CNR Institutional Research Information System

GABRIELE, ANNA LIA
 Distribuzione geografica
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Continente #
AS - Asia 3.947
NA - Nord America 1.702
SA - Sud America 743
EU - Europa 689
AF - Africa 53
OC - Oceania 9
Totale 7.143
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Nazione #
SG - Singapore 1.652
US - Stati Uniti d'America 1.632
CN - Cina 962
BR - Brasile 596
HK - Hong Kong 378
VN - Vietnam 355
FR - Francia 259
KR - Corea 185
JP - Giappone 170
IT - Italia 126
IN - India 73
NL - Olanda 67
AR - Argentina 61
DE - Germania 55
GB - Regno Unito 54
BD - Bangladesh 35
EC - Ecuador 30
CA - Canada 29
IL - Israele 28
MX - Messico 23
ID - Indonesia 20
UA - Ucraina 17
PL - Polonia 16
FI - Finlandia 15
VE - Venezuela 15
IQ - Iraq 14
RU - Federazione Russa 14
TR - Turchia 14
ES - Italia 12
ZA - Sudafrica 12
CO - Colombia 11
SA - Arabia Saudita 11
MA - Marocco 10
CL - Cile 9
PE - Perù 9
PY - Paraguay 8
PH - Filippine 7
PK - Pakistan 7
EG - Egitto 6
LT - Lituania 6
AE - Emirati Arabi Uniti 5
AT - Austria 5
AU - Australia 5
KE - Kenya 5
RO - Romania 5
AL - Albania 4
BB - Barbados 4
CH - Svizzera 4
MY - Malesia 4
SE - Svezia 4
TN - Tunisia 4
DZ - Algeria 3
GR - Grecia 3
IR - Iran 3
LB - Libano 3
NP - Nepal 3
OM - Oman 3
TW - Taiwan 3
UY - Uruguay 3
UZ - Uzbekistan 3
AZ - Azerbaigian 2
BA - Bosnia-Erzegovina 2
BY - Bielorussia 2
CG - Congo 2
CR - Costa Rica 2
CZ - Repubblica Ceca 2
HN - Honduras 2
HR - Croazia 2
IE - Irlanda 2
JM - Giamaica 2
JO - Giordania 2
MD - Moldavia 2
NZ - Nuova Zelanda 2
PA - Panama 2
AM - Armenia 1
BE - Belgio 1
BG - Bulgaria 1
BO - Bolivia 1
BS - Bahamas 1
CD - Congo 1
CI - Costa d'Avorio 1
CM - Camerun 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EE - Estonia 1
ET - Etiopia 1
GH - Ghana 1
GP - Guadalupe 1
HU - Ungheria 1
KI - Kiribati 1
KZ - Kazakistan 1
LU - Lussemburgo 1
LV - Lettonia 1
LY - Libia 1
MK - Macedonia 1
ML - Mali 1
MZ - Mozambico 1
NG - Nigeria 1
NO - Norvegia 1
PF - Polinesia Francese 1
Totale 7.133
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Città #
Singapore 1.023
Santa Clara 715
Hefei 405
Hong Kong 373
San Jose 192
Seoul 185
Lauterbourg 180
Tokyo 141
Beijing 122
Ho Chi Minh City 121
Ashburn 109
Hanoi 99
Los Angeles 58
New York 41
Buffalo 35
São Paulo 34
Frankfurt am Main 29
Dallas 27
Minamishinagawa 27
Orem 24
Rio de Janeiro 22
Bengaluru 16
Haiphong 15
Helsinki 15
Porto Alegre 15
Belo Horizonte 13
Milan 13
Naples 13
Guayaquil 11
Warsaw 11
Atlanta 10
Hải Dương 10
Montreal 10
Rome 10
Brasília 9
Campinas 9
Phoenix 9
Quito 9
Toronto 9
Betim 8
Chennai 8
Da Nang 8
Elk Grove Village 8
Baghdad 7
Düsseldorf 7
Goiânia 7
Guangzhou 7
Jakarta 7
Maceió 7
New Delhi 7
Nuremberg 7
Biên Hòa 6
Brooklyn 6
Bắc Ninh 6
Can Tho 6
Curitiba 6
Hyderabad 6
Istanbul 6
London 6
Quận Một 6
Sorocaba 6
Boardman 5
Bologna 5
Buenos Aires 5
Caracas 5
Chicago 5
Dhaka 5
Guarulhos 5
Johannesburg 5
Manchester 5
Riyadh 5
Salvador 5
Sumaré 5
Turin 5
Amsterdam 4
Araraquara 4
Asunción 4
Birmingham 4
Bridgetown 4
Casablanca 4
Catanduva 4
Catanzaro 4
Council Bluffs 4
Denver 4
Ha Long 4
Houston 4
Joinville 4
Kyiv 4
Las Vegas 4
Lima 4
Lấp Vò 4
Mexico City 4
Mumbai 4
Nairobi 4
Ninh Bình 4
Porto Seguro 4
Quilmes 4
Recife 4
Santa Maria 4
Santo André 4
Totale 4.486
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Nome #
Mapping Soil and Leaf Micronutrients Distribution in an Olive (Olea europaea L.) Orchard 118
Studying potentially toxic trace elements in soil-plant system: a case study of an olive orchard in southern Italy (Calabria) 86
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis 85
PROGETTO ALGENCAL -Sistema innovativo per la coltura di microalghe in fotobioreattori per la produzione di energia da fonte rinnovabile e di altri prodotti -1.SISTEMA DI PRODUZIONE DELLA BIOMASSA ALGALE 81
Mutational screening of the eIF2B5 gene in sib pairs affected by multiple sclerosis. 78
Ophthalmological manifestations in segmental neurofibromatosis type I 78
ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION 72
Accounting for compositional nature of soil constituents in digital mapping of organic carbon 71
Condizioni nutrizionali di un oliveto e distribuzione spaziale degli elementi nutritivi nel sistema suolo pianta. 70
Natural history of neurofibromatosis type 2 with onset before the age of 1 year 69
Seizures and epilepsy in neurofibromatosis type 1 (NF1): a genotype-phenotype study. 68
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis. 67
Mutational Screening in Patient with Charcot-Marie-Tooth Disease Type 2A 65
Studying the spatial structure of potentially toxic trace elements (PTEs) using multivariate geostatistics in an olive orchard of southern Italy 64
New spastin (SPG4) mutations in patients with Hereditary Spastic Paraplegia 63
PROGETTO ALGENCAL Sistema innovativo per la coltura di microalghe in fotobioreattori per la produzione di energia da fonte rinnovabile e di altri prodotti. 6. IMPATTI AMBIENTALI 61
A novel mutation in the 3 UTR of SPG4 gene identified in an apparently sporadic patient affected by spastic paraplegia. 60
NOTCH3 gene mutations in twins with CADASIL 58
Estimating soil organic carbon with soil Vis-NIR spectroscopy: a comparison of different algorithms in two forest areas 56
ACCOUNTING FOR COMPOSITIONAL NATURE OF SOIL COSTITUENTS IN DIGITAL MAPPING OF ORGANIC CARBON 56
Spinal neurofibromatosis with central nervous system involvement in a set of twin girls and a boy: Further expansion of the phenotype 55
A novel locus for dHMN with pyramidal features maps to chromosome 4q34.3-q35.2. 54
Assessing soil pollution by beryllium contamination in an olive orchard of southern Italy 53
Clinical and genetic study of an Italian family linked to SPG26 locus 52
Gene symbol: NOTCH3 51
Experimental plant for the cultivation of microalgae in photobioreactors for energy production 51
NOTCH3 gene analysis in two couples of twins 50
NEUROFIBROMATOSIS TYPE 2 (NF2) IN A CHILD UNDER 1 YEAR OF AGE: A CLINICAL AND MOLECULAR STUDY 48
Rapporto Tecnico semestrale sullo stato di avanzamento intermedio (RTI) del progetto di ricerca "Progetto di un sistema energetico avanzato completo, basato sulla coltura massiva di microalghe in fotobioreattori, trasparenti per la produzione, in condizioni di competitività ed ecosostenibilità, di energia da fonte rinnovabile e di altri prodotti" (PON01_02061). Report semestrale- Stato di avanzamento: n.04, dal 1aprile 2013 al 30 settembre 2013 (IV SAL). 48
Rapporto Tecnico semestrale sullo stato di avanzamento intermedio (RTI) del progetto di ricerca "Progetto di un sistema energetico avanzato completo, basato sulla coltura massiva di microalghe in fotobioreattori, trasparenti per la produzione, in condizioni di competitività ed ecosostenibilità, di energia da fonte rinnovabile e di altri prodotti" (PON01_02061). Report semestrale- Stato di avanzamento: n.03, dal 1 ottobre 2012 al 31 marzo 2013 (III SAL). 47
Modelling seasonal variations of natural radionuclides in agricultural soils. 47
Identificazione di una nuova mutazione nel sito di splicing del gene Sbf2 responsabile di Charcot-Marie-Tooth autosomica recessiva (CMT4B2) 46
Identificazione Di Una Nuova Mutazione Nel Gene PMP22 In Un Paziente Affetto Da HNPP 46
NEUROCUTANEOUS MELANOSIS IN A WOMAN WITH MULTIPLE BRAIN MELANOCYTOMAS, CUTANEOUS MELANOCYTOSIS AND ORAL INVOLVEMENT 46
Rapporto Tecnico semestrale sullo stato di avanzamento intermedio (RTI) del progetto di ricerca "Progetto di un sistema energetico avanzato completo, basato sulla coltura massiva di microalghe in fotobioreattori, trasparenti per la produzione, in condizioni di competitività ed ecosostenibilità, di energia da fonte rinnovabile e di altri prodotti" (PON01_02061). Report semestrale- Stato di avanzamento: n.05, dal 1 ottobre 2013 al 31 marzo 2014 (V SAL). 46
Modelling seasonal variations of natural radionuclides in agricultural soils 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
Geochemistry analysis of rare earth elements of southern Italy soils. 45
A new insertion of CC in exon 4 of PMP22 gene in a patient with Ereditary Neuropathy with Liability to Pressure Palsies (HNPP) 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
Neurofibromatosis type 1 and infantile spasms. 43
Spastin Gene Mutations In Italian Patients With Pure And Complicated Forms Of Spastic Paraplegia 42
Rapporto Tecnico semestrale sullo stato di avanzamento intermedio (RTI) del progetto di ricerca "Progetto di un sistema energetico avanzato completo, basato sulla coltura massiva di microalghe in fotobioreattori, trasparenti per la produzione, in condizioni di competitività ed ecosostenibilità, di energia da fonte rinnovabile e di altri prodotti" (PON01_02061). Report semestrale- Stato di avanzamento: n.06, dal 1 aprile 2014 al 30 settembre 2014 (VI SAL). 42
Analisi mutazionale del gene NF1 in pazienti del sud Italia affetti da Neurofibromatosi di tipo I: identificazione di 21 nuove mutazioni 42
Nevus vascularis mixtus (cutaneous vascular twin nevi) associated with intracranial vascular malformation of the Dyke-Davidoff-Masson type in two patients. 42
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1 42
Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus. 41
Alpha-thalassemia in a southern Italian population (detection by a non-radioactive procedure). 41
Assessment of trace elements in olive leaves in a southern Italy region. 41
Influence of soil properties on potentially harmful elements (PHEs). 40
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3. 39
Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia 39
Seizures and epilepsy in neurofibromatosis type 1 (NF1): a genotype-phenotype study. 38
Neurofibromatosis type 1 and infantile spasms. 38
Earliest clinical manifestations and natural history of neurofibromatosis type 2 (NF2) in childhood: a study of 24 patients. 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
Juvenile Huntington's disease presenting as progressive myoclonic epilepsy. 36
The role of mri in the NOTCH3 gene screening of apparently sporadic CADASIL 36
Caratterizzazione dei portatori sani SMA con Real time PCR 36
Nuove mutazioni identificate nel gene della spastina in soggetti affetti da Paraplegia Spastica Ereditaria 35
Comparison of different techniques for detecting 17p12 duplication in CMT1A. 35
Seizures and Epilepsy in the Setting of Neurofibromatosis Type 1 (NF1): a Population-Based, Genotype-Phenotype Study 35
Tre nuove mutazioni nel gene SPG4 identificate in pazienti affetti da paraparesi spastica ereditaria 35
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
Studio clinico e genetico di una famiglia italiana affetta da una nuova forma di Paraparesi Spastica autosomica dominante complicata 34
A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL. 34
A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and magnetic resonance spectroscopic findings. 34
SUGGESTIVE EVIDENCE FOR LINKAGE TO CHROMOSOME 4qter FOR AUTOSOMAL DOMINANT DISTAL MOTOR NEURONOPATHY 33
Clinical and genetic study of an Italian family with Autosomal Recessive Spastic Paraplegia associated with dysarthria and hearing loss. 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 simple method for diagnosis of autosomal recessive spinal muscular atrophy by denaturing high-performance liquid chromatography 32
A novel locus for Autosomal Dominant Distal Motor Neuronopathy maps to chromosome 4q-ter 32
NOTCH3 gene mutations and mtDNA variations 32
DISTINGUISHING APPARENTLY SPORADIC CADASIL FROM OTHER LEUCOENCEPHALOPATHIES:THE ROLE OF MAGNETIC RESONANCE IMAGING IN THE NOTCH3 GENE SCREENING 31
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1. 31
Further evidence of genetic heterogeneity in autosomal dominant distal motor neuronopathy 31
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy 31
Aspetti epidemiologici del deficit di G6PD in provincia di Cosenza. Dati preliminari 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
Abnormally high levels of SOD1 mRNA in a patient with amyotrophic lateral sclerosis. 30
Analysis of the (CAG)n repeat at the IT15 locus in a population from Calabria (southern Italy). 30
A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis 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
Totale 4.497
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Categoria #
all - tutte 23.747
article - articoli 7.827
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 31.574
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202448 0 0 0 0 0 0 0 0 5 4 26 13
2024/20252.810 17 19 238 119 713 33 30 63 31 92 737 718
2025/20264.291 243 483 372 732 707 122 653 298 317 248 104 12
Totale 7.149