statistiche ricercatore

Nome	#
A rare mutation in MYH7 gene occurs with overlapping phenotype	90
A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers	77
Clinical and genetic features of CMT2T in Italian patients confirm the importance of MME pathogenic variants in idiopathic, late‐onset axonal neuropathies	74
Sporadic chronic progressive external ophthalmoplegia with single large mitochondrial DNA deletion and neurogenic findings	68
DEVELOPMENT AND VALIDATION OF A BIOMARKERS PANEL TO CAPTURE PATHOPHYSIOLOGICAL HETEROGENEITY OF GBS AND CIDP PATIENTS	63
Abnormal sensorimotor cortex and thalamo-cortical networks in familial adult myoclonic epilepsy type 2: pathophysiology and diagnostic implications	38
Neurophysiological and behavioural correlates of ocrelizumab therapy on manual dexterity in patients with primary progressive multiple sclerosis	38
Comparison of the diagnostic accuracy of the 2021 EAN/PNS and 2010 EFNS/PNS diagnostic criteria for chronic inflammatory demyelinating polyradiculoneuropathy	34
Awareness of bone strength in patients with neuromuscular disorders: ERN EURO-NMD clinician survey and European patient survey	18
Split Hand Syndrome in Charcot–Marie–Tooth Disease Type X1 (CMTX1): A Clinical, Neurophysiological, and Radiological Study	5
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)	4
Totale	509

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	26	0	0	0	8	0	0	2	4	2	3	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	225	3	10	6	13	21	17	24	39	30	9	29	24
2025/2026	142	58	25	28	31	0	0	0	0	0	0	0	0
Totale													509