statistiche ricercatore

Nome	#
A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function.	160
Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients	151
Cardioembolic stroke in Danon disease.	133
Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure.	117
Generalized lysosome-associated membrane protein-2 defect explains multisystem clinical involvement and allows leukocyte diagnostic screening in Danon disease	105
Dominant optic atrophy caused by a novel OPA1 mutation: Disruption of the mitochondrial network with preserved bioenergetics.	100
Electrophysiological, neuro-hormonal and neuropsychological response to immunotherapy in a case of atypical Morvan syndrome with limbic seizures	67
Multisystemic LAMP-2 defect in Danon disease.	66
Multisystem primary defect of LAMP-2 in Danon disease	56
Optimized protocols for the analysis of mithocondrial respiratory chain enzymes in cells and tissues	33
Totale	988

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	70	0	0	0	0	0	0	0	0	0	15	29	26
2019/2020	192	25	6	11	9	17	11	19	24	14	32	15	9
2020/2021	194	4	14	2	15	31	23	3	14	23	16	28	21
2021/2022	146	2	8	25	12	12	15	3	15	10	2	12	30
2022/2023	190	26	20	10	39	17	32	0	15	17	0	12	2
2023/2024	69	3	11	15	3	5	17	3	6	1	5	0	0
Totale													988