CNR Institutional Research Information System

MAGARIELLO, ANGELA
 Distribuzione geografica
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Continente #
AS - Asia 4.383
NA - Nord America 2.109
EU - Europa 1.035
SA - Sud America 754
AF - Africa 66
OC - Oceania 11
Totale 8.358
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Nazione #
US - Stati Uniti d'America 2.003
SG - Singapore 1.757
CN - Cina 1.087
BR - Brasile 615
HK - Hong Kong 435
IT - Italia 399
VN - Vietnam 381
FR - Francia 274
KR - Corea 217
JP - Giappone 195
NL - Olanda 81
IN - India 76
GB - Regno Unito 70
BD - Bangladesh 67
DE - Germania 60
AR - Argentina 55
CA - Canada 38
IL - Israele 34
FI - Finlandia 31
MX - Messico 31
EC - Ecuador 27
ID - Indonesia 26
PL - Polonia 26
VE - Venezuela 16
ZA - Sudafrica 16
IQ - Iraq 15
UA - Ucraina 15
JM - Giamaica 12
MA - Marocco 12
PY - Paraguay 12
TR - Turchia 12
EG - Egitto 11
SA - Arabia Saudita 11
SE - Svezia 11
CO - Colombia 10
PK - Pakistan 10
CL - Cile 9
ES - Italia 9
IR - Iran 9
AT - Austria 8
IE - Irlanda 8
HN - Honduras 7
PE - Perù 7
RU - Federazione Russa 7
UZ - Uzbekistan 7
AU - Australia 6
PH - Filippine 6
AE - Emirati Arabi Uniti 5
BY - Bielorussia 5
KE - Kenya 5
MY - Malesia 5
OM - Oman 5
TN - Tunisia 5
AZ - Azerbaigian 4
SV - El Salvador 4
TT - Trinidad e Tobago 4
BG - Bulgaria 3
CH - Svizzera 3
CR - Costa Rica 3
KG - Kirghizistan 3
MD - Moldavia 3
RO - Romania 3
TW - Taiwan 3
CI - Costa d'Avorio 2
DZ - Algeria 2
GR - Grecia 2
JO - Giordania 2
LT - Lituania 2
NI - Nicaragua 2
NP - Nepal 2
NZ - Nuova Zelanda 2
PT - Portogallo 2
RE - Reunion 2
SI - Slovenia 2
SN - Senegal 2
SY - Repubblica araba siriana 2
UY - Uruguay 2
AL - Albania 1
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BE - Belgio 1
BF - Burkina Faso 1
BO - Bolivia 1
BS - Bahamas 1
CD - Congo 1
CG - Congo 1
CM - Camerun 1
CY - Cipro 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EE - Estonia 1
ET - Etiopia 1
GE - Georgia 1
GP - Guadalupe 1
GT - Guatemala 1
HR - Croazia 1
KI - Kiribati 1
KZ - Kazakistan 1
Totale 8.345
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Città #
Singapore 1.129
Santa Clara 785
Hefei 528
Hong Kong 431
San Jose 225
Seoul 217
Lauterbourg 196
Tokyo 160
Ashburn 142
Beijing 139
Ho Chi Minh City 116
Hanoi 100
Los Angeles 75
São Paulo 40
Rome 38
New York 37
Dallas 36
Minamishinagawa 35
Buffalo 31
Milan 30
Frankfurt am Main 28
Helsinki 25
Taranto 25
Naples 23
Orem 21
Rio de Janeiro 21
Bengaluru 19
Warsaw 18
Council Bluffs 17
Bologna 15
Brooklyn 14
Haiphong 14
Hải Dương 14
Da Nang 13
Belo Horizonte 12
Brasília 12
Montreal 12
Phoenix 12
Porto Alegre 12
Amsterdam 11
Atlanta 11
Kingston 11
Boardman 10
Denver 10
Elk Grove Village 10
London 10
Guangzhou 9
Guayaquil 9
Manchester 9
Mexico City 9
Quito 9
Stockholm 9
Chennai 8
Curitiba 8
Dublin 8
Nuremberg 8
Betim 7
Can Tho 7
Houston 7
Johannesburg 7
Memphis 7
Mumbai 7
New Delhi 7
Nha Trang 7
Quận Một 7
Riyadh 7
Shanghai 7
Thái Bình 7
Toronto 7
Baghdad 6
Boston 6
Brescia 6
Bắc Ninh 6
Campinas 6
Caracas 6
Düsseldorf 6
Jakarta 6
Maceió 6
Ottaviano 6
Poplar 6
Seattle 6
The Bronx 6
Turin 6
Uberlândia 6
Ankara 5
Asunción 5
Biên Hòa 5
Buenos Aires 5
Florence 5
Fort Lauderdale 5
Goiânia 5
Juiz de Fora 5
Ninh Bình 5
Philadelphia 5
Portsmouth 5
Quận Bình Thạnh 5
Recife 5
San Antonio 5
San Francisco 5
Sorocaba 5
Totale 5.237
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Nome #
Cibo e invecchiamento attivo. Una riflessione condivisa per raccomandazioni di policy inclusive 135
Percezione, identità e senso di appartenenza 118
Social agriculture for life quality and environmental sustainability 114
L’AGRICOLTURA SOCIALE PER LA QUALITÀ DELLA VITA E LA SOSTENIBILITÀ AMBIENTALE 100
LC-MALDI-TOF ISD MS analysis is an effective, simple and rapid method of investigation for histones characterization: Application to EBV lymphoblastoid cell lines 94
L’Agricoltura sociale per la qualità della vita e la sostenibilità ambientale 94
RAPID IDENTIFICATION OF PATHOGENIC VARIANTS IN NEUROFIBROMATOSIS DISEASE BY GENE-PANEL SEQUENCING. 92
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis 85
NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders 85
Plants in Menstrual Diseases: A Systematic Study from Italian Folk Medicine on Current Approaches 84
Exome sequencing reveals two FA2H mutations in a family with a complicated form of Hereditary Spastic Paraplegia and psychiatric impairments 80
Mutational screening of the eIF2B5 gene in sib pairs affected by multiple sclerosis. 79
Targeted NGS-panel can improve the simultaneous identification of CNVs and SNVs in Mendelian diseases 79
ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION 73
IDENTITA' FEMMINILE E SCLEROSI MULTIPLA 71
Seizures and epilepsy in neurofibromatosis type 1 (NF1): a genotype-phenotype study. 69
Una piattaforma array CGH custom per l'identificazione di CNV in pazienti affetti da Sindromi Neurocutanee ed altri disordini neurologici: validazione della regione d'interesse per la Neurofibromatosi di tipo 1 69
Two Novel Cysteine-Sparing Notch3 Mutations In Patients With CADASIL 67
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis. 67
Mutational Screening in Patient with Charcot-Marie-Tooth Disease Type 2A 65
A novel missense mutation (p.Arg309His) in the nuclear localization signal sequence of spastin protein causes a complicated form of Hereditary Spastic Paraplegia 65
New spastin (SPG4) mutations in patients with Hereditary Spastic Paraplegia 63
Exome sequencing reveals two FA2H mutations in a non-consanguineous Italian family 63
Influence of functional polymorphism in MAO-A on neural network responsible of spatial working memory 61
A novel mutation in the 3 UTR of SPG4 gene identified in an apparently sporadic patient affected by spastic paraplegia. 60
Characterization of Histone post-translational modifications using a Top-Down, label-free, LC- MALDI-TOF Mass Spectrometry approach. 60
NOTCH3 gene mutations in twins with CADASIL 59
First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegia. 59
CHARGE syndrome and ALS: a clinical and genetic study of a family from Southern Italy. 58
Awareness, Identity, and Place Attachment Among Young People Living in a Calabrian Reclamation Landscape 58
VarHunter: a platform to process and analyze data from patients with neurological diseases 57
A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness 57
A novel locus for dHMN with pyramidal features maps to chromosome 4q34.3-q35.2. 55
Report of an ALS case associated with a new mutation in the TARDBP gene 54
Kinesins in neurological inherited diseases: a novel motor-domain mutation in KIF5A gene in a patient from Southern Italy affected by hereditary spastic paraplegia. 54
Gene symbol: NOTCH3 53
NOTCH3 PROTEIN LOCALIZATION IN (SKIN) FIBROBLASTS FROM CADASIL PATIENTS : AN IMMUNOFLUORESCENCE STUDY 53
Il paesaggio della bonifica della piana di Sibari: note preliminari 53
Horizontal gaze palsy with progressive scoliosis: two novel ROBO3 mutations in a compound heterozygous sporadic case 53
NOTCH3 gene analysis in two couples of twins 52
Clinical and genetic study of an Italian family linked to SPG26 locus 52
FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis. 52
Genetically-dependent modulation of serotonergic inactivation in the human ventrolateral prefrontal cortex 52
Genetically-dependent modulation of serotonergic inactivation in the human prefrontal cortex. 49
NEUROFIBROMATOSIS TYPE 2 (NF2) IN A CHILD UNDER 1 YEAR OF AGE: A CLINICAL AND MOLECULAR STUDY 48
Identificazione Di Una Nuova Mutazione Nel Gene PMP22 In Un Paziente Affetto Da HNPP 47
A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies. 47
Clinical and molecular investigation in an unusual Rett Syndrome case 45
A Novel Mutation In The X-Linked Cyclin-Dependent Kinase-Like 5 (CDKL5) Gene Associated With A Severe Rett Phenotype. 45
Monoamine Oxidase-A Genetic Variations Influence Brain Activity Associated with Inhibitory Control: New Insight into the Neural Correlates of Impulsivity 45
Natural History of Neurofibromatosis Type 2 (NF2) in the Paediatric Age: a Prospective Clinical (and Molecular) Study 45
ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION 44
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1 44
Spastin Gene Mutations In Italian Patients With Pure And Complicated Forms Of Spastic Paraplegia 43
From Hippocrates to Italian Traditional Medicine: Ethnopharmacological Evidence for a Potential Pharmacological Perspective in the Management of Polycystic Ovary Syndrome 43
Exome sequencing reveals two compound heterozygous DDHD2 mutations in a non consanguineous family with ARHSP-TCC 43
Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus. 42
L’Agricoltura sociale per la qualità della vita e la sostenibilità ambientale: uno studio di caso. 42
Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia 42
Analisi mutazionale del gene NF1 in pazienti del sud Italia affetti da Neurofibromatosi di tipo I: identificazione di 21 nuove mutazioni 42
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3. 41
Comparison of NOTCH3 expression in fibroblasts from CADASIL patients versus normal controls 41
Monoamine oxidase-a genetic variations influence brain activity associated with inhibitory control: new insight into the neural correlates of impulsivity 41
R521C mutation in the FUS gene in a large Italian family 40
Ventro-Lateral Prefrontal activity during working-memory processing is modulated by Monoamine oxidase-A genetic variation 40
Horizontal gaze palsy with progressive scoliosis: two novel ROBO3 mutations in a compound heterozygous sporadic case 40
Genetic analysis of TARDBP gene in a color of South Italian ALS patients 40
Amyotrophic lateral sclerosis: a new missense mutation in the SOD1 gene. 40
Polymorphisms and mutational analysis of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy. 39
MAO A VNTR polymorphism and variation in human morphology: a VBM study 38
Seizures and epilepsy in neurofibromatosis type 1 (NF1): a genotype-phenotype study. 38
Nuove mutazioni identificate nel gene della spastina in soggetti affetti da Paraplegia Spastica Ereditaria 37
Juvenile Huntington's disease presenting as progressive myoclonic epilepsy. 37
Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum 37
Comparison of different techniques for detecting 17p12 duplication in CMT1A. 37
Assenza di correlazione tra sclerosi multipla familiare (SM) e mutazioni nel gene eIF2B5. 37
NOTCH3 PROTEIN LOCALIZATION IN SKIN FIBROBLASTS FROM CADASIL PATIENTS : AN IMMUNOFLUORESCENCE MICROSCOPY STUDY 37
Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis 37
Charcot-Marie-Tooth disease tipe 2A associate with two novel MFN2 mutations 37
Mutational screening of GJB1, MPZ and PMP22 genes in a cohort of CMT patients from Southern Italy 36
The role of mri in the NOTCH3 gene screening of apparently sporadic CADASIL 36
EXOME SEQUENCING REVEALS TWO COMPOUND HETEROZYGOUS DDHD2 MUTATIONS IN A NON CONSANGUINEOUS SICILIAN FAMILY WITH ARHSP-TCC 36
A simple method for diagnosis of autosomal recessive spinal muscular atrophy by denaturing high-performance liquid chromatography 36
A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL. 36
CADASIL: extended polymorphisms and mutational analysis of the NOTCH3 gene. 35
Seizures and Epilepsy in the Setting of Neurofibromatosis Type 1 (NF1): a Population-Based, Genotype-Phenotype Study 35
Monoamine Oxidase-A genetic variation and the medial temporal lobe response to affective stimuli 35
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis. 35
Tre nuove mutazioni nel gene SPG4 identificate in pazienti affetti da paraparesi spastica ereditaria 35
A Clinical And Molecular Study In Children Under 1 Year Of Age Affected By Neurofibromatosis Type 2 34
Charcot-Marie-Tooth X-linked: five novel mutations in Italian patients 34
SUGGESTIVE EVIDENCE FOR LINKAGE TO CHROMOSOME 4qter FOR AUTOSOMAL DOMINANT DISTAL MOTOR NEURONOPATHY 34
SPASTIN GENE MUTATIONS IN ITALIAN PATIENTS WITH A PURE AND COMPLICATED FORMS OF SPASTIC PARAPLEGIA. 34
The p.Arg416Cys mutation in SPG3a gene associated with a pure form of spastic paraplegia. 34
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1. 33
CADASIL: molecular screening of the NOTCH3 gene in a large cohort of patients affected by leukoencephalopathy. 33
Clinical and genetic study of an Italian family with Autosomal Recessive Spastic Paraplegia associated with dysarthria and hearing loss. 33
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy 32
A novel SPG3A mutation in an Italian patient with Hereditary Spastic Paraplegia 32
Further evidence of genetic heterogeneity in autosomal dominant distal motor neuronopathy 32
Totale 5.233
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Categoria #
all - tutte 28.293
article - articoli 12.414
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 192
Totale 40.899
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202455 0 0 0 0 0 0 0 0 9 7 18 21
2024/20253.162 23 23 244 128 797 80 22 56 100 113 848 728
2025/20265.028 328 580 466 798 782 168 753 274 362 282 140 95
2026/2027191 191 0 0 0 0 0 0 0 0 0 0 0
Totale 8.436