CINECA IRIS Institutional Research Information System

RAMENGHI, Ugo
 Distribuzione geografica
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Continente #
NA - Nord America 7.877
EU - Europa 5.719
AS - Asia 3.615
SA - Sud America 399
AF - Africa 78
OC - Oceania 43
Continente sconosciuto - Info sul continente non disponibili 4
Totale 17.735
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Nazione #
US - Stati Uniti d'America 7.688
CN - Cina 1.472
IT - Italia 1.370
SG - Singapore 1.029
IE - Irlanda 714
SE - Svezia 704
DE - Germania 562
FR - Francia 490
UA - Ucraina 401
FI - Finlandia 397
BR - Brasile 301
KR - Corea 301
GB - Regno Unito 231
AT - Austria 209
IN - India 200
PL - Polonia 176
CA - Canada 144
VN - Vietnam 139
JP - Giappone 109
HK - Hong Kong 95
NL - Olanda 89
ID - Indonesia 77
ES - Italia 67
GR - Grecia 65
RU - Federazione Russa 64
TR - Turchia 61
BE - Belgio 50
TW - Taiwan 41
AU - Australia 37
MX - Messico 27
AR - Argentina 26
CH - Svizzera 26
PE - Perù 25
SN - Senegal 25
EG - Egitto 18
CL - Cile 15
DK - Danimarca 14
EC - Ecuador 14
CZ - Repubblica Ceca 13
CO - Colombia 12
NO - Norvegia 11
RO - Romania 11
IR - Iran 10
IL - Israele 9
MY - Malesia 9
IQ - Iraq 8
LT - Lituania 8
PH - Filippine 8
PT - Portogallo 8
HU - Ungheria 7
MA - Marocco 7
SA - Arabia Saudita 7
DZ - Algeria 6
NZ - Nuova Zelanda 6
PK - Pakistan 6
TH - Thailandia 6
ZA - Sudafrica 6
BD - Bangladesh 5
HR - Croazia 5
TT - Trinidad e Tobago 5
UZ - Uzbekistan 5
BG - Bulgaria 4
BO - Bolivia 4
BY - Bielorussia 4
LU - Lussemburgo 4
LV - Lettonia 4
NG - Nigeria 4
CU - Cuba 3
EU - Europa 3
HN - Honduras 3
NP - Nepal 3
RS - Serbia 3
SI - Slovenia 3
TN - Tunisia 3
AE - Emirati Arabi Uniti 2
CY - Cipro 2
EE - Estonia 2
GM - Gambi 2
GT - Guatemala 2
JO - Giordania 2
KE - Kenya 2
LB - Libano 2
MU - Mauritius 2
PS - Palestinian Territory 2
SK - Slovacchia (Repubblica Slovacca) 2
A1 - Anonimo 1
AN - Antille olandesi 1
AZ - Azerbaigian 1
BN - Brunei Darussalam 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
IS - Islanda 1
JM - Giamaica 1
LK - Sri Lanka 1
LY - Libia 1
NI - Nicaragua 1
OM - Oman 1
PR - Porto Rico 1
PY - Paraguay 1
SO - Somalia 1
Totale 17.733
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Città #
Chandler 1.031
Beijing 968
Dublin 711
Singapore 600
Santa Clara 454
Houston 417
Torino 277
Fairfield 274
Ashburn 269
Jacksonville 267
Villeurbanne 265
Princeton 239
Medford 233
Nyköping 208
Dearborn 197
Columbus 195
Ann Arbor 194
Wilmington 189
Vienna 186
Warsaw 168
Milan 141
Woodbridge 137
Fremont 134
Seattle 132
Redwood City 122
Cambridge 99
Dong Ket 96
Pisa 89
Boston 87
Pune 83
Hong Kong 76
Boardman 73
Toronto 70
Guangzhou 60
Turin 60
Rome 58
Jakarta 56
New York 50
Shanghai 44
Helsinki 40
Verona 40
Hefei 36
Nanjing 36
Los Angeles 35
Falls Church 34
San Diego 32
Norwalk 31
Tainan City 30
San Mateo 29
Brussels 28
Nuremberg 27
Washington 27
São Paulo 26
Tokyo 25
London 22
Paris 22
The Dalles 22
Athens 21
Hangzhou 21
Lachine 21
Düsseldorf 20
Genoa 19
Zhengzhou 18
Bethesda 17
Lima 17
Philadelphia 17
Silver Spring 17
Tianjin 16
Chicago 15
Des Moines 15
Florence 15
Mumbai 15
Dronten 14
Kunming 14
Ottawa 14
Takamatsu 14
Bologna 13
Chengdu 13
Dallas 13
Istanbul 13
Mountain View 13
Padova 13
Piemonte 13
Nürnberg 12
Changsha 11
Hanover 11
Pittsburgh 11
Redmond 11
Rio de Janeiro 11
Wuhan 11
Buenos Aires 10
Cairo 10
Chongqing 10
Edinburgh 10
Frankfurt am Main 10
Madrid 10
Munich 10
Phoenix 10
Santiago 10
Cincinnati 9
Totale 10.139
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Nome #
Reticulocyte Parameters: Markers of Early Response to Oral Treatment in Children With Severe Iron-deficiency Anemia 571
Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation 485
A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferation 460
Autoimmune neutropenia of childhood secondary to other autoimmune disorders: Data from the Italian neutropenia registry 443
Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients 401
Efficacy of intravenous immunoglobulin therapy in giant cell hepatitis with autoimmune hemolytic anemia: A multicenter study 276
Spontaneous remission in a Diamond-Blackfan anaemia patient due to a revertant uniparental disomy ablating a de novo RPS19 mutation 273
Molecular approaches to diagnose Diamond-Blackfan anemia: The EuroDBA experience 254
A 20-year long term experience of the Italian Diamond-Blackfan Anaemia Registry: RPS and RPL genes, different faces of the same disease? 237
Porpora trombocitopenica idiopatica (immune) (PTI) acuta in eta pediatrica. Linee guida AIEOP per la diagnosi ed il trattamento 232
Functional evaluation of circulating hematopoietic progenitors in Noonan syndrome 190
Absolute reticulocyte count and reticulocyte hemoglobin content as predictors of early response to exclusive oral iron in children with iron deficiency anemia 190
High frequency of ribosomal protein gene deletions in Italian Diamond-Blackfan anemia patients detected by multiplex ligation-dependent probe amplification assay 185
Immunophenotypic Profiling of Erythroid Progenitor-Derived Extracellular Vesicles in Diamond-Blackfan Anaemia: A New Diagnostic Strategy 172
Ribosomal RNA analysis in the diagnosis of Diamond-Blackfan Anaemia 160
Diamond-Blackfan anemia: genotype-phenotype correlation in Italian patients with RPL5 and RPL11 mutations 153
Multiplex Ligation-dependent Probe Amplification (MLPA) enhances molecular diagnosis of Diamond Blackfan Anemia due to RPS19 deficiency 148
A functional assay for the clinical annotation of genetic variants of uncertain significance in Diamond–Blackfan anemia 146
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 137
Analysis of seven ribosomal protein genes in Italian Diamond Blackfan anemia patients 131
Efficacy of combined intravenous immunoglobulins and steroids in children with primary immune thrombocytopenia and persistent bleeding symptoms 128
Paroxysmal Nocturnal Hemoglobinuria Clones in Children with Acquired Aplastic Anemia: A Multicentric Study. 126
Analysis of the carbonyl compounds produced in beta thalassaemic erythrocytes by oxidative stress. 125
Anemia sideropenica nel III millennio: "nuovi" parametri di monitoraggio della risposta terapeutica 123
High frequency of RPL5 and RPL11 gene mutation in Italians patients with Diamond-Blackfan anemia (DBA) 122
Variations of the UNC13D gene in patients with autoimmune lymphoproliferative syndrome. 120
A new database for ribosomal protein genes which are mutated in Diamond-Blackfan Anemia 119
Acute pulmonary failure after the first administration of recombinant human granulocyte-macrophage colony-stimulating factor. 116
Identification of point mutations and large intragenic deletions in Fanconi anemia using next-generation sequencing technology 116
Interactions between RPS19, mutated in Diamond-Blackfan anemia, and the PIM-1 oncoprotein 111
ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization. 110
Somatic mosaicism and variable expressivity in Diamond Blackfan anemia (DBA): a gross deletion involving the 19q13 locus in a patient with transient anemia 109
MUTAZIONI IN PROTEINE RIBOSOMIALI IN PAZIENTI ITALIANI CON ANEMIA DI BLACKFAN DIAMOND 109
GH, prolactin and microangiopathy in insulin-dependent diabetes. 107
Acute non-lymphatic leukemia in children 107
Reduction of CFU-GM and Circulating Hematopoietic Progenitors in a Subgroup of Children With Chronic Neutropenia Associated With Severe Infections and Delayed Recovery 107
X-linked thrombocytopenia and Wiskott Aldrich syndrome are allelic diseases with mutations in the WASP gene 106
UN DATABASE PER L’ANEMIA DI DIAMOND-BLACKFAN 106
Administration of vitamin E in heterozygous beta-thalassaemia: the effect on red blood cell survival. 104
Neutropenie: considerazioni su una casistica monocentrica 102
Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family 102
Increased plasma corticosteroid-binding globulin in insulin-dependent pubertal diabetics: relationships with other glycoproteins, growth hormone and prolactin. 101
Haematopoietic stem cell transplantation for Diamond Blackfan anaemia: a report from the Italian Association of Paediatric Haematology and Oncology Registry. 101
Anemia di Diamond Blackfan (DBA) : Studio dell’espressione genica. 100
Diamond-Blackfan anemia: report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian population. 99
Deficiency of the Fas apoptosis pathway without Fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation 97
Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic Analysis 97
High levels of osteopontin associated with polymorphisms in its gene are a risk factor for development of autoimmunity/lymphoproliferation 96
Cell cycle analysis in the diagnosis of Fanconi\'s anemia 94
Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature 94
Le basi genetiche di una ribosomopatia: un database per l'anemia di Diamond-Blackfan 94
Fibroblasts from patients with Diamond-Blackfan anaemia show abnormal expression of genes involved in protein synthesis and amino acid metabolism 94
Pyrimidine 5'-nucleotidase acquired deficiency in beta-thalassemia: involvement of enzyme-SH groups in the inactivation process. 93
Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in children. 93
Analysis of telomeres in peripheral blood cells from patients with bone marrow failure 93
Detection of faecal SARS-CoV-2 RNA in a prospective cohort of children with multisystem inflammatory syndrome (MIS-C) 92
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. 91
Use of pegylated granulocyte-colony stimulating factor in childhood severe aplastic anemia 91
Co-stimulatory signal delivered by CD73 molecule to human CD45RAhiCD45ROlo (naive) CD8+ T lymphocytes. 90
Anemie ” eds, McGraw-Hill, Milano 1998, p 95-133. 90
Serum glycoproteins and insulin-dependent juvenile diabetes mellitus. 89
Pro-hemolytic effect of aldehydic products of lipid peroxidation. 89
Diamond Blackfan anaemia in the Italian population 89
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 89
Diagnosis and management of acquired aplastic anemia in childhood. Guidelines from the Marrow Failure Study Group of the Pediatric Haemato-Oncology Italian Association (AIEOP) 89
Defective function of Fas in T cells from paediatric patients with autoimmune thyroid diseases. 88
Defective function of Fas in patients with type 1 diabetes associated with other autoimmune diseases 88
Multicentre Italian study of SARS-CoV-2 infection in children and adolescents, preliminary data as at 10 April 2020 88
Compound heterozygosity for two new TERT mutations in a patient with aplastic anemia 87
HUMAN PHERIPHERAL BLOOD GRANULOCYTES AND MYELOID LEUKEMIC CELL LINES EXPRESS BOTH TRANSCRIPTS ENCODING FOR STEM CELL FACTOR 87
Autoimmune lymphoproliferative syndrome. [Malattia autoimmune linfoproliferativa] 87
La scelta vita/morte del linfocita.112: 297-309, 1998. 87
Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia 87
Diamond-Blackfan Anemia: an Overview 87
Covid-19 in children: Expressions of type i/ii/iii interferons, trim28, setdb1, and endogenous retroviruses in mild and severe cases 87
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 86
Umbilical cord blood stem cell transplantation. 84
Usefulness of the acidified glycerol lysis test in hereditary spherocytosis. 84
Successful use of antihistamines in severe hypereosinophilia 84
CIRCULATING FOLLICULAR HELPER T CELLS IN CHILDREN WITH IMMUNE THROMBOCYTOPENIC PURPURA 84
Acute childhood idiopathic thrombocytopenic purpura: AIEOP consensus guidelines for diagnosis and treatment. Associazione Italiana di Ematologia e Oncologia Pediatrica. 83
Effect of eradication of Helicobacter pylori in children with chronic immunethrombocytopenia: A prospective, controlled, multicenter study. 83
Flow cytometric evaluation of circulating CD34+ cell counts and apoptotic rate in children with acquired aplastic anemia and myelodysplasia 82
Deficiency of the Fas apoptosis pathway without Fas gene mutations is a familial trait predisposing to development of autoimmune diseases and cancer. 82
Co-inherited mutations of Fas and caspase-10 in development of the autoimmune lymphoproliferative syndrome 81
Rituximab (anti-CD20 monoclonal antibody) in children with chronic refractory symptomatic immune thrombocytopenic purpura: efficacy and safety of treatment 81
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
Mutations in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemia. 79
A comprehensive diagnostic surveillance protocol for idiopathic (de novo) and secondary myelodisplastic syndromes in childhood 78
Loss of GATA-1 full length as a cause of Diamond-Blackfan anemia phenotype. 78
Effect of stem cell factor on colony growth from acquired and constitutional (Fanconi) aplastic anemia 77
Cyclosporin A response and dependence in children with acquired aplastic anaemia: a multicentre retrospective study with long-term observation follow-up 77
Sequelae of COVID-19 in Hospitalized Children: A 4-Months Follow-Up 77
Long-term bone marrow cultures in Diamond-Blackfan anemia reveal a defect of both granulomacrophage and erythroid progenitors 76
Cell adhesion molecule expression in cord blood CD34+ cells 74
Therapeutic use of cefotiam in bacterial infections in pediatrics. 73
Expansion of cord blood progenitors and use for hemopoietic reconstitution. 73
Dissecting the transcriptional phenotype of ribosomal protein deficiency: implications for Diamond-Blackfan Anemia. 73
Le anemie ipoplastiche congenite e acquisite. Prospettive in pediatria, 89: 67-74, 1993. 73
In vitro growth and regulation of bone marrow enriched CD34+ hemopoietic progenitors in Diamond Blackfan anemia 72
Totale 12.711
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Categoria #
all - tutte 59.559
article - articoli 0
book - libri 0
conference - conferenze 4.515
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 64.074
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020220 0 0 0 0 0 0 0 0 0 0 128 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
2024/20252.868 44 259 161 361 784 236 107 150 415 276 75 0
Totale 18.328