Mitchell GA - Search Results

1

Clinical heterogeneity in cobalamin C variant of combined homocystinuria and methylmalonic aciduria.

Mitchell GA, Watkins D, Melançon SB, Rosenblatt DS, Geoffroy G, Orquin J, Homsy MB, Dallaire L. Mitchell GA, et al. J Pediatr. 1986 Mar;108(3):410-5. doi: 10.1016/s0022-3476(86)80882-4. J Pediatr. 1986. PMID: 3950820

2

Erysipeloid in an infant.

Lacroix J, Delage G, Mitchell G. Lacroix J, et al. J Pediatr. 1981 Nov;99(5):745-6. doi: 10.1016/s0022-3476(81)80400-3. J Pediatr. 1981. PMID: 7299551 No abstract available.

3

The Influence of Binocular Vision Symptoms on Computerized Neurocognitive Testing of Adolescents With Concussion.

Peiffer AJ, MacDonald J, Duerson D, Mitchell G, Hartwick ATE, McDaniel CE. Peiffer AJ, et al. Clin Pediatr (Phila). 2020 Oct;59(11):961-969. doi: 10.1177/0009922820927477. Epub 2020 Jun 1. Clin Pediatr (Phila). 2020. PMID: 32476458

4

Factors Affecting Non-Enzymatic Protein Acylation by trans-3-Methylglutaconyl Coenzyme A.

Jennings EA, Macdonald MM, Romenskaia I, Yang H, Mitchell GA, Ryan RO. Jennings EA, et al. Among authors: mitchell ga. Metabolites. 2024 Jul 31;14(8):421. doi: 10.3390/metabo14080421. Metabolites. 2024. PMID: 39195517 Free PMC article.

5

Insulin therapy in acute decompensation of holocarboxylase synthetase deficiency with hyperglycemia and ketoacidosis.

Demaret T, Joyal JS, Karalis A, Parente F, Delrue MA, Mitchell GA. Demaret T, et al. Among authors: mitchell ga. Mol Genet Metab Rep. 2024 Mar 21;39:101073. doi: 10.1016/j.ymgmr.2024.101073. eCollection 2024 Jun. Mol Genet Metab Rep. 2024. PMID: 38550975 Free PMC article.

6

The MMACHC variant c.158T>C: Mild clinical and biochemical phenotypes and marked hydroxocobalamin response in cblC patients.

Demaret T, Bédard K, Soucy JF, Watkins D, Allard P, Levtova A, O'Brien A, Brunel-Guitton C, Rosenblatt DS, Mitchell GA. Demaret T, et al. Among authors: mitchell ga. Mol Genet Metab. 2024 May;142(1):108345. doi: 10.1016/j.ymgme.2024.108345. Epub 2024 Feb 10. Mol Genet Metab. 2024. PMID: 38387306

7

TUFM variants lead to white matter abnormalities mimicking multiple sclerosis.

Chen S, Mitchell GA, Soucy JF, Gauthier J, Brais B, La Piana R. Chen S, et al. Among authors: mitchell ga. Eur J Neurol. 2023 Oct;30(10):3400-3403. doi: 10.1111/ene.15982. Epub 2023 Jul 19. Eur J Neurol. 2023. PMID: 37433570

8

A bouncing cosmology from VECROs.

Brandenberger R, Mitchell GA. Brandenberger R, et al. Among authors: mitchell ga. Eur Phys J C Part Fields. 2023;83(4):308. doi: 10.1140/epjc/s10052-023-11501-2. Epub 2023 Apr 20. Eur Phys J C Part Fields. 2023. PMID: 37096219 Free PMC article.

9

Deciphering a novel complex inversion affecting F8 in a family with severe haemophilia A by optical genome mapping.

Fahiminiya S, Oikonomopoulos S, Rivard GE, Gandhi M, Scott P, Montpetit A, Chen SH, Park K, Vezina C, Ragoussis J, Carvalho CMB, Mitchell GA, Soucy JF, Gauthier J. Fahiminiya S, et al. Among authors: mitchell ga. Haemophilia. 2023 May;29(3):921-924. doi: 10.1111/hae.14771. Epub 2023 Mar 10. Haemophilia. 2023. PMID: 36897533 Free PMC article. No abstract available.

10

The multiple facets of acetyl-CoA metabolism: Energetics, biosynthesis, regulation, acylation and inborn errors.

Wang Y, Yang H, Geerts C, Furtos A, Waters P, Cyr D, Wang S, Mitchell GA. Wang Y, et al. Among authors: mitchell ga. Mol Genet Metab. 2023 Jan;138(1):106966. doi: 10.1016/j.ymgme.2022.106966. Epub 2022 Nov 30. Mol Genet Metab. 2023. PMID: 36528988 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

264 results

Search Page

Filters