SCOLARI, FRANCESCO
 Distribuzione geografica
Continente #
NA - Nord America 14.957
EU - Europa 14.167
AS - Asia 4.018
Continente sconosciuto - Info sul continente non disponibili 25
OC - Oceania 23
SA - Sud America 18
AF - Africa 16
Totale 33.224
Nazione #
US - Stati Uniti d'America 14.899
PL - Polonia 5.795
UA - Ucraina 3.552
CN - Cina 2.533
IT - Italia 1.721
DE - Germania 1.129
HK - Hong Kong 993
FI - Finlandia 729
IE - Irlanda 492
GB - Regno Unito 318
FR - Francia 253
VN - Vietnam 216
IN - India 78
TR - Turchia 77
SG - Singapore 70
SE - Svezia 53
CA - Canada 51
NL - Olanda 26
EU - Europa 25
AU - Australia 23
BE - Belgio 21
IR - Iran 19
RU - Federazione Russa 13
CH - Svizzera 12
JP - Giappone 12
BR - Brasile 7
MU - Mauritius 7
RO - Romania 7
ES - Italia 6
LV - Lettonia 6
PE - Perù 6
MK - Macedonia 5
MX - Messico 5
UG - Uganda 4
AM - Armenia 3
BG - Bulgaria 3
GR - Grecia 3
HR - Croazia 3
HU - Ungheria 3
PT - Portogallo 3
RS - Serbia 3
SA - Arabia Saudita 3
SK - Slovacchia (Repubblica Slovacca) 3
AL - Albania 2
AT - Austria 2
CI - Costa d'Avorio 2
CZ - Repubblica Ceca 2
ID - Indonesia 2
KR - Corea 2
MY - Malesia 2
PH - Filippine 2
AR - Argentina 1
AZ - Azerbaigian 1
BO - Bolivia 1
CL - Cile 1
CR - Costa Rica 1
EC - Ecuador 1
GH - Ghana 1
IL - Israele 1
JO - Giordania 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
LT - Lituania 1
LU - Lussemburgo 1
MA - Marocco 1
PA - Panama 1
SD - Sudan 1
TH - Thailandia 1
VE - Venezuela 1
Totale 33.224
Città #
Warsaw 5.782
Jacksonville 2.271
Fairfield 2.016
Woodbridge 1.999
Houston 1.152
Hong Kong 985
Princeton 972
Ann Arbor 928
Cambridge 868
Ashburn 852
Wilmington 770
Seattle 731
Nanjing 724
Dublin 486
Chandler 400
Nanchang 289
Helsinki 288
Beijing 266
Des Moines 226
Dong Ket 216
New York 187
Hebei 176
Milan 176
Shenyang 176
Changsha 156
Brescia 135
Dearborn 127
San Diego 114
Jiaxing 108
Tianjin 106
Hangzhou 82
Jinan 82
Verona 74
Kocaeli 60
Kunming 56
Shanghai 55
Phoenix 51
Rome 47
Lanzhou 41
Toronto 41
San Francisco 39
Ningbo 36
London 35
Norwalk 30
Zhengzhou 30
San Mateo 28
Taizhou 22
Augusta 21
Leawood 21
Washington 19
Los Angeles 18
Palermo 18
Serio 18
Haikou 17
Orange 17
Bologna 16
Kilburn 16
Monmouth Junction 16
Torino 16
Ardabil 15
Brussels 15
Taiyuan 13
Fuzhou 12
Pavia 12
Catania 11
Changchun 11
Guangzhou 11
Boardman 10
Chiswick 10
Melbourne 10
Frankfurt am Main 9
Lappeenranta 9
Napoli 9
Padova 9
Radomsko 9
Redmond 9
Redwood City 9
Tokyo 9
Venezia 9
Canberra 8
Cremona 8
Hefei 8
Amsterdam 7
Florence 7
Lancaster 7
Novara 7
Trieste 7
Turin 7
Bari 6
Bergamo 6
Dallas 6
Lugano 6
Menlo Park 6
Mountain View 6
Naples 6
Caserta 5
Cazzago San Martino 5
Central 5
Islington 5
Lima 5
Totale 25.048
Nome #
Trattamento del linfocele postoperatorio mediante instillazione su guida ecografica di polivinil-pirrolidone iodico. Casistica personale. 754
GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway 242
Genetic drivers of kidney defects in the digeorge syndrome 240
Deciphering Variability of PKD1 and PKD2 in an Italian Cohort of 643 Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD) 225
Suprarenal aortic cross-clamping in the elective surgery of abdominal aortic aneurysms. Lessons from 68 cases out of consecutive survey of 746 abdominal aortic substitutions. 210
Insufficienza renale acuta e o subacuta richiedente dialisi in corso di malattia ateroembolica renale: impatto sulla sopravvivenza del paziente e del rene. 206
Lack of association between dialysis modality and outcomes in atheroembolic renal disease 200
Genome-wide association study identifies susceptibility loci for IgA nephropathy 197
Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor-dependent idiopathic nephrotic syndrome. 196
The pathophysiology of IgA nephropathy 195
The importance of skin biopsy in the diverse clinical manifestations of cholesterol embolism. 194
PREDICTORS OF RENAL AND PATIENT OUTCOMES IN ATHEROEMBOLIC RENAL DISEASE: A PROSPECTIVE STUDY. 193
Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci. 192
Uromodulin storage diseases: clinical aspects and mechanisms. 192
Coexistence of Different Circulating Anti-PodocyteAntibodies in Membranous Nephropathy 192
CHOLESTEROL CRYSTAL EMBOLISM: A RECOGNIZABLE CAUSE OF RENAL DISEASE 191
Autoimmunity in membranous nephropathy targets aldose reductase and SOD2 189
A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13. 188
The rediscovery of uromodulin (Tamm-Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease. 187
The Case | Cystic renal disease, nephrogenic diabetes insipidus, and polycytemia. 185
Active focal segmental glomerulosclerosis is associated with massive oxidation of plasma albumin 183
Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective study 183
Genetic studies of IgA nephropathy: past, present, and future. 183
IgA nephropathy--the case for a genetic basis becomes stronger. 183
Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations. 183
Mutations in DSTYK and dominant urinary tract malformations. 183
Familial aggregation of primary glomerulonephritis in an Italian population isolate: Valtrompia study 182
Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds 182
Genetic approaches to human renal agenesis/hypoplasia and dysplasia. 181
Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33. 181
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome. 181
Defective intracellular trafficking of uromodulin mutant isoforms 179
Renal outcome in patients with congenital anomalies of the kidney and urinary tract. 179
IgA nephropathy: the presence of familial disease does not confer an increased risk for progression 178
Liver biopsy discloses a new apolipoprotein A-I hereditary amyloidosis in several unrelated Italian families 178
Atheroembolic renal disease 177
Search for genetic association between IgA nephropathy and candidate genes selected by function or by gene mapping at loci IGAN2 and IGAN3 176
Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritis 175
Urinary secretion and extracellular aggregation of mutant uromodulin isoforms 175
Infertility and hypergonadotropic hypogonadism as first evidence of hereditary apolipoprotein A-I amyloidosis 173
Malattia cistica della midollare (MCKD), Nefropatia iperuricemica familiare giovanile (FJHN) e Glomerulocisti (GCKD) sono causate da mutazioni dello stesso gene (UMOD) che determinano alterazioni del trasporto cellulare di uromodulina. 170
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics. 169
The Case ∣ Familial occurrence of retinitis pigmentosa, deafness, and nephropathy. 167
Autosomal Dominant tubulointerstitial Kidney Disease with Adult onset due to a novel Renin Mutation Mapping in the Mature protein 167
Phenotypic expansion of DGKE-associated diseases. 166
Correction to: Tocilizumab for patients with COVID-19 pneumonia. The single-arm TOCIVID-19 prospective trial 166
Copy number disorders are a Common Cause of Congenital Kidney Malformations 165
Rituximab in Children with Steroid-Dependent Nephrotic Syndrome: A Multicenter, Open-Label, Noninferiority, Randomized Controlled Trial. 165
Cis and trans regulatory elements in NPHS2 promoter: implications in proteinuria and progression of renal diseases 165
Genomic Mismatch at LIMS1 Locus and Kidney Allograft Rejection. 157
IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22–23 156
A model to predict disease progression in patients with autosomal dominant polycystic kidney disease (ADPKD): the ADPKD Outcomes Model 151
Glomerular Autoimmune Multicomponents of Human Lupus Nephritis In Vivo (2): Planted Antigens. 151
Glomerular autoimmune multicomponents of human lupus nephritis in vivo: α-enolase and annexin AI 149
LES FORMES FAMILIALES DE NÉPHROPATHIE À IgA ÉTUDES CLINIQUE ET GÉNÉTIQUE 143
Uromodulin: from monogenic to multifactorial diseases. 142
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens 141
Glomerular clusterin is associated with PKC-alpha/beta regulation and good outcome of membranous glomerulonephritis in humans 137
Berger's Disease 137
ORO-FACIO-DIGITAL SYNDROME 137
AUTOSOMAL DOMINANT MEDULLARY CYSTIC KIDNEY DISEASE 136
The progression from obesity to type 2 diabetes in Alström syndrome. 133
Repetitive fragmentation products of albumin and alpha1-antitrypsin in glomerular diseases associated with nephrotic syndrome. 132
The copy number variation landscape of congenital anomalies of the kidney and urinary tract. 122
Non-collagen genes role in digenic Alport syndrome 119
A prospective randomized trial on azathioprine addition to cyclosporine versus cyclosporine monotherapy at steroid withdrawal, 6 months after renal transplantation. 117
IDENTIFICATION OF A NEW LOCUS FOR MEDULLARY CYSTIC DISEASE ON CHROMOSOME 16 114
Low cerebrovascular event rate in subjects with patent foramen ovale and different clinical presentations: results from a prospective non randomized study on a population including patients with and without patent foramen ovale closure. 111
Myroides odoratimimus urinary tract infection in an immunocompromised patient: An emerging multidrug-resistant micro-organism 110
Tubulointerstitial nephritis is a dominant feature of hereditary apolipoprotein A-I amyloidosis. 109
A high calcium-phosphate product is associated with high C-reactive protein concentrations in hemodialysis patients. 108
A large TSC2 and PKD1 gene deletion is associated with renal and extrarenal signs of autosomal dominant polycystic kidney disease 107
Predictors of renal and patient outcomes in atheroembolic renal disease: a prospective study. 101
Searching for IgA nephropathy candidate genes: genetic studies combined with high throughput innovative investigations 100
Viral hepatitis in HBsAg-positive renal transplant patients treated with cyclosporin and steroids. 100
Liver disease in renal transplant patients treated with azathioprine or ciclosporin. 99
La sindrome oro-facio-digitale tipo 1: una causa infrequente di malattia cistica renale a carattere ereditario. 99
Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin. 98
Familial IgM mesangial nephropathy: a morphologic and immunogenetic study of three pedigrees. 98
Clustering familiare di differenti forme di glomerulonefrite primitiva: studio Valtrompia: 98
Direct characterization of target podocyte antigens and auto-antibodies in human membranous glomerulonephritis: Alfa-enolase and borderline antigens. 95
Immunogenetics of Henoch-Schoenlein disease. 95
Early histopathologic changes predicting long-term kidney transplant survival. 94
The challenge of diagnosing atheroembolic renal disease: clinical features and prognostic factors 94
Antiphospholipid syndrome and glomerular thrombosis in the absence of overt lupus nephritis 94
Von Hippel-Lindau syndrome presenting as pancreatic cysts 94
Familial occurrence of primary glomerulonephritis: evidence for a role of genetic factors. 94
Oral-Facial-Digital Syndrome Type I: an unusual cause of hereditary cystic kidney disease. 93
Correction of metabolic acidosis increases serum albumin concentrations and decreases kinetically evaluated protein intake in haemodialysis patients: a prospective study. 93
Spermatogenic and steroidogenic impairment of the testicle characterizes the hereditary leucine-75-proline apolipoprotein a-I amyloidosis. 93
La Sindrome Oro-Digito-Facciale di tipo I (OFD-I): una causa infrequente di malattia cistica renale a carattere ereditario. 92
Viral infection in kidney-transplanted patients. 92
ACE inhibition is renoprotective among obese patients with proteinuria. 92
Short-term effects of rituximab in children with steroid- and calcineurin-dependent nephrotic syndrome: a randomized controlled trial. 91
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations 91
Atheroembolic renal disease. 90
A long term, randomized clinical trial to evaluate the effects of ramipril on the evolution of renal function in chronic nephropathies. 89
Two different types of renal involvement in tuberous sclerosis complex. 88
Are HLA class II and immunoglobulin constant region genes involved in the pathogenesis of mixed cryoglobulinemia type II after hepatitis C virus infection? 88
Major COL4A5 gene rearrangements in patients with juvenile type Alport syndrome. 88
Totale 15.315
Categoria #
all - tutte 138.541
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 138.541


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019560 0 0 0 0 0 0 0 0 0 0 0 560
2019/20209.715 1.613 430 433 1.039 568 1.096 708 1.057 623 1.043 423 682
2020/20217.415 193 738 243 954 251 1.086 292 967 1.003 680 677 331
2021/20223.102 136 746 27 101 55 95 171 202 173 340 284 772
2022/20231.968 519 20 32 102 118 645 6 146 193 17 89 81
2023/20242.267 104 49 154 244 77 274 122 80 1.025 45 63 30
Totale 33.770