SCOLARI, FRANCESCO
 Distribuzione geografica
Continente #
NA - Nord America 15.561
EU - Europa 14.926
AS - Asia 6.613
Continente sconosciuto - Info sul continente non disponibili 25
OC - Oceania 23
SA - Sud America 22
AF - Africa 19
Totale 37.189
Nazione #
US - Stati Uniti d'America 15.495
PL - Polonia 5.796
UA - Ucraina 3.552
CN - Cina 2.558
IT - Italia 1.944
HK - Hong Kong 1.854
SG - Singapore 1.270
DE - Germania 1.158
FI - Finlandia 762
TR - Turchia 504
IE - Irlanda 492
RU - Federazione Russa 428
GB - Regno Unito 319
FR - Francia 254
VN - Vietnam 217
IN - India 78
ID - Indonesia 67
CA - Canada 58
SE - Svezia 54
NL - Olanda 43
CZ - Repubblica Ceca 28
EU - Europa 25
AU - Australia 23
BE - Belgio 21
IR - Iran 19
CH - Svizzera 14
JP - Giappone 14
BR - Brasile 9
AT - Austria 7
ES - Italia 7
LV - Lettonia 7
MU - Mauritius 7
RO - Romania 7
PE - Perù 6
MK - Macedonia 5
MX - Messico 5
PK - Pakistan 5
MA - Marocco 4
UG - Uganda 4
AL - Albania 3
AM - Armenia 3
AZ - Azerbaigian 3
BG - Bulgaria 3
GR - Grecia 3
HR - Croazia 3
HU - Ungheria 3
LU - Lussemburgo 3
PH - Filippine 3
PT - Portogallo 3
RS - Serbia 3
SA - Arabia Saudita 3
SK - Slovacchia (Repubblica Slovacca) 3
AR - Argentina 2
BO - Bolivia 2
CI - Costa d'Avorio 2
KG - Kirghizistan 2
KR - Corea 2
LA - Repubblica Popolare Democratica del Laos 2
MY - Malesia 2
PA - Panama 2
CL - Cile 1
CR - Costa Rica 1
EC - Ecuador 1
GH - Ghana 1
IL - Israele 1
JO - Giordania 1
KZ - Kazakistan 1
LK - Sri Lanka 1
LT - Lituania 1
SD - Sudan 1
TH - Thailandia 1
TW - Taiwan 1
UZ - Uzbekistan 1
VE - Venezuela 1
Totale 37.189
Città #
Warsaw 5.782
Jacksonville 2.271
Fairfield 2.016
Woodbridge 1.999
Hong Kong 1.846
Houston 1.152
Singapore 1.000
Princeton 972
Ann Arbor 928
Ashburn 870
Cambridge 868
Wilmington 770
Seattle 732
Nanjing 724
Dublin 486
Istanbul 427
Chandler 400
Helsinki 320
Nanchang 289
Beijing 266
Des Moines 226
Dong Ket 216
Milan 213
Moscow 196
New York 188
Hebei 176
Shenyang 176
Changsha 156
Brescia 139
Dearborn 127
San Diego 114
Jiaxing 108
Tianjin 106
Hangzhou 82
Jinan 82
Verona 78
Shanghai 69
Rome 68
Jakarta 65
Kocaeli 60
Kunming 56
Phoenix 51
Toronto 45
Lanzhou 41
San Francisco 39
Ningbo 36
London 35
Norwalk 30
Zhengzhou 30
San Mateo 28
Los Angeles 26
Brno 25
Palermo 22
Taizhou 22
Augusta 21
Leawood 21
Munich 20
Washington 19
Bologna 18
Serio 18
Haikou 17
Orange 17
Kilburn 16
Monmouth Junction 16
Torino 16
Ardabil 15
Brussels 15
Taiyuan 13
Florence 12
Fuzhou 12
Pavia 12
Boardman 11
Catania 11
Changchun 11
Guangzhou 11
Chiswick 10
Melbourne 10
Naples 10
Frankfurt am Main 9
Lappeenranta 9
Napoli 9
Padova 9
Radomsko 9
Redmond 9
Redwood City 9
Tokyo 9
Trieste 9
Venezia 9
Canberra 8
Cremona 8
Hefei 8
Amsterdam 7
Bari 7
Lancaster 7
Novara 7
Santa Clara 7
Turin 7
Bergamo 6
Cinisello Balsamo 6
Dallas 6
Totale 27.775
Nome #
Trattamento del linfocele postoperatorio mediante instillazione su guida ecografica di polivinil-pirrolidone iodico. Casistica personale. 808
Genetic drivers of kidney defects in the digeorge syndrome 247
GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway 246
Correction to: Tocilizumab for patients with COVID-19 pneumonia. The single-arm TOCIVID-19 prospective trial 241
Deciphering Variability of PKD1 and PKD2 in an Italian Cohort of 643 Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD) 233
Insufficienza renale acuta e o subacuta richiedente dialisi in corso di malattia ateroembolica renale: impatto sulla sopravvivenza del paziente e del rene. 224
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. 219
Lack of association between dialysis modality and outcomes in atheroembolic renal disease 209
Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor-dependent idiopathic nephrotic syndrome. 204
Genome-wide association study identifies susceptibility loci for IgA nephropathy 203
The pathophysiology of IgA nephropathy 203
The importance of skin biopsy in the diverse clinical manifestations of cholesterol embolism. 202
PREDICTORS OF RENAL AND PATIENT OUTCOMES IN ATHEROEMBOLIC RENAL DISEASE: A PROSPECTIVE STUDY. 201
Coexistence of Different Circulating Anti-PodocyteAntibodies in Membranous Nephropathy 200
A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13. 200
Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci. 199
Uromodulin storage diseases: clinical aspects and mechanisms. 198
CHOLESTEROL CRYSTAL EMBOLISM: A RECOGNIZABLE CAUSE OF RENAL DISEASE 197
Autoimmunity in membranous nephropathy targets aldose reductase and SOD2 195
IgA nephropathy--the case for a genetic basis becomes stronger. 193
The rediscovery of uromodulin (Tamm-Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease. 193
The Case | Cystic renal disease, nephrogenic diabetes insipidus, and polycytemia. 193
Genetic studies of IgA nephropathy: past, present, and future. 192
Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective study 191
Genetic approaches to human renal agenesis/hypoplasia and dysplasia. 190
Active focal segmental glomerulosclerosis is associated with massive oxidation of plasma albumin 190
Familial aggregation of primary glomerulonephritis in an Italian population isolate: Valtrompia study 190
Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations. 190
Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds 190
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome. 190
Mutations in DSTYK and dominant urinary tract malformations. 189
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. 188
Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33. 187
Defective intracellular trafficking of uromodulin mutant isoforms 187
IgA nephropathy: the presence of familial disease does not confer an increased risk for progression 185
Atheroembolic renal disease 185
Renal outcome in patients with congenital anomalies of the kidney and urinary tract. 184
Liver biopsy discloses a new apolipoprotein A-I hereditary amyloidosis in several unrelated Italian families 184
Search for genetic association between IgA nephropathy and candidate genes selected by function or by gene mapping at loci IGAN2 and IGAN3 184
Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritis 182
Urinary secretion and extracellular aggregation of mutant uromodulin isoforms 182
Infertility and hypergonadotropic hypogonadism as first evidence of hereditary apolipoprotein A-I amyloidosis 180
Autosomal Dominant tubulointerstitial Kidney Disease with Adult onset due to a novel Renin Mutation Mapping in the Mature protein 179
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics. 177
The Case ∣ Familial occurrence of retinitis pigmentosa, deafness, and nephropathy. 175
Phenotypic expansion of DGKE-associated diseases. 174
Copy number disorders are a Common Cause of Congenital Kidney Malformations 173
Rituximab in Children with Steroid-Dependent Nephrotic Syndrome: A Multicenter, Open-Label, Noninferiority, Randomized Controlled Trial. 172
Cis and trans regulatory elements in NPHS2 promoter: implications in proteinuria and progression of renal diseases 172
Genomic Mismatch at LIMS1 Locus and Kidney Allograft Rejection. 164
IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22–23 163
Glomerular autoimmune multicomponents of human lupus nephritis in vivo: α-enolase and annexin AI 161
Glomerular Autoimmune Multicomponents of Human Lupus Nephritis In Vivo (2): Planted Antigens. 159
A model to predict disease progression in patients with autosomal dominant polycystic kidney disease (ADPKD): the ADPKD Outcomes Model 157
LES FORMES FAMILIALES DE NÉPHROPATHIE À IgA ÉTUDES CLINIQUE ET GÉNÉTIQUE 150
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens 150
Uromodulin: from monogenic to multifactorial diseases. 147
Berger's Disease 145
Glomerular clusterin is associated with PKC-alpha/beta regulation and good outcome of membranous glomerulonephritis in humans 144
ORO-FACIO-DIGITAL SYNDROME 144
AUTOSOMAL DOMINANT MEDULLARY CYSTIC KIDNEY DISEASE 144
Repetitive fragmentation products of albumin and alpha1-antitrypsin in glomerular diseases associated with nephrotic syndrome. 140
The progression from obesity to type 2 diabetes in Alström syndrome. 139
A prospective randomized trial on azathioprine addition to cyclosporine versus cyclosporine monotherapy at steroid withdrawal, 6 months after renal transplantation. 128
The copy number variation landscape of congenital anomalies of the kidney and urinary tract. 126
IDENTIFICATION OF A NEW LOCUS FOR MEDULLARY CYSTIC DISEASE ON CHROMOSOME 16 125
Non-collagen genes role in digenic Alport syndrome 125
Myroides odoratimimus urinary tract infection in an immunocompromised patient: An emerging multidrug-resistant micro-organism 119
A high calcium-phosphate product is associated with high C-reactive protein concentrations in hemodialysis patients. 117
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. 117
Tubulointerstitial nephritis is a dominant feature of hereditary apolipoprotein A-I amyloidosis. 116
A large TSC2 and PKD1 gene deletion is associated with renal and extrarenal signs of autosomal dominant polycystic kidney disease 115
La sindrome oro-facio-digitale tipo 1: una causa infrequente di malattia cistica renale a carattere ereditario. 111
Viral hepatitis in HBsAg-positive renal transplant patients treated with cyclosporin and steroids. 110
Searching for IgA nephropathy candidate genes: genetic studies combined with high throughput innovative investigations 107
Familial IgM mesangial nephropathy: a morphologic and immunogenetic study of three pedigrees. 107
Predictors of renal and patient outcomes in atheroembolic renal disease: a prospective study. 107
Clustering familiare di differenti forme di glomerulonefrite primitiva: studio Valtrompia: 107
The challenge of diagnosing atheroembolic renal disease: clinical features and prognostic factors 106
Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin. 105
Liver disease in renal transplant patients treated with azathioprine or ciclosporin. 105
Antiphospholipid syndrome and glomerular thrombosis in the absence of overt lupus nephritis 102
Familial occurrence of primary glomerulonephritis: evidence for a role of genetic factors. 102
Correction of metabolic acidosis increases serum albumin concentrations and decreases kinetically evaluated protein intake in haemodialysis patients: a prospective study. 101
Immunogenetics of Henoch-Schoenlein disease. 101
Early histopathologic changes predicting long-term kidney transplant survival. 100
La Sindrome Oro-Digito-Facciale di tipo I (OFD-I): una causa infrequente di malattia cistica renale a carattere ereditario. 100
Direct characterization of target podocyte antigens and auto-antibodies in human membranous glomerulonephritis: Alfa-enolase and borderline antigens. 100
Von Hippel-Lindau syndrome presenting as pancreatic cysts 100
Oral-Facial-Digital Syndrome Type I: an unusual cause of hereditary cystic kidney disease. 99
Short-term effects of rituximab in children with steroid- and calcineurin-dependent nephrotic syndrome: a randomized controlled trial. 99
ACE inhibition is renoprotective among obese patients with proteinuria. 99
Atheroembolic renal disease. 99
Spermatogenic and steroidogenic impairment of the testicle characterizes the hereditary leucine-75-proline apolipoprotein a-I amyloidosis. 98
A long term, randomized clinical trial to evaluate the effects of ramipril on the evolution of renal function in chronic nephropathies. 98
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations 98
Viral infection in kidney-transplanted patients. 97
Are HLA class II and immunoglobulin constant region genes involved in the pathogenesis of mixed cryoglobulinemia type II after hepatitis C virus infection? 96
Major COL4A5 gene rearrangements in patients with juvenile type Alport syndrome. 96
Oral-facial-digital syndrome type I: an unusual cause of hereditary cystic kidney disease 96
Totale 16.211
Categoria #
all - tutte 175.923
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 175.923


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20204.536 0 0 0 0 0 0 708 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
2023/20242.792 104 49 154 244 77 274 122 80 1.025 45 63 555
2024/20253.444 48 46 53 839 969 577 912 0 0 0 0 0
Totale 37.739