GIORDANO, Carla
 Distribuzione geografica
Continente #
NA - Nord America 3.968
EU - Europa 1.183
AS - Asia 420
SA - Sud America 29
AF - Africa 24
OC - Oceania 4
Totale 5.628
Nazione #
US - Stati Uniti d'America 3.937
IT - Italia 576
IN - India 181
SE - Svezia 166
CN - Cina 115
SG - Singapore 115
FI - Finlandia 103
UA - Ucraina 79
DE - Germania 61
GB - Regno Unito 40
AT - Austria 38
CA - Canada 28
BG - Bulgaria 26
IE - Irlanda 25
AR - Argentina 23
FR - Francia 18
TG - Togo 17
BE - Belgio 13
NL - Olanda 12
RO - Romania 9
TR - Turchia 6
ZA - Sudafrica 5
AU - Australia 4
BR - Brasile 4
GR - Grecia 3
PH - Filippine 3
CL - Cile 2
ES - Italia 2
MX - Messico 2
PL - Polonia 2
SC - Seychelles 2
SI - Slovenia 2
BZ - Belize 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
LI - Liechtenstein 1
LU - Lussemburgo 1
MD - Moldavia 1
MK - Macedonia 1
PT - Portogallo 1
RU - Federazione Russa 1
Totale 5.628
Città #
Fairfield 724
Woodbridge 313
Chandler 304
Ashburn 294
Seattle 271
Houston 243
Rome 238
Cambridge 199
Wilmington 181
Ann Arbor 169
Princeton 99
San Paolo di Civitate 92
Dearborn 88
Beijing 85
Lawrence 85
Plano 76
San Diego 58
Boston 55
Singapore 47
Fremont 44
Millbury 36
New York 34
Vienna 34
Des Moines 33
Helsinki 27
Jacksonville 27
Sofia 26
Boardman 23
Federal 23
Dublin 22
Andover 21
Norwalk 20
Lomé 17
Phoenix 16
Falls Church 15
Toronto 15
Parma 14
Milan 13
San Mateo 13
Ottawa 12
Bremen 11
Brussels 11
Los Angeles 11
London 10
Pomezia 10
Bologna 9
Mannheim 8
Hefei 7
Lappeenranta 7
Southend 7
Bühl 6
Salerno 6
Nanjing 5
San Jose 5
Bari 4
Buffalo 4
Chapecó 4
Las Vegas 4
Leawood 4
San Gregorio da Sassola 4
Amsterdam 3
Bengaluru 3
Fiumicino 3
Galway 3
Hyderabad 3
Indiana 3
Kunming 3
Liverpool 3
Modena 3
Ozieri 3
Perugia 3
Pune 3
Redwood City 3
Sigillo 3
Acton 2
Angeles City 2
Ankara 2
Anzola dell'Emilia 2
Berlin 2
Block 2
Blythewood 2
Casalmoro 2
Caserta 2
Chicago 2
Columbus 2
Cuggiono 2
Deiva Marina 2
Duncan 2
Ercolano 2
Ferrara di Monte Baldo 2
Florence 2
Forlì 2
Fort Worth 2
Frankfurt am Main 2
Galdo 2
Giannitsá 2
Grafing 2
Groningen 2
Kranj 2
Laas 2
Totale 4.337
Nome #
A novel LAMP2 mutation associated with severe cardiac hypertrophy and microvascular remodeling in a female with Danon disease: a case report and literature review 147
Afferent nerve ending density in the human laryngeal mucosa: potential implications on endoscopic evaluation of laryngeal sensitivity 131
Neuromuscular magnetic stimulation counteracts muscle decline in ALS patients: results of a randomized, double-blind, controlled study 115
Nonischemic left ventricular scar and cardiac sudden death in the young 114
Novel compound mutations in the mitochondrial translation elongation factor (TSFM) gene cause severe cardiomyopathy with myocardial fibro-adipose replacement 94
Exogenous peptides are able to penetrate human cell and mitochondrial membranes, stabilize mitochondrial tRNA structures, and rescue severe mitochondrial defects 94
Does the epidermal nerve fibre density measured by skin biopsy in patients with peripheral neuropathies correlate with neuropathic pain? 91
Impaired mitochondrial biogenesis is a common feature to myocardial hypertrophy and end-stage ischemic heart failure 89
Laryngeal sensitivity in patients with amyotrophic lateral sclerosis 83
Evaluation of gastrointestinal mtDNA depletion in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE). 82
Sudden cardiac death in younger adults: autopsy diagnosis as a tool for preventive medicine 82
Anti-aminoacyl-tRNA synthetase-related myositis and dermatomyositis: clues for differential diagnosis on muscle biopsy 82
Novel perspectives in redox biology and pathophysiology of failing myocytes: modulation of the intramyocardial redox milieu for therapeutic interventions - A review article from the Working Group of Cardiac Cell Biology, Italian Society of Cardiology 81
Potential role for the VDR agonist elocalcitol in metabolic control: evidences in human skeletal muscle cells 81
Short peptides from leucyl-tRNA synthetase rescue disease-causing mitochondrial tRNA point mutations 80
Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T > C mitochondrial tRNA(Ile) mutation causing hypertrophic cardiomyopathy 79
Severe early onset ethylmalonic encephalopathy with west syndrome 78
A Novel Mutation in ABCA1 Gene Causing Tangier Disease in an Italian Family with Uncommon Neurological Presentation 76
Coronary atherosclerosis and sudden cardiac death in the young: another face of the culprit, another way of striking? 76
TTC19 plays a husbandry role on UQCRFS1 turnover in the biogenesis of mitochondrial respiratory complex III 76
FATAL CONGENITAL MYOPATHY AND GASTROINTESTINAL PSEUDO-OBSTRUCTION DUE TO POLG1 MUTATIONS 76
The phenotypic expression of mitochondrial tRNA-mutations can be modulated by either mitochondrial leucyl-tRNA synthetase or the C-terminal domain thereof 74
New insight into the mechanisms of ectopic fat deposition improvement after bariatric surgery 74
Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy 74
Diagnostic value of persistently low positive TGA-IgA titers in symptomatic chIldren with suspected celiac disease 74
A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy 73
Enhanced ROS production by NADPH oxidase is correlated to changes in antioxidant enzyme activity in human heart failure 69
AAV-mediated Liver-specific MPV17 Expression Restores mtDNA Levels and Prevents Diet-induced Liver Failure 69
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy 68
Small-fibre neuropathy related to bulbar and spinal-onset in patients with ALS 68
Morphologic evidence of diffuse vascular damage in human and in the experimental model of ethylmalonic encephalopathy 66
Cerebral mitochondrial microangiopathy leads to leukoencephalopathy in mitochondrial neurogastrointestinal encephalopathy 66
Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways 66
The isolated carboxy-terminal domain of human mitochondrial leucyl-tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells 65
Cardiomyopathies due to homoplasmic mitochondrial tRNA mutations: morphologic and molecular features 64
Reply: Mitochondrial DNA copy number differentiates the Leber's hereditary optic neuropathy affected individuals from the unaffected mutation carriers 63
Diagnosis of myocardial infarction at autopsy: AECVP reappraisal in the light of the current clinical classification 63
Mitochondrial tRNA mutations manifest not only as hypertrophic cardiomyopathy but also as noncompaction-reply 62
Pantethine treatment is effective in recovering the disease phenotype induced by ketogenic diet in a pantothenate kinase-associated neurodegeneration mouse model 62
Induction of mitochondrial biogenesis is a maladaptive mechanism in mitochondrial cardiomyopathies 62
973 Metabolic Profile of Cisplatin-resistant Phenotype – Studies in Ovarian Carcinoma Cell Lines 62
Inhibition of glucose-6-phosphate dehydrogenase sensitizes cisplatin-resistant cells to death 61
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy 60
Gastrointestinal dysmotility in mitochondrial neurogastrointestinal encephalomyopathy is caused by mitochondrial DNA depletion 60
Searching for genetic modifiers of Leber's hereditary optic neuropathy penetrance 59
Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy 58
Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management 58
Melanopsin-expressing retinal ganglion cells are resistant to cell injury, but not always 58
Pathologic evidence of arrhythmogenic cardiomyopathy and myocarditis in two siblings 56
CXCL13 as biomarker for histological involvement in Sjögren's syndrome 55
Clinical, neurophysiological and skin biopsy study of peripheral neuropathy related to cryoglobulinaemia 54
Pathology of endomyocardial biopsy 53
Blue rubber bleb nevus syndrome and pulmonary hypertension: An unusual association 52
Onset of suspected ulcerative colitis after treatment with tocilizumab in patient with celiac disease and juvenile idiopathic arthritis 52
Mitochondrial Neurogastrointestinal encephalomyopathy: Evidence of mitochondrial DNA depletion in the small intestine 51
Peculiarities of prevalence and morphology of congenital heart disease detected in utero 51
Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation 50
Myopathy complicating lupus pregnancy 50
Monoamine oxidase activity in end-stage heart failure associated with dilated and ischemic cardiomyopathies: a comparison between left and right ventricles 49
NADPH oxidase-dependent redox signaling in human heart failure: Relationship between the left and right ventricle 49
Oncocytic glioblastoma: a glioblastoma showing oncocytic changes and increased mitochondrial DNA copy number 49
Causes of late failure after heart transplantation: A ten-year survey 48
MYOCYTE TRANSDIFFERENTIATION: A POSSIBLE PATHOGENETIC MECHANISM FOR ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 48
Distribution of eosinophils in the gastrointestinal tract of children with no organic disease 47
Myositis in primary Sjögren's syndrome: data from a multicentre cohort 47
Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies. 46
Monoamine oxidase is overactivated in left and right ventricles from ischemic hearts: an intriguing therapeutic target 46
Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction 46
Autophagy occurs in lymphocytes infiltrating sjögren’s syndrome minor salivary glands and correlates with histological severity of salivary gland lesions 45
Sudden cardiac death in the young: a consensus statement on recommended practices for cardiac examination by the pathologist from the Society for Cardiovascular Pathology 44
Patologia del sistema nervoso periferico e tessuto muscolare. 42
Pantothenate kinase-associated neurodegeneration: altered mitochondria membrane potential and defective respiration in Pank2 knock-out mouse model 41
Depletion of mtDNA limited to the external layer of Muscularis propria induces gastrointestinal dysmotility in a MNGIE patient 40
Resection for internal jugular vein thrombosis and cervical lymph nodes' involvement from gastric cancer 40
Myocardial fibrosis: morphologic patterns and role of imaging in diagnosis and prognostication 40
Maintenance therapy with the lowest effective dose of oral viscous budesonide in children with eosinophilic esophagitis 40
Severe rectal prolapse and solitary rectal ulcer in a young anorectic woman with myxoid degeneration of visceral adipose tissue 40
Abdominal lymphadenopathy: hypothesize cat-scratch disease and avoid abdominal excisional biopsy 39
Mitogen-Activated Protein Kinases and Regulation of Mitochondrial Biogenesis in Human Cardiomyopathies 39
Outcome of surgical resection and chemotherapy versus chemotherapy alone for the treatment of isolated primary adrenal lymphoma: a retrospective cohort study of 16 consecutive patients 39
[Mitochondrial diseases]. 36
IS APOPTOSIS A DIAGNOSTIC MARKER OF ACUTE MYOCARDIAL INFARCTION? AN AUTOPSY STUDY COMPARING HISTOLOGICAL, IMMUNOHISTOCHEMICAL, TUNEL, AND DNA ELECTROPHORESIS EVIDENCE 36
Evidence of enteric angiopathy and neuromuscular hypoxia in patients with mitochondrial neurogastrointestinal encephalomyopathy 36
Maladaptive autophagy in the pathogenesis of autoimmune epithelitis in Sjögren's syndrome 35
Axonal mtDNA Copy Number Correlates with the Neurodegenerative Pattern in Optic Nerve Cross-Sections of Leber's Hereditary Optic Neuropathy Patients 34
Increase of mtDNA copy number is a successful compensatory strategy in Leber's Hereditary Optic Neuropathy (LHON) 33
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): position paper on diagnosis, prognosis, and treatment by the MNGIE International Network 31
Lymphadenopathies before and during the pandemic COVID-19: increasing incidence of metastases from solid tumors 30
Induction of mitochondrial biogenesis is a maladaptive mechanism in cardiac remodeling 29
The Biventricular Form of Arrhythmogenic Cardiomyopathy Is the Most frequent Morphologic Substrate of Juvenile Sudden Cardiac Death in Sports 29
A new double immunohistochemistry method to detect mucosal anti-transglutaminase IgA deposits in coeliac children 29
PARALLELISM IN MYOGENIC OXIDATIVE ALTERATIONS BETWEEN UNCOMPLICATED AND COMPLICATED DIVERTICULAR DISEASE 25
[Cardiomyopathies due to defective energy metabolism: morphological and functional features]. 25
Isolated Distal Myopathy of the Upper Limbs Associated With Mitochondrial DNA Depletion and Polymerase gamma Mutations 25
Teaching anatomical pathology in the undergraduate curriculum in Medicine: The experience of 'C Course', Sapienza University, Rome 24
Epstein-Barr virus encoded EBNA2 downregulates ICOSL by inducing miR-24 in B-cell lymphoma 23
Diverticular Disease Worsening Is Associated with Increased Oxidative Stress and Gut Permeability: New Insights by Circulating Biomarkers 22
MITHOCONDRIA-RELATED OXIDATIVE STRESS: AN UNEXPLORED FIELD IN DIVERTICULAR DISEASE 21
Thoracic aorta: anatomy and pathology 21
Role of Plakoglobin Immunohistochemistry in Diagnostic Evaluation of Juvenile Sudden Cardiac Death 21
Totale 5.718
Categoria #
all - tutte 17.363
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 17.363


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019202 0 0 0 0 0 0 0 0 0 0 0 202
2019/20201.365 170 43 11 65 141 196 185 159 148 127 72 48
2020/2021604 52 51 20 31 7 96 12 35 63 151 62 24
2021/20221.073 16 55 122 41 130 40 50 113 73 64 187 182
2022/20231.161 197 286 58 121 119 128 33 71 93 12 27 16
2023/2024745 46 93 34 62 68 111 55 61 26 91 67 31
Totale 5.973