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Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 3 |
2021 | 1 |
2023 | 0 |
Search Results
4 results
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Page 1
ACTN2 mutations cause "Multiple structured Core Disease" (MsCD).
Acta Neuropathol. 2019 Mar;137(3):501-519. doi: 10.1007/s00401-019-01963-8. Epub 2019 Jan 30.
Acta Neuropathol. 2019.
PMID: 30701273
Free PMC article.
Dysregulation of NRAP degradation by KLHL41 contributes to pathophysiology in nemaline myopathy.
Jirka C, Pak JH, Grosgogeat CA, Marchetii MM, Gupta VA.
Jirka C, et al. Among authors: grosgogeat ca.
Hum Mol Genet. 2019 Aug 1;28(15):2549-2560. doi: 10.1093/hmg/ddz078.
Hum Mol Genet. 2019.
PMID: 30986853
Free PMC article.
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Patient experiences and strategies for coping with SLE: A qualitative study.
Case S, Sinnette C, Phillip C, Grosgogeat C, Costenbader KH, Leatherwood C, Feldman CH, Son MB.
Case S, et al. Among authors: grosgogeat c.
Lupus. 2021 Aug;30(9):1405-1414. doi: 10.1177/09612033211016097. Epub 2021 May 20.
Lupus. 2021.
PMID: 34013818
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Homozygous TRPV4 mutation causes congenital distal spinal muscular atrophy and arthrogryposis.
Velilla J, Marchetti MM, Toth-Petroczy A, Grosgogeat C, Bennett AH, Carmichael N, Estrella E, Darras BT, Frank NY, Krier J, Gaudet R, Gupta VA.
Velilla J, et al. Among authors: grosgogeat c.
Neurol Genet. 2019 Mar 7;5(2):e312. doi: 10.1212/NXG.0000000000000312. eCollection 2019 Apr.
Neurol Genet. 2019.
PMID: 31041394
Free PMC article.
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