CNR Institutional Research Information System

CARACCIOLO, MANUELA
 Distribuzione geografica
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Continente #
AS - Asia 1.601
NA - Nord America 1.081
EU - Europa 325
SA - Sud America 268
AF - Africa 25
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 2
Totale 3.304
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Nazione #
US - Stati Uniti d'America 1.043
SG - Singapore 674
CN - Cina 364
BR - Brasile 220
HK - Hong Kong 168
VN - Vietnam 145
FR - Francia 94
NL - Olanda 70
KR - Corea 65
IT - Italia 62
JP - Giappone 58
BD - Bangladesh 37
IN - India 24
GB - Regno Unito 22
AR - Argentina 19
DE - Germania 15
FI - Finlandia 15
MX - Messico 14
CA - Canada 13
ID - Indonesia 12
EC - Ecuador 10
IL - Israele 8
CO - Colombia 7
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
HN - Honduras 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
GT - Guatemala 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
PE - Perù 1
RE - Reunion 1
RO - Romania 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
SO - Somalia 1
SV - El Salvador 1
TZ - Tanzania 1
Totale 3.304
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Città #
Santa Clara 494
Singapore 390
Hong Kong 164
Hefei 146
San Jose 85
Ashburn 71
Beijing 67
Ho Chi Minh City 67
Lauterbourg 67
Seoul 65
Tokyo 50
Los Angeles 32
Dallas 29
Hanoi 21
New York 16
São Paulo 16
Buffalo 15
Orem 13
Minamishinagawa 8
Turku 8
Amsterdam 7
Belo Horizonte 7
Boardman 7
Haiphong 7
Curitiba 6
Warsaw 6
Anoia Superiore 5
Chicago 5
Council Bluffs 5
Helsinki 5
Milan 5
Naples 5
Newark 5
Orlando 5
Phoenix 5
Rio de Janeiro 5
Rome 5
Tashkent 5
Turin 5
Bengaluru 4
Brooklyn 4
Campinas 4
Dhaka 4
Diadema 4
Juiz de Fora 4
Miami 4
Montreal 4
Querétaro 4
Blumenau 3
Brasília 3
Bắc Ninh 3
Campo Grande 3
Chennai 3
Florianópolis 3
London 3
Lấp Vò 3
Nairobi 3
Palhoça 3
Phủ Lý 3
Porto Alegre 3
Providence 3
Quito 3
Quảng Ninh 3
San Antonio 3
Santo André 3
Staten Island 3
Toronto 3
Waco 3
Ấp Tân Phát 3
Abu Dhabi 2
Amman 2
Aparecida de Goiânia 2
Assago 2
Asunción 2
Atlanta 2
Baku 2
Bari 2
Barranquilla 2
Biên Hòa 2
Bogotá 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
Everett 2
Fort Worth 2
Fortaleza 2
Frankfurt am Main 2
Fullerton 2
Grand Rapids 2
Guangzhou 2
Guayaquil 2
Homestead 2
Houston 2
Hải Dương 2
Totale 2.090
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Nome #
MR parkinsonism index predicts vertical supranuclear gaze palsy in patients with PSP-parkinsonism. 95
A new MR imaging index for differentiation of progressive supranuclear palsy-parkinsonism from Parkinson's disease. 94
Magnetic Resonance Parkinsonism Index for evaluating disease progression rate in progressive supranuclear palsy: A longitudinal 2-year study 93
Cst3: fattore di rischio genetico per la Malattia di Alzheimer sporadica? 82
Refining initial diagnosis of Parkinson's disease after follow-up: A 4-year prospective clinical and magnetic resonance imaging study. 78
Disturbo di Alzheimer e tono dell'umore 71
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man 65
Increased cerebellar gray matter volume in head chefs. 60
NOTCH3 gene mutations in twins with CADASIL 59
Imaging counterpart of postural instability and vertical ocular dysfunction in patients with PSP: A multimodal MRI study 59
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. 54
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
A family with dominant optic atrophy and deafness due to a novel Opa1 mutation. 51
Increased glutamate + glutamine levels in the thalamus of patients with essential tremor: A preliminary proton MR spectroscopic study 51
A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy 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 50
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man. 49
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? 48
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 47
The movement time analyser task investigated with functional near infrared spectroscopy: an ecologic approach for measuring hemodynamic response in the motor system 44
Serum levels of interleukin-6 and interleukin-8 are elevated in patients with partial epilepsy 42
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3. 42
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
ADULT ONSET TAY-SACHS ASSOCIATED WITH -HEXOSAMINIDASE A DEFICIENCY: A CASE REPORT FROM SOUTH ITALY 41
Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease 40
D678N mutation in a patient with an early-onset Alzheimer's Disease 40
Thalamic proton MR spectroscopy distinguishes tremor-dominant PD from ET with resting tremor 40
The neuroanatomical correlates of anxiety in a healthy population: differences between the State-Trait Anxiety 1 Inventory and the Hamilton Anxiety Rating Scale 39
High titre of IgM ganglioside GM1 antibodies in patients with multiple sclerosis 39
Linkage analysis in three families from southern Italy with autosomal dominant nocturnal frontal lobe epilepsy . 38
delta thalassemia ed Hb delta variante nella provincia di Cosenza 38
A phenotyphic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation. 36
Fraxe intermediate alleles are associated with Parkinson's disease 35
Depression and epilepsy 35
Osteoporosis in patients affected with thalassemia. Our experience 35
Screening for MELAS mutations in Italian patients having stroke-like episodes. 34
The consanguineity in Calabrian population by genealogic trees 34
Studio clinico e genetico di una famiglia italiana affetta da una nuova forma di Paraparesi Spastica autosomica dominante complicata 34
Depression and Parkinson's disease:a neuropsychological view 33
Clinical and genetic study of an Italian family with Autosomal Recessive Spastic Paraplegia associated with dysarthria and hearing loss. 33
Cognitive impairment in Multiple Sclerosis 32
Molecular characterization of the APP gene in Italian patients with familial Alzheimer disease. 32
Further evidence of genetic heterogeneity in autosomal dominant distal motor neuronopathy 32
Analisi molecolare del promotore del gene PSEN-2 nella Malattia di Alzheimer: uno studio di associazione nella popolazione calabrese 32
Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Italian patients with hereditary spastic paraparesis 32
The association of the regulatory region of the PS-2 gene with Alzheimer s disease. 31
Vitamin E is not a protective factor for Peak-Dose Dyskinesias in Parkinson's disease. 31
Leber s hereditary optic neuropathy associated with multiple sclerosis like picture in a man. 31
Presenilin Enhancer-2 Gene mutations and Familial Alzheimer s Disease 31
Studio clinico-genetico in una famiglia con quadro clinico di neurodegenerazione associata alla Pantotenato Chinasi. 30
Genetic screening of Alzheimer's disease genes in Italian samples yields novel mutations in Presenilin-enhancer 2. 30
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 30
Comparison of different techniques in detecting CMT1A/HNPP duplication/deletion 30
Association of the 5-HT6 receptor gene polymorphism C26TT with Parkinson's disease 29
LRP1- LRPAP1 polymorphisms and risk of sporadic Alzheimer s disease. 29
Analisi di linkage in tre famiglie con Epilessia Frontale Notturna autosomica dominante. 29
The frequency of Limb Girdle Muscular Dystrophy 1C in southern Italy 29
A Novel Lys 130 Gln Mutation of the TAU gene. 28
Mutational analysis of the mitochondrial tRNAleu gene In Italian patients with stroke-like episodes of undetermined origin. 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
CASP-9 exon 1 polymorphism in patients with Multiple Sclerosis. 28
Caspase-9 gene C93T polymorphism and Multiple Sclerosis patients from Southern Italy 28
No evidence of association between the alpha-2 macroglobulin gene and Parkinson's disease in a case-control study 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
Clinical and genetic study of an Italian Family with a new form of Autosomal Dominant Complicated Spastic Paraplegia 26
No evidence of association between the alpha-2 macroglobulin gene and Parkinson's disease ina case-control sample. 25
Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia 25
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
beta pancreatic function in post-puberal thalassemic patients 22
The birth of Paediatrics: the discovery of alcaptonuria 22
PATTERN OF PROTEIN EXPRESSIONS IN SURAL NERVE OF CMT1A PATIENTS WITH CHROMOSOME 17p11.2 DUPLICATION 22
Linkage study in three Italian families with autosomal dominant nocturnal frontal lobe epilepsy . 17
Totale 3.332
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Categoria #
all - tutte 10.786
article - articoli 5.998
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 16.784
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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
2025/20261.799 72 171 151 268 335 74 269 111 142 107 55 44
2026/202777 77 0 0 0 0 0 0 0 0 0 0 0
Totale 3.332