ANGLANI, FRANCA
 Distribuzione geografica
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Continente #
NA - Nord America 13.475
EU - Europa 3.339
AS - Asia 2.145
Continente sconosciuto - Info sul continente non disponibili 14
OC - Oceania 13
AF - Africa 6
SA - Sud America 6
Totale 18.998
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Nazione #
US - Stati Uniti d'America 13.452
CN - Cina 1.517
IT - Italia 1.155
FI - Finlandia 659
SE - Svezia 651
SG - Singapore 425
DE - Germania 325
UA - Ucraina 268
VN - Vietnam 150
GB - Regno Unito 92
IE - Irlanda 54
FR - Francia 28
IN - India 25
CA - Canada 20
NL - Olanda 19
RU - Federazione Russa 15
EU - Europa 13
RO - Romania 12
AU - Australia 9
ES - Italia 9
BE - Belgio 8
MT - Malta 8
PK - Pakistan 6
BR - Brasile 5
CZ - Repubblica Ceca 5
SA - Arabia Saudita 5
TR - Turchia 5
GR - Grecia 4
JP - Giappone 4
LT - Lituania 4
NZ - Nuova Zelanda 4
AL - Albania 3
AT - Austria 3
BG - Bulgaria 3
CH - Svizzera 2
CR - Costa Rica 2
EE - Estonia 2
EG - Egitto 2
HU - Ungheria 2
LU - Lussemburgo 2
NG - Nigeria 2
PL - Polonia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
CI - Costa d'Avorio 1
CL - Cile 1
HR - Croazia 1
IL - Israele 1
IM - Isola di Man 1
IQ - Iraq 1
IR - Iran 1
KH - Cambogia 1
LK - Sri Lanka 1
MK - Macedonia 1
PA - Panama 1
PH - Filippine 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
TW - Taiwan 1
Totale 18.998
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Città #
Chandler 1.661
Fairfield 1.620
Ann Arbor 1.052
Woodbridge 928
Wilmington 874
Houston 837
Jacksonville 811
Ashburn 700
Cambridge 599
Seattle 533
Princeton 509
Medford 394
Beijing 360
Des Moines 341
Nanjing 315
Roxbury 296
Singapore 252
Helsinki 244
San Diego 179
Dong Ket 150
Boardman 147
Guangzhou 138
Padova 131
Hebei 103
Shenyang 103
Nanchang 92
Jiaxing 67
Milan 58
Changsha 55
Norwalk 54
Dublin 48
Rome 46
Tianjin 39
Redwood City 35
Jinan 31
New York 28
Kharkiv 21
Falls Church 20
Borås 19
Parma 19
Ogden 18
London 17
Bologna 16
Ningbo 16
Hefei 14
Redmond 14
Hangzhou 11
Lanzhou 11
Zhengzhou 11
Florence 10
Haikou 10
Kunming 10
Napoli 10
Pune 10
Torino 10
Trieste 10
Washington 10
Dearborn 9
Genoa 9
Palermo 9
Taiyuan 9
Cagliari 8
Costa Mesa 8
Frankfurt am Main 8
Los Angeles 8
Genova 7
Hounslow 7
Indiana 7
Pescara 7
Verona 7
Bari 6
Edinburgh 6
Fuzhou 6
Nürnberg 6
Rockville 6
Timisoara 6
Treviso 6
Falkenstein 5
Senigallia 5
Stra 5
Taizhou 5
Arcevia 4
Baronissi 4
Brescia 4
Brussels 4
Chicago 4
Ciudad Real 4
Easton 4
Grand Rapids 4
Lancenigo 4
Legnano 4
Livorno 4
Melbourne 4
Modena 4
Paris 4
Perugia 4
Phoenix 4
Prato 4
Rovigo 4
San Giuliano Terme 4
Totale 14.358
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Nome #
Cistite incrostata alcalina da Corynebacterium Urealyticum: un caso clinico. 383
Clonaggio, subclonaggio, transfezione, sequenziamento. 245
Inversione pericentrica del cromosoma 17 originante nell'uomo un cromosoma simile a quello del Pan Troglodytes 142
A new disease-causing mutation in the GAP-related domain of the NF1 gene 140
QueryOR: a comprehensive web platform for genetic variant analysis and prioritization 134
The Regenerative Potential of the Kidney: What Can We Learn from Developmental Biology? 128
Glomerular Pathology in Dent Disease and Its Association with Kidney Function 127
Early activation of fibrogenesis in transplanted kidneys: a study on serial renalbiopsies 127
Human proximal tubular cells can form calcium phosphate deposits in osteogenic culture: role of cell death and osteoblast-like transdifferentiation 121
Involvement of the Tubular ClC-Type Exchanger ClC-5 in Glomeruli of human Proteinuric Nephropathies 112
Early activation of fibrogenesis in transplanted kidneys: A study on serial renal biopsies 110
Acquisizione del fenotipo miofibroblastico e transizione epItelio mesenchima in colture primarie di cellule renali umane. 109
Caspase-independent programmed cell death triggers Ca2PO4 deposition in an in vitro model of nephrocalcinosis 109
Identification of GDNF Gene Sequence Variations in Patients with Medullary Sponge Kidney Disease 109
Replication patterns of human X isochromosomes by high-resolution banding 108
Variabilità fenotipica inter ed intrafamiliare nella malattia di Dent di tipo 1. 106
Cell death in ectopic calcification of the kidney 106
Characterization of 28 novel patients expands the mutational and phenotypic spectrum of Lowe syndrome. 103
Interleukin-8 and CXCR1 receptor functional polymorphisms and susceptibility to acute pyelonephritis 102
MO069LRP2 VARIANTS IN DENT DISEASE PATIENTS WITH NO DETECTABLE MUTATION IN CLCN5 AND OCRL GENES 102
Protein uptake at glomerular level: is it just the work of podocytes? 102
An unusual association of contralateral congenital small kidney, reduced renal function and hyperparathyroidism in sponge kidney patients: on the track of the molecular basis 101
Understanding the Pathophysiology of Nephrocalcinosis 100
Locus heterogeneity of Dent's disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutations 99
MP062 EXPLORING ALBUMIN UPTAKE IN HUMAN PODOCYTES: A POSSIBLE INVOLVEMENT FOR THE TUBULAR UPTAKE MACHINERY 98
Family history may be misleading in the diagnosis of Dent's disease 96
Complexity of the 5'UTR region of the CLCN5 gene: eleven 5'UTR ends are differentially expressed in the human kidney. 96
Urine proteome analysis in Dent's disease shows high selective changes potentially involved in chronic renal damage 96
Spontaneous calcification process in primary renal cells from a medullary sponge kidney patient harbouring a GDNF mutation. 93
Encrusted cystitis by Corynebacterium urealyticum: a case report with novel insights into bladder lesions. 93
Hypercalciuria and nephrolithiasis: Expanding the renal phenotype of Donnai-Barrow syndrome 91
Perforin, Granzyme B, and fas ligand for molecular diagnosis of acute renal-allograft rejection: analyses on serial biopsies suggest methodological issues. 90
Dent's disease and prevalence of renal stones in dialysis patients in Northeastern Italy. 90
A PROSPECTIVE STUDY ON THE INCIDENCE AND EVOLUTION ON OF CONGENITAL CMV INFECTION IN A URBAN ITALIAN COMMUNITY. 90
A new screening test for rotavirus infection 89
Nephrolithiasis, kidney failure and bone disorders in Dent disease patients with and without CLCN5 mutations 89
Genes involved in TGF beta 1-driven epithelial-mesenchymal transition of renal epithelial cells are topologically related in the human interactome map 88
ClC-5 and proteinuric nephropathies. 88
GAPDH as housekeeping gene at renal level. 84
Medullary sponge kidney: state of the art. 84
Dent disease: A window into calcium and phosphate transport 84
Mesangial cell proliferation in long-term streptozotocin-induced diabetes mellitus in the rat and the renoprotective activity of heparin 83
Precocious activation of genes of the renin-angiotensin system and the fibrogenic cascade in IgA glomerulonephritis 83
The guanine triphosphatase (GTPase) activating protein (GAP)-related domain of the neurofibromatosis type 1 gene is not mutated in neural crest-derived sporadic tumours. 83
In search of adult renal stem cells 82
Trisomy 4q32 leads to 4qter due to a maternal 4/21 translocation. 82
MP073IN VITRO MODEL OF NEPHROCALCINOSIS: IS APOPTOSIS IN GDNF SILENCED HK2 CELLS THE TRIGGER OF CA2PO4 MINERALIZATION PROCESS? 82
Pregnancy in Alport Syndrome: a report of two differently-evolving cases. 81
Calcium kidney stones are associated with a haplotype of the Calcium-sensing receptor gene regulatory region. 81
Direct effect of chronic cyclosporin (Csa) treatment on collagen III mRNA expression and deposition in rat kidneys 80
Novel mutations of the CLCN5 gene including a complex allele and A 5' UTR mutation in Dent disease 1 80
The renal stem cell system in kidney repair and regeneration 79
Familial clustering of medullary sponge kidney is autosomal dominant with reduced penetrance and variable expressivity. 79
Two unusual cases of Gitelman's syndrome with a complex inheritance: how the phenotype can help interpret the genotype: lesson for the clinical nephrologist 79
Hereditary causes of kidney stones and chronic kidney disease. 78
USE OF PERFORIN (P), GRANZYME B (GB) AND FAS LIGAND (FL) IN RENAL TRANSPLANTATION FOR THE DIAGNOSIS OF ACUTE REJECTION: RT/PCR ANALYSIS OF SERIAL BIOPSIES AND PERIPHERAL BLOOD MONONUCLEARCELLS. 77
A comparative kinetic RT/-PCR strategy for the quantitation of mRNAs in microdissected human renal biopsy specimens 77
An atypical Dent’s disease phenotype caused by co-inheritance of mutations at CLCN5 and OCRL genes 76
Vascular endothelial growth factor expression in microdissected glomeruli of type 2 diabetic patients. 73
Linkage analysis of neurofibromatosis type 1 73
Polimorfismi cromosomici associati a malattie linfomieloproliferative. 73
Genetic Analyses in Dent Disease and Characterization of CLCN5 Mutations in Kidney Biopsies 73
HUMAN PARIETAL EPITHELIAL CELLS EXPRESS TUBULAR PROTEIN UPTAKE SYSTEM IN VIVO 72
RETROSPECTIVE OBSERVATIONAL STUDY FOR EVALUATION OF PREVALENCE AND INCIDENCE OF CHRONIC KIDNEY DISEASE (CKD) IN PATIENTS WITH NEPHROLITHIASIS 72
USE OF PERFORIN (P), GRANZYME B (GB) AND FAS LIGAND(FL) IN RENAL TRANSPLANTATION FOR THE DIAGNOSISOF ACUTE REJECTION: RT/PCR ANALYSIS OF SERIALBIOPSIES AND PERIPHERAL BLOOD MONONUCLEARCELLS. 71
Gene expression analysis in microdissected renal biopsy 71
Vascular endothelial growth factor (VEGF) and VEGF receptors in diabetic nephropathy: expression studies in biopsies of type 2 diabetic patients 71
Linkage Analysis of Neurofibromatosis Type 1. Study of a Homogeneous North Italian Population with Five DNA Markers of Chromosome 17. 70
Nephropathy by Oxalate Deposits: Not Only a Tubular Dysfunction 70
Protein lost and found: not only a tubular matter 70
ANALISI DI MUTAZIONE DELLA REGIONE 5’ UTR DEL GENE CLCN5 E DEI GENI OCRL1 E COLLECTRINA IN PAZIENTI CON MALATTIA DI DENT CLCN5 NEGATIVI 69
Functional polarity of Na+/H+ and Cl-/HCO3- exchangers in a rat cholangiocyte cell line 68
Molecular study in neurofibromatosis type 1: linkage and mutation analysis 68
Intracellular Processing of Transforming Growth Factor–β in Mesangial Cells 67
Molecular biology of the peritoneal membrane: in between morphology and function 67
“Real Time PCR con chimica SYBR Green I e RT/PCR semiquantitativa a confronto per la determinazione dell’espressione genica di fattori di crescita e citochine in differenti tessuti e in sistemi in vivo e in vitro”. 67
Down-regulation of glomerular matrix metalloproteinase-2 gene in human NIDDM. 67
Molecular biology of diabetic glomerulosclerosis 67
From protein uptake to Dent disease: an overview of the CLCN5 gene 67
Linkage analysis of neurofibromatosis 1. Study of a homogeneous North Italian population with five DNA markers of chromosome 17. DNA analysis of genetic diseases: state of art in Italy. 66
Frequency of abnormal karyotypes in relation to the ascertainment method in females referred for suspected sex chromosome abnormality 66
MO063WHOLE EXOME SEQUENCING IN DENT DISESE PATIENTS WITH NO DETECTABLE MUTATIONS IN CLCN5 AND OCRL GENES 66
TGF-beta 1 renal overexpression in diabetic rats and in high glucose mesangial cell cultures: Inhibition by heparinoids. 65
2D-electrophoresis of mitochondrial proteins from cystic fibrosis patients. 64
SCREENING FOR CYSTIC-FIBROSIS GENE-MUTATIONS BY MULTIPLEX DNA AMPLIFICATION 64
Studio dell'antigene H-Y in soggetti con animalie del differenziamento o del comportamento sessuale. 64
ClC5 and Megalin : new insight at glomerular compartment of human proteinuric nephropathies. 64
DNA analysis in CF families by biotinylated probes and polymerase chain reaction technique. 62
Molecular biology of the peritoneal membrane: in between morphology and function 62
CELL DEATH IN NEPHROCALCINOSIS: ROLE OF ANGIOTENSIN II TYPE 2 RECEPTOR AND APOPTOSIS IN PROXIMAL TUBULAR CELLS 62
Identification of a novel splice site mutation of CLCN5 gene and characterization of a new alternative 5' UTR end of ClC-5 mRNA in human renal tissue and leukocytes. 61
LASER-NEPHELOMETER AND LATEX DETERMINATION OF CRP SERUM LEVELS IN A PEDIATRIC POPULATION. 61
Association studies of genetic polymorphisms and complex disease. 61
GENETIC ANALYSIS IN DENT DISEASE AND FUNCTIONAL STUDIES OF CLCN5 MUTATIONS IN PATIENTS’ KIDNEY BIOPSIES 61
DIAGNOSI RAPIDA DI MENINGITE BATTERICA MEDIANTE AGGLUTINAZIONE AL LATTICE E COAGGLUTINAZIONE 60
Genetics and phenotypic heterogeneity of Dent disease: the dark side of the moon 60
Spontaneous calcification process in a primary culture of renal cells from a patient with MSK carrying a GDNF mutation 59
La transizione epitelio-mesenchimale (EMT) in vivo ed in vitro nella fibrosi renale 59
Specific modulatory effect of arachidonic acid on bone cytokine mRNA expression 58
Heparin reduces glomerular infiltration and TGF-beta protein expression by macrophages in puromycin glomerulosclerosis 58
Totale 8.795
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Categoria #
all - tutte 65.918
article - articoli 44.581
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 1.205
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.647
Totale 113.351
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.425 0 92 39 124 249 212 184 311 247 497 308 162
2020/20212.276 115 164 153 132 84 185 55 209 246 263 257 413
2021/20224.050 35 805 189 441 291 153 50 315 139 36 200 1.396
2022/20233.652 810 317 117 339 631 500 22 237 424 20 178 57
2023/20241.598 129 192 154 121 123 136 99 91 49 18 217 269
2024/202569 52 17 0 0 0 0 0 0 0 0 0 0
Totale 19.176