VAZZA, GIOVANNI
 Distribuzione geografica
Continente #
NA - Nord America 157
EU - Europa 48
AS - Asia 11
SA - Sud America 3
AF - Africa 2
Totale 221
Nazione #
US - Stati Uniti d'America 156
IT - Italia 18
FR - Francia 15
CN - Cina 5
DE - Germania 5
JP - Giappone 4
CL - Cile 2
ES - Italia 2
ZA - Sudafrica 2
AE - Emirati Arabi Uniti 1
BR - Brasile 1
CA - Canada 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
FI - Finlandia 1
GB - Regno Unito 1
HK - Hong Kong 1
RO - Romania 1
RU - Federazione Russa 1
SE - Svezia 1
UA - Ucraina 1
Totale 221
Città #
Fairfield 19
Ashburn 14
Buffalo 14
Santa Cruz 10
Padova 8
Cambridge 6
Houston 6
Seattle 6
San Diego 5
Wilmington 5
Woodbridge 5
Brendola 4
Des Moines 4
Chicago 3
Lombard 3
Barcelona 2
Beijing 2
Fort Collins 2
Gorizia 2
Handayama 2
Ann Arbor 1
Boardman 1
Borås 1
Cedar Knolls 1
Central 1
Cologny 1
Dallas 1
Denver 1
Frankfurt am Main 1
Helsinki 1
Henderson 1
Herndon 1
Kirkland 1
Las Vegas 1
Lincolnshire 1
London 1
Los Angeles 1
Monza 1
Moscow 1
Muizenberg 1
Nashville 1
New Orleans 1
Niigata 1
Oak Lawn 1
Ottawa 1
Paris 1
Phoenix 1
Qingdao 1
Recife 1
San Jose 1
Sapporo 1
Shanghai 1
Siena 1
Silverton 1
Tampa 1
University Park 1
Vicenza 1
West Chicago 1
Totale 160
Nome #
Familly with two different cases of post- and pre-natal L1 syndrome; When hydrocephaly become "multidisciplinary headache", file e14fb269-41c8-3de1-e053-1705fe0ac030 117
The GIP/GIPR axis is functionally linked to GH-secretion increase in a significant proportion of gsp(-) somatotropinomas, file e14fb26f-9521-3de1-e053-1705fe0ac030 58
Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network, file e14fb270-2015-3de1-e053-1705fe0ac030 17
Novel mutations in the L1CAM gene support the complexity of L1 syndrome, file e14fb267-8de3-3de1-e053-1705fe0ac030 11
Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlations, file e14fb26f-1e0b-3de1-e053-1705fe0ac030 8
The Methylation Analysis of the Glucose-Dependent Insulinotropic Polypeptide Receptor (GIPR) Locus in GH-Secreting Pituitary Adenomas., file 91af3dc2-4f9e-4058-bd35-440088118776 4
MFN2 KNOCKDOWN CAUSES NEUROMUSCULAR ALTERATIONS DURING ZEBRAFISH (DANIO RERIO) DEVELOPMENT: CHARACTERIZATION AND ANALYSIS OF A NEW MODEL FOR CHARCOT-MARIE-TOOTH TYPE 2A NEUROPATHY, file e14fb267-637f-3de1-e053-1705fe0ac030 4
Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signaling, file e14fb26c-df25-3de1-e053-1705fe0ac030 4
Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder., file e14fb267-9ada-3de1-e053-1705fe0ac030 3
Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants., file e14fb268-5cb8-3de1-e053-1705fe0ac030 1
Diagnosis of Primary Ciliary Dyskinesia by a Targeted Next-Generation Sequencing Panel: Molecular and Clinical Findings in Italian Patients, file e14fb269-40e6-3de1-e053-1705fe0ac030 1
Totale 228
Categoria #
all - tutte 1.012
article - articoli 956
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 1.968


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201912 0 0 0 0 0 0 0 0 0 0 6 6
2019/202027 4 3 1 1 4 1 1 4 3 2 1 2
2020/202117 0 2 2 2 1 1 1 3 3 0 2 0
2021/202254 0 8 3 1 7 2 6 4 0 2 16 5
2022/202367 3 5 17 11 7 8 6 3 0 1 5 1
2023/202438 0 2 1 0 2 10 6 5 8 4 0 0
Totale 228