statistiche ricercatore

Continente	#
EU - Europa	1.370
Totale	1.370

Nazione	#
IT - Italia	1.370
Totale	1.370

Nome	#
PITUITARY HYPOPLASIA AND GROWTH HORMONE DEFICIENCY IN COFFIN-SIRIS SYNDROME	128
A survey on Prader-Willi syndrome in the Italian population: prevalence of historical and clinical signs.	121
Wolfram syndrome (diabetes insipidus, diabetes, optic atrophy, and deafness): clinical and genetic study.	119
Growth hormone secretory pattern in non-obese children and adolescents with Prader-Willi syndrome	117
Further case of metaphyseal acroscyphodysplasia with cone-shaped epiphyses (Bellini disease or metaphyseal dyschondroplasia).	115
The Italian National Survey for Prader-Willi syndrome: an epidemiologic study.	112
Clinical and genetic characterization of Chanarin-Dorfman syndrome	111
Growth hormone secretory pattern in non-obese children and adolescents with Prader-Willi syndrome.	109
Coffin-Siris syndrome and the BAF complex: genotype-phenotype study in 63 patients.	104
Due casi di difficile inquadramento: coreoatetosi e sordità in fratelli	97
A novel Xp22.11 deletion causing a syndrome of craniosynostosis and periventricular nodular heterotopia.	94
Clinical and cytogenetic study of a case of trisomy 1q with familial translocation t(1;5)(q42;p15.3)	84
Adolescenza. Verso un approccio multidisciplinare	59
Totale	1.370

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	85	0	0	0	0	0	0	0	0	0	0	46	39
2019/2020	409	16	13	24	22	47	42	70	22	33	61	38	21
2020/2021	92	4	8	13	8	7	9	4	10	7	11	5	6
2021/2022	166	5	18	4	17	13	11	12	41	5	15	7	18
2022/2023	168	18	20	9	15	17	27	1	15	13	0	30	3
2023/2024	77	4	17	1	14	12	8	6	4	3	5	3	0
Totale													1.370