CNR Institutional Research Information System

MAGARIELLO, ANGELA
 Distribuzione geografica
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Continente #
AS - Asia 4.357
NA - Nord America 1.892
EU - Europa 974
SA - Sud America 752
AF - Africa 65
OC - Oceania 11
Totale 8.051
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Nazione #
US - Stati Uniti d'America 1.814
SG - Singapore 1.757
CN - Cina 1.087
BR - Brasile 614
HK - Hong Kong 435
VN - Vietnam 380
IT - Italia 347
FR - Francia 273
KR - Corea 217
JP - Giappone 195
NL - Olanda 77
IN - India 76
GB - Regno Unito 70
DE - Germania 60
AR - Argentina 54
BD - Bangladesh 43
IL - Israele 34
FI - Finlandia 31
MX - Messico 31
CA - Canada 28
EC - Ecuador 27
ID - Indonesia 26
PL - Polonia 25
VE - Venezuela 16
ZA - Sudafrica 16
IQ - Iraq 15
UA - Ucraina 15
MA - Marocco 12
PY - Paraguay 12
TR - Turchia 12
SA - Arabia Saudita 11
SE - Svezia 11
CO - Colombia 10
EG - Egitto 10
PK - Pakistan 10
CL - Cile 9
ES - Italia 9
IR - Iran 9
AT - Austria 8
IE - Irlanda 8
PE - Perù 7
RU - Federazione Russa 7
UZ - Uzbekistan 7
AU - Australia 6
JM - Giamaica 6
PH - Filippine 6
AE - Emirati Arabi Uniti 5
KE - Kenya 5
OM - Oman 5
TN - Tunisia 5
AZ - Azerbaigian 4
BY - Bielorussia 4
MY - Malesia 4
BG - Bulgaria 3
CH - Svizzera 3
HN - Honduras 3
KG - Kirghizistan 3
MD - Moldavia 3
RO - Romania 3
TT - Trinidad e Tobago 3
TW - Taiwan 3
CI - Costa d'Avorio 2
CR - Costa Rica 2
DZ - Algeria 2
GR - Grecia 2
JO - Giordania 2
LT - Lituania 2
NP - Nepal 2
NZ - Nuova Zelanda 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
KI - Kiribati 1
KZ - Kazakistan 1
LB - Libano 1
LU - Lussemburgo 1
LY - Libia 1
MK - Macedonia 1
Totale 8.041
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Città #
Singapore 1.129
Santa Clara 780
Hefei 528
Hong Kong 431
San Jose 223
Seoul 217
Lauterbourg 196
Tokyo 160
Beijing 139
Ashburn 132
Ho Chi Minh City 116
Hanoi 100
Los Angeles 70
São Paulo 40
Dallas 36
Minamishinagawa 35
New York 35
Rome 30
Frankfurt am Main 28
Buffalo 26
Helsinki 25
Milan 24
Taranto 22
Orem 21
Rio de Janeiro 21
Naples 20
Bengaluru 19
Warsaw 17
Council Bluffs 15
Haiphong 14
Hải Dương 14
Da Nang 13
Belo Horizonte 12
Brasília 12
Porto Alegre 12
Amsterdam 11
Phoenix 11
Brooklyn 10
Denver 10
Elk Grove Village 10
London 10
Montreal 10
Atlanta 9
Guangzhou 9
Guayaquil 9
Manchester 9
Mexico City 9
Quito 9
Stockholm 9
Chennai 8
Curitiba 8
Nuremberg 8
Betim 7
Bologna 7
Can Tho 7
Dublin 7
Johannesburg 7
Mumbai 7
New Delhi 7
Nha Trang 7
Quận Một 7
Riyadh 7
Shanghai 7
Thái Bình 7
Toronto 7
Baghdad 6
Boardman 6
Brescia 6
Bắc Ninh 6
Campinas 6
Caracas 6
Düsseldorf 6
Houston 6
Jakarta 6
Kingston 6
Maceió 6
Ottaviano 6
Poplar 6
Uberlândia 6
Ankara 5
Asunción 5
Biên Hòa 5
Buenos Aires 5
Goiânia 5
Juiz de Fora 5
Memphis 5
Ninh Bình 5
Portsmouth 5
Quận Bình Thạnh 5
Recife 5
San Francisco 5
Sorocaba 5
São José 5
Tashkent 5
Vienna 5
Wilmington 5
Wroclaw 5
Baku 4
Boston 4
Cairo 4
Totale 5.148
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Nome #
Cibo e invecchiamento attivo. Una riflessione condivisa per raccomandazioni di policy inclusive 129
Percezione, identità e senso di appartenenza 114
Social agriculture for life quality and environmental sustainability 111
L’AGRICOLTURA SOCIALE PER LA QUALITÀ DELLA VITA E LA SOSTENIBILITÀ AMBIENTALE 98
LC-MALDI-TOF ISD MS analysis is an effective, simple and rapid method of investigation for histones characterization: Application to EBV lymphoblastoid cell lines 93
L’Agricoltura sociale per la qualità della vita e la sostenibilità ambientale 91
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis 84
Plants in Menstrual Diseases: A Systematic Study from Italian Folk Medicine on Current Approaches 83
Exome sequencing reveals two FA2H mutations in a family with a complicated form of Hereditary Spastic Paraplegia and psychiatric impairments 80
NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders 79
Mutational screening of the eIF2B5 gene in sib pairs affected by multiple sclerosis. 77
Targeted NGS-panel can improve the simultaneous identification of CNVs and SNVs in Mendelian diseases 76
RAPID IDENTIFICATION OF PATHOGENIC VARIANTS IN NEUROFIBROMATOSIS DISEASE BY GENE-PANEL SEQUENCING. 75
ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION 72
Seizures and epilepsy in neurofibromatosis type 1 (NF1): a genotype-phenotype study. 68
IDENTITA' FEMMINILE E SCLEROSI MULTIPLA 68
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
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 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
Influence of functional polymorphism in MAO-A on neural network responsible of spatial working memory 61
Exome sequencing reveals two FA2H mutations in a non-consanguineous Italian family 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
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
Characterization of Histone post-translational modifications using a Top-Down, label-free, LC- MALDI-TOF Mass Spectrometry approach. 56
Awareness, Identity, and Place Attachment Among Young People Living in a Calabrian Reclamation Landscape 55
A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness 55
A novel locus for dHMN with pyramidal features maps to chromosome 4q34.3-q35.2. 54
VarHunter: a platform to process and analyze data from patients with neurological diseases 53
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
Gene symbol: NOTCH3 51
FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis. 51
Il paesaggio della bonifica della piana di Sibari: note preliminari 51
Report of an ALS case associated with a new mutation in the TARDBP gene 51
NOTCH3 gene analysis in two couples of twins 50
Kinesins in neurological inherited diseases: a novel motor-domain mutation in KIF5A gene in a patient from Southern Italy affected by hereditary spastic paraplegia. 50
NEUROFIBROMATOSIS TYPE 2 (NF2) IN A CHILD UNDER 1 YEAR OF AGE: A CLINICAL AND MOLECULAR STUDY 48
Genetically-dependent modulation of serotonergic inactivation in the human ventrolateral prefrontal cortex 47
Horizontal gaze palsy with progressive scoliosis: two novel ROBO3 mutations in a compound heterozygous sporadic case 47
Genetically-dependent modulation of serotonergic inactivation in the human prefrontal cortex. 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
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
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
Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus. 41
Ventro-Lateral Prefrontal activity during working-memory processing is modulated by Monoamine oxidase-A genetic variation 40
From Hippocrates to Italian Traditional Medicine: Ethnopharmacological Evidence for a Potential Pharmacological Perspective in the Management of Polycystic Ovary Syndrome 40
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
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3. 39
Comparison of NOTCH3 expression in fibroblasts from CADASIL patients versus normal controls 39
MAO A VNTR polymorphism and variation in human morphology: a VBM study 38
Horizontal gaze palsy with progressive scoliosis: two novel ROBO3 mutations in a compound heterozygous sporadic case 38
Seizures and epilepsy in neurofibromatosis type 1 (NF1): a genotype-phenotype study. 38
Monoamine Oxidase-A Genetic Variations Influence Brain Activity Associated with Inhibitory Control: New Insight into the Neural Correlates of Impulsivity 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
L’Agricoltura sociale per la qualità della vita e la sostenibilità ambientale: uno studio di caso. 37
Genetic analysis of TARDBP gene in a color of South Italian ALS patients 37
Monoamine oxidase-a genetic variations influence brain activity associated with inhibitory control: new insight into the neural correlates of impulsivity 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
NOTCH3 PROTEIN LOCALIZATION IN SKIN FIBROBLASTS FROM CADASIL PATIENTS : AN IMMUNOFLUORESCENCE MICROSCOPY STUDY 36
Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis 36
Charcot-Marie-Tooth disease tipe 2A associate with two novel MFN2 mutations 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
Tre nuove mutazioni nel gene SPG4 identificate in pazienti affetti da paraparesi spastica ereditaria 35
Mutational screening of GJB1, MPZ and PMP22 genes in a cohort of CMT patients from Southern Italy 34
Comparison of different techniques for detecting 17p12 duplication in CMT1A. 34
EXOME SEQUENCING REVEALS TWO COMPOUND HETEROZYGOUS DDHD2 MUTATIONS IN A NON CONSANGUINEOUS SICILIAN FAMILY WITH ARHSP-TCC 34
Monoamine Oxidase-A genetic variation and the medial temporal lobe response to affective stimuli 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 novel Notch3 gene mutation not involving a cysteine residue in an Italian family with 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
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
MAO-A genetic variations influence the prefrontal cortical activity associated to a response inhibition task 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
Totale 5.039
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Categoria #
all - tutte 25.466
article - articoli 11.167
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 178
Totale 36.811
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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
2025/20264.907 328 580 466 798 782 168 753 274 362 282 114 0
Totale 8.124