IRIS
PUOTI, Gianfranco
 Distribuzione geografica
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Continente #
EU - Europa 5.409
NA - Nord America 3.258
AS - Asia 2.190
SA - Sud America 497
Continente sconosciuto - Info sul continente non disponibili 122
AF - Africa 28
OC - Oceania 6
Totale 11.510
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Nazione #
RU - Federazione Russa 3.303
US - Stati Uniti d'America 3.183
SG - Singapore 784
IE - Irlanda 645
CN - Cina 511
IT - Italia 461
BR - Brasile 436
HK - Hong Kong 351
VN - Vietnam 283
UA - Ucraina 281
GB - Regno Unito 244
DE - Germania 176
FI - Finlandia 83
GR - Grecia 58
KR - Corea 49
IN - India 47
TR - Turchia 47
SE - Svezia 45
CA - Canada 43
FR - Francia 34
AR - Argentina 27
JP - Giappone 25
BD - Bangladesh 21
AT - Austria 17
BE - Belgio 16
EC - Ecuador 14
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
CR - Costa Rica 5
ES - Italia 5
JO - Giordania 5
MA - Marocco 5
AZ - Azerbaigian 4
CO - Colombia 4
EU - Europa 4
HN - Honduras 4
KE - Kenya 4
AL - Albania 3
AU - Australia 3
BG - Bulgaria 3
CL - Cile 3
CZ - Repubblica Ceca 3
LT - Lituania 3
NI - Nicaragua 3
NZ - Nuova Zelanda 3
PT - Portogallo 3
PY - Paraguay 3
SV - El Salvador 3
TN - Tunisia 3
AE - Emirati Arabi Uniti 2
BB - Barbados 2
BY - Bielorussia 2
CH - Svizzera 2
IL - Israele 2
IR - Iran 2
JM - Giamaica 2
PH - Filippine 2
PR - Porto Rico 2
SN - Senegal 2
TH - Thailandia 2
TW - Taiwan 2
BA - Bosnia-Erzegovina 1
BO - Bolivia 1
CG - Congo 1
CI - Costa d'Avorio 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EE - Estonia 1
EG - Egitto 1
ET - Etiopia 1
GP - Guadalupe 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
RO - Romania 1
SC - Seychelles 1
UY - Uruguay 1
Totale 11.392
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Città #
Moscow 1.166
Dublin 642
Jacksonville 420
Santa Clara 362
Hong Kong 345
San Jose 274
Singapore 272
Ashburn 264
Chandler 196
Council Bluffs 196
Princeton 99
Ho Chi Minh City 95
Milan 84
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
Bremen 26
Da Nang 26
Los Angeles 25
San Mateo 25
The Dalles 25
Naples 22
Des Moines 21
Dallas 19
Bengaluru 16
Shenyang 16
Brussels 15
Miano 15
Rio de Janeiro 15
Zhengzhou 14
Haiphong 13
Redwood City 13
Brasília 12
Hangzhou 12
Nuremberg 12
San Francisco 12
Siano 12
Frankfurt am Main 11
Hebei 11
Helsinki 11
Rome 11
Atlanta 10
Curitiba 9
Houston 9
Memphis 9
North Bergen 9
Tianjin 9
Tokyo 9
Vienna 9
Belo Horizonte 8
Guangzhou 8
Napoli 8
Ningbo 8
Taiyuan 8
Tashkent 8
Carrboro 7
Hải Dương 7
Kochi 7
Lanzhou 7
London 7
Montreal 7
Orem 7
Quito 7
Toronto 7
Boydton 6
Duque de Caxias 6
Falkenstein 6
Guidonia 6
Mountain View 6
Phoenix 6
Porto Alegre 6
Ranchi 6
Urtijëi 6
Auburn Hills 5
Baghdad 5
Caxias do Sul 5
Changsha 5
Chicago 5
Dhaka 5
Fairfield 5
Guarulhos 5
Ipoh 5
Kansas City 5
Norwalk 5
Shanghai 5
Taizhou 5
Totale 5.917
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Nome #
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations 190
Creutzfeldt-Jakob disease (CJD) in italian patients with PRNP V210I mutation: an epidemiological and clinical evaluation 187
12-months prospective Pentraxin-3 and metabolomic evaluation in multiple sclerosis patients treated with glatiramer acetate 184
Sporadic human prion diseases: molecular insights and diagnosis 179
Atypical Progressive Multifocal Leukoencephalopathy in a Kidney Transplant Recipient With Improving Symptoms After Immunocompetence Recovery 177
Alemtuzumab-Related Lymphocyte Subset Dynamics and Disease Activity or Autoimmune Adverse Events: Real-World Evidence 174
A comparison of Tau and 14-3-3 protein in the diagnosis of Creitzfeldt-Jakob disease 174
Delayed post‐hypoxic leukoencephalopathy with a peculiar autoantibody association 168
A Novel Missense Mutation in CAV3 Gene in an Italian Family With Persistent hyperCKemia, Myalgia and Hypercholesterolemia: Double-trouble 165
Is the pathology of posterior cortical atrophy clinically predictable? 160
A cluster of progranulin C157KfsX97 mutation in southern Italy- clinical characterization and genetic correlations 155
Co-existence of PrP D Types 1 and 2 in Sporadic Creutzfeldt-Jakob Disease of the VV Subgroup: Phenotypic and Prion Protein Characteristics 154
Amyloid-beta42 interacts mainly with insoluble prion protein in the Alzheimer brain 148
A novel insertional mutation in the prion protein gene: clinical and bio-molecular findings. 147
Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene 146
Myopathic changes in neurofibromatosis type 1 145
A novel SLC20A2 gene mutation causing primary familial brain calcification in an Ukrainian patient. 139
A case of Kohlmeier-Degos disease with dramatic neurological involvment 138
Systematic Review on the Role of Lobar Cerebral Microbleeds in Cognition 138
Minimally invasive percutaneous treatment for osteoid osteoma of the Spine. A case report 137
Deterioramento Cognitivo Minimo: analisi dei fattori di rischio e del tasso di progressione verso la demenza 134
Rehabilitation of gesture imitation: a case study with fMRI. 131
Coexistence of cavernous hemangioma and other vascular malformations of the orbit. A report of three cases 131
Human prion diseases: Surgical lessons learned from iatrogenic prion transmission 127
Clinical and Genetic Heterogeneity in a Large Family with Pseudoxanthoma Elasticum: MTHFR and SERPINE1 Variants as Possible Disease Modifiers in Developing Ischemic Stroke 127
LA NEUROMIELITE OTTICA È UN’ ASSOCIAZIONE SINDROMICA COMUNE A PATOLOGIE ETEROGENEE 126
Non-alcoholic acute Wernicke's encephalopathy: Role of MRI in non typical cases. 126
Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion 126
Protease-sensitive prions with 144-bp insertion mutations 125
A mutation in the 5'-UTR of GRN gene associated with frontotemporal lobar degeneration: phenotypic variability and possible pathogenetic mechanisms 124
Expanding the spectrum of SPTLC1-related disorders beyond hereditary sensory and autonomic neuropathies: a novel case of the distinct "S331 syndrome" 124
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) 124
CORRELATI CLINICO-STRUMENTALI IN UN CASO DI CREUTZFELD- JACOB A LUNGA SOPRAVVIVENZA. 124
Fas-L expression in sporadic Creutzfeldt-Jakob disease: an immunohistochemistry study 123
Studio clinico, neuropatologico e bio-molecolare della malattia di Creutzfeldt-Jakob associata a mutazione V210I del gene della proteina prionica 123
Migraine as possible red flag of PFO presence in suspected demyelinating disease 123
Dalla malattia di Schilder all’adrenoleucodistrofia; una breve storia di un secolo di ricerca neuropatologica clinica esemplare 122
A peculiar report of rare multifocal "ganglio-glioneurocytoma" 122
Fas-L is expressed in sporadic Creutzfeldt-Jakob Disease 121
Heidenhain variant of Creutzfeldt-Jakob disease with the co-occurrence of two differents types of prion proteins 119
Creutzfeldt-Jakob disease: topography of PrPres immunoreactivity 119
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein. 118
A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease 117
The Rise of the GRN C157KfsX97 Mutation in Southern Italy: Going Back to the Fall of the Western Roman Empire 114
Creutzfeldt-Jakob disease: Carnoy's fixative improves the immunohistochemistry of the proteinase K-resistant prion protein 112
phenotypic heterogeneity in Creutzfeldt-Jakob disease associated with a new prion protein mutation 112
Microglia and complement in the cortex of Creutzfeldt-Jakob disease and comparison with Alzheimer’s disease 111
Insertional mutation in prion protein gene presenting with schizophrenia 109
Hereditary cerebral hemorrhage with amyloidosis associated with E693K mutation of APP 107
Variably Protease-sensitive Prionopathy in an Apparent Cognitively Normal 93-Year-Old 107
Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene 107
Synthetic Aβ peptides acquire prion-like properties in the brain 107
Progressive multifocal leukoencephalopathy presenting with bilateral myoclonus: a case report 107
Characterization of prion disease associated with a two-octapeptide repeat insertion 107
Slowly progressive JC positive multifocal leukoencephalopathy not associated with overt immunodeficency, oncohaematological disorder nor immunosoppressive therapies 106
Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPSc. 106
Experimental Therapy with Quinacrine in Creutzfeldt-Jakob disease 105
Large anterior temporal Virchow–Robin spaces: Evaluating MRI features over the years—Our experience and literature review 105
MRI "fogging" in cerebellar ischaemia: case report 104
Heidenhain Variant of Sporadic Creutzfeldt-Jakob Disease With the Co-Occurrence of Two Different Types of Prion Protein 103
Creutzfeldt-Jakob Disease 103
SPORADIC CEREUTZFELDT-JAKOB DISEASE WITH MM1-TYPE PRION PROTEIN AND PLAQUES 102
Variably Protease-Sensitive Prionopathy: a Novel Disease of the Prion Protein 102
Tauopathies: a new phenotype with epilepsy and severe cerebellar involvement 102
Disordini di movimento nella patologia neurologica dell’anziano 102
Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain 101
Experimental therapy with quinacrine in Creutzfeldt-Jakob diseases 100
Predictive factors of volumetric reduction in lumbar disc herniation treated by O2-O3 chemiodiscolysis 99
Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her son 98
Creutzfeldt-Jakob disease (CJD) associated with V210I PRNP mutation: phenotypic and molecular genetic analysis 98
Creutzfeldt-Jakob disease: Distinct PrPres types induce different microglial reaction patterns 98
Heidenhain variant in two patients with inherited V210I Creutzfeldt-Jakob disease 98
The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease. 97
“Borderline” idiopathic CD4+ T-cell lymphocytopenia presenting with atypical progressive multifocal leukoencephalopathy 96
Sporadic Creutzfeldt-Jakob disease in a native Puerto Rican patient 95
Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutation 94
Tau protein in a novel prion disease with GSS features 94
NOVEL HUMAN PRION DISEASE AFFECTING 3 PRION CODON 129 GENOTYPES: THE SPORADIC FORM OF GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE? 94
Plasma Small Extracellular Vesicle Cathepsin D Dysregulation in GRN/C9orf72 and Sporadic Frontotemporal Lobar Degeneration 93
Singular cases of Alzheimer's disease disclose new and old genetic "acquaintances" 92
Sporadic cCreutzfeldt-Jakob disease: coexistence of type 1 and type 2 PrPSc in the same brain 91
Topografic distribution of PrPres in Creutzfeldt-Jakob disease as revealed by immunohistochemistry 90
Global-local information processing in an unusual patient with posterior cortical atrophy 90
Sporadic Creutzfeldt - Jakob disease’ 89
Plasma Small Extracellular Vesicles with Complement Alterations in GRN/C9orf72 and Sporadic Frontotemporal Lobar Degeneration 89
New-onset refractory status epilepticus mimicking herpes virus encephalitis 88
Early Onset Atypical Dementia Associated with a Novel Seven Octapeptide Repeat Insertion in the Prion Protein Gene 88
Distinct types of PrPres induce different microglial reaction in sporadic Creutzfeldt-Jakob disease 87
Creutzfeldt-Jakob disease with one extra-repeat insertion in PRNP 87
Molecular Bases of Phenotypic Heterogeneity in Prion Diseases 87
Sporadic Creutzfeldt-Jakob disease: coexistence of biochemically distinct types of PrPSc in the same brain 87
Insertional mutation in prion protein gene presenting with schizophrenic-like symptoms 86
tion in the prion protein genme presenting with schizophrenia 85
TOPOGRAPHIC DISTRIBUTION OF PRP-Res IN CREUTZFELDT-JAKOB DISEASE AS REVEALED BY IMMUNOHISTOCHEMISTRY 85
Dramatic neurological debut in a case of Köhlmeier-Degos disease 85
Protease-Sensitive Prionopathy in a Cognitively Normal 93 Year Old 84
Phenotypic Heterogeneity and Type-1/2 PrPSc Co-Occurrence in Creutzfeldt-Jakob Disease Associated With a new Mutation of PRNP 83
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 82
Unusual CLIPPERS presentation and role of MRI examination in the proper diagnostic assessment: A case report. 79
Serum miRNAs as biomarkers in Neurofibromatosis 1: New promising findings. 20
Totale 11.510
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Categoria #
all - tutte 40.869
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 40.869
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022500 0 0 0 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
2026/2027997 41 120 401 435 0 0 0 0 0 0 0 0
Totale 11.510