AURICCHIO, LUIGI
 Distribuzione geografica
Continente #
NA - Nord America 354
EU - Europa 169
AS - Asia 70
AF - Africa 17
Totale 610
Nazione #
US - Stati Uniti d'America 339
IT - Italia 47
SG - Singapore 44
DE - Germania 33
UA - Ucraina 30
CN - Cina 25
NL - Olanda 17
CI - Costa d'Avorio 16
FI - Finlandia 16
CA - Canada 15
IE - Irlanda 11
GB - Regno Unito 7
BE - Belgio 4
SE - Svezia 2
FR - Francia 1
IN - India 1
KE - Kenya 1
SI - Slovenia 1
Totale 610
Città #
Chandler 99
Singapore 34
Jacksonville 31
Ottawa 15
Princeton 14
Santa Clara 14
Boston 13
Amsterdam 12
Millbury 12
Nanjing 10
Naples 9
Napoli 9
Woodbridge 8
Los Angeles 6
Wilmington 6
Nanchang 5
Ashburn 4
Waanrode 4
Des Moines 3
Milan 3
Munich 3
Norwalk 3
Rome 3
Ansbach 2
Boardman 2
Changsha 2
Formia 2
Helsinki 2
Kronberg 2
Lawrence 2
Morcone 2
Orange 2
Salerno 2
Shenyang 2
Torre Annunziata 2
Ann Arbor 1
Beijing 1
Benevento 1
Bournemouth 1
Castellammare di Stabia 1
Dublin 1
Groningen 1
Guangzhou 1
Indiana 1
Kunming 1
Nairobi 1
Redwood City 1
San Francisco 1
San Mateo 1
Sant'Anastasia 1
Spodnja Volicina 1
Tianjin 1
Washington 1
Totale 362
Nome #
Transglutaminase 1 deficiency and corneocyte collapse: an indication for targeted molecular screening in autosomal recessive congenital ichthyosis. 56
Cutaneous manifestations as presenting sign of autoimmune lymphoproliferative syndrome in childhood 55
Diagnostic accuracy of the atopy patch test in children with food allergy-related gastrointestinal symptoms. 50
Diagnostic accuracy of atopy patch test using fresh food or commercial food antigen extracts in children with food allergy presenting with gastrointestinal symptoms. 47
Patch test with fresh food in children with atopic dermatitis and a case of allergic contact dermatitis to cod 44
Nail dystrophy associated with heterozygous mutation of the Nude/SCID FOXN1 (WHN) gene. 41
Tungiasis: Case Report of a Traveller to Kenya 39
Acquired digital fibrokeratoma: two case reports 39
Comments to: Compound heterozygotes for filaggrin gene mutations do not always show severe atopic dermatitis 37
Identification of two mutation within the transglutaminase 1 gene patients with lamellar ichthyosis. 34
Different TGM1 mutation spectra in Italian and Portuguese patients with autosomal recessive congenital ichthyosis: evidence of founder effects in Portugal. 34
Allergic contact dermatitis due to garlic (Allium sativum). 33
Possible role of galactose-1-P-uridyl transferase activity deficiency in red blood cells in the development of the presenile and senile cataract. 31
Multi-Gene Next-Generation Sequencing for Molecular Diagnosis of Autosomal Recessive Congenital Ichthyosis: A Genotype-Phenotype Study of Four Italian Patients 30
Transglutaminase 1 Gene Mutations in Italian Patients with Autosomal Recessive Lamellar Ichthyosis 29
Ocular findings and skin histology in a group of patients with X-linked ichthyosis 26
Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry 12
Comprehensive Molecular Analysis of Disease-Related Genes as First-Tier Test for Early Diagnosis, Classification, and Management of Patients Affected by Nonsyndromic Ichthyosis 11
Totale 648
Categoria #
all - tutte 2.787
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 2.787


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202022 0 0 0 0 6 0 2 0 0 0 3 11
2020/202171 10 7 4 6 8 7 9 1 8 2 8 1
2021/202287 0 0 0 9 0 2 1 2 11 14 14 34
2022/2023196 20 39 0 9 24 21 1 18 35 16 8 5
2023/202489 4 14 12 4 2 10 0 18 0 5 7 13
2024/202574 21 13 2 10 28 0 0 0 0 0 0 0
Totale 648