BELSITO, Angela
 Distribuzione geografica
Continente #
NA - Nord America 899
EU - Europa 698
AS - Asia 123
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
SA - Sud America 1
Totale 1.724
Nazione #
US - Stati Uniti d'America 897
IE - Irlanda 273
UA - Ucraina 112
GB - Regno Unito 99
DE - Germania 64
SG - Singapore 61
CN - Cina 45
IT - Italia 45
FI - Finlandia 28
FR - Francia 23
SE - Svezia 17
BE - Belgio 14
GR - Grecia 12
TR - Turchia 9
IN - India 3
AT - Austria 2
CA - Canada 2
CZ - Repubblica Ceca 2
HK - Hong Kong 2
JP - Giappone 2
PL - Polonia 2
AU - Australia 1
CH - Svizzera 1
CL - Cile 1
ES - Italia 1
EU - Europa 1
KE - Kenya 1
KR - Corea 1
LT - Lituania 1
NL - Olanda 1
RO - Romania 1
Totale 1.724
Città #
Dublin 273
Chandler 204
Jacksonville 175
Ann Arbor 64
Santa Clara 64
Singapore 48
Woodbridge 39
Bremen 32
Princeton 32
Medford 28
Boardman 25
Caserta 20
Roxbury 19
Wilmington 15
Beijing 14
Brussels 14
San Mateo 14
Cambridge 12
Auburn Hills 8
Nanjing 8
Jinan 5
Los Angeles 5
New York 5
Mountain View 4
Des Moines 3
Düsseldorf 3
Norwalk 3
Portici 3
Brno 2
Columbus 2
Haikou 2
Helsinki 2
Hong Kong 2
Pune 2
Seattle 2
Shenyang 2
Zhengzhou 2
Andover 1
Apo 1
Ashburn 1
Bologna 1
Canberra 1
Chicago 1
Cluj-napoca 1
Foggia 1
Gragnano 1
Groningen 1
Gunzenhausen 1
Kocaeli 1
Kraków 1
Kunming 1
Ladispoli 1
Luoyang 1
Madrid 1
Marano Di Napoli 1
Massa 1
Nairobi 1
Nanchang 1
Naples 1
New Delhi 1
Ningbo 1
North Bay 1
Nova Siri 1
Seoul 1
Stockholm 1
Taiyuan 1
Tappahannock 1
Tianjin 1
Vilnius 1
Warsaw 1
Winnipeg 1
Yueqing 1
Totale 1.192
Nome #
Association between HLA-A26 and CMV infection in heart transplantation recipients 97
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes 84
Erythrocyte genotyping for transfusion-dependent patients at the Azienda Universitaria Policlinico of Naples 80
Identification and characterization of a novel member of the dystrobrevin gene family 74
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene 68
Multiple heterozygosity for different muscle genes is not rare among individuals with pauci-symptomatic hyperCKemia 66
Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein 65
Candidate-gene testing for orphan limb-girdle muscular dystrophies 63
Identification of the Syrian hamster cardiomyopathy gene 63
The fourth component of the sarcoglycan complex 60
Dystrophin gene scanning by DHPLC of DMD carriers without deletions or duplications 60
Interaction of vault particles with estrogen receptor in the MCF-7 breast cancer cell 59
Blood transfusions and adverse acute events: a retrospective study from 214 transfusion-dependent pediatric patients comparing transfused blood components by apheresis or by whole blood 57
Identification of a DNA binding protein cooperating with estrogen receptor as RIZ (retinoblastoma interacting zinc finger protein) 55
Double carrier status in CANP3 and beta-sarcoglycan genes results in a mild disease phenotype 55
Gamma1- and gamma2-syntrophins, two novel dystrophin-binding proteins localized in neuronal cells 53
Gene redundancies in the dystrophin-associated protein complex 53
Potential adverse reactions associated with apheresis multicomponent (MAC) donors 53
Analysis of caveolin-3 (CAV-3) gene in patients with limb-girdle muscular dystrophies and/or isolated hyperCKemia 52
Clinical outcome of transfusions with extended red blood cell matching in β-thalassemia patients: A single-center experience 51
Aspetti clinici, genetici ed epidemiologici delleDistrofie muscolari dei Cingoli nel Sud Italia 50
Erythrocyte Genotyping With Hea Beadchip Kit: Our Experience At Azienda Ospedaliera Universitaria, Second University Of Naples 50
The retinoblastoma-interacting zinc-finger protein RIZ is a downstream effector of estrogen action 48
Results of an educational program to promote the use of apheresis in the hospitals of region Campania 47
Clinical, genetic and epidemiological aspects of limb-girdle muscular dystrophies in Southern Italy 47
Emerging strategies of blood group genotyping for patients with hemoglobinopathies 47
Blood group genotyping for patients with autoimmune hemolytic anemia 46
Identification of candidate genes for limb-girdle muscular dystrophies: the yeast two hybrid approach 39
Identification and analysis of candidate genes for Limb-Girdle Muscular Dystrophies 38
REPORT OF ADVERSE TRANSFUSION REACTIONS: EMOCOMPONENTS VIA APHERESIS VS WHOLE BLOOD INPEDIATRIC PATIENTS 37
Risultati del programma educativo utilizzato per promuovere l’aferesi 33
Implementation Of Productive Apheresis Improves Platelet Transfusion Safety Of Polytransfused Pediatric Patients 32
Totale 1.782
Categoria #
all - tutte 7.487
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 7.487


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020121 0 0 0 0 32 6 35 9 17 8 9 5
2020/2021224 23 3 29 7 42 2 33 27 5 32 16 5
2021/2022229 16 3 1 3 69 1 3 6 8 39 18 62
2022/2023642 45 42 3 60 86 44 0 41 292 5 11 13
2023/2024145 16 3 7 15 55 7 1 4 0 2 20 15
2024/2025106 2 5 8 6 85 0 0 0 0 0 0 0
Totale 1.782