GARONE, CATERINA
 Distribuzione geografica
Continente #
NA - Nord America 407
EU - Europa 344
AS - Asia 210
Totale 961
Nazione #
US - Stati Uniti d'America 402
CN - Cina 166
IE - Irlanda 85
FR - Francia 63
FI - Finlandia 52
IT - Italia 52
KR - Corea 39
SE - Svezia 29
PL - Polonia 24
DE - Germania 16
BE - Belgio 11
GR - Grecia 10
CA - Canada 5
VN - Vietnam 3
CZ - Repubblica Ceca 1
GB - Regno Unito 1
HK - Hong Kong 1
IN - India 1
Totale 961
Città #
Beijing 128
Chandler 91
Dublin 85
Villeurbanne 60
Torino 45
Medford 42
Houston 27
Princeton 26
Warsaw 24
Ann Arbor 17
Dearborn 17
Brussels 11
Wilmington 11
Athens 9
Hefei 9
Ashburn 8
Kunming 8
Boardman 6
Nanjing 5
Toronto 5
Munich 4
Norwalk 4
Chongqing 3
Dong Ket 2
Jinan 2
Nanchang 2
Bologna 1
Boston 1
Brno 1
Central District 1
Changsha 1
Des Moines 1
Fuzhou 1
Guangzhou 1
Harbin 1
Hebei 1
Milan 1
Nea Smyrni 1
New York 1
Noisy-le-sec 1
Nürnberg 1
Rome 1
Rossano Veneto 1
Seattle 1
Shenzhen 1
Verona 1
Walthamstow 1
Totale 672
Nome #
Unusual diagnosis in a child suffering from juvenile Alexander disease: clinical and imaging report. 57
Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy. 52
Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4. 52
Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing. 49
Mitochondrial encephalomyopathy due to a novel mutation in ACAD9. 47
Requirement of enhanced Survival Motoneuron protein imposed during neuromuscular junction maturation. 45
Preliminary report on effects of oxcarbazepine-treatment on serum lipid levels in children. 43
Prospective study on long-term treatment with oxcarbazepine in pediatric epilepsy. 42
Metabolic disorders of fetal life: glycogenoses and mitochondrial defects of the mitochondrial respiratory chain. 41
No kinetic interaction between levetiracetam and cyclosporine: a case report. 41
Metabolic myopathies. 40
Fever as a seizure precipitant factor in Panayiotopoulos syndrome: a clinical and genetic study. 40
MPV17 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA Deletions. 39
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions. 38
Historical perspective on mitochondrial medicine. 36
Open prospective study on oxcarbazepine in epilepsy in children: a preliminary report. 35
Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN). 35
A new case of idiopathic hemiplegia hemiconvulsion syndrome. 34
Levetiracetam or oxcarbazepine as monotherapy in newly diagnosed benign epilepsy of childhood with centrotemporal spikes (BECTS): an open-label, parallel group trial. 34
Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia. 34
Intracerebral large artery disease in Aicardi-Goutières syndrome implicates SAMHD1 in vascular homeostasis. 33
CoQ(10) deficiencies and MNGIE: two treatable mitochondrial disorders. 32
FA2H-related disorders: a novel c.270+3A>T splice-site mutation leads to a complex neurodegenerative phenotype. 32
SAFA: A new measure to evaluate psychiatric symptoms detected in a sample of children and adolescents affected by eating disorders. Correlations with risk factors. 31
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus. 28
Topiramate: effects on serum lipids and lipoproteins levels in children. 23
Totale 1.013
Categoria #
all - tutte 2.598
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 2.598


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201931 0 0 0 0 0 1 1 14 1 0 12 2
2019/2020103 0 0 0 27 1 33 17 6 2 15 2 0
2020/202145 7 1 1 5 4 4 1 1 8 0 5 8
2021/202291 0 1 1 4 1 1 6 7 6 1 17 46
2022/2023268 27 1 0 20 48 77 34 19 34 2 4 2
2023/202458 10 31 2 4 8 3 0 0 0 0 0 0
Totale 1.013