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Clinical study of ferredoxin-reductase-related mitochondriopathy: Genotype-phenotype correlation and proposal of ancestry-based carrier screening in the Mexican population.
Campbell T, Slone J, Metzger H, Liu W, Sacharow S, Yang A, Moosajee M, La Morgia C, Carelli V, Palombo F, Lines MA, Innes AM, Levy RJ, Neilson D, Longo N, Huang T. Campbell T, et al. Genet Med Open. 2023 Nov 11;2:100841. doi: 10.1016/j.gimo.2023.100841. eCollection 2024. Genet Med Open. 2023. PMID: 39669623 Free PMC article.
FDXR variants cause adrenal insufficiency and atypical sexual development.
Pignatti E, Slone J, Gómez Cano MÁ, Campbell TM, Vu J, Sauter KS, Pandey AV, Martínez-Azorín F, Alonso-Riaño M, Neilson DE, Longo N, du Toit T, Voegel CD, Huang T, Flück CE. Pignatti E, et al. Among authors: campbell tm. JCI Insight. 2024 Jun 17;9(14):e179071. doi: 10.1172/jci.insight.179071. JCI Insight. 2024. PMID: 38885337 Free PMC article.
Nivolumab to restore T-cell fitness in CAR-T refractory multiple myeloma.
Waldschmidt JM, Sotudeh N, Arora S, Vijaykumar T, Anand P, Stuart H, Frede J, Campbell TB, Kaiser S, Zheng X, Munshi NC, Anderson KC, Einsele H, Yee AJ, Knoechel B, Lohr JG, Raje NS. Waldschmidt JM, et al. Among authors: campbell tb. Blood Adv. 2025 Jan 15:bloodadvances.2024015285. doi: 10.1182/bloodadvances.2024015285. Online ahead of print. Blood Adv. 2025. PMID: 39813623
The novel T107I Inherited prion disease can present as a clinical and biomarker mimic of familial Alzheimer's disease.
Holm-Mercer L, Coysh T, Mok TH, Rudge P, Reisz Z, Troakes C, Al-Sarraj S, Campbell T, Hosszu LLP, Bieschke J, Zhang F, Wadsworth JDF, Smith C, Jenkinson J, Rittman T, Brandner S, Jaunmuktane Z, Collinge J, Mead S. Holm-Mercer L, et al. Among authors: campbell t. J Neurogenet. 2025 Jan 9:1-7. doi: 10.1080/01677063.2024.2440395. Online ahead of print. J Neurogenet. 2025. PMID: 39789805 Free article.
1,955 results