CNR Institutional Research Information System

UNGARO, CARMINE
 Distribuzione geografica
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Continente #
AS - Asia 3.611
NA - Nord America 1.575
EU - Europa 686
SA - Sud America 586
AF - Africa 43
OC - Oceania 6
Totale 6.507
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Nazione #
US - Stati Uniti d'America 1.521
SG - Singapore 1.480
CN - Cina 909
BR - Brasile 483
HK - Hong Kong 340
VN - Vietnam 294
FR - Francia 249
KR - Corea 190
IT - Italia 174
JP - Giappone 174
IN - India 55
NL - Olanda 51
GB - Regno Unito 48
DE - Germania 44
AR - Argentina 41
IL - Israele 29
BD - Bangladesh 24
FI - Finlandia 24
CA - Canada 20
MX - Messico 19
EC - Ecuador 18
ID - Indonesia 18
IQ - Iraq 16
ZA - Sudafrica 15
SA - Arabia Saudita 14
AT - Austria 13
PL - Polonia 13
VE - Venezuela 13
UA - Ucraina 12
CL - Cile 9
CO - Colombia 9
PK - Pakistan 9
RU - Federazione Russa 9
ES - Italia 8
TR - Turchia 8
MA - Marocco 7
PY - Paraguay 7
EG - Egitto 6
HN - Honduras 6
MY - Malesia 6
PH - Filippine 6
SE - Svezia 6
AE - Emirati Arabi Uniti 5
OM - Oman 5
BG - Bulgaria 4
GR - Grecia 4
IE - Irlanda 4
IR - Iran 4
KZ - Kazakistan 4
PE - Perù 4
UZ - Uzbekistan 4
BY - Bielorussia 3
KE - Kenya 3
LU - Lussemburgo 3
MD - Moldavia 3
NP - Nepal 3
AU - Australia 2
DZ - Algeria 2
ET - Etiopia 2
JM - Giamaica 2
JO - Giordania 2
LT - Lituania 2
NZ - Nuova Zelanda 2
RO - Romania 2
SI - Slovenia 2
SY - Repubblica araba siriana 2
TH - Thailandia 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
UY - Uruguay 2
AL - Albania 1
AO - Angola 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BE - Belgio 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BS - Bahamas 1
CG - Congo 1
CH - Svizzera 1
CI - Costa d'Avorio 1
CM - Camerun 1
CR - Costa Rica 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
EE - Estonia 1
GE - Georgia 1
GP - Guadalupe 1
HU - Ungheria 1
KG - Kirghizistan 1
KI - Kiribati 1
LB - Libano 1
LC - Santa Lucia 1
ML - Mali 1
PA - Panama 1
PF - Polinesia Francese 1
RE - Reunion 1
TJ - Tagikistan 1
TW - Taiwan 1
Totale 6.507
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Città #
Singapore 928
Santa Clara 642
Hefei 440
Hong Kong 339
San Jose 253
Seoul 190
Lauterbourg 168
Tokyo 143
Beijing 118
Ashburn 98
Ho Chi Minh City 91
Hanoi 87
Los Angeles 48
Dallas 32
Minamishinagawa 31
New York 28
São Paulo 27
Buffalo 24
Frankfurt am Main 23
Orem 21
Helsinki 20
Milan 18
Naples 18
Bengaluru 17
Rio de Janeiro 16
Haiphong 13
Rome 12
Warsaw 12
Belo Horizonte 10
Vienna 10
Brasília 9
Brooklyn 9
Curitiba 9
Guangzhou 9
Porto Alegre 9
Amsterdam 8
Can Tho 8
Chicago 8
Da Nang 8
Hải Dương 8
Manchester 8
Phoenix 8
Riyadh 8
Anoia Superiore 7
Atlanta 7
Betim 7
Dhaka 7
Elk Grove Village 7
Guayaquil 7
Johannesburg 7
Montreal 7
Nuremberg 7
Catanzaro 6
London 6
New Delhi 6
Padova 6
Quito 6
Quận Một 6
Toronto 6
Baghdad 5
Bari 5
Buenos Aires 5
Campinas 5
Goiânia 5
Joinville 5
Portsmouth 5
Rende 5
Sorocaba 5
Bắc Ninh 4
Campo Grande 4
Caxias do Sul 4
Concepción 4
Dublin 4
Düsseldorf 4
Fortaleza 4
Kyiv 4
Lanús 4
Lappeenranta 4
Luzzi 4
Maceió 4
Maracaibo 4
Mumbai 4
Nha Trang 4
Querétaro 4
Seattle 4
Shanghai 4
Stockholm 4
Sumaré 4
Thái Bình 4
Turin 4
Vũng Tàu 4
Araraquara 3
Araçatuba 3
Asunción 3
Athens 3
Bahía Blanca 3
Barquisimeto 3
Birmingham 3
Biên Hòa 3
Bogotá 3
Totale 4.255
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Nome #
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis 84
Relazione tecnica sui risultati dei monitoraggi del Mercurio in aria ambiente e nelle deposizioni 82
Mutational screening of the eIF2B5 gene in sib pairs affected by multiple sclerosis. 77
Conventional MRI and NOTCH3 gene screening in sporadic CADASIL. 76
ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION 72
Gene Symbol: MECP2. Disease: Rett Syndrome. 69
Seizures and epilepsy in neurofibromatosis type 1 (NF1): a genotype-phenotype study. 68
Alternative Splicing of ALS Genes: Misregulation and Potential Therapies 68
Two Novel Cysteine-Sparing Notch3 Mutations In Patients With CADASIL 67
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis. 67
Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) 66
Mutational Screening in Patient with Charcot-Marie-Tooth Disease Type 2A 65
Caratterizzazione dell’Aerosol atmosferico presso l’Osservatorio Climatico-Ambientale di alta quota sito in Monte Curcio (Sila Grande, Calabria) 64
A novel missense mutation (p.Arg309His) in the nuclear localization signal sequence of spastin protein causes a complicated form of Hereditary Spastic Paraplegia 63
New spastin (SPG4) mutations in patients with Hereditary Spastic Paraplegia 63
A novel mutation in the 3 UTR of SPG4 gene identified in an apparently sporadic patient affected by spastic paraplegia. 60
Genetic investigation of amyotrophic lateral sclerosis patients in south Italy: a two-decade analysis 60
Notch3 protein expression in skin fibroblasts from CADASIL patients 59
NOTCH3 gene mutations in twins with CADASIL 58
First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegia. 58
CHARGE syndrome and ALS: a clinical and genetic study of a family from Southern Italy. 57
ALS and CHARGE syndrome: a clinical and genetic study 56
A novel locus for dHMN with pyramidal features maps to chromosome 4q34.3-q35.2. 54
Discovery novel variations in Sleep-related Hypermotor Epilepsy (SHE) using Next Generation Sequencing approach 54
Clinical and genetic study of an Italian family linked to SPG26 locus 52
NOTCH3 PROTEIN LOCALIZATION IN (SKIN) FIBROBLASTS FROM CADASIL PATIENTS : AN IMMUNOFLUORESCENCE STUDY 52
The spectrum of ROBO3 mutations in Horizontal Gaze Palsy With Progressive Scoliosis: an update 52
Gene symbol: NOTCH3 51
FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis. 51
NOTCH3 gene analysis in two couples of twins 50
Clinical features and genetic analysis of two siblings with Startle disease in a family of South Italy 49
NEUROFIBROMATOSIS TYPE 2 (NF2) IN A CHILD UNDER 1 YEAR OF AGE: A CLINICAL AND MOLECULAR STUDY 48
Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report 48
Mercury toxicity and amyotrophic lateral sclerosis 48
A novel S379A TARDBP mutation associated to late-onset sporadic ALS 48
A large Italian family with R521C mutation in the FUS/TLS gene 47
Identificazione Di Una Nuova Mutazione Nel Gene PMP22 In Un Paziente Affetto Da HNPP 46
Clinical and molecular investigation in an unusual Rett Syndrome case 45
A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies. 45
Horizontal gaze palsy with progressive scoliosis: is scoliosis linked to ROBO3 mutations? 45
A Systems Biology Approach for Personalized Medicine in Refractory Epilepsy 44
Natural History of Neurofibromatosis Type 2 (NF2) in the Paediatric Age: a Prospective Clinical (and Molecular) Study 44
ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION 43
A Novel Mutation In The X-Linked Cyclin-Dependent Kinase-Like 5 (CDKL5) Gene Associated With A Severe Rett Phenotype. 43
Spastin Gene Mutations In Italian Patients With Pure And Complicated Forms Of Spastic Paraplegia 42
A novel mutation in the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene associated with a severe Rett phenotype. 42
Exome sequencing reveals two compound heterozygous DDHD2 mutations in a non consanguineous family with ARHSP-TCC 42
Analisi mutazionale del gene NF1 in pazienti del sud Italia affetti da Neurofibromatosi di tipo I: identificazione di 21 nuove mutazioni 42
Clinical, genetic and magnetic resonance findings in an Italian patient affected by l-2-hydroxyglutaric aciduria 41
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1 40
Amyotrophic lateral sclerosis: a new missense mutation in the SOD1 gene. 40
R521C mutation in the FUS gene in a large Italian family 39
Establishing a national network for atmospheric mercury monitoring: preliminary spatial and temporal insights from Italy 39
Comparison of NOTCH3 expression in fibroblasts from CADASIL patients versus normal controls 39
Seizures and epilepsy in neurofibromatosis type 1 (NF1): a genotype-phenotype study. 38
Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia 38
Polymorphisms and mutational analysis of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy. 37
Assenza di correlazione tra sclerosi multipla familiare (SM) e mutazioni nel gene eIF2B5. 37
Genetic analysis of TARDBP gene in a color of South Italian ALS patients 37
The role of mri in the NOTCH3 gene screening of apparently sporadic CADASIL 36
NOTCH3 PROTEIN LOCALIZATION IN SKIN FIBROBLASTS FROM CADASIL PATIENTS : AN IMMUNOFLUORESCENCE MICROSCOPY STUDY 36
Charcot-Marie-Tooth disease tipe 2A associate with two novel MFN2 mutations 36
Horizontal Gaze Palsy With Progressive Scoliosis: Two Novel ROBO3 Mutations in a Compound Heterozygous Sporadic Case 36
Nuove mutazioni identificate nel gene della spastina in soggetti affetti da Paraplegia Spastica Ereditaria 35
Seizures and Epilepsy in the Setting of Neurofibromatosis Type 1 (NF1): a Population-Based, Genotype-Phenotype Study 35
L-2-Hydroxyglutaric aciduria: a case report. 35
Tre nuove mutazioni nel gene SPG4 identificate in pazienti affetti da paraparesi spastica ereditaria 35
Comparison of different techniques for detecting 17p12 duplication in CMT1A. 34
SPASTIN GENE MUTATIONS IN ITALIAN PATIENTS WITH A PURE AND COMPLICATED FORMS OF SPASTIC PARAPLEGIA. 34
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis. 34
A pathogenic rare mutation on exon 22 of the NOTCH3 gene disclosed in an Italian patient affected by CADASIL 34
SUGGESTIVE EVIDENCE FOR LINKAGE TO CHROMOSOME 4qter FOR AUTOSOMAL DOMINANT DISTAL MOTOR NEURONOPATHY 33
Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum 33
Clinical and genetic study of an Italian family with Autosomal Recessive Spastic Paraplegia associated with dysarthria and hearing loss. 33
The p.Arg416Cys mutation in SPG3a gene associated with a pure form of spastic paraplegia. 33
Clinical, genetic and MRI findings in a patient affected by L-2-Hydroxyglutaric aciduria 33
A Clinical And Molecular Study In Children Under 1 Year Of Age Affected By Neurofibromatosis Type 2 32
Charcot-Marie-Tooth X-linked: five novel mutations in Italian patients 32
CADASIL: extended polymorphisms and mutational analysis of the NOTCH3 gene. 32
A novel SPG3A mutation in an Italian patient with Hereditary Spastic Paraplegia 32
Abnormally High Level of SOD1 mRNA in a patient with Amyotrophic Lateral Sclerosis 32
A novel locus for Autosomal Dominant Distal Motor Neuronopathy maps to chromosome 4q-ter 32
DISTINGUISHING APPARENTLY SPORADIC CADASIL FROM OTHER LEUCOENCEPHALOPATHIES:THE ROLE OF MAGNETIC RESONANCE IMAGING IN THE NOTCH3 GENE SCREENING 31
Riscontro di nuova mutazione sul gene NOTCH 3 della CADASIL 31
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1. 31
Rare pathogenic CADASIL-causing mutation on exon 22 of the NOTCH3 gene disclosed for the first time in an Italian patient 31
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy 31
CADASIL: molecular screening of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy. 31
Huntington disease like 2 in Southern Italy: screening of JPH3 and other genes involved in huntington like phenotypes. 31
Angiogenin Gene And Amyotrophic Lateral Sclerosis In Southern Italy 30
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy 30
A Novel Notch3 Gene Mutation In A Patient With Cadasil From Southern Italy 30
Identification of four novel pathogenic mutations in patients from Southern Italy with CADASIL 30
A CLINICAL AND MOLECULAR STUDY IN A CHILD UNDER 1 YEAR OF AGE AFFECTED BY NEUROFIBROMATOSIS TYPE 2 30
Comparison of different techniques in detecting CMT1A/HNPP duplication/deletion 30
Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Italian patients with hereditary spastic paraparesis 30
First Evidence of a Pathogenic Insertion in the NOTCH3 Gene Causing CADASIL 30
FUS gene analysis in Amyotrophic Lateral Sclerosis in South Italy. 29
A NOVEL MISSENSE MUTATION OF THE NF2 GENE IN A SEVERELY AFFECTED BOY AND HIS HEALTHY FATHER 29
Neurofibromatosis Type 2 (Nf2) In Children Under 1 Year Of Age: A Clinical And Molecular Study 29
Totale 4.432
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Categoria #
all - tutte 20.952
article - articoli 8.801
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 191
Totale 29.944
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202425 0 0 0 0 0 0 0 0 5 0 12 8
2024/20252.602 9 14 198 109 648 43 67 69 53 86 702 604
2025/20263.924 264 415 362 641 633 142 602 222 319 252 72 0
Totale 6.551