Bicocca Open Archive

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COMBI, ROMINA
 Distribuzione geografica
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Continente #
NA - Nord America 5.025
EU - Europa 2.256
AS - Asia 573
SA - Sud America 7
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 2
Totale 7.869
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Nazione #
US - Stati Uniti d'America 4.931
IT - Italia 508
DE - Germania 450
SE - Svezia 409
CN - Cina 366
IE - Irlanda 273
UA - Ucraina 211
GB - Regno Unito 113
CA - Canada 94
HK - Hong Kong 69
AT - Austria 64
FI - Finlandia 59
DK - Danimarca 47
VN - Vietnam 45
FR - Francia 36
IN - India 28
TR - Turchia 27
RU - Federazione Russa 25
BE - Belgio 23
PL - Polonia 15
IR - Iran 8
NL - Olanda 8
JP - Giappone 7
IL - Israele 6
KR - Corea 5
TW - Taiwan 5
EU - Europa 4
SG - Singapore 4
CL - Cile 3
ES - Italia 3
GR - Grecia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BG - Bulgaria 2
BR - Brasile 2
CH - Svizzera 2
NO - Norvegia 2
PT - Portogallo 2
AE - Emirati Arabi Uniti 1
AU - Australia 1
EC - Ecuador 1
HU - Ungheria 1
NZ - Nuova Zelanda 1
PE - Perù 1
PH - Filippine 1
PK - Pakistan 1
Totale 7.869
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Città #
Ann Arbor 1.371
Woodbridge 449
Fairfield 434
Houston 357
Chandler 354
Frankfurt am Main 343
Wilmington 277
Dublin 272
Jacksonville 225
Milan 208
Ashburn 205
Dearborn 156
Cambridge 150
Seattle 144
New York 130
Princeton 105
Nanjing 84
Hong Kong 69
Vienna 62
Lawrence 42
Ottawa 40
Altamura 39
Beijing 38
Lachine 37
Nanchang 37
Guangzhou 33
Shanghai 32
Fremont 30
San Diego 30
Boardman 24
Dong Ket 23
Brussels 21
Helsinki 20
Shenyang 20
Hebei 17
Andover 16
Kraków 15
Chicago 13
Norwalk 13
Tianjin 13
Detroit 12
Jinan 12
Falls Church 11
Hangzhou 11
Rome 11
Toronto 11
Jiaxing 10
Auburn Hills 7
Gelsenkirchen 7
Los Angeles 7
Mountain View 7
Zhengzhou 7
Hefei 6
Hyderabad 6
Kocaeli 6
Monza 6
Taizhou 6
University Park 6
Changsha 5
Daejeon 5
Edmonton 5
Kunming 5
Changchun 4
Grafing 4
Huizen 4
Kaohsiung 4
Lanzhou 4
Laurel 4
Leawood 4
Melegnano 4
Napoli 4
Ningbo 4
Philadelphia 4
Ronchis 4
Trieste 4
Costa Mesa 3
Fuzhou 3
Kiev 3
Lyngby 3
Maniago 3
Nürnberg 3
Pianoro 3
Poviglio 3
Prescot 3
Udine 3
Vimercate 3
Zanjan 3
Ansbach 2
Bareggio 2
Berlin 2
Carate Brianza 2
Caserta 2
Chengdu 2
Cinisello Balsamo 2
Desio 2
Genova 2
Kiel 2
London 2
Madrid 2
Magenta 2
Totale 6.231
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Nome #
CHRNA2 and nocturnal frontal lobe epilepsy: Identification and characterization of a novel loss of function mutation 336
Analysis of human papillomavirus (HPV) 16 variants associated with cervical infection in Italian women 281
Simultaneous overexpression of human E5NT and ENTPD1 protects porcine endothelial cells against H2O2-induced oxidative stress and cytotoxicity in vitro 271
Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutation 220
Potassium channels in the neuronal homeostasis and neurodegenerative pathways underlying Alzheimer's disease: An update 220
Long Non-Coding RNAs and Related Molecular Pathways in the Pathogenesis of Epilepsy 219
Understanding the basis of Ehlers-Danlos syndrome in the era of the next-generation sequencing 215
A novel KCNJ2 mutation identified in an autistic proband affects the single channel properties of Kir2.1 211
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) 207
The synergistic relationship between Alzheimer's disease and sleep disorders: An update 206
Variants in CHRNB2 and CHRNA4 identified in patients with insular epilepsy 198
Functional Characterization of a CRH Missense Mutation Identified in an ADNFLE Family 194
Maternal polymorphisms for methyltetrahydrofolate reductase (MTHFR) and methioninesynthetasi-reductase (MTRR) and risk of children with down syndrome: A geographic effect? 192
Sleep disorder-related headaches 191
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy 189
Clinical and genetic evaluation of a family showing both autism and epilepsy 185
Molecular and imaging biomarkers in Alzheimer’s disease: A focus on recent insights 184
Maternal polymorphisms for methyltetrahydrofolate reductase and methionine synthetase reductase and risk of children with Down syndrome 181
Patient-Derived Induced Pluripotent Stem Cells (iPSCs) and Cerebral Organoids for Drug Screening and Development in Autism Spectrum Disorder: Opportunities and Challenges 177
Potassium channels and human epileptic phenotypes: An updated overview 167
Identification and functional characterisation of a new KCNJ2 mutation 158
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy 154
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 152
Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone gene 151
Genetic architecture and molecular, imaging and prodromic markers in dementia with lewy bodies: State of the art, opportunities and challenges 150
Distinct pools of cancer stem-like cells coexist within human glioblastomas and display different tumorigenicity and independent genomic evolution 147
A de novo mutation in an Italian sporadic patient affected by Nocturnal frontal lobe epilepsy 144
Nocturnal frontal lobe epilepsy and the acetylcholine receptor. 143
Autosomal dominant nocturnal frontal lobe epilepsy - A critical overview 139
Maternal heterodisomy/isodisomy and paternal supernumerary ring of chromosome 7 in a child with Silver-Russel syndrome 139
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy 136
Does the Type of Multisystem Atrophy, Parkinsonism, or Cerebellar Ataxia Impact on the Nature of Sleep Disorders? 136
Gene Symbol: SCN1A 133
CHRNA2 mutations are rare in the NFLE population: Evaluation of a large cohort of Italian patients 133
Clinical and genetic evaluation of a family showing both autism and epilepsy 130
Mutations of the orexin system, a regulator of sleep arousal, are not a common cause of ADNFLE. 128
Evidence of the existence of at least a fourth locus for ADNFLE 124
Restless legs syndrome and painful legs/moving toes 122
Clinical and genetic familial study of 61 children showing different epileptic phenotypes. 120
Can SARS-CoV-2 Infection Exacerbate Alzheimer’s Disease? An Overview of Shared Risk Factors and Pathogenetic Mechanisms 120
A rescuable folding defective Nav1.1 (SCN1A) Na+channel mutant causes GEFS+: common mechanism in Nav1.1 related epilepsies? 119
aCGH analysis of two families showing both autism and epilepsy 119
Two new susceptibility loci for ADNFLE 114
Compound heterozygosity with dominance in the CRH (Corticotropin Releasing Hormone)promoter in a case of nocturnal frontal lobe epilepsy 112
Two new putative loci for ADNFLE identified in an Italian family suggest a digenic inheritance for the disease 109
Nocturnal Frontal Lobe Epilepsy 103
Familiar Febrile Seizures and Mutations in the Nav1.1 Sodium Channel 98
Role of the SCN1A gene in the pathogenesis of familial febrile seizures and GEFS+ 94
Corticotropin releasing hormone in frontal lobe epilepsy 81
Ricerca di mutazioni in una famiglia ADNFLE. 79
Study of the genetic basis of autosomal dominant nocturnal frontal lobe epilepsy 74
Ricerca di mutazioni in pazienti affetti da NFLE 70
TSPO Modulates Oligomeric Amyloid-β-Induced Monocyte Chemotaxis: Relevance for Neuroinflammation in Alzheimer's Disease 61
Exome Sequencing in an ADSHE Family: VUS Identification and Limits 51
Totale 8.287
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Categoria #
all - tutte 21.171
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 21.171
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019396 0 0 0 0 0 0 0 0 0 83 146 167
2019/20201.612 160 68 92 142 145 181 265 132 177 105 106 39
2020/20211.554 92 78 144 137 132 149 134 136 130 157 125 140
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
2023/2024704 33 33 33 43 97 220 172 22 43 8 0 0
Totale 8.287