GAUDIO, ANDREA
 Distribuzione geografica
Continente #
EU - Europa 511
AS - Asia 148
NA - Nord America 53
SA - Sud America 12
AF - Africa 6
Totale 730
Nazione #
IT - Italia 487
SG - Singapore 58
US - Stati Uniti d'America 52
CN - Cina 41
VN - Vietnam 32
AR - Argentina 5
FR - Francia 5
BR - Brasile 4
DE - Germania 4
GB - Regno Unito 3
IQ - Iraq 3
NL - Olanda 3
BD - Bangladesh 2
CO - Colombia 2
FI - Finlandia 2
HK - Hong Kong 2
IN - India 2
KZ - Kazakistan 2
UZ - Uzbekistan 2
ZA - Sudafrica 2
AO - Angola 1
BW - Botswana 1
EC - Ecuador 1
EG - Egitto 1
ES - Italia 1
IE - Irlanda 1
JP - Giappone 1
KG - Kirghizistan 1
LT - Lituania 1
MX - Messico 1
NG - Nigeria 1
PK - Pakistan 1
RO - Romania 1
RU - Federazione Russa 1
SK - Slovacchia (Repubblica Slovacca) 1
TR - Turchia 1
UA - Ucraina 1
Totale 730
Città #
Genoa 394
Vado Ligure 71
Singapore 30
San Jose 19
Beijing 10
Ho Chi Minh City 9
Hanoi 8
Ashburn 6
Frankfurt am Main 4
Haiphong 4
Lauterbourg 4
Amsterdam 2
Baghdad 2
Bordighera 2
Chicago 2
City of London 2
Council Bluffs 2
Da Nang 2
Los Angeles 2
Prato 2
Almaty 1
Bishkek 1
Bursa 1
Bắc Ninh 1
Bến Tre 1
Cairo 1
Campo Quijano 1
Cape Town 1
Casilda 1
Changshu 1
Chennai 1
Chumbicha 1
Columbia 1
Concord 1
Conway 1
Curitiba 1
Dublin 1
El Viso de San Juan 1
Francisco I. Madero 1
Gaborone 1
Hangzhou 1
Helsinki 1
Hong Kong 1
Johannesburg 1
Kharian 1
Lappeenranta 1
London 1
Luanda 1
Manizales 1
Medellín 1
Milan 1
Morón 1
Mosul 1
Murom 1
New York 1
Nậm Dinh 1
Ouro Fino 1
Paracuru 1
Paris 1
Phú Nhuận 1
Quận Chín 1
Rosario 1
Shijiazhuang 1
Tashkent 1
Tatuí 1
Temecula 1
Tena 1
Thrissur 1
Thái Nguyên 1
Tokyo 1
Tornaľa 1
Ust-Kamenogorsk 1
West Haven 1
Yangiyer 1
Totale 631
Nome #
ROLE OF MME IN LATE ONSET AXONAL CMT: ANALYSIS OF AN ITALIAN CMT2 COHORT 117
A PROPOSAL FOR IMPROVEMENT OF ACMG GUIDELINES FOR VARIANTS EVALUATION IN CHARCOT-MARIE-TOOTH DISEASE MOLECULAR DIAGNOSIS 113
Clinical and genetic features of CMT2T in Italian patients confirm the importance of MME pathogenic variants in idiopathic, late‐onset axonal neuropathies 108
Next-generation sequencing in Charcot-Marie-Tooth: a proposal for improvement of ACMG guidelines for variant evaluation 95
Early Onset Inherited Peripheral Neuropathies: The Experience of a Specialized Referral Center for Genetic Diagnosis Achievement 87
Case report: Episodic ataxia without ataxia? 75
Harmonizing Genetic Testing for Parkinson's Disease: Results of the PARKNET Multicentric Study 58
The neurological core features of the infantile-onset multisystem neurologic, endocrine, and pancreatic disease: A novel nonsense mutation in an Italian family 52
Case report: A single novel calpain 3 gene variant associated with mild myopathy 44
Totale 749
Categoria #
all - tutte 2.434
article - articoli 2.434
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 4.868


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202466 0 0 2 23 2 3 3 2 7 9 2 13
2024/2025271 6 7 5 26 23 18 23 51 27 23 38 24
2025/2026412 67 27 28 46 55 21 59 37 34 38 0 0
Totale 749