IRIS Institutional Research Information System - OPENBS Open Archive UniBS

MORI, Luigi
 Distribuzione geografica
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Continente #
NA - Nord America 1.011
EU - Europa 624
AS - Asia 249
AF - Africa 1
OC - Oceania 1
SA - Sud America 1
Totale 1.887
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Nazione #
US - Stati Uniti d'America 1.010
CN - Cina 168
DE - Germania 166
UA - Ucraina 124
PL - Polonia 98
IT - Italia 63
FI - Finlandia 52
GB - Regno Unito 40
HK - Hong Kong 34
IN - India 27
RU - Federazione Russa 26
IE - Irlanda 19
FR - Francia 16
SE - Svezia 11
BE - Belgio 8
SG - Singapore 7
TR - Turchia 6
VN - Vietnam 4
IR - Iran 2
AR - Argentina 1
AU - Australia 1
CA - Canada 1
JP - Giappone 1
NL - Olanda 1
SD - Sudan 1
Totale 1.887
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Città #
Fairfield 134
Warsaw 98
Jacksonville 95
Woodbridge 82
Chandler 78
Ann Arbor 73
Ashburn 73
Cambridge 65
Seattle 65
Houston 59
Wilmington 47
Princeton 40
Beijing 38
Hong Kong 34
Helsinki 33
Nanjing 32
New York 31
Brescia 24
Dublin 19
Hebei 13
Shenyang 13
Tianjin 10
Des Moines 9
Brussels 8
Nanchang 8
Changsha 7
Jiaxing 7
Kocaeli 6
Milan 6
Ningbo 6
San Diego 6
Zhengzhou 6
Jinan 5
Nürnberg 5
Dong Ket 4
Hangzhou 4
San Francisco 4
Shanghai 4
Kunming 3
Lanzhou 3
London 3
Varallo Pombia 3
Verona 3
Fuzhou 2
Grafing 2
Guangzhou 2
Indiana 2
Kilburn 2
Lodi 2
Palermo 2
Prescot 2
Redmond 2
Rocca Di Papa 2
Taizhou 2
Treviso 2
Amsterdam 1
Ardabil 1
Bergamo 1
Boardman 1
Canberra 1
Cevo 1
Changchun 1
Frankfurt am Main 1
Gunzenhausen 1
Haikou 1
Hanover 1
Hyderabad 1
Islington 1
Lappeenranta 1
Los Angeles 1
Montichiari 1
New Bedfont 1
Norwalk 1
Palermiti 1
Paris 1
Pars 1
Phoenix 1
Pune 1
Redwood City 1
Salerno 1
Santa Clara 1
Singapore 1
Sochi 1
Tokyo 1
Toronto 1
Tower Hamlets 1
Walnut 1
Totale 1.322
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Nome #
Genetic mutation screening in an Italian cohort of nonsyndromic pheochromocytoma/paraganglioma patients 241
Genetic mutation screening in an Italian cohort of non-syndromic pheochromocytoma/paraganglioma patients. 138
Should we screen non-syndromic pheochromocytoma paraganglioma patients for succinate dehydrogenase mutations? 121
Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome 110
MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma. 109
Relationship Between Different Subpopulations of Circulating CD4+ T-lymphocytes and Microvascular Structural Alterations in Humans 109
Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas. 101
Relationship between different subpopulations of circulating CD4+ T lymphocytes and microvascular or systemic oxidative stress in humans 100
p.Ser891Ala RET gene mutations in medullary thyroid cancer: Phenotypical and genealogical characterization of 28 apparently unrelated kindreds and founder effect uncovering in Northern Italy 98
BASSA PENETRANZA E SPICCATA VARIABILITÀ FENOTIPICA IN UNA NUOVA MUTAZIONE CON EFFETTO FONDATORE ASSOCIATA A FEOCROMOCITOMA/PARAGANGLIOMA. 95
Revised sequence of the alpha 1B adrenergic receptor promoter region. 93
Clinically guided genetic screening in a large cohort of Italian patients with pheochromocytomas and/or functional or non-functional paragangliomas. 92
RELATIONSHIP BETWEEN MICROVASCULAR STRUCTURE AND T REGULATORY LYMPHOCYTES OF SMALL RESISTANCE ARTERIES 86
RELATIONSHIP BETWEEN MICROVASCULAR T REGULATORY LYMPHOCYTES AND CIRCULATING LYMPHOCYTES 77
PHEOCHROMOCYTOMA MAY OCCUR IN KINDREDS WITH RET MUTATION ASSOCIATED WITH FAMILIAL MEDULLARY THYROID CARCINOMA (SER891ALA) 70
ASYMPTOMATIC BILATERAL PHEOCHROMOCYTOMA IN VHL MUTATION (VAL84LEU) CARRIER IDENTIFIED BY FAMILY GENETIC SCREENING 68
Differential activation of inflammatory and hypoxic pathways in visceral and subcutaneous adipose tissue in obese women. 67
Screening genetico per determinare la frequenza di grosse delezioni nei geni SDHx e VHL in una coorte italiana di pazienti affetti da Feocromocitoma/Paraganglioma. 65
Gene polymorphism of the 5-lipoxygenase (ALOX) pathway is not consistently associated with juvenile stroke or carotid atherosclerosis phenotypes in the Italian population 53
Clinical and dermoscopic changes of acquired melanocytic nevi of patients treated with afamelanotide 34
Totale 1.927
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Categoria #
all - tutte 7.496
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 7.496
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019104 0 0 0 0 0 0 0 0 0 0 50 54
2019/2020550 69 19 19 61 37 54 54 61 42 72 36 26
2020/2021288 6 31 7 35 12 42 6 34 38 42 21 14
2021/2022170 8 21 2 10 7 13 10 10 8 26 14 41
2022/2023236 23 6 3 13 27 44 0 31 41 2 22 24
2023/2024164 13 5 19 25 14 35 8 5 36 3 1 0
Totale 1.927