LAMP, MERIT
 Distribuzione geografica
Continente #
EU - Europa 1.284
AS - Asia 144
NA - Nord America 75
SA - Sud America 13
AF - Africa 3
OC - Oceania 1
Totale 1.520
Nazione #
IT - Italia 1.261
US - Stati Uniti d'America 69
SG - Singapore 51
CN - Cina 35
VN - Vietnam 32
BR - Brasile 12
BD - Bangladesh 10
FR - Francia 9
CA - Canada 4
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
BA - Bosnia-Erzegovina 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 1.520
Città #
Genova 659
Genoa 368
Rapallo 130
Vado Ligure 80
San Jose 24
Singapore 21
Ho Chi Minh City 16
Bordighera 11
Lauterbourg 8
Milan 6
Beijing 5
Hanoi 5
Los Angeles 5
Ashburn 4
Tokyo 4
Buffalo 3
Montreal 3
Amsterdam 2
Barcelona 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
Benton Harbor 1
Biên Hòa 1
Brampton 1
Brisbane 1
Brooklyn 1
Caetanópolis 1
Can Tho 1
Caxias do Sul 1
Chongqing 1
City of London 1
Copenhagen 1
Cranston 1
Dar es Salaam 1
Des Moines 1
Dublin 1
Erval Grande 1
Frankfurt am Main 1
Gainesville 1
Ha Long 1
Haiphong 1
Hayward 1
Helsinki 1
Itirapina 1
Jaguariaíva 1
Johannesburg 1
Mariano Roque Alonso 1
Maricá 1
Memphis 1
Mexico City 1
Mission 1
Nairobi 1
Namdong-gu 1
Navoiy 1
Orem 1
Oxon Hill 1
Phú Thọ 1
Plano 1
Porto Alegre 1
Quảng Ngãi 1
Quận Bình Thạnh 1
Rancho Palos Verdes 1
Reno 1
Rio de Janeiro 1
Rome 1
Rouen 1
Samambaia 1
San Bernardino 1
San Francisco 1
Santa Rosa 1
Scranton 1
Stockholm 1
Swedesboro 1
Thessaloniki 1
Tianjin 1
Turin 1
Vinhedo 1
Yirkā 1
Zurich 1
Totale 1.429
Nome #
Spinocerebellar ataxia 17: full phenotype in a 41 CAG/CAA repeats carrier. 216
Twenty years of molecular analyses in amyotrophic lateral sclerosis: genetic landscape of Italian patients 208
Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise" 171
A novel mutation of Twinkle in Perrault syndrome: A not rare diagnosis? 171
Two novel cases of compound heterozygous mutations in mitofusin2: Finding out the inheritance. 168
Neuroimaging features in C9orf72 and TARDBP double mutation with FTD phenotype. 162
Contribution of copy number variations in CMT1X: a retrospective study. 157
Role of MAPT in Pure Motor Neuron Disease: Report of a Recurrent Mutation in Italian Patients. 151
Quiz page february 2015: renal colic in an adolescent. 146
Totale 1.550
Categoria #
all - tutte 4.849
article - articoli 4.849
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 9.698


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20217 0 0 0 0 0 0 0 0 0 0 0 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
2025/2026377 72 6 13 28 66 19 54 17 20 39 19 24
Totale 1.550