Bicocca Open Archive

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COMBI, ROMINA
 Distribuzione geografica
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Continente #
NA - Nord America 6.403
EU - Europa 2.954
AS - Asia 2.464
SA - Sud America 388
AF - Africa 31
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 3
Totale 12.249
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Nazione #
US - Stati Uniti d'America 6.246
SG - Singapore 849
CN - Cina 763
IT - Italia 635
DE - Germania 498
SE - Svezia 435
RU - Federazione Russa 394
HK - Hong Kong 365
BR - Brasile 309
IE - Irlanda 273
UA - Ucraina 225
VN - Vietnam 173
GB - Regno Unito 150
CA - Canada 120
AT - Austria 71
FI - Finlandia 71
IN - India 54
KR - Corea 53
DK - Danimarca 48
FR - Francia 46
TR - Turchia 44
ID - Indonesia 43
AR - Argentina 33
BD - Bangladesh 27
MX - Messico 27
NL - Olanda 26
PL - Polonia 26
BE - Belgio 23
ZA - Sudafrica 19
EC - Ecuador 17
JP - Giappone 16
ES - Italia 14
IR - Iran 12
CL - Cile 10
IQ - Iraq 10
IL - Israele 8
PK - Pakistan 7
AZ - Azerbaigian 6
SA - Arabia Saudita 6
VE - Venezuela 6
TW - Taiwan 5
AE - Emirati Arabi Uniti 4
EU - Europa 4
PE - Perù 4
CO - Colombia 3
EG - Egitto 3
GR - Grecia 3
HN - Honduras 3
JO - Giordania 3
LT - Lituania 3
MA - Marocco 3
PY - Paraguay 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BG - Bulgaria 2
BO - Bolivia 2
CH - Svizzera 2
CR - Costa Rica 2
KE - Kenya 2
LB - Libano 2
LK - Sri Lanka 2
NO - Norvegia 2
NP - Nepal 2
PH - Filippine 2
PT - Portogallo 2
UZ - Uzbekistan 2
AL - Albania 1
AU - Australia 1
BW - Botswana 1
BY - Bielorussia 1
CZ - Repubblica Ceca 1
DM - Dominica 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
HU - Ungheria 1
JM - Giamaica 1
KI - Kiribati 1
KZ - Kazakistan 1
MY - Malesia 1
NZ - Nuova Zelanda 1
OM - Oman 1
PA - Panama 1
PS - Palestinian Territory 1
RS - Serbia 1
SN - Senegal 1
SV - El Salvador 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
TN - Tunisia 1
UY - Uruguay 1
Totale 12.249
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Città #
Ann Arbor 1.371
Ashburn 507
Singapore 506
Woodbridge 449
Fairfield 434
Hong Kong 365
Houston 363
Chandler 354
Frankfurt am Main 351
Wilmington 278
Dublin 272
Milan 263
Jacksonville 226
New York 158
Dearborn 156
Cambridge 150
Seattle 150
Santa Clara 136
Princeton 105
Beijing 100
Hefei 100
Nanjing 85
Dallas 79
Los Angeles 76
Vienna 65
Chicago 52
Shanghai 52
Seoul 48
Lawrence 42
Ho Chi Minh City 41
Buffalo 40
Guangzhou 40
Ottawa 40
Altamura 39
Jakarta 38
Lachine 37
Nanchang 37
Hanoi 34
Moscow 34
Council Bluffs 31
San Diego 31
Fremont 30
São Paulo 28
Boardman 25
Helsinki 25
Shenyang 24
Dong Ket 23
Brussels 21
The Dalles 20
Hebei 17
Munich 17
Toronto 17
Andover 16
Kraków 15
Brooklyn 14
Rio de Janeiro 14
Detroit 13
Hangzhou 13
Norwalk 13
Rome 13
Stockholm 13
Tianjin 13
Jinan 12
London 12
Falls Church 11
Jiaxing 11
Kent 11
Montreal 11
Phoenix 11
Chennai 10
Hyderabad 10
Biên Hòa 9
Boston 9
Changsha 9
Poplar 9
Tokyo 9
Warsaw 9
Zhengzhou 9
Da Nang 8
Dhaka 8
Elk Grove Village 8
Johannesburg 8
Quito 8
Salt Lake City 8
Ankara 7
Atlanta 7
Auburn Hills 7
Brasília 7
Denver 7
Gelsenkirchen 7
Mexico City 7
Miami 7
Monza 7
Mountain View 7
Orem 7
Philadelphia 7
Baku 6
Kocaeli 6
Taizhou 6
University Park 6
Totale 8.437
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Nome #
CHRNA2 and nocturnal frontal lobe epilepsy: Identification and characterization of a novel loss of function mutation 487
Analysis of human papillomavirus (HPV) 16 variants associated with cervical infection in Italian women 401
Simultaneous overexpression of human E5NT and ENTPD1 protects porcine endothelial cells against H2O2-induced oxidative stress and cytotoxicity in vitro 384
A novel KCNJ2 mutation identified in an autistic proband affects the single channel properties of Kir2.1 329
Molecular and imaging biomarkers in Alzheimer’s disease: A focus on recent insights 302
Variants in CHRNB2 and CHRNA4 identified in patients with insular epilepsy 299
Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutation 298
Understanding the basis of Ehlers-Danlos syndrome in the era of the next-generation sequencing 295
Identification of two mutations in cis in the SCN1A gene in a family showing genetic epilepsy with febrile seizures plus (GEFS+) and idiopathic generalized epilepsy (IGE) 292
Potassium channels in the neuronal homeostasis and neurodegenerative pathways underlying Alzheimer's disease: An update 291
Long Non-Coding RNAs and Related Molecular Pathways in the Pathogenesis of Epilepsy 290
Patient-Derived Induced Pluripotent Stem Cells (iPSCs) and Cerebral Organoids for Drug Screening and Development in Autism Spectrum Disorder: Opportunities and Challenges 286
Functional Characterization of a CRH Missense Mutation Identified in an ADNFLE Family 275
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy 272
Sleep disorder-related headaches 269
Maternal polymorphisms for methyltetrahydrofolate reductase (MTHFR) and methioninesynthetasi-reductase (MTRR) and risk of children with down syndrome: A geographic effect? 266
The synergistic relationship between Alzheimer's disease and sleep disorders: An update 248
Clinical and genetic evaluation of a family showing both autism and epilepsy 245
Genetic architecture and molecular, imaging and prodromic markers in dementia with lewy bodies: State of the art, opportunities and challenges 244
TSPO Modulates Oligomeric Amyloid-β-Induced Monocyte Chemotaxis: Relevance for Neuroinflammation in Alzheimer's Disease 240
Maternal polymorphisms for methyltetrahydrofolate reductase and methionine synthetase reductase and risk of children with Down syndrome 240
Potassium channels and human epileptic phenotypes: An updated overview 238
Restless legs syndrome and painful legs/moving toes 235
Nocturnal frontal lobe epilepsy and the acetylcholine receptor 233
A de novo mutation in an Italian sporadic patient affected by Nocturnal frontal lobe epilepsy 223
Distinct pools of cancer stem-like cells coexist within human glioblastomas and display different tumorigenicity and independent genomic evolution 218
Can SARS-CoV-2 Infection Exacerbate Alzheimer’s Disease? An Overview of Shared Risk Factors and Pathogenetic Mechanisms 215
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy 206
Identification and functional characterisation of a new KCNJ2 mutation 206
Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone gene 203
Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated families 203
Gene Symbol: SCN1A 201
Autosomal dominant nocturnal frontal lobe epilepsy - A critical overview 198
Maternal heterodisomy/isodisomy and paternal supernumerary ring of chromosome 7 in a child with Silver-Russel syndrome 191
aCGH analysis of two families showing both autism and epilepsy 187
Does the Type of Multisystem Atrophy, Parkinsonism, or Cerebellar Ataxia Impact on the Nature of Sleep Disorders? 185
Clinical and genetic familial study of 61 children showing different epileptic phenotypes. 184
Clinical and genetic evaluation of a family showing both autism and epilepsy 180
Epigenetics in Alzheimer’s Disease: A Critical Overview 178
CHRNA2 mutations are rare in the NFLE population: Evaluation of a large cohort of Italian patients 178
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy 177
Two new susceptibility loci for ADNFLE 175
A rescuable folding defective Nav1.1 (SCN1A) Na+channel mutant causes GEFS+: common mechanism in Nav1.1 related epilepsies? 175
Mutations of the orexin system, a regulator of sleep arousal, are not a common cause of ADNFLE. 172
Evidence of the existence of at least a fourth locus for ADNFLE 169
Role of the SCN1A gene in the pathogenesis of familial febrile seizures and GEFS+ 168
Familiar Febrile Seizures and Mutations in the Nav1.1 Sodium Channel 162
Exome Sequencing in an ADSHE Family: VUS Identification and Limits 160
Two new putative loci for ADNFLE identified in an Italian family suggest a digenic inheritance for the disease 160
Restless Leg Syndrome Through the Magnifying Glass of Genetics 159
Compound heterozygosity with dominance in the CRH (Corticotropin Releasing Hormone)promoter in a case of nocturnal frontal lobe epilepsy 158
Study of the genetic basis of autosomal dominant nocturnal frontal lobe epilepsy 150
Ricerca di mutazioni in una famiglia ADNFLE. 148
Ricerca di mutazioni in pazienti affetti da NFLE 145
Nocturnal Frontal Lobe Epilepsy 144
Corticotropin releasing hormone in frontal lobe epilepsy 139
Totale 12.676
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Categoria #
all - tutte 40.292
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 40.292
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021971 0 0 0 0 0 149 134 136 130 157 125 140
2021/2022967 83 97 145 120 60 93 22 66 39 50 58 134
2022/20231.413 156 428 131 153 101 212 6 77 87 5 41 16
2023/2024808 33 33 33 43 97 220 172 22 43 9 7 96
2024/20251.937 112 216 192 79 168 82 79 83 182 305 135 304
2025/20262.348 495 363 374 468 581 67 0 0 0 0 0 0
Totale 12.676