TARLARINI, CLAUDIA
 Distribuzione geografica
Continente #
EU - Europa 363
NA - Nord America 214
AS - Asia 127
OC - Oceania 6
AF - Africa 3
Totale 713
Nazione #
US - Stati Uniti d'America 211
GB - Regno Unito 118
DE - Germania 83
IT - Italia 45
CN - Cina 40
SE - Svezia 40
SG - Singapore 31
IE - Irlanda 18
IN - India 18
FI - Finlandia 11
RU - Federazione Russa 11
HK - Hong Kong 10
CZ - Repubblica Ceca 9
KR - Corea 9
BE - Belgio 7
AU - Australia 6
ID - Indonesia 6
TR - Turchia 6
FR - Francia 5
JP - Giappone 5
NL - Olanda 4
UA - Ucraina 4
CA - Canada 3
PT - Portogallo 3
ES - Italia 2
AE - Emirati Arabi Uniti 1
BJ - Benin 1
DK - Danimarca 1
GR - Grecia 1
IR - Iran 1
MU - Mauritius 1
NO - Norvegia 1
SC - Seychelles 1
Totale 713
Città #
Southend 95
Chandler 39
Frankfurt am Main 26
Wilmington 25
Seattle 19
Princeton 18
Dublin 16
Milan 16
Singapore 16
New York 14
Farnborough 10
Ashburn 9
Beijing 8
Des Moines 7
Nanjing 7
Helsinki 5
Hong Kong 5
Houston 5
Bengaluru 4
Cagliari 4
Ningbo 4
Norwalk 4
Redwood City 4
Shanghai 4
Waanrode 4
Boardman 3
Brussels 3
Nürnberg 3
Phoenix 3
Prague 3
San Diego 3
Trento 3
Ankara 2
Bitonto 2
Brisbane 2
Chicago 2
Enfield 2
Jakarta 2
Menlo Park 2
Monza 2
Mountain View 2
Nottingham 2
Olhão 2
Redmond 2
Santa Clara 2
Sheffield 2
Tagami 2
Tianjin 2
Toronto 2
Woodbridge 2
Zhengzhou 2
Absecon 1
Adelaide 1
Applecross 1
Arlington 1
Bari 1
Berlin 1
Bologna 1
Cambridge 1
Canberra 1
Central 1
Central District 1
Centro 1
Changsha 1
Charlotte 1
Chelmsford 1
College Park 1
Dearborn 1
Dubai 1
Edinburgh 1
Falls Church 1
Florence 1
Frankfurt (Oder) 1
Guangzhou 1
Haikou 1
Hanover 1
Hebei 1
Herndon 1
Izmir 1
Jiaxing 1
Kristiansand 1
Las Vegas 1
London 1
Mahé 1
Medford 1
Mohali 1
Mumbai 1
Nanchang 1
Olomouc 1
Pardis 1
Piano Di Sorrento 1
Pittsburgh 1
Porto 1
Rho 1
Rochester 1
Ryde 1
Saint Paul 1
Saint Petersburg 1
San Jose 1
Seoul 1
Totale 476
Nome #
MOLECULAR AND GENETIC CHARACTERIZATION OF ALS PATIENTS 232
De novo MGC4607 gene heterozygous missense variants in a child with multiple cerebral cavernous malformations 91
Amyotrophic lateral sclerosis in pregnancy is associated with a vascular endothelial growth factor promoter genotype 85
Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progression 79
Phenotypic heterogeneity in a SOD1 G93D Italian ALS family : an example of human model to study a complex disease 78
Urinary neopterin, a new marker of the neuroinflammatory status in amyotrophic lateral sclerosis 67
Wide phenotypic spectrum of the TARDBP gene : homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject 66
Neurophysiological indices in amyotrophic lateral sclerosis correlate with functional outcome measures, staging and disease progression 38
Taste changes in amyotrophic lateral sclerosis and effects on quality of life 34
Totale 770
Categoria #
all - tutte 2.842
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.842


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202048 0 0 0 0 6 3 4 3 16 8 6 2
2020/202153 2 2 0 2 8 7 2 7 2 1 11 9
2021/2022113 10 5 6 4 15 6 11 4 6 12 3 31
2022/2023149 15 16 18 16 18 31 1 7 22 0 5 0
2023/2024121 3 10 10 21 35 6 4 9 4 0 8 11
2024/202532 7 25 0 0 0 0 0 0 0 0 0 0
Totale 770