IRIS Institutional Research Information System - OPENBS Open Archive UniBS

SCOLARI, FRANCESCO
 Distribuzione geografica
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Continente #
NA - Nord America 14.661
EU - Europa 14.051
AS - Asia 2.892
Continente sconosciuto - Info sul continente non disponibili 25
OC - Oceania 23
SA - Sud America 15
AF - Africa 14
Totale 31.681
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Nazione #
US - Stati Uniti d'America 14.608
PL - Polonia 5.793
UA - Ucraina 3.552
CN - Cina 2.472
IT - Italia 1.598
DE - Germania 1.118
FI - Finlandia 720
IE - Irlanda 493
GB - Regno Unito 330
FR - Francia 252
VN - Vietnam 216
TR - Turchia 77
IN - India 75
SE - Svezia 53
CA - Canada 46
BE - Belgio 42
EU - Europa 25
NL - Olanda 25
AU - Australia 23
IR - Iran 19
CH - Svizzera 12
RU - Federazione Russa 11
HK - Hong Kong 8
BR - Brasile 7
JP - Giappone 7
MU - Mauritius 7
RO - Romania 7
LV - Lettonia 6
MK - Macedonia 5
MX - Messico 5
PE - Perù 5
ES - Italia 4
UG - Uganda 4
AM - Armenia 3
BG - Bulgaria 3
CZ - Repubblica Ceca 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
ID - Indonesia 2
MY - Malesia 2
PH - Filippine 2
AR - Argentina 1
AZ - Azerbaigian 1
BO - Bolivia 1
CR - Costa Rica 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 31.681
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Città #
Warsaw 5.782
Jacksonville 2.271
Fairfield 2.016
Woodbridge 1.999
Houston 1.152
Princeton 972
Ann Arbor 928
Cambridge 868
Ashburn 796
Wilmington 770
Nanjing 724
Seattle 722
Dublin 487
Chandler 400
Nanchang 289
Helsinki 287
Beijing 264
Des Moines 226
Dong Ket 216
Hebei 176
Shenyang 176
Changsha 156
Milan 153
Brescia 132
Dearborn 127
San Diego 114
Jiaxing 108
Tianjin 106
Hangzhou 82
Jinan 82
Verona 74
Kocaeli 60
Kunming 56
Phoenix 51
London 46
Lanzhou 41
Rome 40
San Francisco 39
Toronto 39
Brussels 36
Ningbo 36
Norwalk 30
Zhengzhou 29
San Mateo 28
Taizhou 22
Augusta 21
Leawood 21
Washington 19
Serio 18
Haikou 17
Orange 17
Monmouth Junction 16
Torino 16
Ardabil 15
Chiswick 13
Palermo 13
Taiyuan 13
Fuzhou 12
Pavia 12
Catania 11
Changchun 11
Guangzhou 11
Bologna 10
Melbourne 10
Napoli 9
Radomsko 9
Redmond 9
Redwood City 9
Venezia 9
Canberra 8
Hefei 8
Boardman 7
Islington 7
Lancaster 7
New Bedfont 7
Novara 7
Padova 7
Trieste 7
Amsterdam 6
Bari 6
Bergamo 6
Dallas 6
Lugano 6
Menlo Park 6
Mountain View 6
New York 6
Caserta 5
Cazzago San Martino 5
Central 5
Chicago 5
Cremona 5
Florence 5
Hanover 5
Mantova 5
Nocera Inferiore 5
Paris 5
Sydney 5
Tokyo 5
Walnut 5
Bangalore 4
Totale 23.711
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Nome #
Trattamento del linfocele postoperatorio mediante instillazione su guida ecografica di polivinil-pirrolidone iodico. Casistica personale. 734
GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway 239
Genetic drivers of kidney defects in the digeorge syndrome 231
Deciphering Variability of PKD1 and PKD2 in an Italian Cohort of 643 Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD) 221
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. 208
Lack of association between dialysis modality and outcomes in atheroembolic renal disease 196
Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor-dependent idiopathic nephrotic syndrome. 196
The importance of skin biopsy in the diverse clinical manifestations of cholesterol embolism. 194
The pathophysiology of IgA nephropathy 193
Coexistence of Different Circulating Anti-PodocyteAntibodies in Membranous Nephropathy 190
PREDICTORS OF RENAL AND PATIENT OUTCOMES IN ATHEROEMBOLIC RENAL DISEASE: A PROSPECTIVE STUDY. 189
Uromodulin storage diseases: clinical aspects and mechanisms. 189
Insufficienza renale acuta e o subacuta richiedente dialisi in corso di malattia ateroembolica renale: impatto sulla sopravvivenza del paziente e del rene. 189
CHOLESTEROL CRYSTAL EMBOLISM: A RECOGNIZABLE CAUSE OF RENAL DISEASE 188
Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci. 187
Autoimmunity in membranous nephropathy targets aldose reductase and SOD2 187
The Case | Cystic renal disease, nephrogenic diabetes insipidus, and polycytemia. 186
A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13. 186
Genetic studies of IgA nephropathy: past, present, and future. 184
Genome-wide association study identifies susceptibility loci for IgA nephropathy 184
The rediscovery of uromodulin (Tamm-Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease. 183
IgA nephropathy--the case for a genetic basis becomes stronger. 181
Mutations in DSTYK and dominant urinary tract malformations. 181
Familial aggregation of primary glomerulonephritis in an Italian population isolate: Valtrompia study 180
Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds 180
Genetic approaches to human renal agenesis/hypoplasia and dysplasia. 179
Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations. 179
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome. 179
Active focal segmental glomerulosclerosis is associated with massive oxidation of plasma albumin 178
Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33. 178
Defective intracellular trafficking of uromodulin mutant isoforms 177
Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective study 177
Renal outcome in patients with congenital anomalies of the kidney and urinary tract. 177
Liver biopsy discloses a new apolipoprotein A-I hereditary amyloidosis in several unrelated Italian families 176
Atheroembolic renal disease 175
Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritis 175
IgA nephropathy: the presence of familial disease does not confer an increased risk for progression 174
Search for genetic association between IgA nephropathy and candidate genes selected by function or by gene mapping at loci IGAN2 and IGAN3 174
Urinary secretion and extracellular aggregation of mutant uromodulin isoforms 173
Infertility and hypergonadotropic hypogonadism as first evidence of hereditary apolipoprotein A-I amyloidosis 171
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics. 166
The Case ∣ Familial occurrence of retinitis pigmentosa, deafness, and nephropathy. 166
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. 164
Phenotypic expansion of DGKE-associated diseases. 164
Copy number disorders are a Common Cause of Congenital Kidney Malformations 163
Autosomal Dominant tubulointerstitial Kidney Disease with Adult onset due to a novel Renin Mutation Mapping in the Mature protein 162
Cis and trans regulatory elements in NPHS2 promoter: implications in proteinuria and progression of renal diseases 162
Rituximab in Children with Steroid-Dependent Nephrotic Syndrome: A Multicenter, Open-Label, Noninferiority, Randomized Controlled Trial. 161
IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22–23 152
Genomic Mismatch at LIMS1 Locus and Kidney Allograft Rejection. 151
Glomerular Autoimmune Multicomponents of Human Lupus Nephritis In Vivo (2): Planted Antigens. 149
Glomerular autoimmune multicomponents of human lupus nephritis in vivo: α-enolase and annexin AI 143
A model to predict disease progression in patients with autosomal dominant polycystic kidney disease (ADPKD): the ADPKD Outcomes Model 142
LES FORMES FAMILIALES DE NÉPHROPATHIE À IgA ÉTUDES CLINIQUE ET GÉNÉTIQUE 140
Uromodulin: from monogenic to multifactorial diseases. 140
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens 139
Glomerular clusterin is associated with PKC-alpha/beta regulation and good outcome of membranous glomerulonephritis in humans 135
Berger's Disease 135
ORO-FACIO-DIGITAL SYNDROME 135
AUTOSOMAL DOMINANT MEDULLARY CYSTIC KIDNEY DISEASE 134
Repetitive fragmentation products of albumin and alpha1-antitrypsin in glomerular diseases associated with nephrotic syndrome. 130
The progression from obesity to type 2 diabetes in Alström syndrome. 130
The copy number variation landscape of congenital anomalies of the kidney and urinary tract. 118
Non-collagen genes role in digenic Alport syndrome 116
Correction to: Tocilizumab for patients with COVID-19 pneumonia. The single-arm TOCIVID-19 prospective trial 116
IDENTIFICATION OF A NEW LOCUS FOR MEDULLARY CYSTIC DISEASE ON CHROMOSOME 16 113
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. 109
A prospective randomized trial on azathioprine addition to cyclosporine versus cyclosporine monotherapy at steroid withdrawal, 6 months after renal transplantation. 108
Myroides odoratimimus urinary tract infection in an immunocompromised patient: An emerging multidrug-resistant micro-organism 104
Tubulointerstitial nephritis is a dominant feature of hereditary apolipoprotein A-I amyloidosis. 103
A large TSC2 and PKD1 gene deletion is associated with renal and extrarenal signs of autosomal dominant polycystic kidney disease 102
Searching for IgA nephropathy candidate genes: genetic studies combined with high throughput innovative investigations 100
A high calcium-phosphate product is associated with high C-reactive protein concentrations in hemodialysis patients. 99
Predictors of renal and patient outcomes in atheroembolic renal disease: a prospective study. 99
Liver disease in renal transplant patients treated with azathioprine or ciclosporin. 98
Viral hepatitis in HBsAg-positive renal transplant patients treated with cyclosporin and steroids. 98
Familial IgM mesangial nephropathy: a morphologic and immunogenetic study of three pedigrees. 96
Oral-Facial-Digital Syndrome Type I: an unusual cause of hereditary cystic kidney disease. 95
Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin. 95
Clustering familiare di differenti forme di glomerulonefrite primitiva: studio Valtrompia: 95
Correction of metabolic acidosis increases serum albumin concentrations and decreases kinetically evaluated protein intake in haemodialysis patients: a prospective study. 94
Immunogenetics of Henoch-Schoenlein disease. 93
Von Hippel-Lindau syndrome presenting as pancreatic cysts 93
The challenge of diagnosing atheroembolic renal disease: clinical features and prognostic factors 92
Antiphospholipid syndrome and glomerular thrombosis in the absence of overt lupus nephritis 92
Direct characterization of target podocyte antigens and auto-antibodies in human membranous glomerulonephritis: Alfa-enolase and borderline antigens. 91
Early histopathologic changes predicting long-term kidney transplant survival. 90
Familial occurrence of primary glomerulonephritis: evidence for a role of genetic factors. 90
ACE inhibition is renoprotective among obese patients with proteinuria. 90
La sindrome oro-facio-digitale tipo 1: una causa infrequente di malattia cistica renale a carattere ereditario. 90
La Sindrome Oro-Digito-Facciale di tipo I (OFD-I): una causa infrequente di malattia cistica renale a carattere ereditario. 89
Viral infection in kidney-transplanted patients. 89
Short-term effects of rituximab in children with steroid- and calcineurin-dependent nephrotic syndrome: a randomized controlled trial. 88
Spermatogenic and steroidogenic impairment of the testicle characterizes the hereditary leucine-75-proline apolipoprotein a-I amyloidosis. 87
Major COL4A5 gene rearrangements in patients with juvenile type Alport syndrome. 87
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations 87
Atheroembolic renal disease. 87
Two different types of renal involvement in tuberous sclerosis complex. 86
Predictors of renal and patient outcomes in atheroembolic renal disease: a prospective study 86
Sarcoma di Kaposi (SK) in corso di trapianto renale. Esperienza clinica in 7 casi. 86
Totale 14.932
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Categoria #
all - tutte 109.819
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 109.819
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20192.910 0 0 0 0 0 233 273 564 208 451 621 560
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
2022/20231.999 519 20 32 102 118 645 10 151 196 21 97 88
2023/2024689 107 52 164 250 93 23 0 0 0 0 0 0
Totale 32.223