IRIS
IOLASCON, ACHILLE
 Distribuzione geografica
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Continente #
NA - Nord America 839
EU - Europa 693
AS - Asia 341
AF - Africa 2
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 1
SA - Sud America 1
Totale 1.879
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Nazione #
US - Stati Uniti d'America 833
IE - Irlanda 258
CN - Cina 247
UA - Ucraina 201
SE - Svezia 153
IN - India 46
TR - Turchia 46
FI - Finlandia 32
GB - Regno Unito 26
DE - Germania 6
CA - Canada 5
IT - Italia 5
FR - Francia 4
RU - Federazione Russa 3
CZ - Repubblica Ceca 2
EU - Europa 2
PL - Polonia 2
BE - Belgio 1
EG - Egitto 1
ET - Etiopia 1
IR - Iran 1
KR - Corea 1
MX - Messico 1
NZ - Nuova Zelanda 1
PE - Perù 1
Totale 1.879
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Città #
Dublin 257
Chandler 163
Jacksonville 140
Dearborn 114
Nanjing 93
Nyköping 89
San Mateo 36
Nanchang 28
Princeton 28
Wilmington 25
Beijing 24
Boardman 24
Shenyang 16
Tianjin 15
Hebei 11
Kunming 11
Changsha 9
Des Moines 9
Hangzhou 8
Jiaxing 8
Ashburn 7
Ann Arbor 6
Woodbridge 6
Helsinki 5
New York 5
Jinan 4
Toronto 4
Zhengzhou 4
Auburn Hills 3
Changchun 3
Hefei 3
Lanzhou 3
London 3
Augusta 2
Brno 2
Leawood 2
West Lafayette 2
Aiello Del Friuli 1
Airdrie 1
Burlington 1
Chimbote 1
Chongqing 1
Dunedin 1
Foggia 1
Frankfurt am Main 1
Guangzhou 1
Hanover 1
Kontich 1
Milan 1
Monterrey 1
Naples 1
Napoli 1
Ningbo 1
Paris 1
Redwood City 1
Saint Petersburg 1
Seoul 1
Shanghai 1
Shaoxing 1
Stevenage 1
Swords 1
Taizhou 1
Washington 1
Totale 1.198
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Nome #
P27KIP1 accumulation is associated with retinoic induced neuroblastoma differentiation: evidence of a decreased proteasome-dependent degradation 87
Congenital dyserythropoietic anemia type II: exclusion of seven candidate genes. 81
Incidence and outcome of hospital acquired malnutrition in children. 81
Red blood cell membrane defects Rev. 78
Inheredited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle piastrine 76
Analysis of CDKN2A, CDKN2B, CDKN2C and Cyclin Ds gene status in hepatoblastoma. 75
MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness. 74
Localization of the gene responsible for Fechtner syndrome in a region <600 Kb on 22q11-q13 74
Glucose-6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemia. 73
Osteoporosis in b-thalassaemia major patients: analysis of the genetic background 71
Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibition 70
Thrombophilia in thalassemia major patients: analysis of genetic predisposing factors. 69
Caspase 3 and 8 deficiency in human neuroblastoma. 68
Gilbert’s syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II) 68
Mutations in MYH9 result in the May-Hegglin anomaly and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. 67
Neonatal hyperbilirubinemia and Gilbert's syndrome. 67
Natural history of congenital dyserythropoietic anemia type II (CDA II) 66
Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approach. 65
Neuroblastoma in Two Siblings Support the Role of 1p36 Deletion in Tumor Development. 64
Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1. 63
The "stomatin" gene and protein in overhydrated hereditary stomatocytosis. 62
Association of breast cancer and polymorphisms of interleukin-10 and tumor necrosis factor-alpha genes. 62
Anemia diseritopoietica congenitas 61
RECOMBINANT ERYTHROPOIETIN THERAPY AS AN ALTERNATIVE TO BLOOD TRANSFUSIONS IN INFANTS WITH HEREDITARY SPHEROCYTOSIS. 60
Bone marrow transplantation in a case of severe, type II congenital dyserythropoietic anemia (CDA II) 55
Reduced Expression of Transforming Growth Factor-Beta Receptor Type III in High Stages Neuroblastoma. 53
Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlation. 49
Erythroid membrane proteomic 48
Totale 1.887
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Categoria #
all - tutte 7.335
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 7.335
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201942 0 0 0 0 0 0 0 0 0 0 13 29
2019/2020431 102 63 9 8 57 59 65 3 30 1 34 0
2020/2021240 28 2 28 0 31 37 29 3 30 52 0 0
2021/2022119 28 0 0 0 6 1 0 12 13 20 11 28
2022/2023703 33 24 23 57 45 82 0 76 333 4 17 9
2023/202452 14 6 5 5 11 5 0 2 0 2 2 0
Totale 1.887