disorders.
Rosenblatt DS. Rosenblatt DS. J Nutr Sci Vitaminol (Tokyo). 1992;Spec No:593-6. doi: 10.3177/jnsv.38.special_593. J Nutr Sci Vitaminol (Tokyo). 1992. PMID: 1297820 Review. No abstract available.
Inherited defects of vitamin B12 metabolism.
Cooper BA, Rosenblatt DS. Cooper BA, et al. Among authors: rosenblatt ds. Annu Rev Nutr. 1987;7:291-320. doi: 10.1146/annurev.nu.07.070187.001451. Annu Rev Nutr. 1987. PMID: 3300737 Review. No abstract available.
Inherited disorders of vitamin B12 metabolism.
Rosenblatt DS, Cooper BA. Rosenblatt DS, et al. Blood Rev. 1987 Sep;1(3):177-82. doi: 10.1016/0268-960x(87)90033-6. Blood Rev. 1987. PMID: 3332101 Review.
251 results