CNR Institutional Research Information System

CARACCIOLO, MANUELA
 Distribuzione geografica
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Continente #
AS - Asia 1.582
NA - Nord America 989
EU - Europa 317
SA - Sud America 264
AF - Africa 25
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 2
Totale 3.181
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Nazione #
US - Stati Uniti d'America 958
SG - Singapore 674
CN - Cina 363
BR - Brasile 218
HK - Hong Kong 167
VN - Vietnam 145
FR - Francia 94
NL - Olanda 70
KR - Corea 65
JP - Giappone 58
IT - Italia 54
IN - India 24
GB - Regno Unito 22
BD - Bangladesh 20
AR - Argentina 19
DE - Germania 15
FI - Finlandia 15
MX - Messico 14
ID - Indonesia 12
EC - Ecuador 10
CA - Canada 9
IL - Israele 8
CO - Colombia 6
PL - Polonia 6
SE - Svezia 6
UZ - Uzbekistan 6
ZA - Sudafrica 6
AE - Emirati Arabi Uniti 5
ES - Italia 5
PK - Pakistan 5
PY - Paraguay 5
AT - Austria 4
IQ - Iraq 4
KE - Kenya 4
MA - Marocco 4
RU - Federazione Russa 4
TR - Turchia 4
CR - Costa Rica 3
DZ - Algeria 3
NP - Nepal 3
UA - Ucraina 3
AU - Australia 2
AZ - Azerbaigian 2
CH - Svizzera 2
CL - Cile 2
EG - Egitto 2
GE - Georgia 2
IE - Irlanda 2
IR - Iran 2
JO - Giordania 2
LV - Lettonia 2
OM - Oman 2
PA - Panama 2
SA - Arabia Saudita 2
TH - Thailandia 2
TN - Tunisia 2
TW - Taiwan 2
UY - Uruguay 2
VE - Venezuela 2
XK - ???statistics.table.value.countryCode.XK??? 2
BG - Bulgaria 1
BZ - Belize 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
EE - Estonia 1
GR - Grecia 1
HN - Honduras 1
HR - Croazia 1
HU - Ungheria 1
IS - Islanda 1
KG - Kirghizistan 1
LK - Sri Lanka 1
LU - Lussemburgo 1
MD - Moldavia 1
MM - Myanmar 1
MZ - Mozambico 1
NI - Nicaragua 1
RE - Reunion 1
RO - Romania 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
SO - Somalia 1
TZ - Tanzania 1
Totale 3.181
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Città #
Santa Clara 494
Singapore 390
Hong Kong 163
Hefei 146
San Jose 84
Beijing 67
Ho Chi Minh City 67
Lauterbourg 67
Seoul 65
Ashburn 63
Tokyo 50
Los Angeles 30
Dallas 24
Hanoi 21
São Paulo 16
Buffalo 14
New York 13
Orem 13
Minamishinagawa 8
Turku 8
Amsterdam 7
Belo Horizonte 7
Haiphong 7
Curitiba 6
Warsaw 6
Anoia Superiore 5
Council Bluffs 5
Helsinki 5
Naples 5
Newark 5
Phoenix 5
Rio de Janeiro 5
Tashkent 5
Bengaluru 4
Brooklyn 4
Campinas 4
Chicago 4
Dhaka 4
Diadema 4
Juiz de Fora 4
Montreal 4
Querétaro 4
Rome 4
Turin 4
Blumenau 3
Boardman 3
Brasília 3
Bắc Ninh 3
Campo Grande 3
Chennai 3
Florianópolis 3
London 3
Lấp Vò 3
Miami 3
Milan 3
Nairobi 3
Orlando 3
Palhoça 3
Phủ Lý 3
Porto Alegre 3
Quito 3
Quảng Ninh 3
Santo André 3
Waco 3
Ấp Tân Phát 3
Abu Dhabi 2
Amman 2
Aparecida de Goiânia 2
Assago 2
Asunción 2
Baku 2
Bari 2
Barranquilla 2
Biên Hòa 2
Bến Tre 2
Cape Town 2
Chengdu 2
Colombo 2
Da Nang 2
Delhi 2
Dublin 2
Düsseldorf 2
Ebersbach an der Fils 2
Fortaleza 2
Frankfurt am Main 2
Guangzhou 2
Guayaquil 2
Homestead 2
Houston 2
Hải Dương 2
Isidro Casanova 2
Jakarta 2
Johannesburg 2
Joinville 2
Kolkata 2
Lappeenranta 2
Madrid 2
Manchester 2
Marseille 2
Monte Grande 2
Totale 2.053
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Nome #
MR parkinsonism index predicts vertical supranuclear gaze palsy in patients with PSP-parkinsonism. 91
Magnetic Resonance Parkinsonism Index for evaluating disease progression rate in progressive supranuclear palsy: A longitudinal 2-year study 91
Cst3: fattore di rischio genetico per la Malattia di Alzheimer sporadica? 80
A new MR imaging index for differentiation of progressive supranuclear palsy-parkinsonism from Parkinson's disease. 79
Refining initial diagnosis of Parkinson's disease after follow-up: A 4-year prospective clinical and magnetic resonance imaging study. 71
Disturbo di Alzheimer e tono dell'umore 70
NOTCH3 gene mutations in twins with CADASIL 58
Increased cerebellar gray matter volume in head chefs. 56
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man 56
Refining initial diagnosis of Parkinson's disease after follow-up: A 4-year prospective clinical and magnetic resonance imaging study 54
Thalamic neurometabolic alterations in tremulous Parkinson's disease: A preliminary proton MR spectroscopy study. 53
Color vision impairment: a preliminar comparison among Idiopathic Prkinson, Essential Tremor, Parkinsonism, Early Parkinson's Disease 53
Clinical and genetic study of an Italian family linked to SPG26 locus 52
Increased glutamate + glutamine levels in the thalamus of patients with essential tremor: A preliminary proton MR spectroscopic study 51
Imaging counterpart of postural instability and vertical ocular dysfunction in patients with PSP: A multimodal MRI study 51
A family with dominant optic atrophy and deafness due to a novel Opa1 mutation. 50
In vivo evidence for decreased scyllo-inositol levels in the supplementary motor area of patients with Progressive Supranuclear Palsy: A proton MR spectroscopy study 50
Color vision in multiple sclerosis. A preliminar investigation on 80 Calabrian males 49
A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy 48
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man. 46
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? 45
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 43
DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex. 42
Gly269Ser mutation in compound heterozygosity with Leu127Arg is associated with adult onset of Tay-Sachs: a case report from south Italy 41
The movement time analyser task investigated with functional near infrared spectroscopy: an ecologic approach for measuring hemodynamic response in the motor system 41
ADULT ONSET TAY-SACHS ASSOCIATED WITH -HEXOSAMINIDASE A DEFICIENCY: A CASE REPORT FROM SOUTH ITALY 40
Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease 40
Serum levels of interleukin-6 and interleukin-8 are elevated in patients with partial epilepsy 40
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3. 39
Thalamic proton MR spectroscopy distinguishes tremor-dominant PD from ET with resting tremor 39
Linkage analysis in three families from southern Italy with autosomal dominant nocturnal frontal lobe epilepsy . 38
D678N mutation in a patient with an early-onset Alzheimer's Disease 38
delta thalassemia ed Hb delta variante nella provincia di Cosenza 38
The neuroanatomical correlates of anxiety in a healthy population: differences between the State-Trait Anxiety 1 Inventory and the Hamilton Anxiety Rating Scale 38
A phenotyphic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation. 36
High titre of IgM ganglioside GM1 antibodies in patients with multiple sclerosis 36
Fraxe intermediate alleles are associated with Parkinson's disease 35
Studio clinico e genetico di una famiglia italiana affetta da una nuova forma di Paraparesi Spastica autosomica dominante complicata 34
Depression and epilepsy 33
Osteoporosis in patients affected with thalassemia. Our experience 33
Clinical and genetic study of an Italian family with Autosomal Recessive Spastic Paraplegia associated with dysarthria and hearing loss. 33
The consanguineity in Calabrian population by genealogic trees 32
Analisi molecolare del promotore del gene PSEN-2 nella Malattia di Alzheimer: uno studio di associazione nella popolazione calabrese 32
The association of the regulatory region of the PS-2 gene with Alzheimer s disease. 31
Depression and Parkinson's disease:a neuropsychological view 31
Further evidence of genetic heterogeneity in autosomal dominant distal motor neuronopathy 31
Vitamin E is not a protective factor for Peak-Dose Dyskinesias in Parkinson's disease. 31
Screening for MELAS mutations in Italian patients having stroke-like episodes. 31
Leber s hereditary optic neuropathy associated with multiple sclerosis like picture in a man. 31
Studio clinico-genetico in una famiglia con quadro clinico di neurodegenerazione associata alla Pantotenato Chinasi. 30
Molecular characterization of the APP gene in Italian patients with familial Alzheimer disease. 30
Genetic screening of Alzheimer's disease genes in Italian samples yields novel mutations in Presenilin-enhancer 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
Association of the 5-HT6 receptor gene polymorphism C26TT with Parkinson's disease 29
Cognitive impairment in Multiple Sclerosis 29
Analisi di linkage in tre famiglie con Epilessia Frontale Notturna autosomica dominante. 29
Presenilin Enhancer-2 Gene mutations and Familial Alzheimer s Disease 29
The frequency of Limb Girdle Muscular Dystrophy 1C in southern Italy 29
A Novel Lys 130 Gln Mutation of the TAU gene. 28
A longitudinal evaluation of cadasil progression by diffusion magnetic resonance imaging. 28
Twenty novel mutations revealed by DHPLC analysis of the Neurofibromatosis Type 1 (NF1) gene in Southern Italian NF1 Patients 28
CAG repeat lenght and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocity 28
CASP-9 exon 1 polymorphism in patients with Multiple Sclerosis. 28
No evidence of association between the alpha-2 macroglobulin gene and Parkinson's disease in a case-control study 27
LRP1- LRPAP1 polymorphisms and risk of sporadic Alzheimer s disease. 27
Clinical and genetic study of an Italian Family with a new form of Autosomal Dominant Complicated Spastic Paraplegia 27
Variations in two lipid metabolizing genes and susceptibility to sporadic Alzheimer s disease. 27
Identificazione di marcatori nel gene della presenilina-2 predittivi di malattia di alzheimer familiare. 27
Identification of Pen-2 gene mutations in Italian patients with Familial Alzheimer s Disease 27
Identificazione di una nuova mutazione nel gene OPA1 in una famiglia affetta da atrofia ottica e sordità. 27
CAG repeat length and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocità. 26
The consanguineity in Calabrian population by genealogic trees 26
Mutational analysis of the mitochondrial tRNAleu gene In Italian patients with stroke-like episodes of undetermined origin. 26
Caspase-9 gene C93T polymorphism and Multiple Sclerosis patients from Southern Italy 26
No evidence of association between the alpha-2 macroglobulin gene and Parkinson's disease ina case-control sample. 24
Clinical and genetic study of an Italian Family with a new form of Autosomal Dominant Complicated Spastic Paraplegia 24
The frequency of limb girdle muscular dystrophy 1c in southern Italy 24
Hb G-San Josè homozygosis in a calabrian family 24
Clinic and genetic study in a family with a clinical picture of pantothenase kinase-associated neurodegeneration . 23
The birth of Paediatrics: the discovery of alcaptonuria 22
Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia 21
PATTERN OF PROTEIN EXPRESSIONS IN SURAL NERVE OF CMT1A PATIENTS WITH CHROMOSOME 17p11.2 DUPLICATION 21
beta pancreatic function in post-puberal thalassemic patients 20
Linkage study in three Italian families with autosomal dominant nocturnal frontal lobe epilepsy . 17
Totale 3.209
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Categoria #
all - tutte 9.844
article - articoli 5.463
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 15.307
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202419 0 0 0 0 0 0 0 0 3 0 11 5
2024/20251.437 7 3 97 43 498 35 18 43 39 62 317 275
2025/20261.753 72 171 151 268 335 74 269 111 142 107 53 0
Totale 3.209