CRIS Current Research Information System

GARONE, CATERINA
 Distribuzione geografica
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Continente #
EU - Europa 3.530
NA - Nord America 3.069
AS - Asia 1.021
AF - Africa 69
SA - Sud America 17
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 2
Totale 7.712
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Nazione #
US - Stati Uniti d'America 3.055
IT - Italia 1.828
GB - Regno Unito 475
CN - Cina 365
SG - Singapore 317
DE - Germania 311
SE - Svezia 184
UA - Ucraina 171
FR - Francia 142
IN - India 141
VN - Vietnam 135
IE - Irlanda 94
FI - Finlandia 74
RU - Federazione Russa 69
NL - Olanda 55
ZA - Sudafrica 32
EE - Estonia 30
ES - Italia 21
TG - Togo 16
CH - Svizzera 15
SC - Seychelles 13
CA - Canada 11
ID - Indonesia 11
JP - Giappone 9
AT - Austria 8
BE - Belgio 8
BR - Brasile 8
JO - Giordania 8
ME - Montenegro 8
BG - Bulgaria 7
CL - Cile 6
IR - Iran 6
LB - Libano 6
AL - Albania 5
AE - Emirati Arabi Uniti 4
CI - Costa d'Avorio 4
HK - Hong Kong 4
CZ - Repubblica Ceca 3
HU - Ungheria 3
MZ - Mozambico 3
PK - Pakistan 3
RO - Romania 3
TR - Turchia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AU - Australia 2
CR - Costa Rica 2
GR - Grecia 2
LK - Sri Lanka 2
MC - Monaco 2
MT - Malta 2
MY - Malesia 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
PL - Polonia 2
SM - San Marino 2
UZ - Uzbekistan 2
AZ - Azerbaigian 1
BO - Bolivia 1
BS - Bahamas 1
CO - Colombia 1
KR - Corea 1
KW - Kuwait 1
LT - Lituania 1
LU - Lussemburgo 1
NG - Nigeria 1
PT - Portogallo 1
SK - Slovacchia (Repubblica Slovacca) 1
VE - Venezuela 1
Totale 7.712
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Città #
Southend 409
Fairfield 299
Singapore 290
Santa Clara 282
Chandler 260
Ashburn 188
Bologna 159
Woodbridge 148
Wilmington 142
Seattle 141
Princeton 134
Houston 131
Jacksonville 124
Milan 109
Rome 104
Cambridge 101
Dublin 94
Ann Arbor 85
Dong Ket 78
Boardman 77
Helsinki 69
Westminster 61
Padova 53
Naples 46
Redmond 46
Berlin 45
Turin 35
Nanjing 34
Florence 27
Jinan 26
Des Moines 25
San Diego 23
Saint Petersburg 22
Bagnacavallo 20
Mülheim 19
Guangzhou 18
Medford 18
Modena 17
Palermo 17
Lomé 16
Nanchang 16
Norwalk 16
Verona 16
Shenyang 15
Catania 14
Genoa 14
Redwood City 14
Dearborn 13
Mahé 13
Shanghai 13
Zhengzhou 13
Changsha 12
Falls Church 12
Moscow 12
New York 12
Parma 12
Reggio Emilia 12
Tianjin 12
Beijing 11
Jakarta 11
Toronto 10
Vicenza 10
Tokyo 9
Amman 8
Bari 8
Brussels 8
Falkenstein 8
Jiaxing 8
Podgorica 8
San Mateo 8
Amsterdam 7
Andover 7
Bern 7
Cagliari 7
Forlì 7
Haikou 7
Hangzhou 7
Hebei 7
Ningbo 7
Olalla 7
Paris 7
Sofia 7
Vienna 7
Altamura 6
Bergamo 6
Brescia 6
Bühl 6
Kunming 6
Lanzhou 6
Pisa 6
Pune 6
Reggio Calabria 6
San Lazzaro di Savena 6
Trieste 6
Ancona 5
Ardabil 5
Bondeno 5
Buffalo 5
Caserta 5
Edinburgh 5
Totale 4.527
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Nome #
Pelizaeus-Merzbacher: aspetti clinici, genetici e di neuroimaging 540
EFFICACIA DEL LEVETIRACETAM IN UN CASO DI ESES SECONDARIO A DISPLASIA CORTICALE. 471
Regressione psicomotoria, tetraparesi spastica, atrofia cerebellare: un nuovo caso di leucodistrofia neuroassonale? 406
Eventi parossistici epilettici e non-epilettici: un caso clinico emblematico per la diagnosi differenziale. 393
A new case of idiopathic hemiplegia hemiconvulsion syndrome 178
Malformazioni dello sviluppo del lobo temporale, epilessia ed autismo 155
FA2H-related disorders: a novel c.270+3A>T splice-site mutation leads to a complex neurodegenerative phenotype. 149
Deoxynucleoside Therapy for Thymidine Kinase 2–Deficient Myopathy 149
Preliminary report on effects of oxcarbazepine-treatment on serum lipid levels in children. 133
Complicanze neurologiche a lungo termine 133
An unusual diagnosis in a child suffering from juvenile Alexander disease: a clinical and imaging report. 132
Novel compound heterozygous pathogenic variants in nucleotide-binding protein like protein (NUBPL) cause leukoencephalopathy with multi-systemic involvement 130
Fever as a seizure precipitant factor in Panayiotopoulos syndrome: A clinical and genetic study 129
The Transcriptome of SH-SY5Y at Single-Cell Resolution: A CITE-Seq Data Analysis Workflow 128
Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes 127
Intracerebral large artery disease in Aicardi-Goutières syndrome implicates SAMHD1 in vascular homeostasis 125
Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN). 122
SAFA: A new measure to evaluate psychiatric symptoms detected in a sample of children and adolescents affected by eating disorders. Correlations with risk factors. 121
Topiramate: effects on serum lipids and lipoproteins levels in children. 114
Evidence of enteric angiopathy and neuromuscular hypoxia in patients with mitochondrial neurogastrointestinal encephalomyopathy 114
No kinetic interaction between levetiracetam and cyclosporine: a case report. 113
Prospective study on long-term treatment with oxcarbazepine in pediatric epilepsy. 112
Levetiracetam or oxcarbazepine as monotherapy in newly diagnosed benign epilepsy of childhood with centrotemporal spikes (BECTS): an open-label, parallel group trial. 111
EPILESSIE DEL LOBO OCCIPITALE IN ETA’ PEDIATRICA 109
Clinical and pharmacological approaches of status epilepticus in children: Personal experience. Minerva Psichiatrica 106
Lo stroke in età pediatrica 103
Unusual brain lesion in a case of restrictive anorexia nervosa. 100
Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies 100
Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy 99
Deoxycytidine and Deoxythymidine Treatment for Thymidine Kinase 2 Deficiency 98
Efficacia e tollerabilità dell'oxcarbazepina in età pediatrica: studio prospettico 97
I disturbi del comportamento alimentare in età evolutiva 97
Epilessia del lobo temporale sintomatica: evoluzione clinica, neuropsicologica e neuroradiologica 97
Epilessie Miocloniche: forme idiopatiche Benigne 96
From the Structural and (Dys)Function of ATP Synthase to Deficiency in Age-Related Diseases 94
Open prospective study on oxcarbazepine monotherapy in children with epilepsy: a preliminary report. 92
NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAs 92
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus 91
Le cefalee in età evolutiva 91
I Disturbi del Comportamento Alimentare in età evolutiva 89
Mitochondrial Neurogastrointestinal Encephalomyopathy: Into the Fourth Decade, What We Have Learned So Far 89
A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement Disorder 81
Towards a therapy for mitochondrial disease: An update 80
Metabolic disorders of fetal life: Glycogenoses and mitochondrial defects of the mitochondrial respiratory chain 79
Retrospective natural history of thymidine kinase 2 deficiency 78
Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome 78
COQ7 defect causes prenatal onset of mitochondrial CoQ10 deficiency with cardiomyopathy and gastrointestinal obstruction 76
CoQ 10 deficiencies and MNGIE: Two treatable mitochondrial disorders 73
Fhl1 W122S causes loss of protein function and late-onset mild myopathy 72
Deoxynucleoside stress exacerbates the phenotype of a mouse model of mitochondrial neurogastrointestinal encephalopathy 71
FGF21 underlies a hormetic response to metabolic stress in methylmalonic acidemia 70
Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family 67
Deoxypyrimidine monophosphate bypass therapy for thymidine kinase 2 deficiency 67
Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia 67
Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing 66
MPV17 mutations causing adult-onset multisystemic disorder with multiple mitochondrial DNA deletions 65
Sindrome 22q13:descrizione di due casi clinici 63
TMEM14C is required for erythroid mitochondrial heme metabolism 63
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions 60
Sindrome de Landau Kleffner et troubles specifique du language: description de deux cases dans la meme famille 59
Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4 59
SARS-CoV-2 infection in patients with primary mitochondrial diseases: Features and outcomes in Italy 58
Mitochondrial metabolism in neural stem cells and implications for neurodevelopmental and neurodegenerative diseases 57
Historical perspective on mitochondrial medicine 56
Requirement of enhanced Survival Motoneuron protein imposed during neuromuscular junction maturation 56
Mitochondrial encephalomyopathy due to a novel mutation in ACAD9 55
Metabolic myopathies 51
A late-stage assembly checkpoint of the human mitochondrial ribosome large subunit 46
Tissue-specific oxidative stress and loss of mitochondria in CoQ-deficient Pdss2 mutant mice 31
Expanding the Clinical Spectrum of UBTF-Related Neurodevelopmental Disorder 30
Deoxyguanosine kinase deficiency: natural history and liver transplant outcome 21
mtDNA maintenance: Disease and therapy 17
Totale 7.897
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Categoria #
all - tutte 20.125
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 20.125
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020962 0 0 0 0 0 93 190 218 204 130 60 67
2020/20211.007 193 79 34 54 44 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
2024/20251.529 130 310 278 174 473 164 0 0 0 0 0 0
Totale 7.897