statistiche ricercatore

Continente	#
NA - Nord America	1.174
EU - Europa	910
AS - Asia	114
SA - Sud America	4
OC - Oceania	2
Continente sconosciuto - Info sul continente non disponibili	1
Totale	2.205

Nome	#
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients	278
Cerebellum and neuropsychiatric disorders: insights from ARSACS	211
Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrum	204
Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsies.	188
null	182
Tarlov cysts: clinical evaluation of an italian cohort of patients.	180
Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene.	172
A new thymidine phosphorylase mutation causing elongation of the protein underlies mitochondrial neurogastrointestinal encephalomyopathy	156
The first Italian patient with oculopharyngodistal myopathy: Case report and considerations on differential diagnosis.	152
Clinical and biochemical improvement following HSCT in a patient with MNGIE: 1-year follow-up.	144
Hand muscles corticomotor excitability in hereditary spastic paraparesis type 4.	132
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome	127
Neurophthalmologic and Orthoptic Ambulatory Assessments Reveal Ocular and Visual Changes in Patients With Early Alzheimer and Parkinson's Disease	80
Vitamin D levels in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)	38
Totale	2.244

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	126	0	0	0	0	0	0	0	0	0	0	66	60
2019/2020	481	52	22	34	84	33	41	39	54	57	27	16	22
2020/2021	312	15	28	22	24	18	28	11	44	22	44	32	24
2021/2022	208	17	33	6	9	19	6	18	6	13	19	21	41
2022/2023	263	20	16	41	28	23	52	8	22	25	16	7	5
2023/2024	243	4	2	27	18	7	71	90	7	5	10	2	0
Totale													2.244