BIANCO, ANNA MONICA ROSARIA
 Distribuzione geografica
Continente #
EU - Europa 1.975
NA - Nord America 1.954
AS - Asia 294
AF - Africa 9
Continente sconosciuto - Info sul continente non disponibili 5
SA - Sud America 5
OC - Oceania 1
Totale 4.243
Nazione #
US - Stati Uniti d'America 1.953
PL - Polonia 1.269
IT - Italia 216
SE - Svezia 174
CN - Cina 119
HK - Hong Kong 94
DE - Germania 79
UA - Ucraina 73
FI - Finlandia 42
TR - Turchia 34
BG - Bulgaria 29
IE - Irlanda 27
BE - Belgio 20
KR - Corea 20
VN - Vietnam 16
GB - Regno Unito 11
CH - Svizzera 10
FR - Francia 9
SN - Senegal 8
NL - Olanda 7
BR - Brasile 5
EU - Europa 5
AT - Austria 4
IN - India 3
SG - Singapore 3
JP - Giappone 2
RO - Romania 2
AL - Albania 1
BD - Bangladesh 1
CA - Canada 1
DZ - Algeria 1
ES - Italia 1
HR - Croazia 1
IR - Iran 1
KZ - Kazakistan 1
NZ - Nuova Zelanda 1
Totale 4.243
Città #
Warsaw 1.262
Fairfield 268
Chandler 207
Woodbridge 203
Houston 186
Ann Arbor 180
Ashburn 137
Wilmington 128
Seattle 103
Hong Kong 94
Jacksonville 78
Trieste 78
Cambridge 77
Princeton 51
Dearborn 45
Sofia 29
Dublin 27
Beijing 24
Izmir 24
Seoul 19
Brussels 17
Dong Ket 16
Helsinki 16
Boardman 14
San Diego 12
Grafing 11
Bremen 9
Nanjing 9
Dakar 8
Nürnberg 8
Des Moines 7
Hebei 7
Jinan 7
Shanghai 7
Udine 7
Bern 6
Kraków 6
Washington 6
Falls Church 5
Boydton 4
Edinburgh 4
Fremont 4
Guangzhou 4
Hangzhou 4
Hefei 4
Kocaeli 4
Kunming 4
Los Angeles 4
Phoenix 4
Redmond 4
Redwood City 4
Romainville 4
Vienna 4
Zurich 4
Baotou 3
Dongguan 3
Fuzhou 3
Paris 3
Pune 3
Venezia 3
Waanrode 3
Bologna 2
Brescia 2
Campi Bisenzio 2
Chongqing 2
Columbus 2
Dallas 2
Düsseldorf 2
Grafenhausen 2
Laurel 2
Mcallen 2
Messina 2
Mestre 2
Milan 2
Muenster 2
New York 2
Portogruaro 2
Salvador 2
San Lazzaro di Savena 2
São Paulo 2
Torino 2
Wuhan 2
Xian 2
Almaty 1
Amsterdam 1
Anguillara Sabazia 1
Ankara 1
Auckland 1
Augusta 1
Berlin 1
Buffalo 1
Cagliari 1
Campinas 1
Camponogara 1
Camposampiero 1
Castelnuovo Rangone 1
Cervignano Del Friuli 1
Charlotte 1
Chengdu 1
Chicago 1
Totale 3.540
Nome #
Genetic profiling of autoinflammatory disorders in patients with periodic fever: a prospective study 420
Fever tree revisited: From malaria to autoinflammatory diseases 332
The diagnostic challenge of very early-onset enterocolitis in an infant with XIAP deficiency 326
Altered pattern of tumor necrosis factor-Alpha production in peripheral blood monocytes from Crohn's disease basic study 290
Type i interferon-mediated autoinflammation due to DNase II deficiency 290
Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome results. 289
Neither hereditary periodic fever nor periodic fever, aphthae, pharingitis, adenitis: Undifferentiated periodic fever in a tertiary pediatric center 266
Iron signature in asbestos-induced malignant pleural mesothelioma: A population-based autopsy study. 188
Genetic profile of patients with early onset inflammatory bowel disease 163
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype 154
F402L variant in NLRP12 in subjects with undiagnosed periodic fevers and in healthy controls 149
Curcumin and inflammatory bowel disease: Potential andlimits of innovative treatments 141
A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defect. 138
Diagnostic Approach to Monogenic Inflammatory Bowel Disease in Clinical Practice: A Ten-Year Multicentric Experience 134
Putative modifier genes in mevalonate kinase deficiency 132
Family history in early-onset inflammatory bowel disease 127
Novel NOD2 Mutation in Early-Onset Inflammatory Bowel Phenotype 119
Protective Role of BST2 Polymorphisms in Mother-to-Child Transmission of HIV-1 and Adult AIDS Progression 110
null 109
Expression and association data strongly support JARID2 involvement in nonsyndromic cleft lip with or without cleft palate. 108
Diagnostic approach to monogenic inflammatory bowel disease in clinical practice: a 10-year multi-centric experience 87
The Challenge of Next Generation Sequencing in a Boy with Severe Mononucleosis and EBV-related Lymphoma 74
The Genetic Diagnosis of Ultrarare DEEs: An Ongoing Challenge 63
MYO5B Gene Mutations: A Not Negligible Cause of Intrahepatic Cholestasis of Infancy with Normal Gamma-glutamyl Transferase Phenotype 56
Could the MED13 mutations manifest as a Kabuki-like syndrome? 50
Notch Signaling Regulation in Autoinflammatory Diseases 41
What Is the Exact Contribution of PITX1 and TBX4 Genes in Clubfoot Development? An Italian Study 35
Genetic bases of C7 deficiency: systematic review and report of a novel deletion determining functional hemizygosity 33
Totale 4.424
Categoria #
all - tutte 9.094
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 9.094


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019207 0 0 0 0 0 0 0 0 0 0 131 76
2019/20201.039 52 56 66 153 83 145 129 83 96 56 74 46
2020/2021665 59 71 71 68 67 58 59 47 43 70 11 41
2021/2022415 13 18 18 27 28 34 19 12 48 36 38 124
2022/2023597 60 83 47 84 61 92 3 58 62 5 24 18
2023/2024318 18 20 18 24 22 48 74 62 22 10 0 0
Totale 4.424