DI ROCCO, MAJA
 Distribuzione geografica
Continente #
EU - Europa 616
NA - Nord America 113
AS - Asia 106
Continente sconosciuto - Info sul continente non disponibili 26
SA - Sud America 14
AF - Africa 1
Totale 876
Nazione #
IT - Italia 601
US - Stati Uniti d'America 100
SG - Singapore 50
VN - Vietnam 22
CN - Cina 20
BR - Brasile 9
FR - Francia 7
CA - Canada 6
AR - Argentina 4
BD - Bangladesh 3
HK - Hong Kong 3
MX - Messico 3
NL - Olanda 3
IQ - Iraq 2
OM - Oman 2
BG - Bulgaria 1
BH - Bahrain 1
BZ - Belize 1
CR - Costa Rica 1
EC - Ecuador 1
GB - Regno Unito 1
GR - Grecia 1
IN - India 1
JM - Giamaica 1
JP - Giappone 1
KE - Kenya 1
PK - Pakistan 1
PR - Porto Rico 1
RO - Romania 1
SE - Svezia 1
Totale 850
Città #
Genoa 282
Genova 194
Rapallo 60
Vado Ligure 60
San Jose 32
Singapore 29
Ashburn 25
Lauterbourg 7
Beijing 5
Ho Chi Minh City 4
Montreal 4
Hanoi 3
São Paulo 3
Boardman 2
Córdoba 2
Haiphong 2
Hong Kong 2
Los Angeles 2
Milan 2
Muscat 2
Summerville 2
Thái Bình 2
Albuquerque 1
Amsterdam 1
Aracaju 1
Arroio Grande 1
Athens 1
Baghdad 1
Belize City 1
Biên Hòa 1
Brasília 1
Brooklyn 1
Buffalo 1
Can Tho 1
Capitol Heights 1
Charlotte 1
Cincinnati 1
City of London 1
Croton-on-Hudson 1
Dallas 1
Dhaka 1
East White Plains 1
Erbil 1
Forlì 1
Greeley 1
Guangzhou 1
Guayaquil 1
Gustavo Adolfo Madero 1
Houston 1
Hưng Yên 1
Kearny 1
Kingston 1
Leander 1
Manama 1
Mexico City 1
Miami 1
Montclair 1
Nairobi 1
Naples 1
New York 1
Orem 1
Othón P. Blanco 1
Oxford 1
Pazardzhik 1
Phoenix 1
Porto Alegre 1
Queens 1
Quận Bình Thạnh 1
Rawalpindi 1
Resistencia 1
San Francisco 1
San José 1
Santa Clara 1
Santa Rosa Beach 1
Shenzhen 1
Slatina 1
Stockholm 1
São José dos Pinhais 1
São Lourenço da Mata 1
Thu Dau Mot 1
Tokyo 1
Toronto 1
Viedma 1
Warren 1
Yên Bái 1
Totale 789
Nome #
Widening the Heterogeneity of Leigh Syndrome: Clinical, Biochemical, and Neuroradiologic Features in a Patient Harboring a NDUFA10 Mutation 167
Epileptic Encephalopathy, Myoclonus-Dystonia, and Premature Pubarche in Siblings with a Novel C-Terminal Truncating Mutation in ATRX Gene 163
ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases 162
LONG-TERM OUTCOME IN CEREBRAL ARTERIA ISCHEMIC STROKE (AIS) DUE TO VARICELLA ZOSTER VIRUS (VZV) IN CHILDREN 115
Erratum: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia (Brain (2021) 144:5 (1422-1434) DOI: 10.1093/brain/awab041) 102
Pontocerebellar hypoplasia: Clinical, pathologic, and genetic studies 90
The shrunken, bright cerebellum: A characteristic MRI finding in congenital disorders of glycosylation type 1a 77
Totale 876
Categoria #
all - tutte 3.369
article - articoli 3.369
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 6.738


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/202255 0 0 3 3 8 9 1 13 4 6 2 6
2022/202371 5 8 3 6 6 14 0 7 10 0 12 0
2023/202475 10 5 1 8 3 9 5 9 4 1 4 16
2024/2025187 13 12 6 13 16 11 27 34 3 6 27 19
2025/2026288 45 6 10 23 56 17 39 18 24 19 12 19
2026/202745 24 14 7 0 0 0 0 0 0 0 0 0
Totale 876