statistiche ricercatore

Nome	#
Clinical features and outcomes of elderly hospitalised patients with chronic obstructive pulmonary disease, heart failure or both	349
Transabdominal ultrasound guided AAV9-GFP delivery in fetal pigs: a translational and minimally invasive model for in utero fetal gene therapy	148
Homozygous mutations in C1QBP as cause of progressive external ophthalmoplegia (PEO) and mitochondrial myopathy with multiple mtDNA deletions	122
Gene Therapy for Mitochondrial Diseases: Current Status and Future Perspective	119
A novel homozygous MSTO1 mutation in Ashkenazi Jewish siblings with ataxia and myopathy	118
Emerging variants, unique phenotypes, and transcriptomic signatures: an integrated study of COASY-associated diseases	92
AAV-mediated liver-specific MPV17 expression restores mtdna levels and prevents diet-induced liver failure	38
AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndrome	25
Loss of ETHE1, a mitochondrial dioxygenase, causes fatal sulfide toxicity in ethylmalonic encephalopathy	23
Transcription Factor EB Controls Metabolic Flexibility during Exercise	14
Proteome adaptations in Ethe1-deficient mice indicate a role in lipid catabolism and cytoskeleton organization via post-translational protein modifications	11
Chronic exposure to sulfide causes accelerated degradation of cytochrome c oxidase in ethylmalonic encephalopathy	9
Totale	1.068

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	4	0	0	0	0	0	0	0	0	0	0	0	4
2021/2022	26	1	3	3	0	1	3	0	3	1	0	4	7
2022/2023	48	6	3	5	4	7	6	2	3	5	0	7	0
2023/2024	24	1	1	2	4	8	0	2	0	0	1	2	3
2024/2025	109	5	6	1	11	10	10	8	10	10	11	10	17
2025/2026	845	37	258	82	50	57	44	79	40	54	61	75	8
Totale													1.068

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