IRIS
CIFALDI, CRISTINA
 Distribuzione geografica
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Continente #
NA - Nord America 1.771
EU - Europa 260
AS - Asia 151
SA - Sud America 3
AF - Africa 1
Totale 2.186
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Nazione #
US - Stati Uniti d'America 1.771
SG - Singapore 91
IT - Italia 76
IE - Irlanda 52
CN - Cina 39
DE - Germania 33
RU - Federazione Russa 32
FR - Francia 16
GB - Regno Unito 15
SE - Svezia 9
KR - Corea 7
NL - Olanda 7
UA - Ucraina 7
BE - Belgio 5
IN - India 4
BR - Brasile 3
CZ - Repubblica Ceca 3
IR - Iran 3
JP - Giappone 2
KG - Kirghizistan 2
AE - Emirati Arabi Uniti 1
AT - Austria 1
CH - Svizzera 1
EG - Egitto 1
ES - Italia 1
FI - Finlandia 1
HK - Hong Kong 1
PL - Polonia 1
VN - Vietnam 1
Totale 2.186
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Città #
Houston 535
Wilmington 475
Fairfield 104
Woodbridge 98
Singapore 85
Chandler 76
Ashburn 61
Seattle 54
Ann Arbor 46
Cambridge 41
Dublin 37
Rome 34
Santa Clara 26
Medford 25
Beijing 18
Lawrence 11
Menlo Park 9
Dearborn 8
Engelhard 8
Milan 8
San Diego 7
Seoul 7
Munich 6
New York 6
St. George 6
Amsterdam 5
Brussels 5
Center 5
Moscow 5
Monte Vista 4
Redwood City 4
Boardman 3
Brno 3
Creede 3
Nanjing 3
Palo Alto 3
Casalecchio di Reno 2
Chiswick 2
Council Bluffs 2
Del Norte 2
Guangzhou 2
Hefei 2
Prescot 2
Pune 2
Shenzhen 2
São Paulo 2
Tokyo 2
Acton 1
Al Mansurah 1
Americana 1
Atlanta 1
Augusta 1
Berlin 1
Boston 1
Central District 1
Chengdu 1
Chongqing 1
Falls Church 1
Geneva 1
Genoa 1
Gunzenhausen 1
Jacksonville 1
Kilburn 1
Krasnoyarsk 1
Kunming 1
L'isle-d'abeau 1
Lappeenranta 1
Las Vegas 1
London 1
Marcianise 1
Nanning 1
Quzhou 1
Rubiana 1
Salt Lake City 1
San Francisco 1
San Mateo 1
Torino 1
Turin 1
Varese 1
Velletri 1
Vienna 1
Wandsworth 1
Wuhan 1
Zhengzhou 1
Totale 1.893
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Nome #
Novel X-linked inhibitor of apoptosis mutation in very early-onset inflammatory bowel disease child successfully treated with HLA-haploidentical hemapoietic stem cells transplant after removal of αβ+T and B cells 396
Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies 248
Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies. Front Immunol. 2019 Apr 11;10:316. doi: 10.3389/fimmu.2019.00316. eCollection 2019. Erratum in: Front Immunol. 2019 May 31;10:1184. 246
JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long-known gene 179
First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia 165
Diagnostic Approach to Monogenic Inflammatory Bowel Disease in Clinical Practice: A Ten-Year Multicentric Experience 158
Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child with Intermittent Neutropenia 150
Novel Compound Heterozygous Mutations in IL-7 Receptor α Gene in a 15-Month-Old Girl Presenting With Thrombocytopenia, Normal T Cell Count and Maternal Engraftment. 144
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function 137
Corrigendum : Targeted NGS platforms for genetic screening and gene discovery in primary immunodeficiencies (Frontiers in Immunology (2019) 10 (316) DOI: 10.3389/fimmu.2019.00316) 136
Partial T cell defects and expanded CD56bright NK cells in an SCID patient carrying hypomorphic mutation in the IL2RG gene 89
Targeted treatment of autoimmune cytopenias in primary immunodeficiencies 49
Natural history of Ras-associated autoimmune leukoproliferative disorder: A 20-year follow-up of a NRAS-mutated patient excluding a malignant progression 35
Gastric cancer, inflammatory bowel disease and polyautoimmunity in a 17-year-old boy: CTLA-4 deficiency successfully treated with Abatacept 32
Corrigendum: Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult Patient 24
Gut mucosal and fecal microbiota profiling combined to intestinal immune system in neonates affected by intestinal ischemic injuries 22
Characterization of AR-CGD female patient with a novel homozygous deletion in CYBC1 gene presenting with unusual clinical phenotype 20
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease 16
Case Report: Crossing a rugged road in a primary immune regulatory disorder 14
Totale 2.260
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Categoria #
all - tutte 7.877
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 7.877
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020556 0 0 0 0 31 35 62 85 123 95 63 62
2020/2021720 65 73 58 67 72 98 107 105 20 32 17 6
2021/2022172 4 15 10 4 46 4 6 13 23 2 7 38
2022/2023218 13 25 6 16 18 53 35 24 21 0 5 2
2023/2024131 17 19 8 11 8 36 8 4 1 0 0 19
2024/2025221 16 103 41 30 31 0 0 0 0 0 0 0
Totale 2.260