statistiche ricercatore

Nome	#
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome	75
Expanding the spectrum of clinical severity of AICA-ribosiduria: Report of two siblings with mild phenotype caused by a novel pathogenic variant in ATIC gene	21
Benign Hereditary Chorea as a Manifestation of HPCA Mutation	13
Identification of bi-allelic LFNG variants in three patients and further clinical and molecular refinement of spondylocostal dysostosis 3	12
Joubert syndrome-derived induced pluripotent stem cells show altered neuronal differentiation in vitro	8
Prenatal findings in oral-facial-digital syndrome type VI: Report of three cases and literature review	8
Heterozygous APTX mutation associated with atypical multiple system atrophy-like phenotype: A case report	5
Establishment of three Joubert syndrome-derived induced pluripotent stem cell (iPSC) lines harbouring compound heterozygous mutations in CC2D2A gene	3
Totale	145

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	14	2	0	0	0	0	1	1	2	3	2	2	1
2020/2021	19	1	1	2	1	1	2	0	3	1	4	1	2
2021/2022	12	0	8	0	0	0	0	1	0	0	0	1	2
2022/2023	28	1	0	1	2	0	5	8	3	4	1	3	0
2023/2024	64	3	2	1	6	3	9	3	0	10	0	15	12
2024/2025	3	3	0	0	0	0	0	0	0	0	0	0	0
Totale													145