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Protective role of the mitochondrial fusion protein OPA1 in hypertension.
Robert P, Nguyen PMC, Richard A, Grenier C, Chevrollier A, Munier M, Grimaud L, Proux C, Champin T, Lelièvre E, Sarzi E, Vessières E, Henni S, Prunier D, Reynier P, Lenaers G, Fassot C, Henrion D, Loufrani L. Robert P, et al. Among authors: prunier d. FASEB J. 2021 Jul;35(7):e21678. doi: 10.1096/fj.202000238RRR. FASEB J. 2021. PMID: 34133045
Laboratory medicine unveiling an unusual cause of D-lactic acidosis as the trigger of decompensation of a rare inborn error of metabolism.
Lefèvre CR, Sacaze E, Damaj L, Rollier P, Lenski M, Le Stradic C, Bendavid C, Reynier P, Dieu X, Prunier D, Moreau C, Homedan C. Lefèvre CR, et al. Among authors: prunier d. Clin Chem Lab Med. 2023 Jun 19;61(12):e263-e267. doi: 10.1515/cclm-2023-0425. Print 2023 Nov 27. Clin Chem Lab Med. 2023. PMID: 37327352 No abstract available.
Congenital hypothyroidism and hearing loss without inner ear malformation: Think TPO.
Ziegler A, Denommé-Pichon AS, Boucher S, Bouzamondo N, Colin E, Dieu X, Jean Yves T, Bouhours N, Rouleau S, Coutant R, Rodien P, Prunier D, Bonneau D. Ziegler A, et al. Among authors: prunier d. Clin Genet. 2021 Apr;99(4):604-606. doi: 10.1111/cge.13902. Epub 2020 Dec 27. Clin Genet. 2021. PMID: 33368191 No abstract available.