statistiche ricercatore

Nome	#
Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia	132
Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T > C mutation	114
Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian families	102
The novel mitochondrial tRNAAsn gene mutation m.5709T>C produces ophthalmoparesis and respiratory impairment	93
Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G > A mitochondrial DNA mutation :aA case report	92
CNS involvement in a cohort of pediatric patients affected with mitochondrial disorders caused by heterogeneous biochemical and genetic defects	91
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	35
Mycophenolate mofetil as induction and long-term maintaining treatment in childhood : primary angiitis of the central nervous system	29
Long-Term Efficacy and Safety of Mycophenolate Mofetil in Childhood Primary Central Nervous System Vasculitis	28
Totale	716

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	90	13	5	5	9	1	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	4	4	0	0	0	0	0	0	0	0	0	0	0
Totale													716

IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca