Bicocca Open Archive

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COMBI, ROMINA
 Distribuzione geografica
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Continente #
NA - Nord America 8.565
EU - Europa 3.453
AS - Asia 3.361
SA - Sud America 505
Continente sconosciuto - Info sul continente non disponibili 445
AF - Africa 74
OC - Oceania 6
Totale 16.409
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Nazione #
US - Stati Uniti d'America 8.094
SG - Singapore 1.139
IT - Italia 955
CN - Cina 847
DE - Germania 506
SE - Svezia 437
RU - Federazione Russa 403
HK - Hong Kong 388
CA - Canada 387
VN - Vietnam 377
BR - Brasile 363
IE - Irlanda 276
UA - Ucraina 229
GB - Regno Unito 187
IN - India 113
FR - Francia 103
BD - Bangladesh 76
FI - Finlandia 76
AT - Austria 71
TR - Turchia 69
KR - Corea 67
ID - Indonesia 54
DK - Danimarca 48
AR - Argentina 43
IQ - Iraq 36
PL - Polonia 36
MX - Messico 34
ES - Italia 32
NL - Olanda 30
EC - Ecuador 28
ZA - Sudafrica 27
PH - Filippine 25
BE - Belgio 24
PK - Pakistan 22
CO - Colombia 21
JP - Giappone 20
SA - Arabia Saudita 17
VE - Venezuela 16
CL - Cile 14
JM - Giamaica 13
IR - Iran 12
CR - Costa Rica 11
MY - Malesia 10
UZ - Uzbekistan 10
NP - Nepal 9
OM - Oman 9
AZ - Azerbaigian 8
CH - Svizzera 8
IL - Israele 8
MA - Marocco 8
AE - Emirati Arabi Uniti 7
EG - Egitto 7
TW - Taiwan 7
ET - Etiopia 6
JO - Giordania 6
LB - Libano 6
LT - Lituania 6
TH - Thailandia 6
UY - Uruguay 6
BO - Bolivia 5
PE - Perù 5
TN - Tunisia 5
EU - Europa 4
GR - Grecia 4
HN - Honduras 4
KE - Kenya 4
NI - Nicaragua 4
PT - Portogallo 4
PY - Paraguay 4
BG - Bulgaria 3
CZ - Repubblica Ceca 3
DZ - Algeria 3
GT - Guatemala 3
PA - Panama 3
SV - El Salvador 3
SY - Repubblica araba siriana 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AL - Albania 2
AU - Australia 2
BH - Bahrain 2
BY - Bielorussia 2
BZ - Belize 2
DO - Repubblica Dominicana 2
HU - Ungheria 2
KG - Kirghizistan 2
LK - Sri Lanka 2
LY - Libia 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
PR - Porto Rico 2
RS - Serbia 2
SN - Senegal 2
AO - Angola 1
BB - Barbados 1
BJ - Benin 1
BW - Botswana 1
DM - Dominica 1
GA - Gabon 1
GH - Ghana 1
HR - Croazia 1
Totale 15.957
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Città #
Ann Arbor 1.371
Ashburn 801
Singapore 618
Woodbridge 449
Fairfield 434
San Jose 387
Hong Kong 384
Houston 377
Milan 374
Frankfurt am Main 358
Chandler 354
Wilmington 278
Dublin 275
Toronto 252
Jacksonville 230
New York 195
Council Bluffs 156
Dearborn 156
Santa Clara 154
Seattle 152
Cambridge 151
Chicago 116
Los Angeles 110
Beijing 106
Princeton 105
Hefei 100
Dallas 93
Hanoi 93
Ho Chi Minh City 91
Boardman 87
Nanjing 86
Vienna 65
Seoul 59
Columbus 58
Shanghai 55
The Dalles 52
Rome 51
Lauterbourg 45
Buffalo 44
Jakarta 42
Lawrence 42
Ottawa 41
Guangzhou 40
Orem 40
Altamura 39
Lachine 37
Nanchang 37
Moscow 36
São Paulo 33
San Diego 32
Fremont 31
Helsinki 30
Phoenix 30
Shenyang 25
Brooklyn 23
Dong Ket 23
London 23
Montreal 22
Brussels 21
Atlanta 20
Chennai 19
Da Nang 19
Hebei 17
Munich 17
Andover 16
Rio de Janeiro 16
Warsaw 16
Denver 15
Detroit 15
Kraków 15
Boston 14
Naples 14
Norwalk 14
Stockholm 14
Falls Church 13
Figino 13
Hangzhou 13
Tianjin 13
Biên Hòa 12
Haiphong 12
Jinan 12
Johannesburg 12
Kent 12
Ankara 11
Baghdad 11
Hyderabad 11
Jiaxing 11
Tokyo 11
Washington 11
Quito 10
Salt Lake City 10
Changsha 9
Dhaka 9
Monza 9
Philadelphia 9
Poplar 9
San Francisco 9
Turin 9
Zhengzhou 9
Baltimore 8
Totale 10.488
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Nome #
CHRNA2 and nocturnal frontal lobe epilepsy: Identification and characterization of a novel loss of function mutation 601
Analysis of human papillomavirus (HPV) 16 variants associated with cervical infection in Italian women 464
Simultaneous overexpression of human E5NT and ENTPD1 protects porcine endothelial cells against H2O2-induced oxidative stress and cytotoxicity in vitro 457
A novel KCNJ2 mutation identified in an autistic proband affects the single channel properties of Kir2.1 418
Potassium channels in the neuronal homeostasis and neurodegenerative pathways underlying Alzheimer's disease: An update 418
Variants in CHRNB2 and CHRNA4 identified in patients with insular epilepsy 386
Patient-Derived Induced Pluripotent Stem Cells (iPSCs) and Cerebral Organoids for Drug Screening and Development in Autism Spectrum Disorder: Opportunities and Challenges 382
Molecular and imaging biomarkers in Alzheimer’s disease: A focus on recent insights 371
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) 370
Long Non-Coding RNAs and Related Molecular Pathways in the Pathogenesis of Epilepsy 362
Understanding the basis of Ehlers-Danlos syndrome in the era of the next-generation sequencing 361
Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutation 354
Sleep disorder-related headaches 344
TSPO Modulates Oligomeric Amyloid-β-Induced Monocyte Chemotaxis: Relevance for Neuroinflammation in Alzheimer's Disease 342
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy 341
Functional Characterization of a CRH Missense Mutation Identified in an ADNFLE Family 331
Genetic architecture and molecular, imaging and prodromic markers in dementia with lewy bodies: State of the art, opportunities and challenges 323
Clinical and genetic evaluation of a family showing both autism and epilepsy 306
Potassium channels and human epileptic phenotypes: An updated overview 304
Restless legs syndrome and painful legs/moving toes 303
Maternal polymorphisms for methyltetrahydrofolate reductase (MTHFR) and methioninesynthetasi-reductase (MTRR) and risk of children with down syndrome: A geographic effect? 302
Can SARS-CoV-2 Infection Exacerbate Alzheimer’s Disease? An Overview of Shared Risk Factors and Pathogenetic Mechanisms 300
Nocturnal frontal lobe epilepsy and the acetylcholine receptor 293
The synergistic relationship between Alzheimer's disease and sleep disorders: An update 293
Maternal polymorphisms for methyltetrahydrofolate reductase and methionine synthetase reductase and risk of children with Down syndrome 283
Epigenetics in Alzheimer’s Disease: A Critical Overview 277
Identification and functional characterisation of a new KCNJ2 mutation 273
A de novo mutation in an Italian sporadic patient affected by Nocturnal frontal lobe epilepsy 272
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy 271
Distinct pools of cancer stem-like cells coexist within human glioblastomas and display different tumorigenicity and independent genomic evolution 271
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 263
Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone gene 259
aCGH analysis of two families showing both autism and epilepsy 255
Gene Symbol: SCN1A 251
Autosomal dominant nocturnal frontal lobe epilepsy - A critical overview 249
Exome Sequencing in an ADSHE Family: VUS Identification and Limits 248
Restless Leg Syndrome Through the Magnifying Glass of Genetics 234
Maternal heterodisomy/isodisomy and paternal supernumerary ring of chromosome 7 in a child with Silver-Russel syndrome 232
Does the Type of Multisystem Atrophy, Parkinsonism, or Cerebellar Ataxia Impact on the Nature of Sleep Disorders? 231
A rescuable folding defective Nav1.1 (SCN1A) Na+channel mutant causes GEFS+: common mechanism in Nav1.1 related epilepsies? 229
Clinical and genetic familial study of 61 children showing different epileptic phenotypes. 229
Role of the SCN1A gene in the pathogenesis of familial febrile seizures and GEFS+ 226
Two new susceptibility loci for ADNFLE 222
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy 222
Clinical and genetic evaluation of a family showing both autism and epilepsy 221
Ricerca di mutazioni in una famiglia ADNFLE. 219
Familiar Febrile Seizures and Mutations in the Nav1.1 Sodium Channel 219
CHRNA2 mutations are rare in the NFLE population: Evaluation of a large cohort of Italian patients 215
Study of the genetic basis of autosomal dominant nocturnal frontal lobe epilepsy 211
Mutations of the orexin system, a regulator of sleep arousal, are not a common cause of ADNFLE. 207
Ricerca di mutazioni in pazienti affetti da NFLE 205
Evidence of the existence of at least a fourth locus for ADNFLE 203
Two new putative loci for ADNFLE identified in an Italian family suggest a digenic inheritance for the disease 202
Compound heterozygosity with dominance in the CRH (Corticotropin Releasing Hormone)promoter in a case of nocturnal frontal lobe epilepsy 197
Nocturnal Frontal Lobe Epilepsy 193
Corticotropin releasing hormone in frontal lobe epilepsy 177
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 77
Functional study of a mutant α2 subunit of the neuronal nicotinic acetylcholine receptor linked to sleep-related generalized seizures with cognitive deficit 61
Identification of a novel missense variant in a family with autosomal dominant sleep-related hypermotor epilepsy (ADSHE) 41
Theranostic Innovative Strategies for Brain Diseases: New Insights on Neurovascular Unit-Associated Pathological Changes in Neurodegenerative Disorders and Aging 38
Totale 16.409
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Categoria #
all - tutte 50.777
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 50.777
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022642 0 0 0 120 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
2025/20264.982 495 363 374 468 581 241 563 258 439 443 368 389
2026/20271.099 205 297 562 35 0 0 0 0 0 0 0 0
Totale 16.409