RITELLI, Marco Giuseppe
 Distribuzione geografica
Continente #
NA - Nord America 3.167
EU - Europa 1.764
AS - Asia 517
AF - Africa 45
SA - Sud America 37
OC - Oceania 33
Continente sconosciuto - Info sul continente non disponibili 1
Totale 5.564
Nazione #
US - Stati Uniti d'America 3.091
FR - Francia 422
DE - Germania 312
IT - Italia 312
CN - Cina 202
GB - Regno Unito 112
CZ - Repubblica Ceca 96
RU - Federazione Russa 90
VN - Vietnam 90
PL - Polonia 87
CA - Canada 68
IN - India 55
NL - Olanda 54
IE - Irlanda 43
SE - Svezia 43
UA - Ucraina 40
JP - Giappone 31
ZA - Sudafrica 30
AU - Australia 29
KR - Corea 24
ES - Italia 23
HK - Hong Kong 20
CL - Cile 17
FI - Finlandia 17
GR - Grecia 17
TW - Taiwan 17
CH - Svizzera 15
BE - Belgio 14
DK - Danimarca 12
IS - Islanda 12
SG - Singapore 12
AE - Emirati Arabi Uniti 11
AT - Austria 9
BR - Brasile 9
ID - Indonesia 9
IL - Israele 8
IR - Iran 7
TH - Thailandia 7
MX - Messico 6
AR - Argentina 5
MT - Malta 5
TR - Turchia 5
ET - Etiopia 4
HR - Croazia 4
MY - Malesia 4
NO - Norvegia 4
NZ - Nuova Zelanda 4
PH - Filippine 4
RO - Romania 4
BG - Bulgaria 3
GH - Ghana 3
PT - Portogallo 3
BD - Bangladesh 2
CO - Colombia 2
GE - Georgia 2
LV - Lettonia 2
MO - Macao, regione amministrativa speciale della Cina 2
NG - Nigeria 2
PE - Perù 2
QA - Qatar 2
RS - Serbia 2
SD - Sudan 2
SI - Slovenia 2
TN - Tunisia 2
BY - Bielorussia 1
BZ - Belize 1
EC - Ecuador 1
EU - Europa 1
FO - Isole Faroe 1
HU - Ungheria 1
LT - Lituania 1
ML - Mali 1
NP - Nepal 1
OM - Oman 1
PA - Panama 1
PK - Pakistan 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
VE - Venezuela 1
Totale 5.564
Città #
Fairfield 338
Ashburn 299
Houston 230
Buffalo 186
Woodbridge 183
Seattle 175
Ann Arbor 120
Cambridge 109
Wilmington 95
Dong Ket 83
Warsaw 76
Brescia 69
Los Angeles 49
Beijing 42
Dublin 41
Paris 36
Chicago 29
Shanghai 29
Stockholm 28
Phoenix 26
Las Vegas 25
Wuhan 25
Nuremberg 24
Ottawa 24
San Diego 23
Muizenberg 21
Nürnberg 20
Clearwater 19
Milan 17
Rome 17
Boardman 14
Helsinki 13
New York 13
Sydney 13
University Park 13
Kopavogur 12
Amsterdam 11
Bengaluru 11
Brooklyn 11
Council Bluffs 11
London 11
Nanjing 11
Dearborn 10
Moscow 10
Tokyo 10
Albino 9
Albuquerque 9
Reseda 9
Champaign 8
Córdoba 8
Guangzhou 8
Hangzhou 8
Henderson 8
Padova 8
Saint Louis 8
San Francisco 8
Atlanta 7
Madison 7
Taipei 7
Dallas 6
Easton 6
Frankfurt am Main 6
Hamilton 6
Milpitas 6
Mountain View 6
Nanchang 6
Portland 6
Provo 6
Rezzato 6
Riva 6
San Jose 6
Singapore 6
Toronto 6
Arlington 5
Bethesda 5
Boulder 5
Chengdu 5
Florence 5
Hong Kong 5
Irvine 5
Jakarta 5
Manchester 5
Nashville 5
Perth 5
Pune 5
Rennes 5
Simi Valley 5
Suzhou 5
Tel Aviv 5
Zurich 5
Bondeno 4
Boston 4
Central 4
Changsha 4
Edmonton 4
Ferryhill 4
Ghent 4
Krimpen Aan Den Ijssel 4
Leawood 4
Minneapolis 4
Totale 2.953
Nome #
Characterization and expression of slc2a10, the zebrafish ortholog of the human gene involved in arterial tortuosity syndrome., file ddc633e3-a947-4e2e-e053-3705fe0a4c80 611
Further delineation of FKBP14-related Ehlers-Danlos syndrome: a patient with early vascular complications and non-progressive kyphoscoliosis, and literature review, file ddc633e3-6bdf-4e2e-e053-3705fe0a4c80 343
Risk Profile of Symptomatic Lacunar Stroke Versus Nonlobar Intracerebral Hemorrhage, file ddc633e3-273a-4e2e-e053-3705fe0a4c80 293
Antithrombotic medications and the etiology of intracerebral hemorrhage: MUCH-Italy., file ddc633e3-0131-4e2e-e053-3705fe0a4c80 283
Clinical and molecular characterization of an 18-month-old infant with autosomal recessive cutis laxa type 1C due to a novel LTBP4 pathogenic variant, and literature review, file ddc633e3-d8b2-4e2e-e053-3705fe0a4c80 247
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: clinical findings and novel COL3A1 mutations, file ddc633e3-a94d-4e2e-e053-3705fe0a4c80 233
Mutations in TGFBR2 gene cause spontaneous cervical artery dissection, file ddc633e3-35de-4e2e-e053-3705fe0a4c80 192
Transcriptome-wide expression profiling in skin fibroblasts of patients with joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type, file ddc633e3-2064-4e2e-e053-3705fe0a4c80 179
Report on a patient with extremely fragile skin, dermatosparaxis, joint hypermobility, short stature, skeletal deformities, and lipomas: a new syndrome?, file ddc633e3-aae4-4e2e-e053-3705fe0a4c80 169
Cellular and molecular mechanisms in the pathogenesis of classical, vascular, and hypermobile ehlers‒danlos syndromes, file ddc633e3-f65d-4e2e-e053-3705fe0a4c80 165
Connective tissue anomalies in patients with spontaneous cervical artery dissection., file ddc633e3-0132-4e2e-e053-3705fe0a4c80 159
A novel homozygous SLC2A9 mutation associated with renal-induced hypouricemia, file ddc633e3-24a3-4e2e-e053-3705fe0a4c80 152
Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular Ehlers-Danlos syndrome, file ddc633e3-8b7d-4e2e-e053-3705fe0a4c80 147
Insights in the etiopathology of galactosyltransferase II (GalT-II) deficiency from transcriptome-wide expression profiling of skin fibroblasts of two sisters with compound heterozygosity for two novel B3GALT6 mutations, file ddc633e3-9bb1-4e2e-e053-3705fe0a4c80 146
Expanding the clinical and mutational spectrum of recessive AEBP1-related classical-like Ehlers-Danlos syndrome, file ddc633e3-c868-4e2e-e053-3705fe0a4c80 145
Molecular genetics and pathogenesis of Ehlers–Danlos syndrome and related connective tissue disorders, file ddc633e4-18ed-4e2e-e053-3705fe0a4c80 132
Clinical and molecular characterization of 40 patients with classic Ehlers--Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations., file ddc633e2-b9bf-4e2e-e053-3705fe0a4c80 121
Molecular Genetics and Pathogenesis of Ehlers–Danlos Syndrome and Related Connective Tissue Disorders. Edited by Marina Colombi and Marco Ritelli, file ddc633e4-1711-4e2e-e053-3705fe0a4c80 117
Recurrent exercise-induced acute renal failure in a young Pakistani man with severe renal hypouricemia and SLC2A9 compound heterozygosity., file ddc633e2-bf76-4e2e-e053-3705fe0a4c80 116
Glucose transporter type 10-lacking in arterial tortuosity syndrome-facilitates dehydroascorbic acid transport, file ddc633e3-1769-4e2e-e053-3705fe0a4c80 112
GLUT10-Lacking in Arterial Tortuosity Syndrome-Is Localized to the Endoplasmic Reticulum of Human Fibroblasts, file ddc633e3-6806-4e2e-e053-3705fe0a4c80 112
Clinical variability in two Macedonian families with Arterial tortuosity syndrome, file ddc633e3-c85e-4e2e-e053-3705fe0a4c80 112
Molecular insights in the pathogenesis of classical Ehlers-Danlos syndrome from transcriptome-wide expression profiling of patients' skin fibroblasts, file ddc633e3-c866-4e2e-e053-3705fe0a4c80 112
Further defining the phenotypic spectrum of B3GAT3 mutations and literature review on linkeropathy syndromes, file ddc633e3-f65f-4e2e-e053-3705fe0a4c80 109
Multisystemic manifestations in a cohort of 75 classical Ehlers-Danlos syndrome patients: natural history and nosological perspectives, file ddc633e4-170f-4e2e-e053-3705fe0a4c80 106
Clinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel TNXB Variant, file ddc633e4-01b5-4e2e-e053-3705fe0a4c80 100
Identification of the novel COL5A1 c.3369_3431dup, p.(Glu1124_Gly1144dup) variant in a patient with incomplete classical Ehlers–Danlos syndrome: The importance of phenotype-guided genetic testing, file ddc633e4-128e-4e2e-e053-3705fe0a4c80 90
Expanding the PURA syndrome phenotype: A child with the recurrent PURA p.(Phe233del) pathogenic variant showing similarities with cutis laxa, file ddc633e4-26c1-4e2e-e053-3705fe0a4c80 80
Abnormal Vasculature Development in Zebrafish Embryos with Reduced Expression of Pantothenate Kinase 2 Gene, file ddc633e4-3f61-4e2e-e053-3705fe0a4c80 80
Molecular characterization and transcriptome-wide expression profiling of two patients affected with spondyloepimetaphyseal dysplasia with joint laxity type, file ddc633e3-aae2-4e2e-e053-3705fe0a4c80 74
Dermal fibroblast-to-myofibroblast transition sustained by αvβ3 integrin-ILK-Snail1/Slug signaling is a common feature for hypermobile Ehlers-Danlos syndrome and hypermobility spectrum disorders, file ddc633e3-8a8d-4e2e-e053-3705fe0a4c80 72
Classic Ehlers-danlos syndrome: clinical and molecular characterisation of 37 patients, file ddc633e3-a94b-4e2e-e053-3705fe0a4c80 68
GLUT10 deficiency leads to oxidative stress and non-canonical αvβ3 integrin-mediated TGFβ signalling associated with extracellular matrix disarray in arterial tortuosity syndrome skin fibroblasts, file ddc633e3-46ca-4e2e-e053-3705fe0a4c80 55
Type V and type III collagen modulate the expression and assembly of fibronectin extracellar matrix in classic and vascular Ehlers-Danlos syndrome fibroblasts, affecting cell survival and migration, file ddc633e3-a949-4e2e-e053-3705fe0a4c80 51
Expanding the clinical and mutational spectrum of B4GALT7-spondylodysplastic Ehlers-Danlos syndrome, file ddc633e4-3d12-4e2e-e053-3705fe0a4c80 48
Matrix metalloproteinases inhibition by doxycycline rescues extracellular matrix organization and partly reverts myofibroblast differentiation in hypermobile ehlers-danlos syndrome dermal fibroblasts: A potential therapeutic target?, file ddc633e4-5ca1-4e2e-e053-3705fe0a4c80 47
Mutations in TGFBR2 gene cause spontaneous cervical artery dissection, file ddc633e3-3479-4e2e-e053-3705fe0a4c80 45
Hereditary alpha-tryptasemia modifies clinical phenotypes among individuals with congenital hypermobility disorders, file ddc633e4-6c5c-4e2e-e053-3705fe0a4c80 45
Aortic rupture after thoracic endovascular repair in a patient with Familial Thoracic Aortic Aneurysm and Dissections type 6 (FTAAD6), file ddc633e2-dd08-4e2e-e053-3705fe0a4c80 40
Serum cholesterol levels, HMG-CoA reductase inhibitors and the risk of intracerebral haemorrhage. the Multicenter Study on Cerebral Haemorrhage in Italy (MUCH-Italy), file ddc633e4-5fac-4e2e-e053-3705fe0a4c80 39
Absence of collagen flowers on electron microscopy and identification of (likely) pathogenic COL5A1 variants in two patients, file ddc633e3-f661-4e2e-e053-3705fe0a4c80 37
Atypical variants in COL1A1 and COL3A1 associated with classical and vascular Ehlers-Danlos syndrome overlap phenotypes: expanding the clinical phenotype based on additional case reports, file d3d96750-a4ae-4ed5-85aa-b828a722c86b 34
Arterial Tortuosity Syndrome: a vitamin C compartmentation disease?, file ddc633e3-57f4-4e2e-e053-3705fe0a4c80 27
GLUT10 deficiency leads to oxidative stress and non-canonical avb3 integrin-mediated TGF signalling associated with extracellular matrix disarray in arterial tortuosity syndrome skin fibroblasts., file ddc633e3-5a2c-4e2e-e053-3705fe0a4c80 25
RNA-Seq of Dermal Fibroblasts from Patients with Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders Supports Their Categorization as a Single Entity with Involvement of Extracellular Matrix Degrading and Proinflammatory Pathomechanisms, file 3847cbe7-c451-4027-b9e4-950b2fa13d30 19
GARFIELD-NGS: Genomic vARiants FIltering by dEep Learning moDels in NGS, file ddc633e4-3b79-4e2e-e053-3705fe0a4c80 19
Connective tissue anomalies in patients with spontaneous cervical artery dissection., file ddc633e2-f828-4e2e-e053-3705fe0a4c80 17
Deciphering disease signatures and molecular targets in vascular Ehlers-Danlos syndrome through transcriptome and miRNome sequencing of dermal fibroblasts, file c14474ff-8c2d-4394-8858-b23e60ffe754 12
Multifaced Roles of the αvβ3 Integrin in Ehlers–Danlos and Arterial Tortuosity Syndromes’ Dermal Fibroblasts, file ddc633e3-9ff5-4e2e-e053-3705fe0a4c80 10
Genotypic categorization of Loeys-Dietz syndrome based on 24 novel families and literature data, file ddc633e4-01b4-4e2e-e053-3705fe0a4c80 9
Antithrombotic medications and the etiology of intracerebral hemorrhage: MUCH-Italy., file ddc633e2-f826-4e2e-e053-3705fe0a4c80 5
Characterization and expression pattern analysis of the facilitative glucose transporter 10 gene (slc2a10) in Danio rerio, file ddc633e2-afe5-4e2e-e053-3705fe0a4c80 4
Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β, file ddc633e4-0367-4e2e-e053-3705fe0a4c80 4
Looking back and beyond the 2017 diagnostic criteria for hypermobile Ehlers-Danlos syndrome: A retrospective cross-sectional study from an Italian reference center, file ea5f6874-3578-4fbd-a29a-aa0c539e3a88 4
Biological insights in the pathogenesis of hypermobile Ehlers-Danlos syndrome from proteome profiling of patients' dermal myofibroblasts, file ddc633e4-365d-4e2e-e053-3705fe0a4c80 3
Gynecologic and obstetric implications of the joint hypermobility syndrome (a.k.a. Ehlers-Danlos syndrome hypermobility type) in 82 Italian patients, file ddc633e2-be5e-4e2e-e053-3705fe0a4c80 2
COL6A5 variants in familial neuropathic chronic itch, file ddc633e3-4b98-4e2e-e053-3705fe0a4c80 2
Application of the 2017 criteria for vascular Ehlers-Danlos syndrome in 50 patients ascertained according to the Villefranche nosology, file ddc633e3-fbf5-4e2e-e053-3705fe0a4c80 2
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: clinical findings and novel COL3A1 mutations., file ddc633e2-b022-4e2e-e053-3705fe0a4c80 1
Recurring and generalized visceroptosis in Ehlers-Danlos syndrome hypermobility type, file ddc633e2-b9b7-4e2e-e053-3705fe0a4c80 1
Nosology and inheritance pattern(s) of joint hypermobility syndrome and Ehlers-Danlos syndrome, hypermobility type: A study of intrafamilial and interfamilial variability in 23 Italian pedigrees., file ddc633e2-b9d0-4e2e-e053-3705fe0a4c80 1
Type III and V collagens modulate the expression and assembly of EDA+ fibronectin in the extracellular matrix of defective Ehlers-Danlos syndrome fibroblasts, file ddc633e2-bc62-4e2e-e053-3705fe0a4c80 1
Delineation of Ehlers–Danlos syndrome phenotype due to the c.934C>T, p.(Arg312Cys) mutation in COL1A1: Report on a three-generation family without cardiovascular events, and literature review, file ddc633e3-5129-4e2e-e053-3705fe0a4c80 1
Spectrum of mucocutaneous, ocular and facial features and delineation of novel presentations in 62 classical Ehlers-Danlos syndrome patients, file ddc633e3-8c61-4e2e-e053-3705fe0a4c80 1
Totale 5.788
Categoria #
all - tutte 4.147.697
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 4.147.697


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019305 0 0 0 0 0 0 0 0 0 73 113 119
2019/2020986 101 63 46 109 91 97 91 88 98 66 67 69
2020/2021921 38 74 62 66 86 95 74 70 60 75 78 143
2021/20221.171 58 91 72 126 107 70 89 70 70 58 255 105
2022/2023911 43 59 222 114 59 110 47 46 40 61 60 50
2023/20241.022 41 58 73 60 92 69 193 269 114 53 0 0
Totale 5.788