GHEZZI, DANIELE
 Distribuzione geografica
Continente #
NA - Nord America 1.058
EU - Europa 420
AS - Asia 249
SA - Sud America 3
OC - Oceania 2
Totale 1.732
Nazione #
US - Stati Uniti d'America 1.044
SG - Singapore 108
DE - Germania 92
CN - Cina 83
SE - Svezia 76
IE - Irlanda 68
RU - Federazione Russa 63
IT - Italia 47
HK - Hong Kong 32
GB - Regno Unito 21
UA - Ucraina 20
CA - Canada 14
FR - Francia 13
ID - Indonesia 12
FI - Finlandia 7
IN - India 7
AT - Austria 5
NL - Olanda 4
BR - Brasile 3
AU - Australia 2
BE - Belgio 2
AE - Emirati Arabi Uniti 1
CZ - Repubblica Ceca 1
IL - Israele 1
IQ - Iraq 1
IR - Iran 1
JP - Giappone 1
PH - Filippine 1
RO - Romania 1
TW - Taiwan 1
Totale 1.732
Città #
Fairfield 154
Chandler 114
Ann Arbor 107
Ashburn 76
Woodbridge 69
Dublin 65
Singapore 64
Cambridge 59
Frankfurt am Main 56
Seattle 53
Houston 48
Wilmington 46
Hong Kong 31
New York 26
Princeton 24
Santa Clara 21
Jacksonville 18
Milan 14
Beijing 13
Altamura 12
Jakarta 12
Lawrence 11
Shanghai 10
Fremont 8
Norwalk 8
Ottawa 8
Nanjing 7
Phoenix 7
Hebei 6
Helsinki 6
Buffalo 5
Toronto 5
Andover 4
Cagliari 4
Changsha 4
Chicago 4
Guangzhou 4
Jinan 4
Shenyang 4
Hangzhou 3
Nanchang 3
Rome 3
San Diego 3
Bel Air 2
Bonndorf 2
Brussels 2
Council Bluffs 2
Dallas 2
Dearborn 2
East Lansing 2
Erfurt 2
Hefei 2
Kunming 2
London 2
Los Angeles 2
Nuremberg 2
Philadelphia 2
Silver Spring 2
São Paulo 2
Upper Marlboro 2
Vitry-sur-Seine 2
Washington 2
Anderson 1
Arnsberg 1
Baghdad 1
Belfast 1
Boardman 1
Boiling Springs 1
Brno 1
Brugherio 1
Chengdu 1
Chongqing 1
Dubai 1
Edinburgh 1
Falls Church 1
Florence 1
Hampton 1
Jiaxing 1
Jinhua 1
Kansas City 1
Lachine 1
Leawood 1
Malmo 1
Manila 1
Medolago 1
Moscow 1
Mountain View 1
Mumbai 1
Ningbo 1
Palermo 1
Parma 1
Pune 1
Puyang Chengguanzhen 1
Queens 1
Quzhou 1
Redmond 1
Salt Lake City 1
Satsuma 1
Strasbourg 1
Sydney 1
Totale 1.279
Nome #
A slowly progressive mitochondrial encephalomyopathy widens the spectrum of AIFM1 disorders 217
Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: Is riboflavin supplementation effective? 159
Identification and characterization of nuclear genes responsible for human mitochondrial disorders: fastkd2, responsible for a neurological disease associated with cox defiency and sdhaf1, encoding a complex II assembly, mutated in SDH-defective leukoencephalopaty 155
LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance 152
Mitochondrial leukoencephalopathy and complex II deficiency associated with a recessive SDHB mutation with reduced penetrance 149
KARS-related diseases: Progressive leukoencephalopathy with brainstem and spinal cord calcifications as new phenotype and a review of literature 144
Compound heterozygous missense and deep intronic variants in NDUFAF6 unraveled by exome sequencing and mRNA analysis 138
New genes and pathomechanisms in mitochondrial disorders unraveled by NGS technologies 136
Clinical, biochemical, and genetic features associated with VARS2-related mitochondrial disease 136
Neurologic phenotypes associated with mutations in RTN4IP1 (OPA10) in children and young adults 132
Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations 128
Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutations 123
Totale 1.769
Categoria #
all - tutte 7.207
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 7.207


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202042 0 0 0 0 0 0 0 0 0 17 16 9
2020/2021228 6 12 35 29 36 24 11 18 12 24 11 10
2021/2022124 14 14 20 6 2 11 9 9 3 8 13 15
2022/2023363 27 129 14 47 19 43 0 31 34 3 10 6
2023/2024189 3 7 1 24 13 46 52 6 11 1 2 23
2024/2025307 14 47 26 14 44 17 16 7 57 65 0 0
Totale 1.769