statistiche ricercatore

Nome	#
CMV-associated axonal sensory-motor Guillain-Barré syndrome in a child: Case report and review of the literature	98
KCNQ2 encephalopathy: A case due to a de novo deletion	80
Letter to the Editor	68
A Case of Congenital Paramyotonia with Atypical Features in a Family with a New Variation of SCN4A Gene	62
A 15-year epileptogenic period after perinatal brain injury	59
Charcot-marie-tooth disease with pyramidal features due to a new mutation of EGR2 gene	54
Peripheral neuropathy and gastroenterologic disorders: an overview on an underrecognized association	53
Novel phenotype in a family with infantile convulsions and paroxysmal choreoathetosis syndrome and PRRT2 gene mutation	44
Hereditary neuropathy with liability to pressure palsy (HNPP): Report of a family with a new point mutation in PMP22 gene	38
Clinical and genetic findings in a series of eight families with arthrogryposis	38
Late diagnosis of severe long-standing autoimmune hypothyroidism after the first lockdown for the Covid-19 pandemic: clinical features and follow-up	32
Aromatic L-Amino-Acid Decarboxylase Deficiency Screening by Analysis of 3-O-Methyldopa in Dried Blood Spots: Results of a Multicentric Study in Neurodevelopmental Disorders	21
Totale	647

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	37	0	0	0	0	1	11	10	3	0	10	2	0
2020/2021	11	0	1	3	0	0	0	1	0	4	0	1	1
2021/2022	32	0	0	0	0	0	0	1	1	4	4	3	19
2022/2023	275	18	33	13	32	37	31	0	17	77	1	12	4
2023/2024	75	2	10	2	3	5	9	9	8	1	3	7	16
2024/2025	108	4	20	15	34	35	0	0	0	0	0	0	0
Totale													647