IRIS
PUOTI, Gianfranco
 Distribuzione geografica
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Continente #
EU - Europa 5.220
NA - Nord America 2.385
AS - Asia 2.117
SA - Sud America 487
AF - Africa 27
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 4
Totale 10.246
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Nazione #
RU - Federazione Russa 3.302
US - Stati Uniti d'America 2.351
SG - Singapore 740
IE - Irlanda 645
CN - Cina 503
BR - Brasile 431
HK - Hong Kong 341
IT - Italia 302
VN - Vietnam 283
UA - Ucraina 281
GB - Regno Unito 235
DE - Germania 168
FI - Finlandia 83
GR - Grecia 58
KR - Corea 49
TR - Turchia 47
SE - Svezia 45
IN - India 41
FR - Francia 32
AR - Argentina 26
JP - Giappone 23
BD - Bangladesh 19
CA - Canada 18
AT - Austria 17
BE - Belgio 15
EC - Ecuador 13
IQ - Iraq 13
PK - Pakistan 12
NL - Olanda 10
MX - Messico 8
UZ - Uzbekistan 8
ID - Indonesia 7
ZA - Sudafrica 7
MY - Malesia 6
PL - Polonia 6
VE - Venezuela 6
JO - Giordania 5
MA - Marocco 5
AZ - Azerbaigian 4
EU - Europa 4
KE - Kenya 4
AL - Albania 3
AU - Australia 3
BG - Bulgaria 3
CO - Colombia 3
CR - Costa Rica 3
CZ - Repubblica Ceca 3
ES - Italia 3
NZ - Nuova Zelanda 3
PT - Portogallo 3
PY - Paraguay 3
TN - Tunisia 3
BY - Bielorussia 2
CL - Cile 2
IL - Israele 2
IR - Iran 2
LT - Lituania 2
NI - Nicaragua 2
PH - Filippine 2
SN - Senegal 2
TH - Thailandia 2
TW - Taiwan 2
AE - Emirati Arabi Uniti 1
BB - Barbados 1
BO - Bolivia 1
CG - Congo 1
CI - Costa d'Avorio 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EG - Egitto 1
ET - Etiopia 1
HU - Ungheria 1
JM - Giamaica 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LY - Libia 1
NP - Nepal 1
OM - Oman 1
PE - Perù 1
UY - Uruguay 1
Totale 10.246
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Città #
Moscow 1.166
Dublin 642
Jacksonville 419
Santa Clara 341
Hong Kong 340
Singapore 268
Chandler 196
San Jose 172
Princeton 96
Ho Chi Minh City 95
Ashburn 91
Beijing 76
Roxbury 75
Ann Arbor 68
Hanoi 65
Medford 64
New York 59
Seoul 45
Wilmington 40
Hefei 37
Boardman 35
Cambridge 34
Nanjing 34
São Paulo 33
Jinan 32
Caserta 30
Woodbridge 30
Munich 28
Bremen 26
Da Nang 26
San Mateo 25
The Dalles 25
Des Moines 21
Milan 19
Bengaluru 16
Dallas 16
Shenyang 16
Brussels 15
Los Angeles 15
Rio de Janeiro 15
Zhengzhou 14
Haiphong 13
Redwood City 13
Hangzhou 12
Nuremberg 12
Siano 12
Hebei 11
Helsinki 11
Brasília 10
Curitiba 9
Naples 9
San Francisco 9
Tianjin 9
Vienna 9
Belo Horizonte 8
Guangzhou 8
Napoli 8
Ningbo 8
Rome 8
Taiyuan 8
Tashkent 8
Hải Dương 7
Lanzhou 7
Quito 7
Tokyo 7
Atlanta 6
Boydton 6
Duque de Caxias 6
Falkenstein 6
Guidonia 6
Houston 6
London 6
Mountain View 6
Orem 6
Porto Alegre 6
Ranchi 6
Auburn Hills 5
Baghdad 5
Caxias do Sul 5
Changsha 5
Dhaka 5
Frankfurt am Main 5
Ipoh 5
Norwalk 5
Taizhou 5
Turku 5
Amman 4
Baku 4
Campinas 4
Can Tho 4
Capua 4
Carapicuíba 4
Chennai 4
Erbil 4
Fairfield 4
Feira de Santana 4
Guarulhos 4
Guayaquil 4
Haikou 4
Jiaxing 4
Totale 5.255
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Nome #
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations 174
12-months prospective Pentraxin-3 and metabolomic evaluation in multiple sclerosis patients treated with glatiramer acetate 173
Atypical Progressive Multifocal Leukoencephalopathy in a Kidney Transplant Recipient With Improving Symptoms After Immunocompetence Recovery 170
Creutzfeldt-Jakob disease (CJD) in italian patients with PRNP V210I mutation: an epidemiological and clinical evaluation 161
Delayed post‐hypoxic leukoencephalopathy with a peculiar autoantibody association 155
Alemtuzumab-Related Lymphocyte Subset Dynamics and Disease Activity or Autoimmune Adverse Events: Real-World Evidence 153
A comparison of Tau and 14-3-3 protein in the diagnosis of Creitzfeldt-Jakob disease 152
A Novel Missense Mutation in CAV3 Gene in an Italian Family With Persistent hyperCKemia, Myalgia and Hypercholesterolemia: Double-trouble 150
Is the pathology of posterior cortical atrophy clinically predictable? 147
A cluster of progranulin C157KfsX97 mutation in southern Italy- clinical characterization and genetic correlations 139
Myopathic changes in neurofibromatosis type 1 138
Amyloid-beta42 interacts mainly with insoluble prion protein in the Alzheimer brain 137
Co-existence of PrP D Types 1 and 2 in Sporadic Creutzfeldt-Jakob Disease of the VV Subgroup: Phenotypic and Prion Protein Characteristics 137
A novel insertional mutation in the prion protein gene: clinical and bio-molecular findings. 136
Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene 131
A novel SLC20A2 gene mutation causing primary familial brain calcification in an Ukrainian patient. 131
A case of Kohlmeier-Degos disease with dramatic neurological involvment 125
Deterioramento Cognitivo Minimo: analisi dei fattori di rischio e del tasso di progressione verso la demenza 124
Rehabilitation of gesture imitation: a case study with fMRI. 121
Systematic Review on the Role of Lobar Cerebral Microbleeds in Cognition 121
Sporadic human prion diseases: molecular insights and diagnosis 120
Minimally invasive percutaneous treatment for osteoid osteoma of the Spine. A case report 120
LA NEUROMIELITE OTTICA È UN’ ASSOCIAZIONE SINDROMICA COMUNE A PATOLOGIE ETEROGENEE 119
Clinical and Genetic Heterogeneity in a Large Family with Pseudoxanthoma Elasticum: MTHFR and SERPINE1 Variants as Possible Disease Modifiers in Developing Ischemic Stroke 119
A mutation in the 5'-UTR of GRN gene associated with frontotemporal lobar degeneration: phenotypic variability and possible pathogenetic mechanisms 117
Coexistence of cavernous hemangioma and other vascular malformations of the orbit. A report of three cases 116
CORRELATI CLINICO-STRUMENTALI IN UN CASO DI CREUTZFELD- JACOB A LUNGA SOPRAVVIVENZA. 116
Human prion diseases: Surgical lessons learned from iatrogenic prion transmission 116
Fas-L expression in sporadic Creutzfeldt-Jakob disease: an immunohistochemistry study 115
Analyses of the Protein Tau to Help Determine Whether the Newly Discovered Protease-Sensitive Prionopathy is the Sporadic Form of Gerstmann-Sträussler-Scheinker Disease (GSS) 113
A peculiar report of rare multifocal "ganglio-glioneurocytoma" 113
Protease-sensitive prions with 144-bp insertion mutations 112
Studio clinico, neuropatologico e bio-molecolare della malattia di Creutzfeldt-Jakob associata a mutazione V210I del gene della proteina prionica 112
Expanding the spectrum of SPTLC1-related disorders beyond hereditary sensory and autonomic neuropathies: a novel case of the distinct "S331 syndrome" 111
Migraine as possible red flag of PFO presence in suspected demyelinating disease 111
Heidenhain variant of Creutzfeldt-Jakob disease with the co-occurrence of two differents types of prion proteins 110
Fas-L is expressed in sporadic Creutzfeldt-Jakob Disease 110
Dalla malattia di Schilder all’adrenoleucodistrofia; una breve storia di un secolo di ricerca neuropatologica clinica esemplare 109
Non-alcoholic acute Wernicke's encephalopathy: Role of MRI in non typical cases. 109
Creutzfeldt-Jakob disease: topography of PrPres immunoreactivity 108
Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion 106
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein. 104
A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease 104
phenotypic heterogeneity in Creutzfeldt-Jakob disease associated with a new prion protein mutation 103
The Rise of the GRN C157KfsX97 Mutation in Southern Italy: Going Back to the Fall of the Western Roman Empire 102
Slowly progressive JC positive multifocal leukoencephalopathy not associated with overt immunodeficency, oncohaematological disorder nor immunosoppressive therapies 100
Insertional mutation in prion protein gene presenting with schizophrenia 100
Creutzfeldt-Jakob disease: Carnoy's fixative improves the immunohistochemistry of the proteinase K-resistant prion protein 99
Progressive multifocal leukoencephalopathy presenting with bilateral myoclonus: a case report 99
Characterization of prion disease associated with a two-octapeptide repeat insertion 99
Hereditary cerebral hemorrhage with amyloidosis associated with E693K mutation of APP 98
Experimental Therapy with Quinacrine in Creutzfeldt-Jakob disease 98
Creutzfeldt-Jakob Disease 97
Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPSc. 95
Heidenhain Variant of Sporadic Creutzfeldt-Jakob Disease With the Co-Occurrence of Two Different Types of Prion Protein 95
Tauopathies: a new phenotype with epilepsy and severe cerebellar involvement 95
Synthetic Aβ peptides acquire prion-like properties in the brain 95
Variably Protease-sensitive Prionopathy in an Apparent Cognitively Normal 93-Year-Old 94
Variably Protease-Sensitive Prionopathy: a Novel Disease of the Prion Protein 94
Experimental therapy with quinacrine in Creutzfeldt-Jakob diseases 94
Microglia and complement in the cortex of Creutzfeldt-Jakob disease and comparison with Alzheimer’s disease 94
MRI "fogging" in cerebellar ischaemia: case report 93
Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain 93
Disordini di movimento nella patologia neurologica dell’anziano 93
Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene 92
Large anterior temporal Virchow–Robin spaces: Evaluating MRI features over the years—Our experience and literature review 91
Creutzfeldt-Jakob disease: Distinct PrPres types induce different microglial reaction patterns 89
Heidenhain variant in two patients with inherited V210I Creutzfeldt-Jakob disease 88
Predictive factors of volumetric reduction in lumbar disc herniation treated by O2-O3 chemiodiscolysis 88
SPORADIC CEREUTZFELDT-JAKOB DISEASE WITH MM1-TYPE PRION PROTEIN AND PLAQUES 87
Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her son 87
Creutzfeldt-Jakob disease (CJD) associated with V210I PRNP mutation: phenotypic and molecular genetic analysis 87
Tau protein in a novel prion disease with GSS features 86
NOVEL HUMAN PRION DISEASE AFFECTING 3 PRION CODON 129 GENOTYPES: THE SPORADIC FORM OF GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE? 86
Global-local information processing in an unusual patient with posterior cortical atrophy 86
Plasma Small Extracellular Vesicle Cathepsin D Dysregulation in GRN/C9orf72 and Sporadic Frontotemporal Lobar Degeneration 85
Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutation 84
“Borderline” idiopathic CD4+ T-cell lymphocytopenia presenting with atypical progressive multifocal leukoencephalopathy 84
The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease. 83
Sporadic Creutzfeldt - Jakob disease’ 82
Sporadic Creutzfeldt-Jakob disease in a native Puerto Rican patient 82
Sporadic cCreutzfeldt-Jakob disease: coexistence of type 1 and type 2 PrPSc in the same brain 81
Topografic distribution of PrPres in Creutzfeldt-Jakob disease as revealed by immunohistochemistry 81
Creutzfeldt-Jakob disease with one extra-repeat insertion in PRNP 80
Early Onset Atypical Dementia Associated with a Novel Seven Octapeptide Repeat Insertion in the Prion Protein Gene 80
New-onset refractory status epilepticus mimicking herpes virus encephalitis 79
tion in the prion protein genme presenting with schizophrenia 79
TOPOGRAPHIC DISTRIBUTION OF PRP-Res IN CREUTZFELDT-JAKOB DISEASE AS REVEALED BY IMMUNOHISTOCHEMISTRY 79
Sporadic Creutzfeldt-Jakob disease: coexistence of biochemically distinct types of PrPSc in the same brain 79
Singular cases of Alzheimer's disease disclose new and old genetic "acquaintances" 79
Plasma Small Extracellular Vesicles with Complement Alterations in GRN/C9orf72 and Sporadic Frontotemporal Lobar Degeneration 79
Molecular Bases of Phenotypic Heterogeneity in Prion Diseases 78
Insertional mutation in prion protein gene presenting with schizophrenic-like symptoms 77
Protease-Sensitive Prionopathy in a Cognitively Normal 93 Year Old 77
Dramatic neurological debut in a case of Köhlmeier-Degos disease 77
Distinct types of PrPres induce different microglial reaction in sporadic Creutzfeldt-Jakob disease 76
Phenotypic Heterogeneity and Type-1/2 PrPSc Co-Occurrence in Creutzfeldt-Jakob Disease Associated With a new Mutation of PRNP 75
Pathological 25 kDa C-Terminal Fragments of TDP-43 Are Present in Lymphoblastoid Cell Lines and Extracellular Vesicles from Patients Affected by Frontotemporal Lobar Degeneration and Neuronal Ceroidolipofuscinosis Carrying a GRN Mutation 73
Unusual CLIPPERS presentation and role of MRI examination in the proper diagnostic assessment: A case report. 72
Totale 10.363
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Categoria #
all - tutte 34.912
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 34.912
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021187 0 0 0 0 0 0 0 0 0 86 77 24
2021/2022557 44 10 3 13 186 2 10 30 21 16 36 186
2022/20231.033 123 5 21 55 92 60 1 42 572 13 23 26
2023/2024432 32 11 18 26 159 61 7 2 2 7 28 79
2024/20251.510 5 20 11 54 244 157 150 119 251 305 112 82
2025/20265.119 140 177 219 305 474 3.069 285 205 180 65 0 0
Totale 10.363