CINECA IRIS Institutional Research Information System

RAMENGHI, Ugo
 Distribuzione geografica
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Continente #
NA - Nord America 6.764
EU - Europa 5.425
AS - Asia 2.510
SA - Sud America 123
AF - Africa 65
OC - Oceania 40
Continente sconosciuto - Info sul continente non disponibili 4
Totale 14.931
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Nazione #
US - Stati Uniti d'America 6.599
CN - Cina 1.336
IT - Italia 1.266
IE - Irlanda 712
SE - Svezia 703
DE - Germania 512
FR - Francia 482
UA - Ucraina 398
FI - Finlandia 384
KR - Corea 301
SG - Singapore 250
GB - Regno Unito 207
AT - Austria 187
PL - Polonia 175
IN - India 173
VN - Vietnam 139
CA - Canada 135
JP - Giappone 104
NL - Olanda 72
GR - Grecia 64
ES - Italia 59
BR - Brasile 53
RU - Federazione Russa 50
TR - Turchia 47
BE - Belgio 41
TW - Taiwan 39
AU - Australia 34
ID - Indonesia 29
SN - Senegal 25
CH - Svizzera 24
AR - Argentina 23
HK - Hong Kong 23
PE - Perù 21
MX - Messico 18
DK - Danimarca 14
EG - Egitto 14
CZ - Repubblica Ceca 13
NO - Norvegia 11
EC - Ecuador 10
IL - Israele 9
RO - Romania 9
IR - Iran 8
MY - Malesia 8
PH - Filippine 8
PT - Portogallo 8
CL - Cile 7
CO - Colombia 6
DZ - Algeria 6
NZ - Nuova Zelanda 6
SA - Arabia Saudita 6
TH - Thailandia 6
PK - Pakistan 5
TT - Trinidad e Tobago 5
HR - Croazia 4
LT - Lituania 4
LU - Lussemburgo 4
MA - Marocco 4
NG - Nigeria 4
ZA - Sudafrica 4
BD - Bangladesh 3
BO - Bolivia 3
BY - Bielorussia 3
CU - Cuba 3
EU - Europa 3
HU - Ungheria 3
LV - Lettonia 3
NP - Nepal 3
RS - Serbia 3
SI - Slovenia 3
BG - Bulgaria 2
CY - Cipro 2
EE - Estonia 2
GM - Gambi 2
IQ - Iraq 2
LB - Libano 2
MU - Mauritius 2
SK - Slovacchia (Repubblica Slovacca) 2
TN - Tunisia 2
UZ - Uzbekistan 2
A1 - Anonimo 1
AE - Emirati Arabi Uniti 1
AN - Antille olandesi 1
CR - Costa Rica 1
IS - Islanda 1
JO - Giordania 1
LK - Sri Lanka 1
LY - Libia 1
NI - Nicaragua 1
PR - Porto Rico 1
PS - Palestinian Territory 1
SO - Somalia 1
SY - Repubblica araba siriana 1
Totale 14.931
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Città #
Chandler 1.031
Beijing 964
Dublin 709
Houston 417
Torino 277
Fairfield 274
Jacksonville 267
Villeurbanne 265
Ashburn 258
Princeton 239
Medford 233
Nyköping 208
Dearborn 197
Ann Arbor 194
Wilmington 189
Vienna 179
Warsaw 167
Singapore 148
Woodbridge 137
Fremont 134
Milan 122
Redwood City 122
Seattle 122
Cambridge 99
Dong Ket 96
Pisa 89
Boston 87
Pune 79
Boardman 73
Toronto 63
Rome 51
New York 50
Turin 47
Verona 40
Shanghai 36
Falls Church 34
Guangzhou 34
Nanjing 34
Los Angeles 32
Norwalk 31
San Diego 31
Helsinki 30
Tainan City 30
San Mateo 29
Washington 27
Hefei 26
Tokyo 23
Paris 22
Athens 21
Lachine 21
Brussels 20
Hangzhou 20
Düsseldorf 19
Bethesda 17
London 17
Philadelphia 17
Genoa 16
Tianjin 16
Des Moines 15
Dronten 14
Florence 14
Lima 14
Ottawa 14
Takamatsu 14
Bologna 13
Chicago 13
Kunming 13
Mountain View 13
Piemonte 13
Zhengzhou 13
Chengdu 12
Nürnberg 12
Hanover 11
Pittsburgh 11
Redmond 11
Silver Spring 11
São Paulo 11
Buenos Aires 10
Dallas 10
Phoenix 10
Wuhan 10
Changsha 9
Cincinnati 9
Columbus 9
Genova 9
Istanbul 9
Madrid 9
Pavia 9
Ankara 8
Bandung 8
Catania 8
Chongqing 8
Detroit 8
Ferrara 8
Jakarta 8
Mumbai 8
Napoli 8
Padova 8
Barcelona 7
Frankfurt am Main 7
Totale 8.669
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Nome #
Reticulocyte Parameters: Markers of Early Response to Oral Treatment in Children With Severe Iron-deficiency Anemia 517
Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation 450
A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferation 408
Autoimmune neutropenia of childhood secondary to other autoimmune disorders: Data from the Italian neutropenia registry 383
Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients 364
Spontaneous remission in a Diamond-Blackfan anaemia patient due to a revertant uniparental disomy ablating a de novo RPS19 mutation 244
Efficacy of intravenous immunoglobulin therapy in giant cell hepatitis with autoimmune hemolytic anemia: A multicenter study 235
Porpora trombocitopenica idiopatica (immune) (PTI) acuta in eta pediatrica. Linee guida AIEOP per la diagnosi ed il trattamento 225
A 20-year long term experience of the Italian Diamond-Blackfan Anaemia Registry: RPS and RPL genes, different faces of the same disease? 220
Molecular approaches to diagnose Diamond-Blackfan anemia: The EuroDBA experience 211
Functional evaluation of circulating hematopoietic progenitors in Noonan syndrome 169
High frequency of ribosomal protein gene deletions in Italian Diamond-Blackfan anemia patients detected by multiplex ligation-dependent probe amplification assay 169
Absolute reticulocyte count and reticulocyte hemoglobin content as predictors of early response to exclusive oral iron in children with iron deficiency anemia 168
Immunophenotypic Profiling of Erythroid Progenitor-Derived Extracellular Vesicles in Diamond-Blackfan Anaemia: A New Diagnostic Strategy 154
Ribosomal RNA analysis in the diagnosis of Diamond-Blackfan Anaemia 142
A functional assay for the clinical annotation of genetic variants of uncertain significance in Diamond–Blackfan anemia 134
Diamond-Blackfan anemia: genotype-phenotype correlation in Italian patients with RPL5 and RPL11 mutations 129
Increased Prevalence of Congenital Heart Disease in Children With Diamond Blackfan Anemia Suggests Unrecognized Diamond Blackfan Anemia as a Cause of Congenital Heart Disease in the General Population: A Report of the Diamond Blackfan Anemia Registry 128
Multiplex Ligation-dependent Probe Amplification (MLPA) enhances molecular diagnosis of Diamond Blackfan Anemia due to RPS19 deficiency 128
Efficacy of combined intravenous immunoglobulins and steroids in children with primary immune thrombocytopenia and persistent bleeding symptoms 109
Paroxysmal Nocturnal Hemoglobinuria Clones in Children with Acquired Aplastic Anemia: A Multicentric Study. 109
Acute pulmonary failure after the first administration of recombinant human granulocyte-macrophage colony-stimulating factor. 108
Analysis of the carbonyl compounds produced in beta thalassaemic erythrocytes by oxidative stress. 108
High frequency of RPL5 and RPL11 gene mutation in Italians patients with Diamond-Blackfan anemia (DBA) 107
Identification of point mutations and large intragenic deletions in Fanconi anemia using next-generation sequencing technology 107
Analysis of seven ribosomal protein genes in Italian Diamond Blackfan anemia patients 107
Variations of the UNC13D gene in patients with autoimmune lymphoproliferative syndrome. 106
Interactions between RPS19, mutated in Diamond-Blackfan anemia, and the PIM-1 oncoprotein 103
Anemia sideropenica nel III millennio: "nuovi" parametri di monitoraggio della risposta terapeutica 102
X-linked thrombocytopenia and Wiskott Aldrich syndrome are allelic diseases with mutations in the WASP gene 101
A new database for ribosomal protein genes which are mutated in Diamond-Blackfan Anemia 99
Administration of vitamin E in heterozygous beta-thalassaemia: the effect on red blood cell survival. 98
Acute non-lymphatic leukemia in children 97
MUTAZIONI IN PROTEINE RIBOSOMIALI IN PAZIENTI ITALIANI CON ANEMIA DI BLACKFAN DIAMOND 95
Increased plasma corticosteroid-binding globulin in insulin-dependent pubertal diabetics: relationships with other glycoproteins, growth hormone and prolactin. 94
Haematopoietic stem cell transplantation for Diamond Blackfan anaemia: a report from the Italian Association of Paediatric Haematology and Oncology Registry. 94
Diamond-Blackfan anemia: report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian population. 93
GH, prolactin and microangiopathy in insulin-dependent diabetes. 92
UN DATABASE PER L’ANEMIA DI DIAMOND-BLACKFAN 89
Anemia di Diamond Blackfan (DBA) : Studio dell’espressione genica. 88
Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic Analysis 88
Reduction of CFU-GM and Circulating Hematopoietic Progenitors in a Subgroup of Children With Chronic Neutropenia Associated With Severe Infections and Delayed Recovery 88
Deficiency of the Fas apoptosis pathway without Fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation 87
ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization. 87
Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family 87
Neutropenie: considerazioni su una casistica monocentrica 86
High levels of osteopontin associated with polymorphisms in its gene are a risk factor for development of autoimmunity/lymphoproliferation 85
Le basi genetiche di una ribosomopatia: un database per l'anemia di Diamond-Blackfan 85
Somatic mosaicism and variable expressivity in Diamond Blackfan anemia (DBA): a gross deletion involving the 19q13 locus in a patient with transient anemia 84
Fibroblasts from patients with Diamond-Blackfan anaemia show abnormal expression of genes involved in protein synthesis and amino acid metabolism 84
Pyrimidine 5'-nucleotidase acquired deficiency in beta-thalassemia: involvement of enzyme-SH groups in the inactivation process. 82
Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in children. 82
Anemie ” eds, McGraw-Hill, Milano 1998, p 95-133. 82
Serum glycoproteins and insulin-dependent juvenile diabetes mellitus. 80
Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature 80
Analysis of telomeres in peripheral blood cells from patients with bone marrow failure 79
Autoimmune lymphoproliferative syndrome. [Malattia autoimmune linfoproliferativa] 79
Diagnosis and management of acquired aplastic anemia in childhood. Guidelines from the Marrow Failure Study Group of the Pediatric Haemato-Oncology Italian Association (AIEOP) 79
Pro-hemolytic effect of aldehydic products of lipid peroxidation. 78
Defective function of Fas in T cells from paediatric patients with autoimmune thyroid diseases. 78
Diamond Blackfan anaemia in the Italian population 77
Defective function of Fas in patients with type 1 diabetes associated with other autoimmune diseases 77
Umbilical cord blood stem cell transplantation. 77
Co-stimulatory signal delivered by CD73 molecule to human CD45RAhiCD45ROlo (naive) CD8+ T lymphocytes. 77
Usefulness of the acidified glycerol lysis test in hereditary spherocytosis. 77
La scelta vita/morte del linfocita.112: 297-309, 1998. 77
Use of pegylated granulocyte-colony stimulating factor in childhood severe aplastic anemia 77
The polymorphisms -318C>T in the promoter and 49A>G in exon 1 of CTLA4 and the risk of aplastic anemia in a Caucasian population 76
Detection of faecal SARS-CoV-2 RNA in a prospective cohort of children with multisystem inflammatory syndrome (MIS-C) 74
Cell cycle analysis in the diagnosis of Fanconi\'s anemia 73
Effect of eradication of Helicobacter pylori in children with chronic immunethrombocytopenia: A prospective, controlled, multicenter study. 73
Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia 73
Diamond-Blackfan anemia: expansion of erythroid progenitors in vitro by IL-9, but exclusion of a significant pathogenetic role for the IL-9 gene and the hematopoietic gene cluster on chromosome 5q. 72
Rituximab (anti-CD20 monoclonal antibody) in children with chronic refractory symptomatic immune thrombocytopenic purpura: efficacy and safety of treatment 72
The cell death-inducing ability of glycoprotein 120 from different HIV strains correlates with their ability to induce CD4 lateral association with CD95 on CD4+ T cells. 72
Deficiency of the Fas apoptosis pathway without Fas gene mutations is a familial trait predisposing to development of autoimmune diseases and cancer. 72
M-07e Cell Bioassay detects stromal cell production of Granulocyte-Macrophage colony stimulating factor and stem cell factor in normal and Diamond-Blackfan anemia bone marrow 71
Flow cytometric evaluation of circulating CD34+ cell counts and apoptotic rate in children with acquired aplastic anemia and myelodysplasia 71
CIRCULATING FOLLICULAR HELPER T CELLS IN CHILDREN WITH IMMUNE THROMBOCYTOPENIC PURPURA 71
Co-inherited mutations of Fas and caspase-10 in development of the autoimmune lymphoproliferative syndrome 70
Compound heterozygosity for two new TERT mutations in a patient with aplastic anemia 69
Acute childhood idiopathic thrombocytopenic purpura: AIEOP consensus guidelines for diagnosis and treatment. Associazione Italiana di Ematologia e Oncologia Pediatrica. 69
Loss of GATA-1 full length as a cause of Diamond-Blackfan anemia phenotype. 68
Cyclosporin A response and dependence in children with acquired aplastic anaemia: a multicentre retrospective study with long-term observation follow-up 68
A comprehensive diagnostic surveillance protocol for idiopathic (de novo) and secondary myelodisplastic syndromes in childhood 67
HUMAN PHERIPHERAL BLOOD GRANULOCYTES AND MYELOID LEUKEMIC CELL LINES EXPRESS BOTH TRANSCRIPTS ENCODING FOR STEM CELL FACTOR 67
Successful use of antihistamines in severe hypereosinophilia 67
Diamond-Blackfan Anemia: an Overview 67
Therapeutic use of cefotiam in bacterial infections in pediatrics. 66
Multicentre Italian study of SARS-CoV-2 infection in children and adolescents, preliminary data as at 10 April 2020 66
L'anemia di diamond blackfan 65
Sequelae of COVID-19 in Hospitalized Children: A 4-Months Follow-Up 65
Covid-19 in children: Expressions of type i/ii/iii interferons, trim28, setdb1, and endogenous retroviruses in mild and severe cases 65
Increased frequency of the glucocorticoid receptor A3669G (rs6198) polymorphism in patients with Diamond-Blackfan anemia. 64
Dissecting the transcriptional phenotype of ribosomal protein deficiency: implications for Diamond-Blackfan Anemia. 64
Exploiting pre-rRNA processing in Diamond Blackfan anemia gene discovery and diagnosis. 64
RPS19 mutations in patients with Diamond-Blackfan anemia 63
Effect of desferrioxamine and hydroxypyridones on hemopoietic progenitors and neuroectodermal tumor cells. 62
Role of inherited defects decreasing Fas function in autoimmunity. 62
Diamond-Blackfan anemia: a congenital defect in erythropoiesis 61
Totale 11.132
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Categoria #
all - tutte 44.742
article - articoli 0
book - libri 0
conference - conferenze 3.447
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 48.189
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.922 0 99 127 195 153 437 233 102 177 179 128 92
2020/20211.811 172 86 143 116 144 139 120 77 225 168 174 247
2021/20222.088 94 62 101 163 74 65 147 191 114 169 410 498
2022/20233.263 324 196 61 305 352 873 230 224 389 85 135 89
2023/20241.450 192 226 103 69 98 224 69 73 19 83 109 185
2024/202560 44 16 0 0 0 0 0 0 0 0 0 0
Totale 15.520