CINECA IRIS Institutional Research Information System

RAMENGHI, Ugo
 Distribuzione geografica
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Continente #
NA - Nord America 5346
EU - Europa 4888
AS - Asia 2007
SA - Sud America 90
AF - Africa 41
OC - Oceania 34
Continente sconosciuto - Info sul continente non disponibili 4
Totale 12410
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Nazione #
US - Stati Uniti d'America 5195
CN - Cina 1276
IT - Italia 1075
SE - Svezia 659
IE - Irlanda 652
DE - Germania 460
FR - Francia 447
UA - Ucraina 388
FI - Finlandia 357
KR - Corea 297
AT - Austria 186
GB - Regno Unito 186
PL - Polonia 175
VN - Vietnam 137
CA - Canada 129
JP - Giappone 92
IN - India 77
GR - Grecia 56
ES - Italia 55
RU - Federazione Russa 40
BE - Belgio 39
BR - Brasile 37
NL - Olanda 36
TR - Turchia 31
AU - Australia 28
SN - Senegal 25
ID - Indonesia 20
AR - Argentina 18
MX - Messico 14
PE - Perù 14
CH - Svizzera 12
HK - Hong Kong 12
DK - Danimarca 9
NO - Norvegia 9
TW - Taiwan 9
CZ - Repubblica Ceca 8
EC - Ecuador 8
IL - Israele 8
PH - Filippine 8
PT - Portogallo 8
CL - Cile 7
CO - Colombia 6
IR - Iran 6
NZ - Nuova Zelanda 6
TH - Thailandia 6
RO - Romania 5
SG - Singapore 5
TT - Trinidad e Tobago 5
HR - Croazia 4
LT - Lituania 4
MY - Malesia 4
ZA - Sudafrica 4
DZ - Algeria 3
EG - Egitto 3
EU - Europa 3
LU - Lussemburgo 3
LV - Lettonia 3
PK - Pakistan 3
SA - Arabia Saudita 3
SI - Slovenia 3
BY - Bielorussia 2
CY - Cipro 2
EE - Estonia 2
GM - Gambi 2
HU - Ungheria 2
IQ - Iraq 2
LB - Libano 2
MU - Mauritius 2
TN - Tunisia 2
A1 - ???statistics.table.value.countryCode.A1??? 1
AE - Emirati Arabi Uniti 1
AN - Antille olandesi 1
BG - Bulgaria 1
IS - Islanda 1
JO - Giordania 1
LK - Sri Lanka 1
NI - Nicaragua 1
NP - Nepal 1
PR - Porto Rico 1
PS - Palestinian Territory 1
SK - Slovacchia (Repubblica Slovacca) 1
SY - Repubblica araba siriana 1
UZ - Uzbekistan 1
Totale 12410
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Città #
Chandler 960
Beijing 954
Dublin 649
Houston 395
Torino 276
Fairfield 274
Jacksonville 261
Villeurbanne 261
Princeton 237
Medford 231
Ann Arbor 194
Dearborn 191
Wilmington 189
Vienna 178
Nyköping 169
Warsaw 167
Woodbridge 137
Fremont 134
Ashburn 130
Redwood City 122
Seattle 119
Cambridge 99
Milan 98
Dong Ket 96
Pisa 89
Boston 80
Boardman 67
Toronto 61
Verona 39
Shanghai 35
Falls Church 34
Guangzhou 34
Norwalk 31
San Diego 29
San Mateo 29
Rome 26
Hefei 25
Nanjing 25
Brussels 20
Hangzhou 20
Lachine 20
Tokyo 20
Turin 18
Düsseldorf 17
Philadelphia 17
Athens 16
Bethesda 16
Paris 16
Tianjin 16
Des Moines 15
Ottawa 14
Takamatsu 14
Helsinki 13
Lima 13
Piemonte 13
Zhengzhou 13
Chengdu 12
Florence 12
Kunming 12
Mountain View 12
Nürnberg 12
Silver Spring 11
Bologna 10
Dallas 10
London 10
Phoenix 10
Redmond 10
Chicago 9
Genova 9
Wuhan 9
Buenos Aires 8
Changsha 8
Chongqing 8
Detroit 8
Jakarta 8
Mumbai 8
Napoli 8
Padova 8
Pittsburgh 8
Hebei 7
Madrid 7
New York 7
Pavia 7
Rotterdam 7
São Paulo 7
Xian 7
Ankara 6
Central District 6
Columbus 6
Ferrara 6
Minoh 6
Moscow 6
Stavanger 6
Atlanta 5
Auburn Hills 5
Barcelona 5
Chaguanas 5
Jinan 5
Los Angeles 5
Salt Lake City 5
Totale 7762
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Nome #
Reticulocyte Parameters: Markers of Early Response to Oral Treatment in Children With Severe Iron-deficiency Anemia 427
Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation 394
A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferation 341
Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients 331
Autoimmune neutropenia of childhood secondary to other autoimmune disorders: Data from the Italian neutropenia registry 252
Porpora trombocitopenica idiopatica (immune) (PTI) acuta in eta pediatrica. Linee guida AIEOP per la diagnosi ed il trattamento 209
Efficacy of intravenous immunoglobulin therapy in giant cell hepatitis with autoimmune hemolytic anemia: A multicenter study 207
Spontaneous remission in a Diamond-Blackfan anaemia patient due to a revertant uniparental disomy ablating a de novo RPS19 mutation 187
A 20-year long term experience of the Italian Diamond-Blackfan Anaemia Registry: RPS and RPL genes, different faces of the same disease? 182
Molecular approaches to diagnose Diamond-Blackfan anemia: The EuroDBA experience 174
Absolute reticulocyte count and reticulocyte hemoglobin content as predictors of early response to exclusive oral iron in children with iron deficiency anemia 159
Functional evaluation of circulating hematopoietic progenitors in Noonan syndrome 155
High frequency of ribosomal protein gene deletions in Italian Diamond-Blackfan anemia patients detected by multiplex ligation-dependent probe amplification assay 152
Immunophenotypic Profiling of Erythroid Progenitor-Derived Extracellular Vesicles in Diamond-Blackfan Anaemia: A New Diagnostic Strategy 137
Ribosomal RNA analysis in the diagnosis of Diamond-Blackfan Anaemia 122
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 120
Multiplex Ligation-dependent Probe Amplification (MLPA) enhances molecular diagnosis of Diamond Blackfan Anemia due to RPS19 deficiency 111
A functional assay for the clinical annotation of genetic variants of uncertain significance in Diamond–Blackfan anemia 109
Diamond-Blackfan anemia: genotype-phenotype correlation in Italian patients with RPL5 and RPL11 mutations 106
Identification of point mutations and large intragenic deletions in Fanconi anemia using next-generation sequencing technology 104
Paroxysmal Nocturnal Hemoglobinuria Clones in Children with Acquired Aplastic Anemia: A Multicentric Study. 101
Analysis of seven ribosomal protein genes in Italian Diamond Blackfan anemia patients 99
Variations of the UNC13D gene in patients with autoimmune lymphoproliferative syndrome. 98
High frequency of RPL5 and RPL11 gene mutation in Italians patients with Diamond-Blackfan anemia (DBA) 96
Analysis of the carbonyl compounds produced in beta thalassaemic erythrocytes by oxidative stress. 93
X-linked thrombocytopenia and Wiskott Aldrich syndrome are allelic diseases with mutations in the WASP gene 93
Efficacy of combined intravenous immunoglobulins and steroids in children with primary immune thrombocytopenia and persistent bleeding symptoms 93
Acute pulmonary failure after the first administration of recombinant human granulocyte-macrophage colony-stimulating factor. 91
Administration of vitamin E in heterozygous beta-thalassaemia: the effect on red blood cell survival. 91
Haematopoietic stem cell transplantation for Diamond Blackfan anaemia: a report from the Italian Association of Paediatric Haematology and Oncology Registry. 91
GH, prolactin and microangiopathy in insulin-dependent diabetes. 86
Increased plasma corticosteroid-binding globulin in insulin-dependent pubertal diabetics: relationships with other glycoproteins, growth hormone and prolactin. 85
Diamond-Blackfan anemia: report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian population. 85
A new database for ribosomal protein genes which are mutated in Diamond-Blackfan Anemia 85
MUTAZIONI IN PROTEINE RIBOSOMIALI IN PAZIENTI ITALIANI CON ANEMIA DI BLACKFAN DIAMOND 84
UN DATABASE PER L’ANEMIA DI DIAMOND-BLACKFAN 81
Anemia di Diamond Blackfan (DBA) : Studio dell’espressione genica. 78
Fibroblasts from patients with Diamond-Blackfan anaemia show abnormal expression of genes involved in protein synthesis and amino acid metabolism 78
Pyrimidine 5'-nucleotidase acquired deficiency in beta-thalassemia: involvement of enzyme-SH groups in the inactivation process. 75
Deficiency of the Fas apoptosis pathway without Fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation 75
Use of pegylated granulocyte-colony stimulating factor in childhood severe aplastic anemia 75
Acute non-lymphatic leukemia in children 75
Somatic mosaicism and variable expressivity in Diamond Blackfan anemia (DBA): a gross deletion involving the 19q13 locus in a patient with transient anemia 74
Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic Analysis 74
Neutropenie: considerazioni su una casistica monocentrica 73
Anemie ” eds, McGraw-Hill, Milano 1998, p 95-133. 73
Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family 71
Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature 70
Le basi genetiche di una ribosomopatia: un database per l'anemia di Diamond-Blackfan 70
Diagnosis and management of acquired aplastic anemia in childhood. Guidelines from the Marrow Failure Study Group of the Pediatric Haemato-Oncology Italian Association (AIEOP) 70
Defective function of Fas in T cells from paediatric patients with autoimmune thyroid diseases. 69
Umbilical cord blood stem cell transplantation. 69
Usefulness of the acidified glycerol lysis test in hereditary spherocytosis. 69
Anemia sideropenica nel III millennio: "nuovi" parametri di monitoraggio della risposta terapeutica 69
Pro-hemolytic effect of aldehydic products of lipid peroxidation. 68
High levels of osteopontin associated with polymorphisms in its gene are a risk factor for development of autoimmunity/lymphoproliferation 68
Analysis of telomeres in peripheral blood cells from patients with bone marrow failure 68
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 67
Serum glycoproteins and insulin-dependent juvenile diabetes mellitus. 66
Autoimmune lymphoproliferative syndrome. [Malattia autoimmune linfoproliferativa] 66
Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia 66
Defective function of Fas in patients with type 1 diabetes associated with other autoimmune diseases 65
Reduction of CFU-GM and Circulating Hematopoietic Progenitors in a Subgroup of Children With Chronic Neutropenia Associated With Severe Infections and Delayed Recovery 65
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 64
La scelta vita/morte del linfocita.112: 297-309, 1998. 64
Loss of GATA-1 full length as a cause of Diamond-Blackfan anemia phenotype. 64
Cell cycle analysis in the diagnosis of Fanconi\'s anemia 63
Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in children. 63
Flow cytometric evaluation of circulating CD34+ cell counts and apoptotic rate in children with acquired aplastic anemia and myelodysplasia 63
Effect of eradication of Helicobacter pylori in children with chronic immunethrombocytopenia: A prospective, controlled, multicenter study. 63
Deficiency of the Fas apoptosis pathway without Fas gene mutations is a familial trait predisposing to development of autoimmune diseases and cancer. 63
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. 62
Therapeutic use of cefotiam in bacterial infections in pediatrics. 61
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. 61
CIRCULATING FOLLICULAR HELPER T CELLS IN CHILDREN WITH IMMUNE THROMBOCYTOPENIC PURPURA 61
Diamond Blackfan anaemia in the Italian population 60
Co-stimulatory signal delivered by CD73 molecule to human CD45RAhiCD45ROlo (naive) CD8+ T lymphocytes. 60
Rituximab (anti-CD20 monoclonal antibody) in children with chronic refractory symptomatic immune thrombocytopenic purpura: efficacy and safety of treatment 59
Increased frequency of the glucocorticoid receptor A3669G (rs6198) polymorphism in patients with Diamond-Blackfan anemia. 59
Co-inherited mutations of Fas and caspase-10 in development of the autoimmune lymphoproliferative syndrome 58
ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization. 58
Diamond-Blackfan Anemia: an Overview 58
Compound heterozygosity for two new TERT mutations in a patient with aplastic anemia 56
A comprehensive diagnostic surveillance protocol for idiopathic (de novo) and secondary myelodisplastic syndromes in childhood 55
L'anemia di diamond blackfan 55
Effect of desferrioxamine and hydroxypyridones on hemopoietic progenitors and neuroectodermal tumor cells. 54
Stem cell factor suppresses apoptosis in neuroblastoma cell lines. 54
Dissecting the transcriptional phenotype of ribosomal protein deficiency: implications for Diamond-Blackfan Anemia. 54
Flt-3 and its ligand are expressed in neural crest-derived tumors and promote survival and proliferation of their cell lines. 54
Search for protein interactors of ribosomal protein S19, mutated in Diamond Blackfan Anemia 53
Diamond-Blackfan anemia: a congenital defect in erythropoiesis 53
Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome. 52
Cyclosporin A response and dependence in children with acquired aplastic anaemia: a multicentre retrospective study with long-term observation follow-up 52
Eltrombopag for children with chronic immune thrombocytopenia (PETIT2): A randomised, multicentre, placebo-controlled trial 52
Sequelae of COVID-19 in Hospitalized Children: A 4-Months Follow-Up 52
Role of inherited defects decreasing Fas function in autoimmunity. 51
Use of recombinant granulocyte colony-stimulating factor in Fanconi’s anemia 51
Management of Chronic Childhood Immune Thrombocytopenic Purpura: AIEOP Consensus Guidelines 51
Are all cases of paediatric essential thrombocythaemia really myeloproliferative neoplasms? Analysis of a large cohort. 51
Covid-19 in children: Expressions of type i/ii/iii interferons, trim28, setdb1, and endogenous retroviruses in mild and severe cases 51
Totale 9452
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Categoria #
all - tutte 20802
article - articoli 0
book - libri 0
conference - conferenze 1799
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 22601
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/20181514 0000 00 0371 7113355047
2018/20191281 412912157 69121 83209 7985268119
2019/20201980 10199125193 151411 228101 17517812692
2020/20211801 17086141116 144139 11877 223166174247
2021/20222073 9462101161 7465 145190 114168406493
2022/20232351 32219660302 348860 2603 0000
Totale 12985