IRIS
SANTACROCE, ROSA
 Distribuzione geografica
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Continente #
EU - Europa 69
NA - Nord America 24
AS - Asia 22
OC - Oceania 1
Totale 116
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Nazione #
IT - Italia 33
US - Stati Uniti d'America 22
IE - Irlanda 15
IN - India 15
CN - Cina 6
NL - Olanda 6
DE - Germania 5
CZ - Repubblica Ceca 3
GB - Regno Unito 3
CA - Canada 2
FR - Francia 2
AU - Australia 1
KR - Corea 1
LT - Lituania 1
MK - Macedonia 1
Totale 116
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Città #
Dublin 14
Foggia 11
Ghisalba 5
Zwolle 5
Coimbatore 4
Bari 3
Bedford 3
Mannheim 3
Medford 3
San Jose 3
Boardman 2
Chicago 2
Columbus 2
Council Bluffs 2
Hamburg 2
Lucera 2
Adelaide 1
Ashburn 1
Baricella 1
Dreux 1
Florence 1
Fontebuona 1
Gangnam-gu 1
Houston 1
Indore 1
Kildare 1
Los Angeles 1
Montreal 1
Naples 1
New Delhi 1
New York 1
Palo del Colle 1
Prague 1
San Severo 1
Skopje 1
Toronto 1
Turin 1
Vilnius 1
Totale 88
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Nome #
Angiopoietin-1 haploinsufficiency affects the endothelial barrier and causes hereditary angioedema, file 2837cc69-0807-4a38-b28a-c4fc6bdf56eb 33
A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α2-antiplasmin) deficiency in an Italian patient, file de2a6390-2f03-8577-e053-3705fe0aa5f3 25
In vitroresidual activity of phenylalanine hydroxylase variants and correlation with metabolic phenotypes in PKU, file de2a638f-65eb-8577-e053-3705fe0aa5f3 18
Double de novo mutations in dilated cardiomyopathy with cardiac arrest, file de2a6390-2f7a-8577-e053-3705fe0aa5f3 12
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism, file 7b800b31-60bc-4b8a-b226-dd6246500364 8
Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema., file de2a6390-e02d-8577-e053-3705fe0aa5f3 5
THE MOLECULAR ORGANIZATION OF ENDOTHELIAL JUNCTIONS IN VASCULAR PERMEABILITY, file de2a6390-eb17-8577-e053-3705fe0aa5f3 4
null, file de2a638e-f88d-8577-e053-3705fe0aa5f3 2
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism, file 0f8fce2d-3f22-4723-9651-5c20f652b7ab 1
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A., file de2a638e-f87d-8577-e053-3705fe0aa5f3 1
Identification of GLA gene deletions in Fabry patients by Multiplex Ligation-dependent Probe Amplification (MLPA), file de2a638e-fc19-8577-e053-3705fe0aa5f3 1
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification, file de2a638e-fcce-8577-e053-3705fe0aa5f3 1
Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia, file de2a638f-778d-8577-e053-3705fe0aa5f3 1
null, file de2a6390-4233-8577-e053-3705fe0aa5f3 1
Towards the genetic basis of cerebral venous thrombosis-the BEAST Consortium: a study protocol., file de2a6390-cdd1-8577-e053-3705fe0aa5f3 1
A New SERPINA-1 Missense Mutation Associated with Alpha-1 Antitrypsin Deficiency and Bronchiectasis, file de2a6390-d647-8577-e053-3705fe0aa5f3 1
The Genetics of Hereditary Angioedema: A Review, file de2a6390-e86f-8577-e053-3705fe0aa5f3 1
Totale 116
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Categoria #
all - tutte 370
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 370
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20228 0 0 3 0 0 0 0 0 0 0 1 4
2022/202378 0 1 10 8 4 15 6 4 16 7 6 1
2023/202423 0 4 1 2 5 2 3 1 2 1 2 0
Totale 116