PATRONE, SERENA
 Distribuzione geografica
Continente #
EU - Europa 1.413
AS - Asia 111
NA - Nord America 25
SA - Sud America 11
AF - Africa 1
Totale 1.561
Nazione #
IT - Italia 1.405
SG - Singapore 46
CN - Cina 30
VN - Vietnam 29
US - Stati Uniti d'America 20
BR - Brasile 7
MX - Messico 5
AR - Argentina 3
HK - Hong Kong 3
ES - Italia 2
GB - Regno Unito 2
CL - Cile 1
DE - Germania 1
IL - Israele 1
JP - Giappone 1
KZ - Kazakistan 1
PL - Polonia 1
RU - Federazione Russa 1
TN - Tunisia 1
UA - Ucraina 1
Totale 1.561
Città #
Genoa 797
Genova 300
Vado Ligure 170
Rapallo 134
Ho Chi Minh City 12
Hanoi 10
Singapore 10
Beijing 8
Ashburn 5
Bordighera 4
Mexico City 4
Hong Kong 3
Manchester 2
New York 2
Almaty 1
Aryanah 1
Biên Hòa 1
Bắc Giang 1
Bắc Ninh 1
Da Nang 1
Dallas 1
Freiburg im Breisgau 1
Fuzhou 1
Guapiaçu 1
Itapetinga 1
Ituzaingó 1
Los Angeles 1
Morón 1
Orem 1
Ouro Fino 1
Petrolina 1
Phoenix 1
Pirapora 1
Querétaro 1
Quận Bình Thạnh 1
Recife 1
San Jose 1
Santiago 1
Santiago del Estero 1
Serpukhov 1
Shijiazhuang 1
Tatuí 1
Tianjin 1
Tokyo 1
Warsaw 1
Yuncheng 1
Totale 1.493
Nome #
Prognostic value of chromosomal imbalances, gene mutations, and BAP1 expression in uveal melanoma 218
Prognostic value of specific chromosome imbalances, mutation profile, and BAP1 expression in uveal melanoma 198
Secondary Somatic Mutations in G-Protein-Related Pathways and Mutation Signatures in Uveal Melanoma 156
Genetic Workup for Charcot–Marie–Tooth Neuropathy: A Retrospective Single-Site Experience Covering 15 Years 144
How many mutations does it take to make a uveal melanoma? 125
An integrated approach to the evaluation of patients with asymptomatic or minimally symptomatic hyperCKemia 101
ROLE OF MME IN LATE ONSET AXONAL CMT: ANALYSIS OF AN ITALIAN CMT2 COHORT 94
A CASE OF BIALLELIC SORD MUTATIONS ASSOCIATED WITH DISTAL WEAKNESS AND HISTOLOGICAL SIGNS OF MYOPATHY 85
A PROPOSAL FOR IMPROVEMENT OF ACMG GUIDELINES FOR VARIANTS EVALUATION IN CHARCOT-MARIE-TOOTH DISEASE MOLECULAR DIAGNOSIS 84
Skeletal muscle involvement in biallelic SORD mutations: case report and review of the literature 75
A misleading presentation of Mohr–Tranebjaerg syndrome: what is hidden behind an axonal neuropathy? 75
Early Onset Inherited Peripheral Neuropathies: The Experience of a Specialized Referral Center for Genetic Diagnosis Achievement 70
Next-generation sequencing in Charcot-Marie-Tooth: a proposal for improvement of ACMG guidelines for variant evaluation 70
Case report: Episodic ataxia without ataxia? 59
null 35
Case report: A single novel calpain 3 gene variant associated with mild myopathy 20
Totale 1.609
Categoria #
all - tutte 5.882
article - articoli 5.414
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 11.296


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202134 0 0 0 0 0 6 1 9 0 6 7 5
2021/2022120 7 8 10 4 3 4 10 17 10 11 20 16
2022/2023154 6 10 1 12 14 24 8 18 20 5 30 6
2023/2024233 17 6 11 43 11 37 13 15 16 14 14 36
2024/2025495 16 28 11 40 61 33 48 101 31 28 48 50
2025/2026401 109 29 56 75 122 10 0 0 0 0 0 0
Totale 1.609