Bicocca Open Archive

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COMBI, ROMINA
 Distribuzione geografica
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Continente #
NA - Nord America 7.971
EU - Europa 3.433
AS - Asia 3.342
SA - Sud America 485
Continente sconosciuto - Info sul continente non disponibili 445
AF - Africa 73
OC - Oceania 6
Totale 15.755
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Nazione #
US - Stati Uniti d'America 7.528
SG - Singapore 1.138
IT - Italia 941
CN - Cina 845
DE - Germania 506
SE - Svezia 437
RU - Federazione Russa 403
HK - Hong Kong 388
VN - Vietnam 376
CA - Canada 373
BR - Brasile 354
IE - Irlanda 276
UA - Ucraina 229
GB - Regno Unito 183
IN - India 113
FR - Francia 103
FI - Finlandia 76
BD - Bangladesh 73
AT - Austria 71
TR - Turchia 68
KR - Corea 67
ID - Indonesia 52
DK - Danimarca 48
AR - Argentina 43
PL - Polonia 36
IQ - Iraq 35
MX - Messico 33
ES - Italia 32
NL - Olanda 29
ZA - Sudafrica 27
EC - Ecuador 25
BE - Belgio 24
PH - Filippine 22
PK - Pakistan 20
JP - Giappone 19
SA - Arabia Saudita 17
CO - Colombia 15
CL - Cile 14
VE - Venezuela 14
IR - Iran 12
CR - Costa Rica 10
JM - Giamaica 10
UZ - Uzbekistan 10
NP - Nepal 9
OM - Oman 9
AZ - Azerbaigian 8
CH - Svizzera 8
IL - Israele 8
MA - Marocco 8
MY - Malesia 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
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
AL - Albania 2
AU - Australia 2
BH - Bahrain 2
BY - Bielorussia 2
BZ - Belize 2
DO - Repubblica Dominicana 2
GT - Guatemala 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
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
Totale 15.306
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Città #
Ann Arbor 1.371
Ashburn 703
Singapore 618
Woodbridge 449
Fairfield 434
Hong Kong 384
Houston 376
Milan 372
Frankfurt am Main 358
Chandler 354
San Jose 304
Wilmington 278
Dublin 275
Toronto 248
Jacksonville 227
New York 191
Dearborn 156
Cambridge 151
Santa Clara 151
Seattle 150
Council Bluffs 146
Chicago 113
Los Angeles 105
Princeton 105
Beijing 104
Hefei 100
Hanoi 93
Dallas 91
Ho Chi Minh City 90
Boardman 86
Nanjing 86
Vienna 65
Seoul 59
Columbus 56
Shanghai 55
The Dalles 52
Rome 48
Lauterbourg 45
Buffalo 43
Jakarta 42
Lawrence 42
Guangzhou 40
Orem 40
Ottawa 40
Altamura 39
Lachine 37
Nanchang 37
Moscow 36
San Diego 32
São Paulo 31
Fremont 30
Helsinki 30
Shenyang 25
Dong Ket 23
London 22
Phoenix 22
Brussels 21
Montreal 21
Brooklyn 20
Chennai 19
Da Nang 19
Atlanta 17
Hebei 17
Munich 17
Andover 16
Rio de Janeiro 16
Warsaw 16
Detroit 15
Kraków 15
Stockholm 14
Boston 13
Falls Church 13
Hangzhou 13
Naples 13
Norwalk 13
Tianjin 13
Biên Hòa 12
Haiphong 12
Jinan 12
Johannesburg 12
Kent 12
Ankara 11
Denver 11
Figino 11
Hyderabad 11
Jiaxing 11
Baghdad 10
Tokyo 10
Changsha 9
Dhaka 9
Monza 9
Poplar 9
Quito 9
San Francisco 9
Turin 9
Washington 9
Zhengzhou 9
Elk Grove Village 8
Manchester 8
Mumbai 8
Totale 10.221
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Nome #
CHRNA2 and nocturnal frontal lobe epilepsy: Identification and characterization of a novel loss of function mutation 586
Analysis of human papillomavirus (HPV) 16 variants associated with cervical infection in Italian women 454
Simultaneous overexpression of human E5NT and ENTPD1 protects porcine endothelial cells against H2O2-induced oxidative stress and cytotoxicity in vitro 447
Potassium channels in the neuronal homeostasis and neurodegenerative pathways underlying Alzheimer's disease: An update 404
A novel KCNJ2 mutation identified in an autistic proband affects the single channel properties of Kir2.1 400
Variants in CHRNB2 and CHRNA4 identified in patients with insular epilepsy 370
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) 364
Molecular and imaging biomarkers in Alzheimer’s disease: A focus on recent insights 360
Patient-Derived Induced Pluripotent Stem Cells (iPSCs) and Cerebral Organoids for Drug Screening and Development in Autism Spectrum Disorder: Opportunities and Challenges 360
Long Non-Coding RNAs and Related Molecular Pathways in the Pathogenesis of Epilepsy 354
Understanding the basis of Ehlers-Danlos syndrome in the era of the next-generation sequencing 353
Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutation 342
Sleep disorder-related headaches 333
TSPO Modulates Oligomeric Amyloid-β-Induced Monocyte Chemotaxis: Relevance for Neuroinflammation in Alzheimer's Disease 331
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy 330
Functional Characterization of a CRH Missense Mutation Identified in an ADNFLE Family 326
Genetic architecture and molecular, imaging and prodromic markers in dementia with lewy bodies: State of the art, opportunities and challenges 306
Maternal polymorphisms for methyltetrahydrofolate reductase (MTHFR) and methioninesynthetasi-reductase (MTRR) and risk of children with down syndrome: A geographic effect? 297
Clinical and genetic evaluation of a family showing both autism and epilepsy 292
Potassium channels and human epileptic phenotypes: An updated overview 291
Restless legs syndrome and painful legs/moving toes 291
Can SARS-CoV-2 Infection Exacerbate Alzheimer’s Disease? An Overview of Shared Risk Factors and Pathogenetic Mechanisms 290
Nocturnal frontal lobe epilepsy and the acetylcholine receptor 283
The synergistic relationship between Alzheimer's disease and sleep disorders: An update 283
Maternal polymorphisms for methyltetrahydrofolate reductase and methionine synthetase reductase and risk of children with Down syndrome 275
Identification and functional characterisation of a new KCNJ2 mutation 266
A de novo mutation in an Italian sporadic patient affected by Nocturnal frontal lobe epilepsy 261
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy 259
Distinct pools of cancer stem-like cells coexist within human glioblastomas and display different tumorigenicity and independent genomic evolution 259
Epigenetics in Alzheimer’s Disease: A Critical Overview 257
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 251
Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone gene 248
aCGH analysis of two families showing both autism and epilepsy 248
Gene Symbol: SCN1A 241
Autosomal dominant nocturnal frontal lobe epilepsy - A critical overview 239
Exome Sequencing in an ADSHE Family: VUS Identification and Limits 237
Restless Leg Syndrome Through the Magnifying Glass of Genetics 228
Maternal heterodisomy/isodisomy and paternal supernumerary ring of chromosome 7 in a child with Silver-Russel syndrome 226
Does the Type of Multisystem Atrophy, Parkinsonism, or Cerebellar Ataxia Impact on the Nature of Sleep Disorders? 222
A rescuable folding defective Nav1.1 (SCN1A) Na+channel mutant causes GEFS+: common mechanism in Nav1.1 related epilepsies? 220
Clinical and genetic familial study of 61 children showing different epileptic phenotypes. 220
Two new susceptibility loci for ADNFLE 213
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy 210
Role of the SCN1A gene in the pathogenesis of familial febrile seizures and GEFS+ 210
CHRNA2 mutations are rare in the NFLE population: Evaluation of a large cohort of Italian patients 210
Clinical and genetic evaluation of a family showing both autism and epilepsy 209
Familiar Febrile Seizures and Mutations in the Nav1.1 Sodium Channel 209
Mutations of the orexin system, a regulator of sleep arousal, are not a common cause of ADNFLE. 203
Study of the genetic basis of autosomal dominant nocturnal frontal lobe epilepsy 200
Evidence of the existence of at least a fourth locus for ADNFLE 198
Ricerca di mutazioni in una famiglia ADNFLE. 198
Two new putative loci for ADNFLE identified in an Italian family suggest a digenic inheritance for the disease 194
Ricerca di mutazioni in pazienti affetti da NFLE 193
Compound heterozygosity with dominance in the CRH (Corticotropin Releasing Hormone)promoter in a case of nocturnal frontal lobe epilepsy 187
Nocturnal Frontal Lobe Epilepsy 182
Corticotropin releasing hormone in frontal lobe epilepsy 165
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 64
Functional study of a mutant α2 subunit of the neuronal nicotinic acetylcholine receptor linked to sleep-related generalized seizures with cognitive deficit 52
Identification of a novel missense variant in a family with autosomal dominant sleep-related hypermotor epilepsy (ADSHE) 35
Theranostic Innovative Strategies for Brain Diseases: New Insights on Neurovascular Unit-Associated Pathological Changes in Neurodegenerative Disorders and Aging 19
Totale 15.755
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Categoria #
all - tutte 49.092
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 49.092
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022884 0 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
2025/20264.982 495 363 374 468 581 241 563 258 439 443 368 389
2026/2027445 205 240 0 0 0 0 0 0 0 0 0 0
Totale 15.755