statistiche ricercatore

Continente	#
NA - Nord America	984
EU - Europa	308
AS - Asia	81
Continente sconosciuto - Info sul continente non disponibili	1
SA - Sud America	1
Totale	1.375

Nome	#
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes	294
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry	229
Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy.	184
Elevated TGF β2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes	175
The genetic basis of undiagnosed muscular dystrophies and myopathies	171
Facioscapulohumeral muscular dystrophy: more complex than it appears	154
D4Z4 reduced allele in myopathic subjects with no FSHD phenotype: why inconsistency between molecular and clinical data should prompt us to further investigations.	120
Phenotype may predict the clinical course of facioscapolohumeral muscular dystrophy	64
Totale	1.391

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	106	0	0	0	0	0	0	0	0	0	18	44	44
2019/2020	322	23	8	12	26	32	59	54	36	27	17	19	9
2020/2021	329	25	5	22	23	37	49	13	44	17	42	40	12
2021/2022	200	13	16	28	7	8	14	10	17	24	11	33	19
2022/2023	209	19	24	24	16	29	18	6	19	30	2	10	12
2023/2024	93	2	9	7	13	27	3	12	16	2	2	0	0
Totale													1.391