LAMP, MERIT
 Distribuzione geografica
Continente #
EU - Europa 1.280
AS - Asia 133
NA - Nord America 46
SA - Sud America 13
AF - Africa 3
OC - Oceania 1
Totale 1.476
Nazione #
IT - Italia 1.258
SG - Singapore 51
US - Stati Uniti d'America 43
CN - Cina 33
VN - Vietnam 32
BR - Brasile 12
FR - Francia 9
JP - Giappone 4
ES - Italia 2
HK - Hong Kong 2
IN - India 2
NL - Olanda 2
PH - Filippine 2
TR - Turchia 2
AU - Australia 1
BD - Bangladesh 1
CA - Canada 1
CH - Svizzera 1
DE - Germania 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
FI - Finlandia 1
GB - Regno Unito 1
GR - Grecia 1
IE - Irlanda 1
IL - Israele 1
IQ - Iraq 1
KE - Kenya 1
KR - Corea 1
MX - Messico 1
PY - Paraguay 1
RU - Federazione Russa 1
SE - Svezia 1
TZ - Tanzania 1
UZ - Uzbekistan 1
ZA - Sudafrica 1
Totale 1.476
Città #
Genova 659
Genoa 368
Rapallo 130
Vado Ligure 80
Singapore 21
Ho Chi Minh City 16
San Jose 15
Bordighera 11
Lauterbourg 8
Milan 6
Hanoi 5
Los Angeles 5
Tokyo 4
Beijing 3
Amsterdam 2
Ashburn 2
Barcelona 2
Buffalo 2
Chennai 2
Da Nang 2
Hong Kong 2
New York 2
Santa Clara 2
São Paulo 2
Baghdad 1
Baguio City 1
Bath 1
Biên Hòa 1
Brampton 1
Brisbane 1
Caetanópolis 1
Can Tho 1
Caxias do Sul 1
Chongqing 1
City of London 1
Copenhagen 1
Dar es Salaam 1
Des Moines 1
Dublin 1
Erval Grande 1
Frankfurt am Main 1
Ha Long 1
Haiphong 1
Helsinki 1
Itirapina 1
Jaguariaíva 1
Johannesburg 1
Mariano Roque Alonso 1
Maricá 1
Memphis 1
Mexico City 1
Nairobi 1
Namdong-gu 1
Navoiy 1
Orem 1
Phú Thọ 1
Plano 1
Porto Alegre 1
Quảng Ngãi 1
Quận Bình Thạnh 1
Reno 1
Rio de Janeiro 1
Rome 1
Rouen 1
Samambaia 1
San Bernardino 1
Santa Rosa 1
Stockholm 1
Thessaloniki 1
Tianjin 1
Turin 1
Vinhedo 1
Yirkā 1
Zurich 1
Totale 1.401
Nome #
Twenty years of molecular analyses in amyotrophic lateral sclerosis: genetic landscape of Italian patients 205
Spinocerebellar ataxia 17: full phenotype in a 41 CAG/CAA repeats carrier. 197
A novel mutation of Twinkle in Perrault syndrome: A not rare diagnosis? 168
Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise" 167
Two novel cases of compound heterozygous mutations in mitofusin2: Finding out the inheritance. 162
Neuroimaging features in C9orf72 and TARDBP double mutation with FTD phenotype. 161
Contribution of copy number variations in CMT1X: a retrospective study. 154
Role of MAPT in Pure Motor Neuron Disease: Report of a Recurrent Mutation in Italian Patients. 147
Quiz page february 2015: renal colic in an adolescent. 145
Totale 1.506
Categoria #
all - tutte 4.651
article - articoli 4.651
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 9.302


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202131 0 0 0 0 0 0 0 0 0 16 8 7
2021/2022121 1 5 10 9 10 7 5 31 8 13 7 15
2022/2023148 10 13 4 13 27 20 0 10 26 0 21 4
2023/202492 8 5 1 13 2 22 7 13 2 1 5 13
2024/2025246 11 16 6 16 25 18 15 54 11 12 33 29
2025/2026333 72 6 13 28 66 19 54 17 20 38 0 0
Totale 1.506