statistiche ricercatore

Nome	#
Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia	144
Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T > C mutation	122
CNS involvement in a cohort of pediatric patients affected with mitochondrial disorders caused by heterogeneous biochemical and genetic defects	120
Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian families	112
Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G > A mitochondrial DNA mutation :aA case report	109
The novel mitochondrial tRNAAsn gene mutation m.5709T>C produces ophthalmoparesis and respiratory impairment	103
Le mycophénolate mofétil en traitement d’induction et traitement d’entretien à long terme dans la prise en charge de la vascularite primitive du système nerveux central chez l’enfant	43
Long-Term Efficacy and Safety of Mycophenolate Mofetil in Childhood Primary Central Nervous System Vasculitis	36
Mycophenolate mofetil as induction and long-term maintaining treatment in childhood : primary angiitis of the central nervous system	35
Totale	824

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	57	0	0	0	0	0	11	5	4	19	9	3	6
2020/2021	103	3	3	16	0	6	8	2	10	26	6	17	6
2021/2022	84	9	3	3	3	3	4	2	3	21	8	8	17
2022/2023	117	12	11	9	13	12	25	0	7	19	5	4	0
2023/2024	57	0	10	3	2	25	0	1	1	0	0	6	9
2024/2025	112	5	19	12	33	38	5	0	0	0	0	0	0
Totale													824

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