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Two-photon absorption properties of multipolar triarylamino/tosylamido 1,1,4,4-tetracyanobutadienes.
Ripoche N, Betou M, Philippe C, Trolez Y, Mongin O, Dudek M, Pokladek Z, Matczyszyn K, Samoc M, Sahnoune H, Halet JF, Roisnel T, Toupet L, Cordier M, Moxey GJ, Humphrey MG, Paul F. Ripoche N, et al. Among authors: philippe c. Phys Chem Chem Phys. 2021 Oct 13;23(39):22283-22297. doi: 10.1039/d1cp03346h. Phys Chem Chem Phys. 2021. PMID: 34585692 Free article.
The E592K variant of SF3B1 creates unique RNA missplicing and associates with high-risk MDS without ring sideroblasts.
Choi IY, Ling JP, Zhang J, Helmenstine E, Walter W, Tsakiroglou P, Bergman RE, Philippe C, Manley JL, Rouault-Pierre K, Li B, Wiseman DH, Batta K, Ouseph MM, Bernard E, Dubner B, Li X, Haferlach T, Koget A, Fazal S, Jain T, Gocke CD, DeZern AE, Dalton WB. Choi IY, et al. Among authors: philippe c. Blood Adv. 2024 May 17:bloodadvances.2023011260. doi: 10.1182/bloodadvances.2023011260. Online ahead of print. Blood Adv. 2024. PMID: 38759096
Lamentations in the night: A systematic review on catathrenia.
Martel Q, Maranci JB, Philippe C, Arnulf I. Martel Q, et al. Among authors: philippe c. Sleep Med Rev. 2024 May 6;75:101944. doi: 10.1016/j.smrv.2024.101944. Online ahead of print. Sleep Med Rev. 2024. PMID: 38718707 Review.
Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur-Chung neurodevelopmental syndrome.
Blanc A, Bonnet C, Wandzel M, Roth V, Duffourd Y, Safraou H, Leheup B, Muller F, D Colne J, Feillet F, Schmitt E, Castro M, Savatt J, Burcheri A, Nemos C, Philippe C, Lambert L. Blanc A, et al. Among authors: philippe c. Am J Med Genet A. 2024 May 6:e63642. doi: 10.1002/ajmg.a.63642. Online ahead of print. Am J Med Genet A. 2024. PMID: 38711237
547 results