statistiche ricercatore

Continente	#
EU - Europa	371
NA - Nord America	320
AS - Asia	156
AF - Africa	14
OC - Oceania	7
SA - Sud America	4
Continente sconosciuto - Info sul continente non disponibili	1
Totale	873

Nome	#
DIABETES MELLITUS: A COMPLEX METABOLIC DISORDER.EXPLORING THE DISEASE THROUGH FRUCTOSAMINE 3-KINASE GENE ANALYSIS	225
PDCD10 gene mutations in multiple cerebral cavernous malformations	150
Role of fructosamine-3-kinase in protecting against the onset of microvascular and macrovascular complications in patients with T2DM	104
De novo MGC4607 gene heterozygous missense variants in a child with multiple cerebral cavernous malformations	91
Amyotrophic lateral sclerosis in pregnancy is associated with a vascular endothelial growth factor promoter genotype	85
Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progression	80
Phenotypic heterogeneity in a SOD1 G93D Italian ALS family : an example of human model to study a complex disease	79
Wide phenotypic spectrum of the TARDBP gene : homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject	66
Possible role of fructosamine 3-kinase genotyping for the management of diabetic patients	62
Totale	942

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	67	0	0	0	5	11	5	5	5	18	11	5	2
2020/2021	100	7	2	0	23	11	11	8	8	6	4	15	5
2021/2022	115	8	7	8	2	15	11	5	1	9	17	3	29
2022/2023	142	13	13	16	10	19	33	0	7	26	0	4	1
2023/2024	94	5	8	11	12	27	3	3	8	0	0	5	12
2024/2025	52	12	33	7	0	0	0	0	0	0	0	0	0
Totale													942

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