statistiche ricercatore

Nome	#
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene.	29
A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease.	6
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region	2
Emergence of Talanin protein associated with human uric acid nephrolithiasis in the Hominidae lineage	1
Epidemiological, clinical, and genetic characteristics of Paget's disease of bone in a rural area of Calabria, Southern Italy	1
Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts	1
Incontinentia Pigmenti Type 2 (IP2): isolation and characterisation of the gene through trascriptional and sequence analysis	1
Common and Rare Variants in TMEM175 Gene Concur to the Pathogenesis of Parkinson's Disease in Italian Patients	1
Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship.	1
Multifactorial disorder: molecular and evolutionary insights of uric acid nephrolithiasis	1
Multiple pathogenic and benign rearrangements arise from an ancient 35-kb genomic duplication involving the NEMO and LAGE2 genes	1
Identification of sixteen novel candidate genes for late onset Parkinson's disease	1
Totale	46

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2023/2024	46	0	0	0	0	0	0	0	0	7	0	3	36
Totale													46

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