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Leonardo Caporali

IRCCS Istituto delle Scienze Neurologiche di Bologna
H指数:30
被引数:4,258

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2026-10-270
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ENLIGHTENme: Translating the Benefits of Self-Administered Daytime Light Supplementation to Older Adults in the Real World

ENLIGHTENme:将自我管理的日间光照补充益处应用于老年人在真实世界中的翻译

2026-09-030
OAAI
The origin of modern North Africans as depicted by a massive survey of mitogenomes

现代北非人起源的描绘:一项大规模线粒体基因组调查

2025-07-250
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Exploratory and comprehensive description of an Italian cohort of patients affected by leber hereditary optic neuropathy carrying the pathogenic variants m.11778G > A/MT-ND4 and m.3460G > A/MT-ND1

对受累于携带致病性变异m.11778G > A/MT-ND4和m.3460G > A/MT-ND1的Leber遗传性视神经病变的意大利队列患者的探索性及全面性描述

2025-01-190
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Pathogenic mitochondrial DNA variants are associated with response to anti-VEGF therapy in ovarian cancer PDX models

卵巢癌PDX模型中致病性线粒体DNA变异与抗VEGF治疗反应相关

2024-12-190
OAAI
Genetic variants of NQO1 affect the expression and activity of the protein, which determines the efficacy of idebenone treatment in Leber's hereditary optic neuropathy
2024-09-010
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AFG3L2 and ACO2-Linked Dominant Optic Atrophy: Genotype-Phenotype Characterization Compared to OPA1 Patients
2024-06-010
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COQ7 defect causes prenatal onset of mitochondrial CoQ10 deficiency with cardiomyopathy and gastrointestinal obstruction
2024-05-035
OAAI
Bi-allelic variants in SNF8 cause a disease spectrum ranging from severe developmental and epileptic encephalopathy to syndromic optic atrophy

SNF8中的双等位基因变体引起的疾病谱从严重的发育性和癫痫性脑病到综合征性视神经萎缩

2024-03-014
OAAI
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy
2024-02-018
OAAI
Anti-VEGF therapy selects for clones resistant to glucose starvation in ovarian cancer xenografts
2023-08-073
OAAI
Childhood-Onset Leber Hereditary Optic Neuropathy-Clinical and Prognostic Insights
2023-05-0112
OAAI