statistiche ricercatore

Nome	#
Neuromuscular syndrome associated with the 3291T→C mutation of mitochondrial DNA: A second case	93
Early-onset liver mtDNA depletion and late-onset proteinuric nephropathy in Mpv17 knockout mice	84
A novel mutation (8342G → A) in the mitochondrial tRNA(Lys) gene associated with progressive external ophthalmoplegia and myoclonus	75
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease	54
Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene	53
Identification of novel mutations in five patients with mitochondrial encephalomyopathy	51
Severe X-Linked Mitochondrial Encephalomyopathy Associated with a Mutation in Apoptosis-Inducing Factor	42
Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: A morphological, biochemical and molecular-genetic study	38
A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentation	37
Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the 5698G→A mitochondrial DNA mutation	37
Monomelic amyotrophy associated with the 7472insC mutation in the mtDNA tRNA Ser(UCN) gene	36
Totale	600

	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	29	1	21	7	0	0	0	0	0	0	0	0	0
Totale													600