IRIS
AMORINI, MARIA
 Distribuzione geografica
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Continente #
NA - Nord America 443
EU - Europa 407
AS - Asia 114
Totale 964
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Nazione #
US - Stati Uniti d'America 443
SE - Svezia 131
IE - Irlanda 110
CN - Cina 77
IT - Italia 52
SG - Singapore 31
GB - Regno Unito 28
FI - Finlandia 25
DE - Germania 18
BE - Belgio 16
UA - Ucraina 16
FR - Francia 7
IN - India 4
IQ - Iraq 2
NL - Olanda 2
AT - Austria 1
HU - Ungheria 1
Totale 964
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Città #
Dublin 110
Chandler 88
Nyköping 52
Ann Arbor 50
Jacksonville 44
Ashburn 41
Beijing 34
Singapore 28
Messina 25
Dearborn 19
Princeton 17
Cambridge 16
Medford 16
Brussels 15
Des Moines 14
Lancaster 12
Boardman 11
Woodbridge 9
Houston 7
Shenyang 7
New York 6
Espoo 5
Jinan 4
Los Angeles 4
Pune 4
San Mateo 4
Barga 3
Helsinki 3
Nanchang 3
Ningbo 3
Bremen 2
Butera 2
Changsha 2
Fuzhou 2
Haikou 2
Hangzhou 2
Hebei 2
Jiaxing 2
Lappeenranta 2
Shanghai 2
Taizhou 2
Washington 2
Wilmington 2
Bitonto 1
Clifton 1
Kunming 1
Lanzhou 1
Munich 1
Nanjing 1
Santa Clara 1
Sopron 1
Strasbourg 1
Tappahannock 1
Vienna 1
Waanrode 1
Zhengzhou 1
Totale 693
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Nome #
Co-inheritance of Hb Hershey [beta70(E14) Ala-->Gly] and Hb La Pommeraie [beta133(H11)Val-->Met] in a Sicilian subject 98
Concomitant inheritance of globin defects: results of a survey family 72
TLR4 and NOD2/CARD15 genetic polymorphisms and their possible role in gastric carcinogenesis. 71
Diagnostica molecolare della fibrosi cistica 71
Uteroglobin-related protein 1 gene -112G/a polymorphism and atopic asthma in Sicilian children. 68
Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease. 67
Filaggrin mutations and Molluscum contagiosum skin infection in patients with atopic dermatitis 64
Mutations in TMEM216 cause Joubert (JBTS2), Meckel (MKS2) and related syndromes 62
Correlation between serum ICAM-1 and oxidative stress in patients with β-thalassemia Major 62
Endocrinopathies, metabolic disorders, and iron overload in major and intermedia thalassemia: Serum ferritin as diagnostic and predictive marker associated with liver and cardiac T2* MRI assessment 61
Molecular analysis of toll-like receptor gene in patients with β-thalassemia 56
CEP290 Mutations Are Frequently Identified in the Oculo-Renal Form of Joubert Syndrome Related Disorders 52
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders 49
Microsatellite-based genotyping of Candida parapsilosis sensu stricto isolates reveals dominance and persistence of a particular epidemiological clone among neonatal intensive care unit patients. 46
Familial Mediterranean fever: genetic and immunological aspects 41
LMNA gene mutation as a model of cardiometabolic dysfunction: From genetic analysis to treatment response. 28
null 23
Totale 991
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Categoria #
all - tutte 4.097
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 4.097
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020121 0 0 0 0 0 28 22 8 12 21 26 4
2020/2021120 12 0 17 11 5 13 2 2 18 19 10 11
2021/2022148 2 8 3 7 3 2 20 3 3 41 16 40
2022/2023325 27 42 14 21 29 25 7 13 134 1 10 2
2023/202494 9 9 2 21 8 21 4 8 0 2 2 8
2024/202552 4 8 2 29 9 0 0 0 0 0 0 0
Totale 991