statistiche ricercatore

Nome	#
Centronuclear myopathies: genotype–phenotype correlation and frequency of defined genetic forms in an Italian cohort	136
Prevalence of Duchenne muscular dystrophy in Italy: a nationwide survey	127
An integrated approach to the evaluation of patients with asymptomatic or minimally symptomatic hyperCKemia	119
A rare mutation in MYH7 gene occurs with overlapping phenotype	109
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase	103
Sporadic chronic progressive external ophthalmoplegia with single large mitochondrial DNA deletion and neurogenic findings	86
Clinical Phenotype of Pediatric and Adult Patients With Spinal Muscular Atrophy With Four SMN2 Copies: Are They Really All Stable?	56
Italian validation of the SMA independence scale–upper limb module	51
Describing phenotypes in FSHD: an update of the comprehensive clinical evaluation form	45
null	35
Centronuclear myopathy related to dynamin 2 mutations: Clinical, morphological, muscle imaging and genetic features of an Italian cohort	33
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: Experience of the FSHD Italian National Registry	29
Totale	929

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	12	0	0	0	0	0	0	0	0	0	5	7	0
2021/2022	56	5	1	0	0	0	3	6	14	5	10	2	10
2022/2023	67	5	7	0	5	8	10	0	3	9	1	19	0
2023/2024	62	6	5	1	6	2	13	5	2	2	1	8	11
2024/2025	200	4	8	3	11	18	8	27	47	12	9	21	32
2025/2026	470	65	11	31	58	70	40	45	27	57	66	0	0
Totale													929