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

Year Number of Results
1963 1
1978 1
1980 1
1986 1
1987 2
1989 1
1993 1
2006 1
2018 3
2019 2
2020 4
2021 2
2022 2
2023 2
2024 0

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21 results

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Page 1
Maple Syrup Urine Disease.
Strauss KA, Puffenberger EG, Carson VJ. Strauss KA, et al. Among authors: carson vj. 2006 Jan 30 [updated 2020 Apr 23]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2006 Jan 30 [updated 2020 Apr 23]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301495 Free Books & Documents. Review.
Branched-chain α-ketoacid dehydrogenase deficiency (maple syrup urine disease): Treatment, biomarkers, and outcomes.
Strauss KA, Carson VJ, Soltys K, Young ME, Bowser LE, Puffenberger EG, Brigatti KW, Williams KB, Robinson DL, Hendrickson C, Beiler K, Taylor CM, Haas-Givler B, Chopko S, Hailey J, Muelly ER, Shellmer DA, Radcliff Z, Rodrigues A, Loeven K, Heaps AD, Mazariegos GV, Morton DH. Strauss KA, et al. Among authors: carson vj. Mol Genet Metab. 2020 Mar;129(3):193-206. doi: 10.1016/j.ymgme.2020.01.006. Epub 2020 Jan 16. Mol Genet Metab. 2020. PMID: 31980395 Free article.
Hypotonia and Failure to Thrive in an 8-month-old Infant.
Muthusami S, Hatchman L, Carson VJ. Muthusami S, et al. Among authors: carson vj. Pediatr Rev. 2023 Nov 1;44(11):644-649. doi: 10.1542/pir.2021-005040. Pediatr Rev. 2023. PMID: 37907420 No abstract available.
TNNT1 nemaline myopathy: natural history and therapeutic frontier.
Fox MD, Carson VJ, Feng HZ, Lawlor MW, Gray JT, Brigatti KW, Jin JP, Strauss KA. Fox MD, et al. Among authors: carson vj. Hum Mol Genet. 2018 Sep 15;27(18):3272-3282. doi: 10.1093/hmg/ddy233. Hum Mol Genet. 2018. PMID: 29931346 Free PMC article.
WiTNNess: An international natural history study of infantile-onset TNNT1 myopathy.
Strauss KA, Carson VJ, Bolettieri E, Everett M, Bollinger A, Bowser LE, Beiler K, Young M, Edvardson S, Fraenkel N, D'Amico A, Bertini E, Lingappa L, Chowdhury D, Lowes LP, Iammarino M, Alfano LN, Brigatti KW. Strauss KA, et al. Among authors: carson vj. Ann Clin Transl Neurol. 2023 Nov;10(11):1972-1984. doi: 10.1002/acn3.51884. Epub 2023 Aug 25. Ann Clin Transl Neurol. 2023. PMID: 37632133 Free PMC article.
Adolescents and rooming-in.
Winkelstein ML, Carson VJ. Winkelstein ML, et al. Among authors: carson vj. Matern Child Nurs J. 1987 Spring;16(1):75-88. Matern Child Nurs J. 1987. PMID: 3649526
Recessive GM3 synthase deficiency: Natural history, biochemistry, and therapeutic frontier.
Bowser LE, Young M, Wenger OK, Ammous Z, Brigatti KW, Carson VJ, Moser T, Deline J, Aoki K, Morlet T, Scott EM, Puffenberger EG, Robinson DL, Hendrickson C, Salvin J, Gottlieb S, Heaps AD, Tiemeyer M, Strauss KA. Bowser LE, et al. Among authors: carson vj. Mol Genet Metab. 2019 Apr;126(4):475-488. doi: 10.1016/j.ymgme.2019.01.013. Epub 2019 Jan 21. Mol Genet Metab. 2019. PMID: 30691927
21 results