Bicocca Open Archive

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COMBI, ROMINA
 Distribuzione geografica
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Continente #
NA - Nord America 7.142
AS - Asia 3.314
EU - Europa 3.167
SA - Sud America 478
AF - Africa 73
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 6
Totale 14.186
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Nazione #
US - Stati Uniti d'America 6.956
SG - Singapore 1.136
CN - Cina 837
IT - Italia 682
DE - Germania 506
SE - Svezia 436
RU - Federazione Russa 403
HK - Hong Kong 388
VN - Vietnam 371
BR - Brasile 352
IE - Irlanda 276
UA - Ucraina 229
GB - Regno Unito 182
CA - Canada 129
IN - India 113
FR - Francia 103
FI - Finlandia 76
AT - Austria 71
TR - Turchia 68
KR - Corea 67
BD - Bangladesh 64
ID - Indonesia 52
DK - Danimarca 48
AR - Argentina 43
PL - Polonia 36
IQ - Iraq 35
MX - Messico 33
ES - Italia 31
NL - Olanda 29
ZA - Sudafrica 27
BE - Belgio 24
EC - Ecuador 23
PH - Filippine 22
PK - Pakistan 20
JP - Giappone 19
SA - Arabia Saudita 17
CO - Colombia 14
CL - Cile 13
VE - Venezuela 13
IR - Iran 12
UZ - Uzbekistan 10
OM - Oman 9
AZ - Azerbaigian 8
IL - Israele 8
MA - Marocco 8
CH - Svizzera 7
CR - Costa Rica 7
EG - Egitto 7
MY - Malesia 7
NP - Nepal 7
TW - Taiwan 7
AE - Emirati Arabi Uniti 6
ET - Etiopia 6
JO - Giordania 6
LB - Libano 6
TH - Thailandia 6
UY - Uruguay 6
BO - Bolivia 5
LT - Lituania 5
PE - Perù 5
TN - Tunisia 5
EU - Europa 4
JM - Giamaica 4
PT - Portogallo 4
PY - Paraguay 4
BG - Bulgaria 3
CZ - Repubblica Ceca 3
DZ - Algeria 3
GR - Grecia 3
HN - Honduras 3
KE - Kenya 3
PA - Panama 3
SY - Repubblica araba siriana 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AU - Australia 2
BH - Bahrain 2
BY - Bielorussia 2
DO - Repubblica Dominicana 2
HU - Ungheria 2
KG - Kirghizistan 2
LK - Sri Lanka 2
LY - Libia 2
NI - Nicaragua 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
RS - Serbia 2
SN - Senegal 2
SV - El Salvador 2
AL - Albania 1
AO - Angola 1
BJ - Benin 1
BW - Botswana 1
DM - Dominica 1
GA - Gabon 1
GH - Ghana 1
HR - Croazia 1
KI - Kiribati 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
ML - Mali 1
Totale 14.179
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Città #
Ann Arbor 1.371
Ashburn 639
Singapore 617
Woodbridge 449
Fairfield 434
Hong Kong 384
Houston 367
Frankfurt am Main 358
Chandler 354
San Jose 278
Wilmington 278
Dublin 275
Milan 266
Jacksonville 227
New York 176
Dearborn 156
Cambridge 150
Seattle 150
Santa Clara 139
Chicago 110
Princeton 105
Beijing 103
Hefei 100
Los Angeles 94
Hanoi 90
Ho Chi Minh City 88
Nanjing 86
Dallas 84
Vienna 65
Council Bluffs 60
Seoul 59
Shanghai 55
The Dalles 52
Lauterbourg 45
Buffalo 43
Jakarta 42
Lawrence 42
Guangzhou 40
Ottawa 40
Altamura 39
Orem 39
Lachine 37
Nanchang 37
Moscow 36
San Diego 31
São Paulo 31
Fremont 30
Helsinki 30
Boardman 25
Shenyang 25
Dong Ket 23
Brussels 21
London 20
Rome 20
Chennai 19
Da Nang 19
Montreal 18
Toronto 18
Hebei 17
Munich 17
Andover 16
Rio de Janeiro 16
Warsaw 16
Kraków 15
Brooklyn 14
Detroit 14
Stockholm 14
Atlanta 13
Hangzhou 13
Norwalk 13
Tianjin 13
Biên Hòa 12
Haiphong 12
Jinan 12
Johannesburg 12
Kent 12
Phoenix 12
Ankara 11
Falls Church 11
Hyderabad 11
Jiaxing 11
Baghdad 10
Tokyo 10
Boston 9
Changsha 9
Dhaka 9
Poplar 9
Quito 9
Zhengzhou 9
Denver 8
Elk Grove Village 8
Manchester 8
Mumbai 8
Salt Lake City 8
Tashkent 8
Auburn Hills 7
Brasília 7
Erbil 7
Gelsenkirchen 7
Lahore 7
Totale 9.453
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Nome #
CHRNA2 and nocturnal frontal lobe epilepsy: Identification and characterization of a novel loss of function mutation 555
Analysis of human papillomavirus (HPV) 16 variants associated with cervical infection in Italian women 440
Simultaneous overexpression of human E5NT and ENTPD1 protects porcine endothelial cells against H2O2-induced oxidative stress and cytotoxicity in vitro 435
A novel KCNJ2 mutation identified in an autistic proband affects the single channel properties of Kir2.1 374
Molecular and imaging biomarkers in Alzheimer’s disease: A focus on recent insights 346
Variants in CHRNB2 and CHRNA4 identified in patients with insular epilepsy 345
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) 339
Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutation 332
Patient-Derived Induced Pluripotent Stem Cells (iPSCs) and Cerebral Organoids for Drug Screening and Development in Autism Spectrum Disorder: Opportunities and Challenges 332
Understanding the basis of Ehlers-Danlos syndrome in the era of the next-generation sequencing 329
Long Non-Coding RNAs and Related Molecular Pathways in the Pathogenesis of Epilepsy 328
Potassium channels in the neuronal homeostasis and neurodegenerative pathways underlying Alzheimer's disease: An update 325
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy 312
TSPO Modulates Oligomeric Amyloid-β-Induced Monocyte Chemotaxis: Relevance for Neuroinflammation in Alzheimer's Disease 311
Functional Characterization of a CRH Missense Mutation Identified in an ADNFLE Family 309
Sleep disorder-related headaches 306
Genetic architecture and molecular, imaging and prodromic markers in dementia with lewy bodies: State of the art, opportunities and challenges 287
Maternal polymorphisms for methyltetrahydrofolate reductase (MTHFR) and methioninesynthetasi-reductase (MTRR) and risk of children with down syndrome: A geographic effect? 286
Clinical and genetic evaluation of a family showing both autism and epilepsy 280
Can SARS-CoV-2 Infection Exacerbate Alzheimer’s Disease? An Overview of Shared Risk Factors and Pathogenetic Mechanisms 273
Maternal polymorphisms for methyltetrahydrofolate reductase and methionine synthetase reductase and risk of children with Down syndrome 271
Nocturnal frontal lobe epilepsy and the acetylcholine receptor 269
The synergistic relationship between Alzheimer's disease and sleep disorders: An update 269
Potassium channels and human epileptic phenotypes: An updated overview 268
Restless legs syndrome and painful legs/moving toes 261
Identification and functional characterisation of a new KCNJ2 mutation 251
Distinct pools of cancer stem-like cells coexist within human glioblastomas and display different tumorigenicity and independent genomic evolution 246
A de novo mutation in an Italian sporadic patient affected by Nocturnal frontal lobe epilepsy 245
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy 242
Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone gene 231
Epigenetics in Alzheimer’s Disease: A Critical Overview 229
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 229
aCGH analysis of two families showing both autism and epilepsy 227
Gene Symbol: SCN1A 226
Autosomal dominant nocturnal frontal lobe epilepsy - A critical overview 224
Maternal heterodisomy/isodisomy and paternal supernumerary ring of chromosome 7 in a child with Silver-Russel syndrome 214
Does the Type of Multisystem Atrophy, Parkinsonism, or Cerebellar Ataxia Impact on the Nature of Sleep Disorders? 212
Exome Sequencing in an ADSHE Family: VUS Identification and Limits 210
Clinical and genetic familial study of 61 children showing different epileptic phenotypes. 208
A rescuable folding defective Nav1.1 (SCN1A) Na+channel mutant causes GEFS+: common mechanism in Nav1.1 related epilepsies? 207
Two new susceptibility loci for ADNFLE 202
Restless Leg Syndrome Through the Magnifying Glass of Genetics 200
Clinical and genetic evaluation of a family showing both autism and epilepsy 198
CHRNA2 mutations are rare in the NFLE population: Evaluation of a large cohort of Italian patients 196
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy 194
Familiar Febrile Seizures and Mutations in the Nav1.1 Sodium Channel 194
Role of the SCN1A gene in the pathogenesis of familial febrile seizures and GEFS+ 192
Mutations of the orexin system, a regulator of sleep arousal, are not a common cause of ADNFLE. 190
Evidence of the existence of at least a fourth locus for ADNFLE 188
Ricerca di mutazioni in una famiglia ADNFLE. 179
Study of the genetic basis of autosomal dominant nocturnal frontal lobe epilepsy 177
Two new putative loci for ADNFLE identified in an Italian family suggest a digenic inheritance for the disease 174
Ricerca di mutazioni in pazienti affetti da NFLE 174
Compound heterozygosity with dominance in the CRH (Corticotropin Releasing Hormone)promoter in a case of nocturnal frontal lobe epilepsy 172
Nocturnal Frontal Lobe Epilepsy 164
Corticotropin releasing hormone in frontal lobe epilepsy 154
Characterization of a novel missense mutation in the α2 subunit of the neuronal nicotinic acetylcholine receptor linked to sleep-related generalized seizures with cognitive deficit 37
Functional study of a mutant α2 subunit of the neuronal nicotinic acetylcholine receptor linked to sleep-related generalized seizures with cognitive deficit 30
Identification of a novel missense variant in a family with autosomal dominant sleep-related hypermotor epilepsy (ADSHE) 24
Totale 14.622
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Categoria #
all - tutte 44.491
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 44.491
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021265 0 0 0 0 0 0 0 0 0 0 125 140
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
2025/20264.294 495 363 374 468 581 241 563 258 439 443 69 0
Totale 14.622