MAZZA, Cinzia
 Distribuzione geografica
Continente #
NA - Nord America 410
EU - Europa 191
AS - Asia 142
OC - Oceania 3
SA - Sud America 1
Totale 747
Nazione #
US - Stati Uniti d'America 408
CN - Cina 80
UA - Ucraina 58
DE - Germania 55
SG - Singapore 36
FI - Finlandia 23
IT - Italia 21
HK - Hong Kong 16
GB - Regno Unito 14
IE - Irlanda 10
TR - Turchia 8
RU - Federazione Russa 6
AU - Australia 3
SE - Svezia 3
CA - Canada 2
BR - Brasile 1
ID - Indonesia 1
IN - India 1
PT - Portogallo 1
Totale 747
Città #
Woodbridge 55
Fairfield 46
Jacksonville 41
Houston 36
Chandler 32
Ashburn 30
Singapore 27
Princeton 20
Seattle 20
Beijing 19
Cambridge 18
Ann Arbor 17
Helsinki 16
Hong Kong 16
Wilmington 15
Nanjing 11
Dublin 10
New York 10
Istanbul 8
Shanghai 7
Changsha 5
Dearborn 5
Hangzhou 5
Nanchang 5
Shenyang 5
Brescia 4
Jinan 4
Lancaster 4
Milan 4
Ningbo 4
Des Moines 3
Hebei 3
Sydney 3
Haikou 2
London 2
Nürnberg 2
Palermo 2
San Francisco 2
Taiyuan 2
Tianjin 2
Verona 2
Baotou 1
Castiglione Delle Stiviere 1
Dallas 1
Eboli 1
Fano 1
Frankfurt am Main 1
Jakarta 1
Lanzhou 1
Leawood 1
Los Angeles 1
Markham 1
New Bedfont 1
Norwalk 1
Nottingham 1
Qingdao 1
Redwood City 1
San Diego 1
Santa Clara 1
São Paulo 1
Taizhou 1
Toronto 1
Zhengzhou 1
Totale 546
Nome #
Monocytes from Wiskott-Aldrich patients differentiate in functional mature dendritic cells with a defect in CD83 expression 131
Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia 114
Atypical presentation of autoimmune lymphoproliferative syndrome due to CASP10 mutation 105
PROSPECTIVE STUDY OF 84 PATIENTS WITH WISKOTT-ALDRICH SYNDROME AND X-RECESSIVE PIASTRINOPENIA: RESULTS OF THE APPLICATION OF COMMON PROTOCOL FOR DIAGNOSIS AND TREATMENT OF WAS/XLT 75
WASP-WIP DEFICIENCIES: NEW INSIGHTS IN WASP-WIP INTERACTION 72
CASE REPORT: IDENTIFICATION OF A PATIENT WITH FAMILIAR MUTATIONS AFFECTING BOTH WASP AND FOXP3 GENES 70
Multi-lineage analysis of X-inactivation in female carriers of genetic alterations in the Wiskott-Aldrich syndrome protein (WASP) gene locus 67
Application of common recommendations for diagnosis and treatment of Wiskott-Aldrich syndrome and X-recessive piastrinopenia: clinical and immunological characteristics of 65 patients with WAS/XLT 67
Combined DOCK8 and CLEC7A mutations causing immunodeficiency in 3 brothers with diarrhea, eczema, and infections 42
Lessons From the Clinic: ADPKD Genetic Test Unraveling Severe Phenotype, Intrafamilial Variability, and New, Rare Causing Genotype 24
Totale 767
Categoria #
all - tutte 4.103
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 4.103


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020125 0 0 0 0 8 19 18 16 11 28 16 9
2020/2021104 1 11 1 14 4 13 3 16 10 16 11 4
2021/202279 4 12 0 5 0 5 4 2 6 9 13 19
2022/202377 10 0 6 0 9 31 0 5 9 1 4 2
2023/2024101 8 0 15 7 7 21 5 8 16 0 0 14
2024/202544 2 1 1 22 18 0 0 0 0 0 0 0
Totale 767