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Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25.
Barbier M, Bahlo M, Pennisi A, Jacoupy M, Tankard RM, Ewenczyk C, Davies KC, Lino-Coulon P, Colace C, Rafehi H, Auger N, Ansell BRE, van der Stelt I, Howell KB, Coutelier M, Amor DJ, Mundwiller E, Guillot-Noël L, Storey E, Gardner RJM, Wallis MJ, Brusco A, Corti O, Rötig A, Leventer RJ, Brice A, Delatycki MB, Stevanin G, Lockhart PJ, Durr A. Barbier M, et al. Among authors: pennisi a. Ann Neurol. 2022 Jul;92(1):122-137. doi: 10.1002/ana.26366. Epub 2022 May 7. Ann Neurol. 2022. PMID: 35411967 Free article.
Mitochondrial myopathy plus due to the variant m.586G > A in MT-TF.
Barcia G, Assouline Z, Pennisi A, Steffann J, Boddaert N, Gitiaux C, Rötig A, Bonnefont JP, Munnich A. Barcia G, et al. Among authors: pennisi a. Mol Genet Metab Rep. 2019 Oct 23;21:100522. doi: 10.1016/j.ymgmr.2019.100522. eCollection 2019 Dec. Mol Genet Metab Rep. 2019. PMID: 31687337 Free PMC article. No abstract available.
Cytochrome c oxidase deficiency caused by biallelic SCO2 mutations in two sibs with cerebellar ataxia and progressive peripheral axonal neuropathy.
Barcia G, Assouline Z, Pennisi A, Gitiaux C, Schiff M, Boddaert N, Munnich A, Bonnefont JP, Rötig A. Barcia G, et al. Among authors: pennisi a. Mol Genet Metab Rep. 2019 Nov 6;21:100528. doi: 10.1016/j.ymgmr.2019.100528. eCollection 2019 Dec. Mol Genet Metab Rep. 2019. PMID: 31844624 Free PMC article. No abstract available.
Improving post-natal detection of mitochondrial DNA mutations.
Barcia G, Assouline Z, Magen M, Pennisi A, Rötig A, Munnich A, Bonnefont JP, Steffann J. Barcia G, et al. Among authors: pennisi a. Expert Rev Mol Diagn. 2020 Oct;20(10):1003-1008. doi: 10.1080/14737159.2020.1820326. Epub 2020 Sep 20. Expert Rev Mol Diagn. 2020. PMID: 32902337
Heterogeneity of PNPT1 neuroimaging: mitochondriopathy, interferonopathy or both?
Pennisi A, Rötig A, Roux CJ, Lévy R, Henneke M, Gärtner J, Teke Kisa P, Sarioglu FC, Yiş U, Konczal LL, Burkardt DD, Wu S, Gaignard P, Besmond C, Hubert L, Rio M, Barcia G, Munnich A, Boddaert N, Schiff M. Pennisi A, et al. J Med Genet. 2022 Feb;59(2):204-208. doi: 10.1136/jmedgenet-2020-107367. Epub 2020 Nov 16. J Med Genet. 2022. PMID: 33199448
Cerebral blood flow and acute episodes of Leigh syndrome in neurometabolic disorders.
Loiselet K, Ruzzenente B, Roux CJ, Barcia G, Pennisi A, Desguerre I, Rötig A, Munnich A, Boddaert N; Paediatric Radiology and Metabolics Group. Loiselet K, et al. Among authors: pennisi a. Dev Med Child Neurol. 2021 Jun;63(6):705-711. doi: 10.1111/dmcn.14814. Epub 2021 Jan 28. Dev Med Child Neurol. 2021. PMID: 33511646 Free article.
Primary mitochondrial disorders and mimics: Insights from a large French cohort.
Rouzier C, Pion E, Chaussenot A, Bris C, Ait-El-Mkadem Saadi S, Desquiret-Dumas V, Gueguen N, Fragaki K, Amati-Bonneau P, Barcia G, Gaignard P, Steffann J, Pennisi A, Bonnefont JP, Lebigot E, Bannwarth S, Francou B, Rucheton B, Sternberg D, Martin-Negrier ML, Trimouille A, Hardy G, Allouche S, Acquaviva-Bourdain C, Pagan C, Lebre AS, Reynier P, Cossee M, Attarian S, Paquis-Flucklinger V; MitoDiag's Network Collaborators; Procaccio V. Rouzier C, et al. Among authors: pennisi a. Ann Clin Transl Neurol. 2024 May 4. doi: 10.1002/acn3.52062. Online ahead of print. Ann Clin Transl Neurol. 2024. PMID: 38703036 Free article.
Expanding the clinical spectrum of MTTF mutations.
Barcia G, Assouline Z, Pennisi A, Steffann J, Boddaert N, Gitiaux C, Rötig A, Bonnefont JP, Munnich A. Barcia G, et al. Among authors: pennisi a. Mol Genet Metab Rep. 2019 Aug 13;21:100501. doi: 10.1016/j.ymgmr.2019.100501. eCollection 2019 Dec. Mol Genet Metab Rep. 2019. PMID: 31463198 Free PMC article.
Evidence of diaphragmatic dysfunction with severe alveolar hypoventilation syndrome in mitochondrial respiratory chain deficiency.
Barcia G, Khirani S, Amaddeo A, Assouline Z, Pennisi A, Boddaert N, Romero N, Desguerre I, Schiff M, Rötig A, Besmond C, Bonnefont JP, Munnich A, Fauroux B. Barcia G, et al. Among authors: pennisi a. Neuromuscul Disord. 2020 Jul;30(7):593-598. doi: 10.1016/j.nmd.2020.06.002. Epub 2020 Jun 10. Neuromuscul Disord. 2020. PMID: 32654952
Biallelic IARS2 mutations presenting as sideroblastic anemia.
Barcia G, Pandithan D, Ruzzenente B, Assouline Z, Pennisi A, Ormieres C, Besmond C, Roux CJ, Boddaert N, Desguerre I, Thorburn DR, Bratkovic D, Munnich A, Bonnefont JP, Rötig A, Steffann J. Barcia G, et al. Among authors: pennisi a. Haematologica. 2021 Apr 1;106(4):1220-1225. doi: 10.3324/haematol.2020.270710. Haematologica. 2021. PMID: 33327715 Free PMC article.
163 results