statistiche ricercatore

Nome	#
Familial mediterranean fever	136
Association of NF1 and neuroblastoma in a pediatric case	116
A very rare cause of a deglutition disorder: achalasia of the cricopharyngeal muscle	111
Fibrodysplasia ossificans progressiva (myositis ossificans progressiva)	106
The Weaver Smith syndrome	98
Behaviour of the renin-aldosterone system in a case of pheochromocytoma	98
The heterogeneity of oral-facial-digital anomalies. Report of a case of Mohr syndrome	98
Facio-Femoral syndrome. Description of a case with monolateral femoral hypoplasia	96
Brachmann-Cornelia de Lange syndrome	96
Jarcho-Levin syndrome. Description of a familial case and review of the literature	93
EEC syndrome:report of two cases in a familiy	93
Smith-Lemli-Opitz syndrome. Description of two cases and review of the literature	93
Freeman-Sheldon syndrome. Description of 2 cases of probable recessive autosomal inheritance.	92
Unusual association of Bourneville's tuberous sclerosis and progressive external ophtalmoplegia	89
Familial hypercjolesterolemia. Study of low density lipoprotein receptors. Treatment with plasmapheresis	88
Picture of the month. Cushing's syndrome due to topical corticosteroids	88
Crouzon's syndrome. Description of a case treated surgically in the fifth month of life	87
Radiological case of the monthe. Pfeiffer's syndrome	87
Mesenteric cysts in childhood. A case with chilous form	86
Confirmed scurvy in childhood. Two more cases	73
Unusual case of oculo-dento-digital dysplasia	70
Totale	1.994

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	16	0	0	0	0	0	0	0	0	0	0	8	8
2021/2022	201	2	22	22	11	25	1	8	56	1	18	6	29
2022/2023	262	26	14	0	17	50	63	0	13	45	1	23	10
2023/2024	96	8	12	1	22	3	14	3	6	4	4	4	15
2024/2025	373	11	30	8	14	55	54	21	104	6	10	32	28
2025/2026	530	70	5	7	32	124	58	125	24	52	32	1	0
Totale													1.994