CRIS Current Research Information System

GARONE, CATERINA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 4.334
NA - Nord America 3.437
AS - Asia 2.544
SA - Sud America 187
AF - Africa 111
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 3
Totale 10.623
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 3.402
IT - Italia 2.293
SG - Singapore 904
CN - Cina 757
GB - Regno Unito 491
DE - Germania 357
VN - Vietnam 289
HK - Hong Kong 201
SE - Svezia 189
UA - Ucraina 175
FR - Francia 169
IN - India 165
NL - Olanda 149
RU - Federazione Russa 139
BR - Brasile 128
KR - Corea 99
IE - Irlanda 97
FI - Finlandia 90
JP - Giappone 45
ES - Italia 41
ZA - Sudafrica 37
AR - Argentina 30
EE - Estonia 30
SC - Seychelles 29
AT - Austria 23
CA - Canada 20
CI - Costa d'Avorio 17
ID - Indonesia 17
CH - Svizzera 16
TG - Togo 16
BE - Belgio 13
PL - Polonia 12
CL - Cile 9
BD - Bangladesh 8
EC - Ecuador 8
JO - Giordania 8
ME - Montenegro 8
MX - Messico 8
BG - Bulgaria 7
LB - Libano 7
AE - Emirati Arabi Uniti 6
IR - Iran 6
AL - Albania 5
AU - Australia 5
CO - Colombia 5
IQ - Iraq 5
LT - Lituania 5
AZ - Azerbaigian 4
PK - Pakistan 4
TR - Turchia 4
VE - Venezuela 4
CR - Costa Rica 3
CZ - Repubblica Ceca 3
HU - Ungheria 3
MA - Marocco 3
MY - Malesia 3
MZ - Mozambico 3
RO - Romania 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BZ - Belize 2
GR - Grecia 2
LK - Sri Lanka 2
MC - Monaco 2
MT - Malta 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
PE - Perù 2
SM - San Marino 2
UZ - Uzbekistan 2
BJ - Benin 1
BN - Brunei Darussalam 1
BO - Bolivia 1
BS - Bahamas 1
BY - Bielorussia 1
KG - Kirghizistan 1
KW - Kuwait 1
KZ - Kazakistan 1
LU - Lussemburgo 1
MD - Moldavia 1
MK - Macedonia 1
NE - Niger 1
NG - Nigeria 1
PA - Panama 1
PH - Filippine 1
PS - Palestinian Territory 1
PT - Portogallo 1
SA - Arabia Saudita 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
SY - Repubblica araba siriana 1
TN - Tunisia 1
XK - ???statistics.table.value.countryCode.XK??? 1
ZM - Zambia 1
Totale 10.623
Salva come PNG Salva come JPEG
Città #
Singapore 610
Southend 409
Fairfield 299
Santa Clara 288
Ashburn 271
Chandler 260
Hefei 203
Hong Kong 200
Bologna 198
Milan 152
Woodbridge 148
Rome 143
Seattle 143
Wilmington 143
Princeton 134
Houston 133
Jacksonville 124
Cambridge 101
Seoul 98
Dublin 97
Ann Arbor 85
Boardman 85
Dong Ket 78
Helsinki 75
Beijing 69
Naples 68
Westminster 61
Ho Chi Minh City 53
Padova 53
Redmond 46
Berlin 45
Turin 44
Tokyo 43
Buffalo 39
Hanoi 39
Los Angeles 39
Dallas 34
Nanjing 34
Florence 28
Jinan 27
Des Moines 25
San Diego 24
New York 23
Redondo Beach 22
Saint Petersburg 22
Catania 21
Modena 21
Palermo 21
Bagnacavallo 20
Parma 20
São Paulo 20
Bengaluru 19
Mülheim 19
Verona 19
Guangzhou 18
Medford 18
Abidjan 17
Shenyang 17
Lomé 16
Nanchang 16
Norwalk 16
Nuremberg 16
Moscow 15
Bari 14
Genoa 14
Redwood City 14
Shanghai 14
Tianjin 14
Toronto 14
Brussels 13
Dearborn 13
Falkenstein 13
Frankfurt am Main 13
Mahé 13
Reggio Emilia 13
Vienna 13
Zhengzhou 13
Ancona 12
Changsha 12
Falls Church 12
Jakarta 12
Brescia 11
Yubileyny 11
Bergamo 10
Da Nang 10
Lappeenranta 10
London 10
Phoenix 10
Vicenza 10
Amsterdam 9
Cagliari 9
Paris 9
Ravenna 9
Treviso 9
Amman 8
Hangzhou 8
Jiaxing 8
Lauterbourg 8
Pisa 8
Podgorica 8
Totale 6.055
Salva come PNG Salva come JPEG
Nome #
Pelizaeus-Merzbacher: aspetti clinici, genetici e di neuroimaging 630
EFFICACIA DEL LEVETIRACETAM IN UN CASO DI ESES SECONDARIO A DISPLASIA CORTICALE. 599
Eventi parossistici epilettici e non-epilettici: un caso clinico emblematico per la diagnosi differenziale. 595
Regressione psicomotoria, tetraparesi spastica, atrofia cerebellare: un nuovo caso di leucodistrofia neuroassonale? 479
COQ7 defect causes prenatal onset of mitochondrial CoQ10 deficiency with cardiomyopathy and gastrointestinal obstruction 204
A new case of idiopathic hemiplegia hemiconvulsion syndrome 200
Deoxynucleoside Therapy for Thymidine Kinase 2–Deficient Myopathy 190
Evidence of enteric angiopathy and neuromuscular hypoxia in patients with mitochondrial neurogastrointestinal encephalomyopathy 188
Malformazioni dello sviluppo del lobo temporale, epilessia ed autismo 184
FA2H-related disorders: a novel c.270+3A>T splice-site mutation leads to a complex neurodegenerative phenotype. 182
Preliminary report on effects of oxcarbazepine-treatment on serum lipid levels in children. 179
The Transcriptome of SH-SY5Y at Single-Cell Resolution: A CITE-Seq Data Analysis Workflow 169
Mitochondrial metabolism in neural stem cells and implications for neurodevelopmental and neurodegenerative diseases 168
Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes 166
Novel compound heterozygous pathogenic variants in nucleotide-binding protein like protein (NUBPL) cause leukoencephalopathy with multi-systemic involvement 166
SAFA: A new measure to evaluate psychiatric symptoms detected in a sample of children and adolescents affected by eating disorders. Correlations with risk factors. 154
Intracerebral large artery disease in Aicardi-Goutières syndrome implicates SAMHD1 in vascular homeostasis 154
An unusual diagnosis in a child suffering from juvenile Alexander disease: a clinical and imaging report. 154
Infantile TK2 Deficiency Causing Mitochondrial Encephalomyopathy With Migrating Focal Seizures 153
Fever as a seizure precipitant factor in Panayiotopoulos syndrome: A clinical and genetic study 152
Complicanze neurologiche a lungo termine 151
Prospective study on long-term treatment with oxcarbazepine in pediatric epilepsy. 148
Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN). 146
Topiramate: effects on serum lipids and lipoproteins levels in children. 142
EPILESSIE DEL LOBO OCCIPITALE IN ETA’ PEDIATRICA 138
Unusual brain lesion in a case of restrictive anorexia nervosa. 137
Expanding the Clinical Spectrum of UBTF-Related Neurodevelopmental Disorder 136
Natural History of Patients With Mitochondrial ATPase Deficiency Due to Pathogenic Variants of MT-ATP6 and MT-ATP8 135
No kinetic interaction between levetiracetam and cyclosporine: a case report. 132
I disturbi del comportamento alimentare in età evolutiva 131
From the Structural and (Dys)Function of ATP Synthase to Deficiency in Age-Related Diseases 130
Efficacia e tollerabilità dell'oxcarbazepina in età pediatrica: studio prospettico 128
Levetiracetam or oxcarbazepine as monotherapy in newly diagnosed benign epilepsy of childhood with centrotemporal spikes (BECTS): an open-label, parallel group trial. 128
Lo stroke in età pediatrica 127
Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies 127
Deoxyguanosine kinase deficiency: natural history and liver transplant outcome 126
Epilessie Miocloniche: forme idiopatiche Benigne 126
Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy 125
Epilessia del lobo temporale sintomatica: evoluzione clinica, neuropsicologica e neuroradiologica 124
Clinical and pharmacological approaches of status epilepticus in children: Personal experience. Minerva Psichiatrica 124
A late-stage assembly checkpoint of the human mitochondrial ribosome large subunit 124
I Disturbi del Comportamento Alimentare in età evolutiva 123
Open prospective study on oxcarbazepine monotherapy in children with epilepsy: a preliminary report. 121
Deoxycytidine and Deoxythymidine Treatment for Thymidine Kinase 2 Deficiency 121
Mitochondrial Neurogastrointestinal Encephalomyopathy: Into the Fourth Decade, What We Have Learned So Far 119
Retrospective natural history of thymidine kinase 2 deficiency 114
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus 113
Le cefalee in età evolutiva 111
NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAs 111
Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family 106
Towards a therapy for mitochondrial disease: An update 104
FGF21 underlies a hormetic response to metabolic stress in methylmalonic acidemia 98
Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome 98
A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement Disorder 97
Metabolic disorders of fetal life: Glycogenoses and mitochondrial defects of the mitochondrial respiratory chain 93
CoQ 10 deficiencies and MNGIE: Two treatable mitochondrial disorders 93
Deoxynucleoside stress exacerbates the phenotype of a mouse model of mitochondrial neurogastrointestinal encephalopathy 91
Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia 85
Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing 84
TMEM14C is required for erythroid mitochondrial heme metabolism 83
Fhl1 W122S causes loss of protein function and late-onset mild myopathy 83
Deoxypyrimidine monophosphate bypass therapy for thymidine kinase 2 deficiency 83
SARS-CoV-2 infection in patients with primary mitochondrial diseases: Features and outcomes in Italy 83
MPV17 mutations causing adult-onset multisystemic disorder with multiple mitochondrial DNA deletions 81
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions 81
Sindrome 22q13:descrizione di due casi clinici 77
Requirement of enhanced Survival Motoneuron protein imposed during neuromuscular junction maturation 75
Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4 74
Sindrome de Landau Kleffner et troubles specifique du language: description de deux cases dans la meme famille 73
Mitochondrial encephalomyopathy due to a novel mutation in ACAD9 73
Historical perspective on mitochondrial medicine 72
Metabolic myopathies 65
mtDNA maintenance: Disease and therapy 45
Tissue-specific oxidative stress and loss of mitochondria in CoQ-deficient Pdss2 mutant mice 42
Totale 10.823
Salva come PNG Salva come JPEG
Categoria #
all - tutte 29.782
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 29.782
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021603 0 0 0 0 0 70 18 84 60 81 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
2025/20261.916 282 370 356 242 461 205 0 0 0 0 0 0
Totale 10.823