GHEZZI, DANIELE
 Distribuzione geografica
Continente #
NA - Nord America 1.025
EU - Europa 369
AS - Asia 170
OC - Oceania 2
SA - Sud America 1
Totale 1.567
Nazione #
US - Stati Uniti d'America 1.011
DE - Germania 85
CN - Cina 76
SE - Svezia 76
IE - Irlanda 68
SG - Singapore 56
IT - Italia 46
RU - Federazione Russa 32
GB - Regno Unito 21
UA - Ucraina 18
HK - Hong Kong 17
CA - Canada 14
FR - Francia 11
ID - Indonesia 8
FI - Finlandia 7
IN - India 7
AU - Australia 2
BE - Belgio 2
AE - Emirati Arabi Uniti 1
BR - Brasile 1
CZ - Repubblica Ceca 1
IL - Israele 1
IR - Iran 1
JP - Giappone 1
NL - Olanda 1
PH - Filippine 1
RO - Romania 1
TW - Taiwan 1
Totale 1.567
Città #
Fairfield 154
Chandler 114
Ann Arbor 107
Ashburn 76
Woodbridge 69
Dublin 65
Cambridge 59
Frankfurt am Main 56
Seattle 53
Houston 48
Singapore 48
Wilmington 46
New York 24
Princeton 24
Santa Clara 20
Jacksonville 18
Hong Kong 16
Milan 14
Beijing 13
Altamura 12
Lawrence 11
Fremont 8
Jakarta 8
Norwalk 8
Ottawa 8
Shanghai 8
Nanjing 7
Phoenix 7
Hebei 6
Helsinki 6
Toronto 5
Andover 4
Cagliari 4
Changsha 4
Guangzhou 4
Jinan 4
Shenyang 4
Hangzhou 3
Nanchang 3
Rome 3
San Diego 3
Bel Air 2
Bonndorf 2
Brussels 2
Dallas 2
Dearborn 2
East Lansing 2
Erfurt 2
Hefei 2
Kunming 2
London 2
Philadelphia 2
Upper Marlboro 2
Washington 2
Anderson 1
Arnsberg 1
Belfast 1
Boardman 1
Boiling Springs 1
Brno 1
Brugherio 1
Chengdu 1
Chongqing 1
Dubai 1
Edinburgh 1
Falls Church 1
Hampton 1
Jiaxing 1
Jinhua 1
Lachine 1
Leawood 1
Malmo 1
Manila 1
Medolago 1
Mountain View 1
Mumbai 1
Ningbo 1
Palermo 1
Parma 1
Pune 1
Queens 1
Quzhou 1
Redmond 1
Satsuma 1
Strasbourg 1
Sydney 1
São Paulo 1
Tacoma 1
Taipei 1
Taizhou 1
Tel Aviv 1
Tianjin 1
Wenzhou 1
Wuhan 1
Xian 1
Zanjan 1
Totale 1.222
Nome #
A slowly progressive mitochondrial encephalomyopathy widens the spectrum of AIFM1 disorders 207
Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: Is riboflavin supplementation effective? 146
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 145
LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance 132
Clinical, biochemical, and genetic features associated with VARS2-related mitochondrial disease 129
KARS-related diseases: Progressive leukoencephalopathy with brainstem and spinal cord calcifications as new phenotype and a review of literature 128
Neurologic phenotypes associated with mutations in RTN4IP1 (OPA10) in children and young adults 124
Compound heterozygous missense and deep intronic variants in NDUFAF6 unraveled by exome sequencing and mRNA analysis 122
New genes and pathomechanisms in mitochondrial disorders unraveled by NGS technologies 122
Mitochondrial leukoencephalopathy and complex II deficiency associated with a recessive SDHB mutation with reduced penetrance 121
Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations 116
Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutations 112
Totale 1.604
Categoria #
all - tutte 5.981
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 5.981


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020213 0 0 0 0 28 24 39 34 46 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
2024/2025142 14 47 26 14 41 0 0 0 0 0 0 0
Totale 1.604