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

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

34 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Premature Ovarian Failure in French Canadian Leigh Syndrome.
Ghaddhab C, Morin C, Brunel-Guitton C, Mitchell GA, Van Vliet G, Huot C. Ghaddhab C, et al. J Pediatr. 2017 May;184:227-229.e1. doi: 10.1016/j.jpeds.2017.02.008. Epub 2017 Mar 8. J Pediatr. 2017. PMID: 28284481
Use of dexamethasone in acute rhabdomyolysis in LPIN1 deficiency.
Yeganeh M, March K, Jones C, Ho G, Selby KA, Chanoine JP, Stockler S, Salvarinova R, Horvath G, Brunel-Guitton C. Yeganeh M, et al. Among authors: brunel guitton c. Mol Genet Metab Rep. 2023 Mar 10;35:100961. doi: 10.1016/j.ymgmr.2023.100961. eCollection 2023 Jun. Mol Genet Metab Rep. 2023. PMID: 36941958 Free PMC article.
Treatment of cobalamin C (cblC) deficiency during pregnancy.
Brunel-Guitton C, Costa T, Mitchell GA, Lambert M. Brunel-Guitton C, et al. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S409-12. doi: 10.1007/s10545-010-9202-7. Epub 2010 Sep 10. J Inherit Metab Dis. 2010. PMID: 20830523
Inborn errors of cytoplasmic triglyceride metabolism.
Wu JW, Yang H, Wang SP, Soni KG, Brunel-Guitton C, Mitchell GA. Wu JW, et al. J Inherit Metab Dis. 2015 Jan;38(1):85-98. doi: 10.1007/s10545-014-9767-7. Epub 2014 Oct 10. J Inherit Metab Dis. 2015. PMID: 25300978 Review.
The 3' addition of CCA to mitochondrial tRNASer(AGY) is specifically impaired in patients with mutations in the tRNA nucleotidyl transferase TRNT1.
Sasarman F, Thiffault I, Weraarpachai W, Salomon S, Maftei C, Gauthier J, Ellazam B, Webb N, Antonicka H, Janer A, Brunel-Guitton C, Elpeleg O, Mitchell G, Shoubridge EA. Sasarman F, et al. Hum Mol Genet. 2015 May 15;24(10):2841-7. doi: 10.1093/hmg/ddv044. Epub 2015 Feb 4. Hum Mol Genet. 2015. PMID: 25652405 Free PMC article.
34 results