IRIS
PUOTI, Gianfranco
 Distribuzione geografica
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Continente #
EU - Europa 5.261
NA - Nord America 2.565
AS - Asia 2.162
SA - Sud America 492
Continente sconosciuto - Info sul continente non disponibili 122
AF - Africa 27
OC - Oceania 6
Totale 10.635
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Nazione #
RU - Federazione Russa 3.302
US - Stati Uniti d'America 2.512
SG - Singapore 769
IE - Irlanda 645
CN - Cina 508
BR - Brasile 433
HK - Hong Kong 349
IT - Italia 332
VN - Vietnam 283
UA - Ucraina 281
GB - Regno Unito 236
DE - Germania 171
FI - Finlandia 83
GR - Grecia 58
KR - Corea 49
TR - Turchia 47
SE - Svezia 45
IN - India 41
CA - Canada 32
FR - Francia 32
AR - Argentina 27
JP - Giappone 25
BD - Bangladesh 20
AT - Austria 17
BE - Belgio 16
EC - Ecuador 13
IQ - Iraq 13
PK - Pakistan 12
NL - Olanda 11
MX - Messico 9
UZ - Uzbekistan 8
ID - Indonesia 7
VE - Venezuela 7
ZA - Sudafrica 7
MY - Malesia 6
PL - Polonia 6
ES - Italia 5
JO - Giordania 5
MA - Marocco 5
AZ - Azerbaigian 4
CO - Colombia 4
CR - Costa Rica 4
EU - Europa 4
KE - Kenya 4
AL - Albania 3
AU - Australia 3
BG - Bulgaria 3
CZ - Repubblica Ceca 3
NZ - Nuova Zelanda 3
PT - Portogallo 3
PY - Paraguay 3
TN - Tunisia 3
BY - Bielorussia 2
CH - Svizzera 2
CL - Cile 2
IL - Israele 2
IR - Iran 2
JM - Giamaica 2
LT - Lituania 2
NI - Nicaragua 2
PH - Filippine 2
SN - Senegal 2
TH - Thailandia 2
TW - Taiwan 2
AE - Emirati Arabi Uniti 1
BA - Bosnia-Erzegovina 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
HN - Honduras 1
HU - Ungheria 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
PR - Porto Rico 1
UY - Uruguay 1
Totale 10.517
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Città #
Moscow 1.166
Dublin 642
Jacksonville 420
Santa Clara 350
Hong Kong 344
Singapore 270
San Jose 217
Chandler 196
Ashburn 131
Princeton 96
Ho Chi Minh City 95
Beijing 78
Roxbury 75
Ann Arbor 68
Hanoi 65
Medford 64
New York 61
Seoul 45
Wilmington 40
Hefei 37
Boardman 35
Cambridge 34
Nanjing 34
São Paulo 33
Jinan 32
Caserta 30
Woodbridge 30
Munich 28
Milan 27
Bremen 26
Da Nang 26
San Mateo 25
The Dalles 25
Des Moines 21
Naples 21
Los Angeles 20
Dallas 18
Bengaluru 16
Shenyang 16
Brussels 15
Rio de Janeiro 15
Zhengzhou 14
Haiphong 13
Redwood City 13
Hangzhou 12
Nuremberg 12
Siano 12
Hebei 11
Helsinki 11
Brasília 10
San Francisco 10
Curitiba 9
Memphis 9
Rome 9
Tianjin 9
Tokyo 9
Vienna 9
Belo Horizonte 8
Frankfurt am Main 8
Guangzhou 8
Houston 8
Napoli 8
Ningbo 8
Taiyuan 8
Tashkent 8
Atlanta 7
Hải Dương 7
Lanzhou 7
London 7
Orem 7
Quito 7
Boydton 6
Duque de Caxias 6
Falkenstein 6
Guidonia 6
Montreal 6
Mountain View 6
Porto Alegre 6
Ranchi 6
Toronto 6
Auburn Hills 5
Baghdad 5
Caxias do Sul 5
Changsha 5
Council Bluffs 5
Dhaka 5
Guarulhos 5
Ipoh 5
Norwalk 5
Shanghai 5
Taizhou 5
Turku 5
Amman 4
Amsterdam 4
Baku 4
Campinas 4
Can Tho 4
Capua 4
Carapicuíba 4
Chennai 4
Totale 5.411
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Nome #
Creutzfeldt-Jakob disease (CJD) in italian patients with PRNP V210I mutation: an epidemiological and clinical evaluation 182
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations 178
12-months prospective Pentraxin-3 and metabolomic evaluation in multiple sclerosis patients treated with glatiramer acetate 176
Atypical Progressive Multifocal Leukoencephalopathy in a Kidney Transplant Recipient With Improving Symptoms After Immunocompetence Recovery 172
Delayed post‐hypoxic leukoencephalopathy with a peculiar autoantibody association 160
A comparison of Tau and 14-3-3 protein in the diagnosis of Creitzfeldt-Jakob disease 158
Alemtuzumab-Related Lymphocyte Subset Dynamics and Disease Activity or Autoimmune Adverse Events: Real-World Evidence 157
Is the pathology of posterior cortical atrophy clinically predictable? 152
A Novel Missense Mutation in CAV3 Gene in an Italian Family With Persistent hyperCKemia, Myalgia and Hypercholesterolemia: Double-trouble 151
Co-existence of PrP D Types 1 and 2 in Sporadic Creutzfeldt-Jakob Disease of the VV Subgroup: Phenotypic and Prion Protein Characteristics 144
A cluster of progranulin C157KfsX97 mutation in southern Italy- clinical characterization and genetic correlations 144
Amyloid-beta42 interacts mainly with insoluble prion protein in the Alzheimer brain 140
A novel insertional mutation in the prion protein gene: clinical and bio-molecular findings. 138
Myopathic changes in neurofibromatosis type 1 138
A novel SLC20A2 gene mutation causing primary familial brain calcification in an Ukrainian patient. 134
Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene 132
Minimally invasive percutaneous treatment for osteoid osteoma of the Spine. A case report 128
Sporadic human prion diseases: molecular insights and diagnosis 127
Deterioramento Cognitivo Minimo: analisi dei fattori di rischio e del tasso di progressione verso la demenza 127
A case of Kohlmeier-Degos disease with dramatic neurological involvment 126
Systematic Review on the Role of Lobar Cerebral Microbleeds in Cognition 126
Rehabilitation of gesture imitation: a case study with fMRI. 122
Coexistence of cavernous hemangioma and other vascular malformations of the orbit. A report of three cases 121
LA NEUROMIELITE OTTICA È UN’ ASSOCIAZIONE SINDROMICA COMUNE A PATOLOGIE ETEROGENEE 121
Clinical and Genetic Heterogeneity in a Large Family with Pseudoxanthoma Elasticum: MTHFR and SERPINE1 Variants as Possible Disease Modifiers in Developing Ischemic Stroke 120
CORRELATI CLINICO-STRUMENTALI IN UN CASO DI CREUTZFELD- JACOB A LUNGA SOPRAVVIVENZA. 119
Fas-L expression in sporadic Creutzfeldt-Jakob disease: an immunohistochemistry study 118
Human prion diseases: Surgical lessons learned from iatrogenic prion transmission 118
A mutation in the 5'-UTR of GRN gene associated with frontotemporal lobar degeneration: phenotypic variability and possible pathogenetic mechanisms 117
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) 117
A peculiar report of rare multifocal "ganglio-glioneurocytoma" 116
Dalla malattia di Schilder all’adrenoleucodistrofia; una breve storia di un secolo di ricerca neuropatologica clinica esemplare 115
Fas-L is expressed in sporadic Creutzfeldt-Jakob Disease 115
Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion 114
Protease-sensitive prions with 144-bp insertion mutations 112
Expanding the spectrum of SPTLC1-related disorders beyond hereditary sensory and autonomic neuropathies: a novel case of the distinct "S331 syndrome" 112
Studio clinico, neuropatologico e bio-molecolare della malattia di Creutzfeldt-Jakob associata a mutazione V210I del gene della proteina prionica 112
Creutzfeldt-Jakob disease: topography of PrPres immunoreactivity 112
Migraine as possible red flag of PFO presence in suspected demyelinating disease 112
Heidenhain variant of Creutzfeldt-Jakob disease with the co-occurrence of two differents types of prion proteins 111
Non-alcoholic acute Wernicke's encephalopathy: Role of MRI in non typical cases. 111
A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease 108
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein. 106
phenotypic heterogeneity in Creutzfeldt-Jakob disease associated with a new prion protein mutation 106
The Rise of the GRN C157KfsX97 Mutation in Southern Italy: Going Back to the Fall of the Western Roman Empire 103
Slowly progressive JC positive multifocal leukoencephalopathy not associated with overt immunodeficency, oncohaematological disorder nor immunosoppressive therapies 102
Progressive multifocal leukoencephalopathy presenting with bilateral myoclonus: a case report 102
Microglia and complement in the cortex of Creutzfeldt-Jakob disease and comparison with Alzheimer’s disease 101
Insertional mutation in prion protein gene presenting with schizophrenia 101
Creutzfeldt-Jakob disease: Carnoy's fixative improves the immunohistochemistry of the proteinase K-resistant prion protein 100
Characterization of prion disease associated with a two-octapeptide repeat insertion 100
Creutzfeldt-Jakob Disease 99
Experimental Therapy with Quinacrine in Creutzfeldt-Jakob disease 99
Hereditary cerebral hemorrhage with amyloidosis associated with E693K mutation of APP 98
Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene 97
Disordini di movimento nella patologia neurologica dell’anziano 97
Synthetic Aβ peptides acquire prion-like properties in the brain 97
MRI "fogging" in cerebellar ischaemia: case report 96
Heidenhain Variant of Sporadic Creutzfeldt-Jakob Disease With the Co-Occurrence of Two Different Types of Prion Protein 96
Variably Protease-sensitive Prionopathy in an Apparent Cognitively Normal 93-Year-Old 95
Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPSc. 95
Variably Protease-Sensitive Prionopathy: a Novel Disease of the Prion Protein 95
Tauopathies: a new phenotype with epilepsy and severe cerebellar involvement 95
Experimental therapy with quinacrine in Creutzfeldt-Jakob diseases 95
Large anterior temporal Virchow–Robin spaces: Evaluating MRI features over the years—Our experience and literature review 95
Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain 94
The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease. 93
Creutzfeldt-Jakob disease: Distinct PrPres types induce different microglial reaction patterns 92
Creutzfeldt-Jakob disease (CJD) associated with V210I PRNP mutation: phenotypic and molecular genetic analysis 91
Heidenhain variant in two patients with inherited V210I Creutzfeldt-Jakob disease 90
Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her son 89
NOVEL HUMAN PRION DISEASE AFFECTING 3 PRION CODON 129 GENOTYPES: THE SPORADIC FORM OF GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE? 89
Predictive factors of volumetric reduction in lumbar disc herniation treated by O2-O3 chemiodiscolysis 89
SPORADIC CEREUTZFELDT-JAKOB DISEASE WITH MM1-TYPE PRION PROTEIN AND PLAQUES 88
“Borderline” idiopathic CD4+ T-cell lymphocytopenia presenting with atypical progressive multifocal leukoencephalopathy 88
Tau protein in a novel prion disease with GSS features 87
Global-local information processing in an unusual patient with posterior cortical atrophy 86
Sporadic Creutzfeldt-Jakob disease in a native Puerto Rican patient 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 85
Sporadic cCreutzfeldt-Jakob disease: coexistence of type 1 and type 2 PrPSc in the same brain 84
Sporadic Creutzfeldt - Jakob disease’ 83
Topografic distribution of PrPres in Creutzfeldt-Jakob disease as revealed by immunohistochemistry 83
Sporadic Creutzfeldt-Jakob disease: coexistence of biochemically distinct types of PrPSc in the same brain 83
Molecular Bases of Phenotypic Heterogeneity in Prion Diseases 82
Creutzfeldt-Jakob disease with one extra-repeat insertion in PRNP 81
tion in the prion protein genme presenting with schizophrenia 81
Early Onset Atypical Dementia Associated with a Novel Seven Octapeptide Repeat Insertion in the Prion Protein Gene 81
Singular cases of Alzheimer's disease disclose new and old genetic "acquaintances" 81
New-onset refractory status epilepticus mimicking herpes virus encephalitis 80
Distinct types of PrPres induce different microglial reaction in sporadic Creutzfeldt-Jakob disease 79
TOPOGRAPHIC DISTRIBUTION OF PRP-Res IN CREUTZFELDT-JAKOB DISEASE AS REVEALED BY IMMUNOHISTOCHEMISTRY 79
Protease-Sensitive Prionopathy in a Cognitively Normal 93 Year Old 79
Plasma Small Extracellular Vesicles with Complement Alterations in GRN/C9orf72 and Sporadic Frontotemporal Lobar Degeneration 79
Dramatic neurological debut in a case of Köhlmeier-Degos disease 78
Phenotypic Heterogeneity and Type-1/2 PrPSc Co-Occurrence in Creutzfeldt-Jakob Disease Associated With a new Mutation of PRNP 77
Insertional mutation in prion protein gene presenting with schizophrenic-like symptoms 77
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 74
Unusual CLIPPERS presentation and role of MRI examination in the proper diagnostic assessment: A case report. 73
Serum miRNAs as biomarkers in Neurofibromatosis 1: New promising findings. 6
Totale 10.635
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Categoria #
all - tutte 38.402
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 38.402
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022513 0 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
2025/20265.269 140 177 219 305 474 3.069 285 205 180 81 93 41
2026/2027122 41 81 0 0 0 0 0 0 0 0 0 0
Totale 10.635