statistiche ricercatore

Nome	#
Clinical and genetic features of CMT2T in Italian patients confirm the importance of MME pathogenic variants in idiopathic, late‐onset axonal neuropathies	140
A rare mutation in MYH7 gene occurs with overlapping phenotype	113
A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers	106
DEVELOPMENT AND VALIDATION OF A BIOMARKERS PANEL TO CAPTURE PATHOPHYSIOLOGICAL HETEROGENEITY OF GBS AND CIDP PATIENTS	95
Sporadic chronic progressive external ophthalmoplegia with single large mitochondrial DNA deletion and neurogenic findings	86
Neurophysiological and behavioural correlates of ocrelizumab therapy on manual dexterity in patients with primary progressive multiple sclerosis	65
Abnormal sensorimotor cortex and thalamo-cortical networks in familial adult myoclonic epilepsy type 2: pathophysiology and diagnostic implications	53
Split Hand Syndrome in Charcot–Marie–Tooth Disease Type X1 (CMTX1): A Clinical, Neurophysiological, and Radiological Study	51
Awareness of bone strength in patients with neuromuscular disorders: ERN EURO-NMD clinician survey and European patient survey	41
Correction to: Long-term treatment of hereditary transthyretin amyloidosis with patisiran: multicentre, real-world experience in Italy(Neurological Sciences, (2024), 10.1007/s10072-024-07494-9)	29
Totale	779

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	7	0	0	0	0	0	0	0	0	0	0	7	0
2021/2022	17	2	0	0	0	0	2	0	6	1	3	0	3
2022/2023	41	2	0	0	3	7	6	0	2	6	0	12	3
2023/2024	58	4	2	3	7	6	11	3	1	2	2	5	12
2024/2025	199	3	10	6	13	14	15	22	36	27	9	24	20
2025/2026	438	52	24	27	32	55	20	46	36	38	46	62	0
Totale													779