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Page 1
Recurrence of Visual Loss in Recessive Leber Hereditary Optic Neuropathy: New Paradigm.
Barboni P, Battista M, Brotto L, Nucci P, Checchin L, Bandello F, Fiorini C, Ormanbekova D, Carelli V, Cascavilla ML, Caporali L. Barboni P, et al. Among authors: ormanbekova d. J Neuroophthalmol. 2024 Feb 21. doi: 10.1097/WNO.0000000000002117. Online ahead of print. J Neuroophthalmol. 2024. PMID: 38381526 No abstract available.
AFG3L2 and ACO2-Linked Dominant Optic Atrophy: Genotype-Phenotype Characterization Compared to OPA1 Patients.
Amore G, Romagnoli M, Carbonelli M, Cascavilla ML, De Negri AM, Carta A, Parisi V, Di Renzo A, Schiavi C, Lenzetti C, Zenesini C, Ormanbekova D, Palombo F, Fiorini C, Caporali L, Carelli V, Barboni P, La Morgia C. Amore G, et al. Among authors: ormanbekova d. Am J Ophthalmol. 2024 Jan 24;262:114-124. doi: 10.1016/j.ajo.2024.01.011. Online ahead of print. Am J Ophthalmol. 2024. PMID: 38278202 Free article.
Recessive MECR pathogenic variants cause an LHON-like optic neuropathy.
Fiorini C, Degiorgi A, Cascavilla ML, Tropeano CV, La Morgia C, Battista M, Ormanbekova D, Palombo F, Carbonelli M, Bandello F, Carelli V, Maresca A, Barboni P, Baruffini E, Caporali L. Fiorini C, et al. Among authors: ormanbekova d. J Med Genet. 2023 Dec 21;61(1):93-101. doi: 10.1136/jmg-2023-109340. J Med Genet. 2023. PMID: 37734847 Free PMC article.
The Italian reappraisal of the most frequent genetic defects in hereditary optic neuropathies and the global top 10.
Fiorini C, Ormanbekova D, Palombo F, Carbonelli M, Amore G, Romagnoli M, d'Agati P, Valentino ML, Barboni P, Cascavilla ML, De Negri A, Sadun F, Carta A, Testa F, Petruzzella V, Guerriero S, Bianchi Marzoli S, Carelli V, La Morgia C, Caporali L. Fiorini C, et al. Among authors: ormanbekova d. Brain. 2023 Sep 1;146(9):e67-e70. doi: 10.1093/brain/awad080. Brain. 2023. PMID: 36913248 Free PMC article. No abstract available.
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder.
Caporali L, Fiorini C, Palombo F, Romagnoli M, Baccari F, Zenesini C, Visconti P, Posar A, Scaduto MC, Ormanbekova D, Battaglia A, Tancredi R, Cameli C, Viggiano M, Olivieri A, Torroni A, Maestrini E, Rochat MJ, Bacchelli E, Carelli V, Maresca A. Caporali L, et al. Among authors: ormanbekova d. Front Genet. 2022 Nov 7;13:953762. doi: 10.3389/fgene.2022.953762. eCollection 2022. Front Genet. 2022. PMID: 36419830 Free PMC article.
Co-occurrence of amyotrophic lateral sclerosis and Leber's hereditary optic neuropathy: is mitochondrial dysfunction a modifier?
Amore G, Vacchiano V, La Morgia C, Valentino ML, Caporali L, Fiorini C, Ormanbekova D, Salvi F, Bartoletti-Stella A, Capellari S, Liguori R, Carelli V. Amore G, et al. Among authors: ormanbekova d. J Neurol. 2023 Jan;270(1):559-564. doi: 10.1007/s00415-022-11355-w. Epub 2022 Sep 6. J Neurol. 2023. PMID: 36066624 Free PMC article. No abstract available.
The Global Durum Wheat Panel (GDP): An International Platform to Identify and Exchange Beneficial Alleles.
Mazzucotelli E, Sciara G, Mastrangelo AM, Desiderio F, Xu SS, Faris J, Hayden MJ, Tricker PJ, Ozkan H, Echenique V, Steffenson BJ, Knox R, Niane AA, Udupa SM, Longin FCH, Marone D, Petruzzino G, Corneti S, Ormanbekova D, Pozniak C, Roncallo PF, Mather D, Able JA, Amri A, Braun H, Ammar K, Baum M, Cattivelli L, Maccaferri M, Tuberosa R, Bassi FM. Mazzucotelli E, et al. Among authors: ormanbekova d. Front Plant Sci. 2020 Dec 21;11:569905. doi: 10.3389/fpls.2020.569905. eCollection 2020. Front Plant Sci. 2020. PMID: 33408724 Free PMC article.
20 results