CRIS Current Research Information System

GARONE, CATERINA
 Distribuzione geografica
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Continente #
EU - Europa 3.898
NA - Nord America 3.090
AS - Asia 1.075
AF - Africa 70
SA - Sud America 20
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 2
Totale 8.159
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Nazione #
US - Stati Uniti d'America 3.075
IT - Italia 2.038
GB - Regno Unito 480
CN - Cina 377
SG - Singapore 354
DE - Germania 329
SE - Svezia 184
UA - Ucraina 172
FR - Francia 150
IN - India 141
VN - Vietnam 135
RU - Federazione Russa 132
IE - Irlanda 95
NL - Olanda 94
FI - Finlandia 81
ZA - Sudafrica 32
ES - Italia 31
EE - Estonia 30
TG - Togo 16
CH - Svizzera 15
SC - Seychelles 13
AT - Austria 12
CA - Canada 12
BR - Brasile 11
ID - Indonesia 11
BE - Belgio 10
JP - Giappone 9
HK - Hong Kong 8
JO - Giordania 8
ME - Montenegro 8
BG - Bulgaria 7
CL - Cile 6
IR - Iran 6
LB - Libano 6
AL - Albania 5
CI - Costa d'Avorio 5
AE - Emirati Arabi Uniti 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
BD - Bangladesh 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 8.159
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Città #
Southend 409
Singapore 302
Fairfield 299
Santa Clara 282
Chandler 260
Ashburn 193
Bologna 186
Woodbridge 148
Seattle 143
Wilmington 142
Milan 135
Princeton 134
Houston 131
Jacksonville 124
Rome 118
Cambridge 101
Dublin 95
Ann Arbor 85
Dong Ket 78
Boardman 77
Helsinki 75
Westminster 61
Naples 53
Padova 53
Redmond 46
Berlin 45
Turin 43
Nanjing 34
Florence 27
Jinan 26
Des Moines 25
San Diego 23
Saint Petersburg 22
Catania 21
Bagnacavallo 20
Mülheim 19
Guangzhou 18
Medford 18
Verona 18
Modena 17
Palermo 17
Parma 17
Lomé 16
Nanchang 16
Norwalk 16
Shenyang 15
Beijing 14
Genoa 14
Moscow 14
Redwood City 14
Shanghai 14
Dearborn 13
Falkenstein 13
Mahé 13
Zhengzhou 13
Changsha 12
Falls Church 12
New York 12
Reggio Emilia 12
Tianjin 12
Brescia 11
Jakarta 11
Nuremberg 11
Toronto 11
Yubileyny 11
Bari 10
Brussels 10
Vicenza 10
Cagliari 9
Tokyo 9
Treviso 9
Amman 8
Bergamo 8
Jiaxing 8
London 8
Paris 8
Podgorica 8
San Mateo 8
Vienna 8
Amsterdam 7
Andover 7
Bern 7
Forlì 7
Haikou 7
Hangzhou 7
Hebei 7
Hong Kong 7
Ningbo 7
Olalla 7
Sofia 7
Altamura 6
Bondeno 6
Bühl 6
Kunming 6
Lanzhou 6
Lauterbourg 6
Pescara 6
Pisa 6
Pistoia 6
Pune 6
Totale 4.698
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Nome #
Pelizaeus-Merzbacher: aspetti clinici, genetici e di neuroimaging 575
EFFICACIA DEL LEVETIRACETAM IN UN CASO DI ESES SECONDARIO A DISPLASIA CORTICALE. 513
Eventi parossistici epilettici e non-epilettici: un caso clinico emblematico per la diagnosi differenziale. 488
Regressione psicomotoria, tetraparesi spastica, atrofia cerebellare: un nuovo caso di leucodistrofia neuroassonale? 434
A new case of idiopathic hemiplegia hemiconvulsion syndrome 180
Malformazioni dello sviluppo del lobo temporale, epilessia ed autismo 159
Deoxynucleoside Therapy for Thymidine Kinase 2–Deficient Myopathy 156
FA2H-related disorders: a novel c.270+3A>T splice-site mutation leads to a complex neurodegenerative phenotype. 151
Complicanze neurologiche a lungo termine 137
Preliminary report on effects of oxcarbazepine-treatment on serum lipid levels in children. 136
An unusual diagnosis in a child suffering from juvenile Alexander disease: a clinical and imaging report. 135
Novel compound heterozygous pathogenic variants in nucleotide-binding protein like protein (NUBPL) cause leukoencephalopathy with multi-systemic involvement 135
Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes 134
Fever as a seizure precipitant factor in Panayiotopoulos syndrome: A clinical and genetic study 133
The Transcriptome of SH-SY5Y at Single-Cell Resolution: A CITE-Seq Data Analysis Workflow 133
Intracerebral large artery disease in Aicardi-Goutières syndrome implicates SAMHD1 in vascular homeostasis 129
SAFA: A new measure to evaluate psychiatric symptoms detected in a sample of children and adolescents affected by eating disorders. Correlations with risk factors. 124
Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN). 123
Evidence of enteric angiopathy and neuromuscular hypoxia in patients with mitochondrial neurogastrointestinal encephalomyopathy 123
Topiramate: effects on serum lipids and lipoproteins levels in children. 117
No kinetic interaction between levetiracetam and cyclosporine: a case report. 116
Prospective study on long-term treatment with oxcarbazepine in pediatric epilepsy. 114
EPILESSIE DEL LOBO OCCIPITALE IN ETA’ PEDIATRICA 112
Levetiracetam or oxcarbazepine as monotherapy in newly diagnosed benign epilepsy of childhood with centrotemporal spikes (BECTS): an open-label, parallel group trial. 112
Clinical and pharmacological approaches of status epilepticus in children: Personal experience. Minerva Psichiatrica 108
Epilessia del lobo temporale sintomatica: evoluzione clinica, neuropsicologica e neuroradiologica 107
Lo stroke in età pediatrica 106
Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies 105
Unusual brain lesion in a case of restrictive anorexia nervosa. 103
Deoxycytidine and Deoxythymidine Treatment for Thymidine Kinase 2 Deficiency 101
I disturbi del comportamento alimentare in età evolutiva 100
Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy 100
Efficacia e tollerabilità dell'oxcarbazepina in età pediatrica: studio prospettico 98
Epilessie Miocloniche: forme idiopatiche Benigne 98
From the Structural and (Dys)Function of ATP Synthase to Deficiency in Age-Related Diseases 98
COQ7 defect causes prenatal onset of mitochondrial CoQ10 deficiency with cardiomyopathy and gastrointestinal obstruction 96
I Disturbi del Comportamento Alimentare in età evolutiva 95
NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAs 95
Open prospective study on oxcarbazepine monotherapy in children with epilepsy: a preliminary report. 93
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus 93
Le cefalee in età evolutiva 92
Mitochondrial Neurogastrointestinal Encephalomyopathy: Into the Fourth Decade, What We Have Learned So Far 90
Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome 83
Towards a therapy for mitochondrial disease: An update 83
A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement Disorder 82
Metabolic disorders of fetal life: Glycogenoses and mitochondrial defects of the mitochondrial respiratory chain 80
Retrospective natural history of thymidine kinase 2 deficiency 80
FGF21 underlies a hormetic response to metabolic stress in methylmalonic acidemia 74
CoQ 10 deficiencies and MNGIE: Two treatable mitochondrial disorders 74
Deoxynucleoside stress exacerbates the phenotype of a mouse model of mitochondrial neurogastrointestinal encephalopathy 74
Fhl1 W122S causes loss of protein function and late-onset mild myopathy 73
Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family 72
Mitochondrial metabolism in neural stem cells and implications for neurodevelopmental and neurodegenerative diseases 70
Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia 69
Deoxypyrimidine monophosphate bypass therapy for thymidine kinase 2 deficiency 68
Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing 67
MPV17 mutations causing adult-onset multisystemic disorder with multiple mitochondrial DNA deletions 66
Sindrome 22q13:descrizione di due casi clinici 64
TMEM14C is required for erythroid mitochondrial heme metabolism 64
SARS-CoV-2 infection in patients with primary mitochondrial diseases: Features and outcomes in Italy 63
Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4 62
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions 62
Sindrome de Landau Kleffner et troubles specifique du language: description de deux cases dans la meme famille 61
Requirement of enhanced Survival Motoneuron protein imposed during neuromuscular junction maturation 58
Historical perspective on mitochondrial medicine 57
Mitochondrial encephalomyopathy due to a novel mutation in ACAD9 57
A late-stage assembly checkpoint of the human mitochondrial ribosome large subunit 53
Metabolic myopathies 52
Expanding the Clinical Spectrum of UBTF-Related Neurodevelopmental Disorder 41
Tissue-specific oxidative stress and loss of mitochondria in CoQ-deficient Pdss2 mutant mice 31
Deoxyguanosine kinase deficiency: natural history and liver transplant outcome 26
mtDNA maintenance: Disease and therapy 20
Infantile TK2 Deficiency Causing Mitochondrial Encephalomyopathy With Migrating Focal Seizures 20
Natural History of Patients With Mitochondrial ATPase Deficiency Due to Pathogenic Variants of MT-ATP6 and MT-ATP8 2
Totale 8.355
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Categoria #
all - tutte 22.153
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 22.153
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020257 0 0 0 0 0 0 0 0 0 130 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
2024/20251.987 130 310 278 174 473 233 170 78 133 8 0 0
Totale 8.355