statistiche ricercatore

Nome	#
Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 gene	106
Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterization	104
Methylated premutation of the FMR1 gene in three sisters: correlating CGG expansion and epigenetic inactivation	76
Reversion to Normal of FMR1 Expanded Alleles: A Rare Event in Two Independent Fragile X Syndrome Families	70
Co-occurrence of fragile x syndrome with a second genetic condition: Three independent cases of double diagnosis	51
Co-occurrence of fragile x syndrome with a second genetic condition: Three independent cases of double diagnosis	49
Mother and Daughter Carrying of the Same Pathogenic Variant in FGFR2 with Discordant Phenotype	40
DNA Methylation, Mechanisms of FMR1 Inactivation and Therapeutic Perspectives for Fragile X Syndrome	30
Rutin Protects Fibroblasts from UVA Radiation through Stimulation of Nrf2 Pathway.	29
Mechanisms of the FMR1 Repeat Instability: How Does the CGG Sequence Expand?	27
Age-Dependent Dysregulation of APP in Neuronal and Skin Cells from Fragile X Individuals	14
Mitochondrial Dysfunction Causes Cell Death in Patients Affected by Fragile-X-Associated Disorders	4
Totale	600

	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
Totale													600

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