RAMENGHI, Ugo
 Distribuzione geografica
Continente #
NA - Nord America 7.788
EU - Europa 5.551
AS - Asia 3.101
SA - Sud America 133
AF - Africa 67
OC - Oceania 43
Continente sconosciuto - Info sul continente non disponibili 4
Totale 16.687
Nazione #
US - Stati Uniti d'America 7.615
CN - Cina 1.448
IT - Italia 1.319
IE - Irlanda 714
SE - Svezia 703
SG - Singapore 654
DE - Germania 524
FR - Francia 487
UA - Ucraina 398
FI - Finlandia 390
KR - Corea 301
GB - Regno Unito 219
AT - Austria 188
IN - India 183
PL - Polonia 176
CA - Canada 143
VN - Vietnam 139
JP - Giappone 105
NL - Olanda 78
ID - Indonesia 77
GR - Grecia 64
ES - Italia 59
RU - Federazione Russa 57
BR - Brasile 53
TR - Turchia 53
BE - Belgio 48
TW - Taiwan 41
AU - Australia 37
HK - Hong Kong 28
AR - Argentina 25
CH - Svizzera 25
SN - Senegal 25
PE - Perù 24
MX - Messico 18
EG - Egitto 16
DK - Danimarca 14
CZ - Repubblica Ceca 13
CO - Colombia 11
NO - Norvegia 11
RO - Romania 11
EC - Ecuador 10
IL - Israele 9
MY - Malesia 9
IR - Iran 8
PH - Filippine 8
PT - Portogallo 8
CL - Cile 7
HU - Ungheria 7
LT - Lituania 7
DZ - Algeria 6
NZ - Nuova Zelanda 6
SA - Arabia Saudita 6
TH - Thailandia 6
HR - Croazia 5
PK - Pakistan 5
TT - Trinidad e Tobago 5
BG - Bulgaria 4
BY - Bielorussia 4
LU - Lussemburgo 4
MA - Marocco 4
NG - Nigeria 4
ZA - Sudafrica 4
BD - Bangladesh 3
BO - Bolivia 3
CU - Cuba 3
EU - Europa 3
IQ - Iraq 3
LV - Lettonia 3
NP - Nepal 3
RS - Serbia 3
SI - Slovenia 3
AE - Emirati Arabi Uniti 2
CY - Cipro 2
EE - Estonia 2
GM - Gambi 2
LB - Libano 2
MU - Mauritius 2
SK - Slovacchia (Repubblica Slovacca) 2
TN - Tunisia 2
UZ - Uzbekistan 2
A1 - Anonimo 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 16.687
Città #
Chandler 1.031
Beijing 968
Dublin 711
Singapore 526
Santa Clara 454
Houston 417
Torino 277
Fairfield 274
Ashburn 267
Jacksonville 267
Villeurbanne 265
Princeton 239
Medford 233
Nyköping 208
Dearborn 197
Columbus 195
Ann Arbor 194
Wilmington 189
Vienna 180
Warsaw 168
Woodbridge 137
Fremont 134
Milan 129
Seattle 125
Redwood City 122
Cambridge 99
Dong Ket 96
Pisa 89
Boston 87
Pune 79
Boardman 73
Toronto 69
Guangzhou 60
Jakarta 56
Rome 54
Turin 54
New York 50
Shanghai 41
Verona 40
Helsinki 36
Nanjing 36
Falls Church 34
Los Angeles 33
Norwalk 31
San Diego 31
Tainan City 30
San Mateo 29
Washington 27
Brussels 26
Hefei 26
Tokyo 24
Paris 22
Athens 21
Hangzhou 21
Lachine 21
London 20
Düsseldorf 19
Zhengzhou 18
Bethesda 17
Lima 17
Philadelphia 17
Genoa 16
Tianjin 16
Chicago 15
Des Moines 15
Florence 15
Mumbai 15
Dronten 14
Kunming 14
Ottawa 14
Takamatsu 14
Bologna 13
Chengdu 13
Mountain View 13
Piemonte 13
Nürnberg 12
Dallas 11
Hanover 11
Hong Kong 11
Padova 11
Pittsburgh 11
Redmond 11
Silver Spring 11
São Paulo 11
Wuhan 11
Buenos Aires 10
Changsha 10
Phoenix 10
Cincinnati 9
Frankfurt am Main 9
Genova 9
Istanbul 9
Madrid 9
Pavia 9
Ankara 8
Bandung 8
Cairo 8
Catania 8
Chongqing 8
Detroit 8
Totale 9.853
Nome #
Reticulocyte Parameters: Markers of Early Response to Oral Treatment in Children With Severe Iron-deficiency Anemia 542
Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation 464
A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferation 440
Autoimmune neutropenia of childhood secondary to other autoimmune disorders: Data from the Italian neutropenia registry 408
Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients 385
Spontaneous remission in a Diamond-Blackfan anaemia patient due to a revertant uniparental disomy ablating a de novo RPS19 mutation 257
Efficacy of intravenous immunoglobulin therapy in giant cell hepatitis with autoimmune hemolytic anemia: A multicenter study 255
A 20-year long term experience of the Italian Diamond-Blackfan Anaemia Registry: RPS and RPL genes, different faces of the same disease? 229
Porpora trombocitopenica idiopatica (immune) (PTI) acuta in eta pediatrica. Linee guida AIEOP per la diagnosi ed il trattamento 228
Molecular approaches to diagnose Diamond-Blackfan anemia: The EuroDBA experience 225
Functional evaluation of circulating hematopoietic progenitors in Noonan syndrome 183
Absolute reticulocyte count and reticulocyte hemoglobin content as predictors of early response to exclusive oral iron in children with iron deficiency anemia 181
High frequency of ribosomal protein gene deletions in Italian Diamond-Blackfan anemia patients detected by multiplex ligation-dependent probe amplification assay 181
Immunophenotypic Profiling of Erythroid Progenitor-Derived Extracellular Vesicles in Diamond-Blackfan Anaemia: A New Diagnostic Strategy 170
Ribosomal RNA analysis in the diagnosis of Diamond-Blackfan Anaemia 151
Diamond-Blackfan anemia: genotype-phenotype correlation in Italian patients with RPL5 and RPL11 mutations 145
A functional assay for the clinical annotation of genetic variants of uncertain significance in Diamond–Blackfan anemia 143
Multiplex Ligation-dependent Probe Amplification (MLPA) enhances molecular diagnosis of Diamond Blackfan Anemia due to RPS19 deficiency 141
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 131
Analysis of seven ribosomal protein genes in Italian Diamond Blackfan anemia patients 127
High frequency of RPL5 and RPL11 gene mutation in Italians patients with Diamond-Blackfan anemia (DBA) 122
Efficacy of combined intravenous immunoglobulins and steroids in children with primary immune thrombocytopenia and persistent bleeding symptoms 122
Paroxysmal Nocturnal Hemoglobinuria Clones in Children with Acquired Aplastic Anemia: A Multicentric Study. 120
Analysis of the carbonyl compounds produced in beta thalassaemic erythrocytes by oxidative stress. 119
Anemia sideropenica nel III millennio: "nuovi" parametri di monitoraggio della risposta terapeutica 115
Acute pulmonary failure after the first administration of recombinant human granulocyte-macrophage colony-stimulating factor. 114
Variations of the UNC13D gene in patients with autoimmune lymphoproliferative syndrome. 111
Identification of point mutations and large intragenic deletions in Fanconi anemia using next-generation sequencing technology 111
Interactions between RPS19, mutated in Diamond-Blackfan anemia, and the PIM-1 oncoprotein 109
A new database for ribosomal protein genes which are mutated in Diamond-Blackfan Anemia 109
MUTAZIONI IN PROTEINE RIBOSOMIALI IN PAZIENTI ITALIANI CON ANEMIA DI BLACKFAN DIAMOND 107
ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization. 106
GH, prolactin and microangiopathy in insulin-dependent diabetes. 104
Acute non-lymphatic leukemia in children 104
Administration of vitamin E in heterozygous beta-thalassaemia: the effect on red blood cell survival. 103
X-linked thrombocytopenia and Wiskott Aldrich syndrome are allelic diseases with mutations in the WASP gene 103
Somatic mosaicism and variable expressivity in Diamond Blackfan anemia (DBA): a gross deletion involving the 19q13 locus in a patient with transient anemia 103
UN DATABASE PER L’ANEMIA DI DIAMOND-BLACKFAN 103
Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family 100
Reduction of CFU-GM and Circulating Hematopoietic Progenitors in a Subgroup of Children With Chronic Neutropenia Associated With Severe Infections and Delayed Recovery 100
Increased plasma corticosteroid-binding globulin in insulin-dependent pubertal diabetics: relationships with other glycoproteins, growth hormone and prolactin. 99
Diamond-Blackfan anemia: report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian population. 99
Neutropenie: considerazioni su una casistica monocentrica 99
Haematopoietic stem cell transplantation for Diamond Blackfan anaemia: a report from the Italian Association of Paediatric Haematology and Oncology Registry. 99
Anemia di Diamond Blackfan (DBA) : Studio dell’espressione genica. 98
Deficiency of the Fas apoptosis pathway without Fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation 96
Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic Analysis 94
Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in children. 92
Le basi genetiche di una ribosomopatia: un database per l'anemia di Diamond-Blackfan 92
Fibroblasts from patients with Diamond-Blackfan anaemia show abnormal expression of genes involved in protein synthesis and amino acid metabolism 92
High levels of osteopontin associated with polymorphisms in its gene are a risk factor for development of autoimmunity/lymphoproliferation 91
Analysis of telomeres in peripheral blood cells from patients with bone marrow failure 89
Co-stimulatory signal delivered by CD73 molecule to human CD45RAhiCD45ROlo (naive) CD8+ T lymphocytes. 89
Use of pegylated granulocyte-colony stimulating factor in childhood severe aplastic anemia 88
Detection of faecal SARS-CoV-2 RNA in a prospective cohort of children with multisystem inflammatory syndrome (MIS-C) 88
Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature 87
Autoimmune lymphoproliferative syndrome. [Malattia autoimmune linfoproliferativa] 87
La scelta vita/morte del linfocita.112: 297-309, 1998. 87
Serum glycoproteins and insulin-dependent juvenile diabetes mellitus. 86
Cell cycle analysis in the diagnosis of Fanconi\'s anemia 86
Defective function of Fas in T cells from paediatric patients with autoimmune thyroid diseases. 86
Compound heterozygosity for two new TERT mutations in a patient with aplastic anemia 86
Pro-hemolytic effect of aldehydic products of lipid peroxidation. 85
Defective function of Fas in patients with type 1 diabetes associated with other autoimmune diseases 85
Anemie ” eds, McGraw-Hill, Milano 1998, p 95-133. 85
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 84
Pyrimidine 5'-nucleotidase acquired deficiency in beta-thalassemia: involvement of enzyme-SH groups in the inactivation process. 83
Diamond Blackfan anaemia in the Italian population 83
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. 83
HUMAN PHERIPHERAL BLOOD GRANULOCYTES AND MYELOID LEUKEMIC CELL LINES EXPRESS BOTH TRANSCRIPTS ENCODING FOR STEM CELL FACTOR 83
Diagnosis and management of acquired aplastic anemia in childhood. Guidelines from the Marrow Failure Study Group of the Pediatric Haemato-Oncology Italian Association (AIEOP) 83
Effect of eradication of Helicobacter pylori in children with chronic immunethrombocytopenia: A prospective, controlled, multicenter study. 82
Diamond-Blackfan Anemia: an Overview 82
Rituximab (anti-CD20 monoclonal antibody) in children with chronic refractory symptomatic immune thrombocytopenic purpura: efficacy and safety of treatment 80
Usefulness of the acidified glycerol lysis test in hereditary spherocytosis. 80
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. 80
Deficiency of the Fas apoptosis pathway without Fas gene mutations is a familial trait predisposing to development of autoimmune diseases and cancer. 80
CIRCULATING FOLLICULAR HELPER T CELLS IN CHILDREN WITH IMMUNE THROMBOCYTOPENIC PURPURA 80
Multicentre Italian study of SARS-CoV-2 infection in children and adolescents, preliminary data as at 10 April 2020 80
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 79
Umbilical cord blood stem cell transplantation. 79
Flow cytometric evaluation of circulating CD34+ cell counts and apoptotic rate in children with acquired aplastic anemia and myelodysplasia 77
Successful use of antihistamines in severe hypereosinophilia 77
Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia 77
Acute childhood idiopathic thrombocytopenic purpura: AIEOP consensus guidelines for diagnosis and treatment. Associazione Italiana di Ematologia e Oncologia Pediatrica. 76
Loss of GATA-1 full length as a cause of Diamond-Blackfan anemia phenotype. 76
Cyclosporin A response and dependence in children with acquired aplastic anaemia: a multicentre retrospective study with long-term observation follow-up 76
Sequelae of COVID-19 in Hospitalized Children: A 4-Months Follow-Up 76
Covid-19 in children: Expressions of type i/ii/iii interferons, trim28, setdb1, and endogenous retroviruses in mild and severe cases 76
Co-inherited mutations of Fas and caspase-10 in development of the autoimmune lymphoproliferative syndrome 75
A comprehensive diagnostic surveillance protocol for idiopathic (de novo) and secondary myelodisplastic syndromes in childhood 74
Therapeutic use of cefotiam in bacterial infections in pediatrics. 72
Long-term bone marrow cultures in Diamond-Blackfan anemia reveal a defect of both granulomacrophage and erythroid progenitors 70
Cell adhesion molecule expression in cord blood CD34+ cells 70
Diamond-Blackfan anemia: a congenital defect in erythropoiesis 70
Mutations in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemia. 69
Management of Chronic Childhood Immune Thrombocytopenic Purpura: AIEOP Consensus Guidelines 69
Increased frequency of the glucocorticoid receptor A3669G (rs6198) polymorphism in patients with Diamond-Blackfan anemia. 69
Role of inherited defects decreasing Fas function in autoimmunity. 68
In vitro growth and regulation of bone marrow enriched CD34+ hemopoietic progenitors in Diamond Blackfan anemia 68
Totale 12.122
Categoria #
all - tutte 52.046
article - articoli 0
book - libri 0
conference - conferenze 4.034
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 56.080


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.348 0 0 0 0 0 437 233 102 177 179 128 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
2024/20251.817 44 259 161 361 784 208 0 0 0 0 0 0
Totale 17.277