IRIS
PUOTI, Gianfranco
 Distribuzione geografica
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Continente #
EU - Europa 1.777
NA - Nord America 1.624
AS - Asia 423
SA - Sud America 6
Continente sconosciuto - Info sul continente non disponibili 4
AF - Africa 1
Totale 3.835
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Nazione #
US - Stati Uniti d'America 1.617
IE - Irlanda 643
IT - Italia 279
UA - Ucraina 278
GB - Regno Unito 218
CN - Cina 213
SG - Singapore 143
DE - Germania 133
FI - Finlandia 76
GR - Grecia 58
SE - Svezia 42
TR - Turchia 32
FR - Francia 20
BE - Belgio 14
IN - India 12
CA - Canada 6
KR - Corea 6
BR - Brasile 5
MY - Malesia 5
NL - Olanda 5
EU - Europa 4
BG - Bulgaria 2
CZ - Repubblica Ceca 2
IR - Iran 2
JP - Giappone 2
PL - Polonia 2
VN - Vietnam 2
BD - Bangladesh 1
BO - Bolivia 1
BY - Bielorussia 1
DK - Danimarca 1
ES - Italia 1
HK - Hong Kong 1
HU - Ungheria 1
ID - Indonesia 1
IQ - Iraq 1
JO - Giordania 1
MA - Marocco 1
MX - Messico 1
RU - Federazione Russa 1
TW - Taiwan 1
Totale 3.835
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Città #
Dublin 640
Jacksonville 419
Chandler 196
Santa Clara 99
Princeton 96
Singapore 91
Roxbury 75
Ann Arbor 68
Medford 64
New York 51
Wilmington 40
Beijing 35
Boardman 35
Cambridge 34
Nanjing 34
Jinan 32
Caserta 30
Woodbridge 30
Bremen 26
San Mateo 25
Des Moines 21
Milan 17
Munich 17
Shenyang 15
Brussels 14
Redwood City 13
Siano 12
Hebei 11
Zhengzhou 11
Ashburn 10
Hangzhou 10
Helsinki 9
Los Angeles 8
Napoli 8
Ningbo 8
Taiyuan 8
Lanzhou 7
Rome 7
Boydton 6
Guidonia 6
Houston 6
Mountain View 6
Ranchi 6
Tianjin 6
Auburn Hills 5
Guangzhou 5
Ipoh 5
Norwalk 5
Capua 4
Fairfield 4
Haikou 4
Jiaxing 4
Limbiate 4
Seoul 4
Taizhou 4
Andover 3
Changsha 3
Cleveland 3
Düsseldorf 3
Kansas City 3
Mumbai 3
Nanchang 3
Solofra 3
Capannelle 2
Dong Ket 2
Duncan 2
Falconara Marittima 2
Farmington 2
Greensboro 2
Gunzenhausen 2
Indianapolis 2
Lissone 2
Menlo Park 2
Miramichi 2
Naples 2
Pellezzano 2
San Gennaro Vesuviano 2
San Severino Marche 2
Sant'antimo 2
Seattle 2
Venice 2
Wuhan 2
Alvorada 1
Amsterdam 1
Aragona 1
Atlanta 1
Bozen 1
Brdo 1
Brno 1
Cagliari 1
Calgary 1
Cambrils 1
Catania 1
Changchun 1
Collegeville 1
Copenhagen 1
Dhaka 1
Ferrandina 1
Fes 1
Florence 1
Totale 2.490
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Nome #
A cluster of progranulin C157KfsX97 mutations in Southern Italy: clinical characterization and genetic correlations 84
Creutzfeldt-Jakob disease (CJD) in italian patients with PRNP V210I mutation: an epidemiological and clinical evaluation 80
Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene 71
Creutzfeldt-Jakob disease: topography of PrPres immunoreactivity 66
Delayed post‐hypoxic leukoencephalopathy with a peculiar autoantibody association 65
Atypical Progressive Multifocal Leukoencephalopathy in a Kidney Transplant Recipient With Improving Symptoms After Immunocompetence Recovery 65
Myopathic changes in neurofibromatosis type 1 64
Studio clinico, neuropatologico e bio-molecolare della malattia di Creutzfeldt-Jakob associata a mutazione V210I del gene della proteina prionica 63
Sporadic human prion diseases: molecular insights and diagnosis 61
A comparison of Tau and 14-3-3 protein in the diagnosis of Creitzfeldt-Jakob disease 60
LA NEUROMIELITE OTTICA È UN’ ASSOCIAZIONE SINDROMICA COMUNE A PATOLOGIE ETEROGENEE 58
CORRELATI CLINICO-STRUMENTALI IN UN CASO DI CREUTZFELD- JACOB A LUNGA SOPRAVVIVENZA. 57
Rehabilitation of gesture imitation: a case study with fMRI. 56
Amyloid-beta42 interacts mainly with insoluble prion protein in the Alzheimer brain 53
Creutzfeldt-Jakob Disease 53
A cluster of progranulin C157KfsX97 mutation in southern Italy- clinical characterization and genetic correlations 50
Protease-sensitive prions with 144-bp insertion mutations 49
Dalla malattia di Schilder all’adrenoleucodistrofia; una breve storia di un secolo di ricerca neuropatologica clinica esemplare 49
12-months prospective Pentraxin-3 and metabolomic evaluation in multiple sclerosis patients treated with glatiramer acetate 49
A novel insertional mutation in the prion protein gene: clinical and bio-molecular findings. 47
phenotypic heterogeneity in Creutzfeldt-Jakob disease associated with a new prion protein mutation 47
Experimental therapy with quinacrine in Creutzfeldt-Jakob diseases 47
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) 47
Insertional mutation in prion protein gene presenting with schizophrenia 46
Human prion diseases: Surgical lessons learned from iatrogenic prion transmission 46
A Novel Missense Mutation in CAV3 Gene in an Italian Family With Persistent hyperCKemia, Myalgia and Hypercholesterolemia: Double-trouble 46
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein. 45
Deterioramento Cognitivo Minimo: analisi dei fattori di rischio e del tasso di progressione verso la demenza 45
Hereditary cerebral hemorrhage with amyloidosis associated with E693K mutation of APP 44
A mutation in the 5'-UTR of GRN gene associated with frontotemporal lobar degeneration: phenotypic variability and possible pathogenetic mechanisms 44
Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene 44
Tauopathies: a new phenotype with epilepsy and severe cerebellar involvement 44
Experimental Therapy with Quinacrine in Creutzfeldt-Jakob disease 44
Non-alcoholic acute Wernicke's encephalopathy: Role of MRI in non typical cases. 43
Heidenhain variant of Creutzfeldt-Jakob disease with the co-occurrence of two differents types of prion proteins 42
Coexistence of cavernous hemangioma and other vascular malformations of the orbit. A report of three cases 42
Creutzfeldt-Jakob disease (CJD) associated with V210I PRNP mutation: phenotypic and molecular genetic analysis 42
Is the pathology of posterior cortical atrophy clinically predictable? 41
Creutzfeldt-Jakob disease: Carnoy's fixative improves the immunohistochemistry of the proteinase K-resistant prion protein 41
A novel SLC20A2 gene mutation causing primary familial brain calcification in an Ukrainian patient. 41
A case of Kohlmeier-Degos disease with dramatic neurological involvment 41
Clinical and Genetic Heterogeneity in a Large Family with Pseudoxanthoma Elasticum: MTHFR and SERPINE1 Variants as Possible Disease Modifiers in Developing Ischemic Stroke 41
Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPSc. 40
NOVEL HUMAN PRION DISEASE AFFECTING 3 PRION CODON 129 GENOTYPES: THE SPORADIC FORM OF GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE? 40
Migraine as possible red flag of PFO presence in suspected demyelinating disease 40
Systematic Review on the Role of Lobar Cerebral Microbleeds in Cognition 40
SPORADIC CEREUTZFELDT-JAKOB DISEASE WITH MM1-TYPE PRION PROTEIN AND PLAQUES 39
MRI "fogging" in cerebellar ischaemia: case report 38
Microglia and complement in the cortex of Creutzfeldt-Jakob disease and comparison with Alzheimer’s disease 38
Heidenhain variant in two patients with inherited V210I Creutzfeldt-Jakob disease 38
Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain 37
Sporadic Creutzfeldt - Jakob disease’ 37
Creutzfeldt-Jakob disease: Distinct PrPres types induce different microglial reaction patterns 37
Fas-L expression in sporadic Creutzfeldt-Jakob disease: an immunohistochemistry study 37
Fas-L is expressed in sporadic Creutzfeldt-Jakob Disease 37
Variably Protease-sensitive Prionopathy in an Apparent Cognitively Normal 93-Year-Old 36
Heidenhain Variant of Sporadic Creutzfeldt-Jakob Disease With the Co-Occurrence of Two Different Types of Prion Protein 36
Synthetic Aβ peptides acquire prion-like properties in the brain 36
Variably Protease-Sensitive Prionopathy: a Novel Disease of the Prion Protein 35
Tau protein in a novel prion disease with GSS features 35
Early Onset Atypical Dementia Associated with a Novel Seven Octapeptide Repeat Insertion in the Prion Protein Gene 35
Co-existence of PrP D Types 1 and 2 in Sporadic Creutzfeldt-Jakob Disease of the VV Subgroup: Phenotypic and Prion Protein Characteristics 34
Large anterior temporal Virchow–Robin spaces: Evaluating MRI features over the years—Our experience and literature review 34
Slowly progressive JC positive multifocal leukoencephalopathy not associated with overt immunodeficency, oncohaematological disorder nor immunosoppressive therapies 33
New-onset refractory status epilepticus mimicking herpes virus encephalitis 33
The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease. 33
Disordini di movimento nella patologia neurologica dell’anziano 33
Expanding the spectrum of SPTLC1-related disorders beyond hereditary sensory and autonomic neuropathies: a novel case of the distinct "S331 syndrome" 33
Protease-Sensitive Prionopathy in a Cognitively Normal 93 Year Old 33
The Rise of the GRN C157KfsX97 Mutation in Southern Italy: Going Back to the Fall of the Western Roman Empire 33
Global-local information processing in an unusual patient with posterior cortical atrophy 32
Sporadic Creutzfeldt-Jakob disease in a native Puerto Rican patient 32
Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion 32
Minimally invasive percutaneous treatment for osteoid osteoma of the Spine. A case report 32
Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her son 31
Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutation 31
Sporadic cCreutzfeldt-Jakob disease: coexistence of type 1 and type 2 PrPSc in the same brain 31
Molecular Bases of Phenotypic Heterogeneity in Prion Diseases 31
Creutzfeldt-Jakob disease with one extra-repeat insertion in PRNP 30
Topografic distribution of PrPres in Creutzfeldt-Jakob disease as revealed by immunohistochemistry 30
TOPOGRAPHIC DISTRIBUTION OF PRP-Res IN CREUTZFELDT-JAKOB DISEASE AS REVEALED BY IMMUNOHISTOCHEMISTRY 30
Insertional mutation in prion protein gene presenting with schizophrenic-like symptoms 30
Sporadic Creutzfeldt-Jakob disease: coexistence of biochemically distinct types of PrPSc in the same brain 30
tion in the prion protein genme presenting with schizophrenia 29
Distinct types of PrPres induce different microglial reaction in sporadic Creutzfeldt-Jakob disease 28
Characterization of prion disease associated with a two-octapeptide repeat insertion 28
Phenotypic Heterogeneity and Type-1/2 PrPSc Co-Occurrence in Creutzfeldt-Jakob Disease Associated With a new Mutation of PRNP 27
Dramatic neurological debut in a case of Köhlmeier-Degos disease 27
A peculiar report of rare multifocal "ganglio-glioneurocytoma" 27
“Borderline” idiopathic CD4+ T-cell lymphocytopenia presenting with atypical progressive multifocal leukoencephalopathy 27
A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease 26
Singular cases of Alzheimer's disease disclose new and old genetic "acquaintances" 26
Progressive multifocal leukoencephalopathy presenting with bilateral myoclonus: a case report 25
Unusual CLIPPERS presentation and role of MRI examination in the proper diagnostic assessment: A case report. 23
Plasma Small Extracellular Vesicles with Complement Alterations in GRN/C9orf72 and Sporadic Frontotemporal Lobar Degeneration 22
Predictive factors of volumetric reduction in lumbar disc herniation treated by O2-O3 chemiodiscolysis 20
Alemtuzumab-Related Lymphocyte Subset Dynamics and Disease Activity or Autoimmune Adverse Events: Real-World Evidence 17
Plasma Small Extracellular Vesicle Cathepsin D Dysregulation in GRN/C9orf72 and Sporadic Frontotemporal Lobar Degeneration 14
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 11
Totale 3.952
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Categoria #
all - tutte 18.842
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 18.842
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020308 0 0 0 0 69 3 76 10 54 33 53 10
2020/2021772 65 3 81 61 213 7 84 69 2 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
2024/2025218 5 20 11 54 128 0 0 0 0 0 0 0
Totale 3.952