statistiche ricercatore

Nome	#
Acute intermittent porphyria : heterogeneity of mutations in the hydroxymethylbilane synthase gene in Italy	144
Molecular analysis of the hydroxymethylbilane synthase (HMBS) gene in Italian patients with acute intermittent porphyria : report of four novel mutations	118
Molecular characterization of porphyrias in Italy : a diagnostic flow-chart	118
Molecular characterisation of the glucose-6-phosphate dehydrogenase (G6PD) Ferrara II variant	106
The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency	97
G6PD Ferrara I has the same two mutations as G6PD A(-) but a distinct biochemical phenotype	97
Hematologically important mutations : acute intermittent porphyria	93
Biochemical and molecular characterization of a new sporadic glucose-6-phosphate dehydrogenase variant described in Italy : G6PD Modena	93
Molecular characterisation of an Italian G6PD variant responsible for chronic non-spherocytic haemolytic anaemia	80
Different origin of nt 1246 glucose-6-phosphate dehydrogenase mutation	77
Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in Italy	75
Totale	1.098

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	110	15	1	6	5	0	19	11	6	12	26	6	3
2020/2021	146	3	5	16	1	13	5	13	8	18	15	33	16
2021/2022	117	13	3	0	5	8	8	15	3	15	10	9	28
2022/2023	188	16	25	18	17	27	42	0	14	21	3	4	1
2023/2024	87	4	10	5	2	23	8	2	6	0	3	11	13
2024/2025	8	8	0	0	0	0	0	0	0	0	0	0	0
Totale													1.098

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