CARECCHIO, Miryam
 Distribuzione geografica
Continente #
EU - Europa 197
NA - Nord America 187
AS - Asia 114
SA - Sud America 11
AF - Africa 2
Totale 511
Nazione #
US - Stati Uniti d'America 181
IE - Irlanda 49
SG - Singapore 40
DE - Germania 37
SE - Svezia 30
IT - Italia 27
CN - Cina 26
HK - Hong Kong 22
UA - Ucraina 16
RU - Federazione Russa 9
BR - Brasile 6
GB - Regno Unito 5
VN - Vietnam 5
AT - Austria 4
CA - Canada 4
CZ - Repubblica Ceca 4
ES - Italia 4
FI - Finlandia 4
IN - India 4
KR - Corea 4
FR - Francia 3
JP - Giappone 3
AR - Argentina 2
BD - Bangladesh 2
BE - Belgio 2
BJ - Benin 2
MX - Messico 2
TR - Turchia 2
CL - Cile 1
CO - Colombia 1
ID - Indonesia 1
IQ - Iraq 1
IR - Iran 1
KG - Kirghizistan 1
KH - Cambogia 1
LT - Lituania 1
NL - Olanda 1
PH - Filippine 1
PL - Polonia 1
UY - Uruguay 1
Totale 511
Città #
Dublin 49
Jacksonville 24
Hong Kong 22
Beijing 15
Ashburn 14
Ann Arbor 12
Dearborn 12
Singapore 12
Chandler 9
Munich 9
New York 8
Wilmington 8
Lawrence 5
Milan 5
Princeton 5
Brno 4
Buffalo 4
Dallas 4
Denver 4
Seoul 4
Boardman 3
Bremen 3
Ho Chi Minh City 3
Los Angeles 3
Novara 3
Piemonte 3
San Mateo 3
Santa Clara 3
Stockholm 3
Tokyo 3
Borgomanero 2
Brooklyn 2
Brussels 2
Cassano Magnago 2
Chennai 2
City of London 2
Cotonou 2
Falkenstein 2
Monmouth Junction 2
Moscow 2
Rome 2
Strasbourg 2
The Dalles 2
Vienna 2
Winnipeg 2
Amsterdam 1
Atlanta 1
Augusta 1
Bishkek 1
Bologna 1
Columbus 1
Dhaka 1
Düsseldorf 1
Frankfurt am Main 1
Genoa 1
Guarapari 1
Hefei 1
Houston 1
Istanbul 1
Itabira 1
Jakarta 1
Jinan 1
Kidderminster 1
Kocaeli 1
Kunming 1
Leawood 1
Manila 1
Mariana 1
Medellín 1
Mexico City 1
Montevideo 1
Montreal 1
Nanjing 1
Nasiriyah 1
New Delhi 1
Orem 1
Phnom Penh 1
Poplar 1
Porto Alegre 1
Posadas 1
Puente Alto 1
Querétaro 1
San Fernando 1
San Francisco 1
Seattle 1
Shanghai 1
Shaoxing 1
Shenyang 1
São Paulo 1
Tarumirim 1
Turku 1
Warsaw 1
Zanjan 1
Totale 337
Nome #
A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b 104
Phenotypic heterogeneity of movement disorders due to intracranial calcifications with or without SLC20A2 mutations 99
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series 92
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson’s disease 89
Short-term videoEEG: Review of a 3-year experience [Short-term videoEEG: Studio retrospettivo di 3 anni di esperienza clinica] 86
Pediatric Onset of Generalized Dystonia, Cognitive Impairment, and Dysmorphic Features in a Patient Carrying Compound Heterozygous GNAL Mutations 54
Totale 524
Categoria #
all - tutte 2.633
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 2.633


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202119 0 0 0 0 0 1 5 0 5 3 5 0
2021/202247 4 0 3 6 7 0 1 1 3 2 9 11
2022/202399 7 9 4 1 5 7 4 5 48 1 6 2
2023/202435 2 4 3 2 5 0 6 0 0 0 6 7
2024/2025104 0 6 4 10 5 7 13 13 19 4 8 15
2025/2026127 16 7 14 43 33 14 0 0 0 0 0 0
Totale 524