MAZZACCARA, CRISTINA
 Distribuzione geografica
Continente #
NA - Nord America 852
EU - Europa 444
AS - Asia 271
OC - Oceania 1
Totale 1568
Nazione #
US - Stati Uniti d'America 836
IT - Italia 256
VN - Vietnam 136
CN - Cina 122
UA - Ucraina 54
IE - Irlanda 42
FI - Finlandia 36
DE - Germania 17
CA - Canada 16
SE - Svezia 13
GB - Regno Unito 8
ES - Italia 6
FR - Francia 5
IR - Iran 5
IN - India 4
PL - Polonia 3
AU - Australia 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
GR - Grecia 1
IL - Israele 1
KR - Corea 1
LV - Lettonia 1
PK - Pakistan 1
SA - Arabia Saudita 1
Totale 1568
Città #
Chandler 262
Dong Ket 136
Millbury 79
Napoli 72
Beijing 41
Princeton 40
Boston 39
Des Moines 37
Lawrence 34
Nanjing 30
Wilmington 27
Jacksonville 21
Ottawa 15
Nanchang 12
Falls Church 11
Oristano 11
Fairfield 10
Milan 10
Shenyang 10
Ercolano 9
Norwalk 9
Ashburn 8
Hebei 8
Monmouth Junction 7
Jiaxing 6
Manduria 6
Woodbridge 6
Augusta 5
Boardman 5
Quarto 5
Trento 5
Ardabil 4
Changsha 4
Mountain View 4
San Mateo 4
Ann Arbor 3
Caserta 3
Como 3
Fiumicino 3
Hangzhou 3
Kunming 3
Redwood City 3
Rome 3
Andover 2
Baltimore 2
Cambridge 2
Dallas 2
Dearborn 2
Formia 2
Kraków 2
Leawood 2
Marano Di Napoli 2
Marcianise 2
Montemesola 2
Montesarchio 2
Mumbai 2
Naples 2
Ragusa 2
Salerno 2
San Francisco 2
San Giorgio a Cremano 2
Seregno 2
Tagliacozzo 2
Vélizy 2
Besançon 1
Brindisi 1
Brno 1
Casoria 1
Chicago 1
Frosinone 1
Giugliano In Campania 1
Guangzhou 1
Jinan 1
Karachi 1
Lanuvio 1
Marano 1
Montoro 1
Nocera Superiore 1
Novara 1
Nürnberg 1
Orange 1
Padova 1
Pagani 1
Pesaro 1
Pescara 1
Phoenix 1
Pisa 1
Qualiano 1
Quartu Sant'elena 1
Redmond 1
Rimini 1
Riyadh 1
Romano Di Lombardia 1
Saint-martin-d'heres 1
San Giorgio A Cremano 1
San Giovanni Rotondo 1
Saviano 1
Schöneck 1
Stuttgart 1
Taizhou 1
Totale 1094
Nome #
Effect of CYP4F2, VKORC1, and CYP2C9 in Influencing Coumarin Dose: A Single-Patient Data Meta-Analysis in More Than 15,000 Individuals 57
Laboratory medicine: health evaluation in elite athletes 51
The mtDNA 15497 G/A polymorphism in cytochrome b in severe obese subjects from Southern Italy. 47
Mitochondrial M.T4216C (P.Y304h) and M.A4917G, (P.N150D) variations In a young patient with Maternally Inherited Diabetes and Deafness 47
Association of H558R Polymorphism In SCN5A Gene With Familial Dilated Cardiomyopathy 47
Comparison of the TaqMan and LightCycler systems in pharmacogenetic testing: evaluation of the CYP2C9*2/*3 polymorphisms. 42
La Farmacogenetica nella terapia anticoagulante orale. Dall’analisi genetica alla pratica clinica 39
Hypermethioninemia in Campania: Results from 10 years of newborn screening 39
Paraoxonase and superoxide dismutase gene polymorphisms and noise-induced hearing loss. 36
Diabete Tipo 1, Tipo 2 e Tipo X 36
Contemporary genetic testing in inherited cardiac disease: Tools, ethical issues, and clinical applications 36
A paraoxonase gene polymorphism, PON 1 (55), as an independent risk factor for increased carotid intima-media tickness in middle-aged women. 35
Molecular analysis has allowed the definitive diagnosis of multiple acyl-CoA dehydrogenase deficiency (MADD) 35
First trimester ultrasound features of X-linked Opitz syndrome and early molecular diagnosis: case report and review of the literature 34
HNP-1 and HBD-1 as biomarkers for the immune systems of elite basketball athletes 33
Athlete's Passport: Prevention of Infections, Inflammations, Injuries and Cardiovascular Diseases 32
Exercise, immune system, nutrition, respiratory and cardiovascular diseases during COVID-19: A complex combination 32
La farmacogenetica nella terapia anticoagulante orale:dall’analisi genetica alla pratica clinica 31
Clinical molecular biology in the assessment and prevention of cardiological risk in case of participation in sports activity and intense physical activity 31
A common polymorphism in the SCN5A gene is associated with dilated cardiomyopathy 30
Successful Pregnancy in a Young Woman with Multiple Acyl-CoA Dehydrogenase Deficiency 27
The Biological Role of Vitamins in Athletes’ Muscle, Heart and Microbiota 27
Il Diabete Mitocondriale: se lo cerchi lo trovi. 26
Methicillin-Resistant Staphylococcus aureus: Risk for General Infection and Endocarditis Among Athletes 26
Yield and clinical significance of genetic screening in elite and amateur athletes 26
Age-Related Reference Intervals of the Main Biochemical and Hematological Parameters in C57BL/6J, 129SV/EV and C3H/HeJ Mouse Strains 25
Nuove variazioni nel genoma mitocondriale in pazienti con diabete mitocondriale del Sud Italia 25
Mitochondrial diabetes in children: seek and you will find it 25
Interpretation of Non-Coding Variants In Inherited Cardiomyopathies Associated To Sudden Death 25
PEGylated helper-dependent adenoviral vector expressing human Apo A-I for gene therapy in LDLR-deficient mice 24
Functional Studies and In Silico Analyses to Evaluate Non-Coding Variants in Inherited Cardiomyopathies 24
A real benefit of an extended neonatal screening 24
Decreased Paraoxonase-2 Expression in Human Carotids During the Progression of Atherosclerosis 23
Effect of high-density lipoprotein cholesterol levels on carotid artery geometry in a Mediterranean female population 23
A paraoxonase gene polymorphism pon 1 (55) as an independent factor for increased carotid imt in women 23
Mitochondrial diabetes in children from Southern Italy 23
A new case of Congenital Hyperinsulinemic Hypoglycemia due to M/SCHAD deficiency: the contribution of metabolic and molecular diagnosis for the management 23
Childhood obesity: an overview of laboratory medicine, exercise and microbiome 22
Association between apolipoprotein E polymorphisms and metabolic syndrome in women. 20
Haplogroup T is an obesity risk factor: mitochondrial DNA haplotyping in a morbid obese population from southern Italy. 20
Warfarin anticoagulant therapy: a Southern Italy pharmacogenetics-based dosing model. 20
Urinary biomarkers: Diagnostic tools for monitoring athletes’ health status 20
Genetic analysis resolves differential diagnosis of a familial syndromic dilated cardiomyopathy: A new case of Alström syndrome 19
Dietary thiols: A potential supporting strategy against oxidative stress in heart failure and muscular damage during sports activity 19
The mtDNA 15497 G/A polymorphism in cytochrome b in severe obese subjects from South Italy 18
Alterazioni del DNA mitocondriale in paziente con patologia neurologica complessa. 18
Sudden cardiac death in young athletes: Literature review of molecular basis 18
The hidden fragility in the heart of the athletes: A review of genetic biomarkers 18
Cardiovascular Involvement in mtDNA Disease: Diagnosis, Management, and Therapeutic Options 18
Valutazione di parametri di ossidazione in placche aterosclerotiche e plasma di pazienti endoarteriectomizzati. 17
Mitochondrial mutation in adult patient with Hypertrophic Cardiomyopathy and renal failure 17
Mitochondrial Mutational Event In An Adult Patient With Renal Failure And Cardiomyopathy 17
Mitochondrial haplogroups and obesity in patients from South Italy 16
Genetic pre-participation screening in selected athletes: a new tool for the prevention of sudden cardiac death? 16
Genotype-phenotype correlation: A triple DNA mutational event in a boy entering sport conveys an additional pathogenicity risk 16
Hepatic Presentation of Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD): Case Report and Systematic Review 16
A new case of M/SCHAD deficiency: The contribution of metabolic findings in directing the definitive genetic diagnosis for an optimal management 15
Metabolic Treatment of Wolfram Syndrome 15
De novo mitochondrial DNA alteration in child with complex neurilogical compromission. 14
Unexplained sudden cardiac arrest in children: clinical and genetic characteristics of survivors 14
NGS Analysis Revealed Digenic Heterozygous GCK and HNF1A Variants in a Child with Mild Hyperglycemia: A Case Report 14
Novel mutations in mitochondrial genome in midd patients from Southern Italy 13
Nuove variazioni nel genoma mitocondriale in pazienti con diabete mitocondriale del sud Italia 13
Genetic Pre-Participation Screening in Selected Athletes: A New Tool for the Prevention of Sudden Cardiac Death? 13
Mitochondrial Haplogroup T is Associated with Severe Obesity in Patients from South Italy. 13
Prenatal diagnosis of HNF1b mutation allows recognition of neonatal dysglycemia 13
Physical activity and thrombophilic risk in a short series 11
Molecular Epidemiology of Mitochondrial Cardiomyopathy: A Search Among Mitochondrial and Nuclear Genes 11
Loss of heterozygosity to identify genes associated with cutaneous malignant melanoma. 10
Potential role of imaging markers in predicting future disease expression of arrhythmogenic cardiomyopathy 9
Protein Thermodynamic Destabilization in the Assessment of Pathogenicity of a Variant of Uncertain Significance in Cardiac Myosin Binding Protein C 8
The role of the Clinical Biochemistry laboratory in the organization of an international sporting event: The 30th Summer Universiade 8
Impact of molecular diagnostics in an asymptomatic amateur athlete found to be affected by hypertrophic cardiomyopathy 7
Multidisciplinary in-depth investigation in a young athlete suffering from syncope caused by myocardial bridge 5
Next-Generation Sequencing Gene Panels in Inheritable Cardiomyopathies and Channelopathies: Prevalence of Pathogenic Variants and Variants of Unknown Significance in Uncommon Genes 2
Totale 1742
Categoria #
all - tutte 3086
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 3086


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/201820 0000 00 12 5921
2018/201977 11568 121 103 6006
2019/2020240 65658 219 611 3274039
2020/2021367 1783426 1220 1712 26444147
2021/2022527 18344 88 1623 6356150174
2022/2023353 82602133 9263 20 0000
Totale 1742