statistiche ricercatore

Continente	#
EU - Europa	627
Totale	627

Nazione	#
IT - Italia	627
Totale	627

Nome	#
Prognostic value of chromosomal imbalances, gene mutations, and BAP1 expression in uveal melanoma	153
Prognostic value of specific chromosome imbalances, mutation profile, and BAP1 expression in uveal melanoma	146
Secondary Somatic Mutations in G-Protein-Related Pathways and Mutation Signatures in Uveal Melanoma	105
How many mutations does it take to make a uveal melanoma?	63
Genetic Workup for Charcot–Marie–Tooth Neuropathy: A Retrospective Single-Site Experience Covering 15 Years	53
ROLE OF MME IN LATE ONSET AXONAL CMT: ANALYSIS OF AN ITALIAN CMT2 COHORT	41
null	35
An integrated approach to the evaluation of patients with asymptomatic or minimally symptomatic hyperCKemia	19
A CASE OF BIALLELIC SORD MUTATIONS ASSOCIATED WITH DISTAL WEAKNESS AND HISTOLOGICAL SIGNS OF MYOPATHY	18
A misleading presentation of Mohr–Tranebjaerg syndrome: what is hidden behind an axonal neuropathy?	17
Early Onset Inherited Peripheral Neuropathies: The Experience of a Specialized Referral Center for Genetic Diagnosis Achievement	7
Case report: Episodic ataxia without ataxia?	3
Skeletal muscle involvement in biallelic SORD mutations: case report and review of the literature	3
Totale	663

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	9	0	0	0	0	0	0	0	0	0	0	5	4
2019/2020	128	3	2	1	5	13	13	18	10	18	21	18	6
2020/2021	50	1	6	1	4	4	6	1	9	0	6	7	5
2021/2022	120	7	8	10	4	3	4	10	17	10	11	20	16
2022/2023	154	6	10	1	12	14	24	8	18	20	5	30	6
2023/2024	183	17	6	11	43	11	37	13	15	16	14	0	0
Totale													663