CRIS Current Research Information System

GARONE, CATERINA
 Distribuzione geografica
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Continente #
EU - Europa 4.708
NA - Nord America 3.928
AS - Asia 3.447
SA - Sud America 234
AF - Africa 135
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 3
Totale 12.463
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Nazione #
US - Stati Uniti d'America 3.878
IT - Italia 2.482
SG - Singapore 1.022
CN - Cina 861
VN - Vietnam 770
GB - Regno Unito 500
DE - Germania 367
FR - Francia 237
HK - Hong Kong 235
SE - Svezia 190
IN - India 187
UA - Ucraina 181
NL - Olanda 160
BR - Brasile 159
RU - Federazione Russa 141
FI - Finlandia 130
KR - Corea 106
IE - Irlanda 100
JP - Giappone 83
ES - Italia 49
ZA - Sudafrica 43
AR - Argentina 34
AT - Austria 32
BD - Bangladesh 31
EE - Estonia 30
CA - Canada 29
SC - Seychelles 29
ID - Indonesia 21
CH - Svizzera 19
CI - Costa d'Avorio 18
TG - Togo 16
IQ - Iraq 15
PL - Polonia 15
BE - Belgio 13
PH - Filippine 13
PK - Pakistan 12
TH - Thailandia 12
CL - Cile 11
EC - Ecuador 11
TR - Turchia 11
MX - Messico 10
JO - Giordania 9
LB - Libano 9
ME - Montenegro 8
BG - Bulgaria 7
TW - Taiwan 7
AE - Emirati Arabi Uniti 6
AL - Albania 6
AU - Australia 6
CO - Colombia 6
IR - Iran 6
MY - Malesia 6
UZ - Uzbekistan 6
VE - Venezuela 6
GR - Grecia 5
LT - Lituania 5
SA - Arabia Saudita 5
AZ - Azerbaigian 4
CR - Costa Rica 4
CZ - Repubblica Ceca 4
HU - Ungheria 4
MA - Marocco 4
SK - Slovacchia (Repubblica Slovacca) 4
BO - Bolivia 3
KE - Kenya 3
MZ - Mozambico 3
NG - Nigeria 3
PE - Perù 3
RO - Romania 3
TN - Tunisia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BZ - Belize 2
DZ - Algeria 2
EG - Egitto 2
HR - Croazia 2
LK - Sri Lanka 2
MC - Monaco 2
MT - Malta 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
PR - Porto Rico 2
PT - Portogallo 2
SM - San Marino 2
AO - Angola 1
BJ - Benin 1
BN - Brunei Darussalam 1
BS - Bahamas 1
BY - Bielorussia 1
ET - Etiopia 1
GH - Ghana 1
JM - Giamaica 1
KG - Kirghizistan 1
KW - Kuwait 1
KZ - Kazakistan 1
LU - Lussemburgo 1
LY - Libia 1
MD - Moldavia 1
MG - Madagascar 1
MK - Macedonia 1
NE - Niger 1
Totale 12.454
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Città #
Singapore 717
Southend 409
Ashburn 307
Santa Clara 302
Fairfield 299
Chandler 260
Hong Kong 219
Bologna 214
Hefei 204
San Jose 194
Ho Chi Minh City 169
Milan 163
Hanoi 151
Rome 151
Woodbridge 148
Seattle 143
Wilmington 143
Houston 134
Princeton 134
Jacksonville 124
Helsinki 115
Cambridge 101
Dublin 100
Seoul 98
Ann Arbor 85
Boardman 85
Dong Ket 78
Beijing 76
Tokyo 76
Naples 71
Lauterbourg 68
Westminster 61
Los Angeles 53
New York 53
Padova 53
Turin 50
Redmond 46
Berlin 45
Buffalo 42
Dallas 40
Da Nang 37
Council Bluffs 36
Nanjing 36
Florence 29
Jinan 28
São Paulo 26
Des Moines 25
Guangzhou 24
San Diego 24
Modena 23
Haiphong 22
Redondo Beach 22
Saint Petersburg 22
Catania 21
Palermo 21
Verona 21
Bagnacavallo 20
Bengaluru 20
Frankfurt am Main 20
Parma 20
Mülheim 19
Abidjan 18
Genoa 18
Medford 18
Nuremberg 18
Shanghai 17
Shenyang 17
Toronto 17
Lomé 16
Nanchang 16
Norwalk 16
Tianjin 16
Moscow 15
Rimini 15
Amsterdam 14
Bari 14
Changsha 14
Redwood City 14
Reggio Emilia 14
Vicenza 14
Brescia 13
Brussels 13
Dearborn 13
Falkenstein 13
London 13
Mahé 13
Phoenix 13
Vienna 13
Zhengzhou 13
Ancona 12
Falls Church 12
Jakarta 12
Madrid 12
Hải Dương 11
Yubileyny 11
Bergamo 10
Chicago 10
Hangzhou 10
Lappeenranta 10
The Dalles 10
Totale 7.035
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Nome #
Pelizaeus-Merzbacher: aspetti clinici, genetici e di neuroimaging 686
Eventi parossistici epilettici e non-epilettici: un caso clinico emblematico per la diagnosi differenziale. 678
EFFICACIA DEL LEVETIRACETAM IN UN CASO DI ESES SECONDARIO A DISPLASIA CORTICALE. 646
Regressione psicomotoria, tetraparesi spastica, atrofia cerebellare: un nuovo caso di leucodistrofia neuroassonale? 519
Evidence of enteric angiopathy and neuromuscular hypoxia in patients with mitochondrial neurogastrointestinal encephalomyopathy 259
COQ7 defect causes prenatal onset of mitochondrial CoQ10 deficiency with cardiomyopathy and gastrointestinal obstruction 254
Deoxynucleoside Therapy for Thymidine Kinase 2–Deficient Myopathy 235
A new case of idiopathic hemiplegia hemiconvulsion syndrome 214
Mitochondrial metabolism in neural stem cells and implications for neurodevelopmental and neurodegenerative diseases 213
Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes 207
Natural History of Patients With Mitochondrial ATPase Deficiency Due to Pathogenic Variants of MT-ATP6 and MT-ATP8 206
The Transcriptome of SH-SY5Y at Single-Cell Resolution: A CITE-Seq Data Analysis Workflow 206
FA2H-related disorders: a novel c.270+3A>T splice-site mutation leads to a complex neurodegenerative phenotype. 204
Deoxyguanosine kinase deficiency: natural history and liver transplant outcome 200
Preliminary report on effects of oxcarbazepine-treatment on serum lipid levels in children. 195
Malformazioni dello sviluppo del lobo temporale, epilessia ed autismo 195
Novel compound heterozygous pathogenic variants in nucleotide-binding protein like protein (NUBPL) cause leukoencephalopathy with multi-systemic involvement 194
Infantile TK2 Deficiency Causing Mitochondrial Encephalomyopathy With Migrating Focal Seizures 193
Prospective study on long-term treatment with oxcarbazepine in pediatric epilepsy. 182
An unusual diagnosis in a child suffering from juvenile Alexander disease: a clinical and imaging report. 179
Fever as a seizure precipitant factor in Panayiotopoulos syndrome: A clinical and genetic study 175
Intracerebral large artery disease in Aicardi-Goutières syndrome implicates SAMHD1 in vascular homeostasis 173
SAFA: A new measure to evaluate psychiatric symptoms detected in a sample of children and adolescents affected by eating disorders. Correlations with risk factors. 167
Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN). 166
From the Structural and (Dys)Function of ATP Synthase to Deficiency in Age-Related Diseases 163
Expanding the Clinical Spectrum of UBTF-Related Neurodevelopmental Disorder 162
Topiramate: effects on serum lipids and lipoproteins levels in children. 161
Complicanze neurologiche a lungo termine 159
NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAs 158
EPILESSIE DEL LOBO OCCIPITALE IN ETA’ PEDIATRICA 154
Unusual brain lesion in a case of restrictive anorexia nervosa. 154
Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies 153
A late-stage assembly checkpoint of the human mitochondrial ribosome large subunit 153
Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy 149
Retrospective natural history of thymidine kinase 2 deficiency 147
Lo stroke in età pediatrica 145
Deoxycytidine and Deoxythymidine Treatment for Thymidine Kinase 2 Deficiency 145
Efficacia e tollerabilità dell'oxcarbazepina in età pediatrica: studio prospettico 143
No kinetic interaction between levetiracetam and cyclosporine: a case report. 142
Clinical and pharmacological approaches of status epilepticus in children: Personal experience. Minerva Psichiatrica 142
I disturbi del comportamento alimentare in età evolutiva 141
Open prospective study on oxcarbazepine monotherapy in children with epilepsy: a preliminary report. 140
Epilessie Miocloniche: forme idiopatiche Benigne 140
Levetiracetam or oxcarbazepine as monotherapy in newly diagnosed benign epilepsy of childhood with centrotemporal spikes (BECTS): an open-label, parallel group trial. 140
Mitochondrial Neurogastrointestinal Encephalomyopathy: Into the Fourth Decade, What We Have Learned So Far 140
I Disturbi del Comportamento Alimentare in età evolutiva 137
Epilessia del lobo temporale sintomatica: evoluzione clinica, neuropsicologica e neuroradiologica 136
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus 128
Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family 127
Le cefalee in età evolutiva 125
Towards a therapy for mitochondrial disease: An update 122
A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement Disorder 120
FGF21 underlies a hormetic response to metabolic stress in methylmalonic acidemia 118
Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome 113
Metabolic disorders of fetal life: Glycogenoses and mitochondrial defects of the mitochondrial respiratory chain 110
CoQ 10 deficiencies and MNGIE: Two treatable mitochondrial disorders 110
Deoxynucleoside stress exacerbates the phenotype of a mouse model of mitochondrial neurogastrointestinal encephalopathy 110
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions 104
SARS-CoV-2 infection in patients with primary mitochondrial diseases: Features and outcomes in Italy 103
TMEM14C is required for erythroid mitochondrial heme metabolism 102
Fhl1 W122S causes loss of protein function and late-onset mild myopathy 102
Deoxypyrimidine monophosphate bypass therapy for thymidine kinase 2 deficiency 101
Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia 100
Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4 98
Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing 97
MPV17 mutations causing adult-onset multisystemic disorder with multiple mitochondrial DNA deletions 91
Mitochondrial encephalomyopathy due to a novel mutation in ACAD9 91
Requirement of enhanced Survival Motoneuron protein imposed during neuromuscular junction maturation 90
Historical perspective on mitochondrial medicine 89
Sindrome 22q13:descrizione di due casi clinici 84
Sindrome de Landau Kleffner et troubles specifique du language: description de deux cases dans la meme famille 82
Metabolic myopathies 77
mtDNA maintenance: Disease and therapy 64
Tissue-specific oxidative stress and loss of mitochondria in CoQ-deficient Pdss2 mutant mice 54
Gene therapy and mRNA drugs approach for mitochondrial OXPHOS deficiencies 32
Totale 12.694
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Categoria #
all - tutte 33.153
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 33.153
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021290 0 0 0 0 0 0 0 0 0 0 72 218
2021/20221.349 94 65 88 107 127 66 33 86 63 92 328 200
2022/20231.357 106 128 70 162 144 98 67 94 223 57 142 66
2023/2024873 70 108 71 77 64 67 46 78 47 77 90 78
2024/20252.539 130 310 278 174 473 233 170 78 133 112 106 342
2025/20263.787 282 370 356 242 461 258 482 130 679 345 182 0
Totale 12.694