statistiche ricercatore

Nome	#
Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 gene	114
Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterization	109
Methylated premutation of the FMR1 gene in three sisters: correlating CGG expansion and epigenetic inactivation	80
Reversion to Normal of FMR1 Expanded Alleles: A Rare Event in Two Independent Fragile X Syndrome Families	75
Co-occurrence of fragile x syndrome with a second genetic condition: Three independent cases of double diagnosis	59
Co-occurrence of fragile x syndrome with a second genetic condition: Three independent cases of double diagnosis	53
Mother and Daughter Carrying of the Same Pathogenic Variant in FGFR2 with Discordant Phenotype	46
Rutin Protects Fibroblasts from UVA Radiation through Stimulation of Nrf2 Pathway.	37
DNA Methylation, Mechanisms of FMR1 Inactivation and Therapeutic Perspectives for Fragile X Syndrome	33
Mechanisms of the FMR1 Repeat Instability: How Does the CGG Sequence Expand?	32
Age-Dependent Dysregulation of APP in Neuronal and Skin Cells from Fragile X Individuals	18
Mitochondrial Dysfunction Causes Cell Death in Patients Affected by Fragile-X-Associated Disorders	10
Totale	666

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	32	0	0	0	0	0	0	0	0	5	5	20	2
2020/2021	38	8	0	2	0	7	5	0	0	1	5	8	2
2021/2022	135	13	49	2	7	2	0	1	6	4	3	26	22
2022/2023	213	36	27	14	24	17	10	17	10	28	3	17	10
2023/2024	182	7	27	7	29	7	32	18	3	3	10	16	23
2024/2025	66	3	8	19	17	19	0	0	0	0	0	0	0
Totale													666

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