statistiche ricercatore

Nome	#
Neuromuscular syndrome associated with the 3291T→C mutation of mitochondrial DNA: A second case	97
Early-onset liver mtDNA depletion and late-onset proteinuric nephropathy in Mpv17 knockout mice	86
A novel mutation (8342G → A) in the mitochondrial tRNA(Lys) gene associated with progressive external ophthalmoplegia and myoclonus	77
Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene	59
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease	57
Identification of novel mutations in five patients with mitochondrial encephalomyopathy	52
Severe X-Linked Mitochondrial Encephalomyopathy Associated with a Mutation in Apoptosis-Inducing Factor	48
Monomelic amyotrophy associated with the 7472insC mutation in the mtDNA tRNA Ser(UCN) gene	40
Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: A morphological, biochemical and molecular-genetic study	39
A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentation	38
Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the 5698G→A mitochondrial DNA mutation	38
Totale	631

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	26	0	0	0	0	0	0	3	5	5	6	7	0
2020/2021	275	2	0	4	138	33	1	1	13	32	6	26	19
2021/2022	116	0	0	14	5	16	7	0	18	21	0	7	28
2022/2023	108	18	6	2	9	15	16	0	17	9	0	15	1
2023/2024	46	2	6	2	6	3	13	2	0	1	0	5	6
2024/2025	60	1	21	9	7	22	0	0	0	0	0	0	0
Totale													631