CASTORI, MARCO
 Distribuzione geografica
Continente #
NA - Nord America 2.584
EU - Europa 535
AS - Asia 343
SA - Sud America 14
AF - Africa 12
Totale 3.488
Nazione #
US - Stati Uniti d'America 2.559
IT - Italia 229
IN - India 126
SG - Singapore 105
CN - Cina 87
SE - Svezia 70
FI - Finlandia 54
UA - Ucraina 53
DE - Germania 34
CA - Canada 20
GB - Regno Unito 15
NL - Olanda 15
RO - Romania 14
AR - Argentina 11
BE - Belgio 11
BG - Bulgaria 11
FR - Francia 11
IE - Irlanda 9
PK - Pakistan 8
MX - Messico 5
MY - Malesia 5
TG - Togo 5
PH - Filippine 4
SA - Arabia Saudita 4
CL - Cile 3
PT - Portogallo 3
CH - Svizzera 2
HU - Ungheria 2
NG - Nigeria 2
SC - Seychelles 2
AE - Emirati Arabi Uniti 1
EG - Egitto 1
HR - Croazia 1
IL - Israele 1
IR - Iran 1
LT - Lituania 1
MU - Mauritius 1
TH - Thailandia 1
ZA - Sudafrica 1
Totale 3.488
Città #
Fairfield 478
Woodbridge 229
Ashburn 218
Seattle 206
Houston 174
Wilmington 161
Cambridge 157
Chandler 140
Rome 83
Ann Arbor 76
Princeton 68
Beijing 67
San Paolo di Civitate 63
Singapore 61
Plano 53
Lawrence 49
Boston 41
San Diego 39
New York 31
Millbury 26
Des Moines 21
Jacksonville 20
Dearborn 19
Fremont 18
Andover 14
Toronto 12
Federal 11
Sofia 11
Bremen 10
Bühl 10
Dublin 10
Norwalk 9
Peshawar 8
London 7
Redmond 7
Bologna 6
Helsinki 6
Horia 6
Pittsburgh 6
Waanrode 6
Lomé 5
Mannheim 5
Milan 5
Boardman 4
Buffalo 4
Falls Church 4
Ottawa 4
Quezon City 4
Brussels 3
Chennai 3
Edmonton 3
Kuala Lumpur 3
Lubbock 3
Maniago 3
Mexico City 3
Padova 3
San Mateo 3
Santa Clara 3
Trento 3
Berlin 2
Fuzhou 2
Guangzhou 2
Hyderabad 2
Indiana 2
Jeddah 2
Kunming 2
Lagos 2
Liège 2
Los Angeles 2
Mathi 2
Naaldwijk 2
Nanjing 2
Paris 2
Porto 2
Prineville 2
Redwood City 2
Rieti 2
Riyadh 2
Romainville 2
San Jose 2
Sannois 2
Suzzara 2
Szeged 2
Worthing 2
Abu Dhabi 1
Baotou 1
Bern 1
Braga 1
Chapel Hill 1
Chiang Mai 1
Chongqing 1
Dallas 1
Fort Worth 1
Frankfurt am Main 1
Frascati 1
Giugliano In Campania 1
Hadera 1
Hangzhou 1
Harrisburg 1
Hefei 1
Totale 2.771
Nome #
The use of piezosurgery in cranial surgery in children 90
Clinical and molecular characterization of a boy with intellectual disability, facial dysmorphism, minor digital anomalies and a complex IL1RAPL1 intragenic rearrangement 87
Prediction and visualization data for the interpretation of sarcomeric and non-sarcomeric DNA variants found in patients with hypertrophic cardiomyopathy 87
Clinical features predicting identification of CDKN2A mutations in Italian patients with familial cutaneous melanoma 86
Re-writing the natural history of pain and related symptoms in the joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type 82
Exploring relationships between joint hypermobility and neurodevelopment in children (4–13 years) with hereditary connective tissue disorders and developmental coordination disorder 79
Oropharyngeal teratoma, oral duplication, cervical diplomyelia and anencephaly in a 22-week fetus: A review of the craniofacial teratoma syndrome 79
Clinical and genetic study of two patients with Zimmermann-Laband syndrome and literature review 76
Biallelic variants in the ciliary gene TMEM67 cause RHYNS syndrome 75
The nosology of Richieri-Costa/Guion-Almeida syndrome(s). 74
Fast and early mandibular osteogenetic distraction in a 24-day-old female newborn with Larsen syndrome. 74
A proposal of rehabilitative approach in the rare disease “De Barsy Syndrome”: case report 74
Unexpected association between joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type and obsessive-compulsive personality disorder. 73
Evaluation of Kinesiophobia and Its Correlations with Pain and Fatigue in Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome Hypermobility Type 72
Quality of Life in the Classic and Hypermobility Types of Elhers-Danlos Syndrome 71
Ehlers-Danlos syndrome hypermobility type and the excess of affected females: Possible mechanisms and perspectives 70
Temporomandibular joint mobility in adult females with Ehlers-Danlos syndrome, hypermobility type (also known as joint hypermobility syndrome) 70
Towards a re-thinking of the clinical significance of generalized joint hypermobility, joint hypermobiity syndrome, and Ehlers-Danlos syndrome, hypermobility type 70
Monozygotic twin discordance for phacomatosis cesioflammea further supports the post-zygotic mutation hypothesis 69
Early ultrasound suspect of thanatophoric dysplasia followed by first trimester molecular diagnosis 68
Foot type analysis based on electronic pedobarography data in individuals with joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type during upright standing. 68
AXIN2 germline mutations are rare in familial melanoma 67
Gynecologic and obstetric implications of the joint hypermobility syndrome (a.k.a. Ehlers-Danlos syndrome hypermobility type) in 82 Italian patients 66
Early mandibular distraction to relieve Robin severe airway obstruction in two siblings with lymphedema-distichiasis syndrome 65
Evaluation of balance and improvement of proprioception by repetitive muscle vibration in a 15-year-old girl with joint hypermobility syndrome 63
Prenatal diagnosis and post-mortem examination in a fetus with thrombocytopenia-absent radius (TAR) syndrome due to compound heterozygosity for a 1q21.1 microdeletion and a RBM8A hypomorphic allele: a case report 63
Adult presentation of arterial tortuosity syndrome in a 51-year-old woman with a novel homozygous c.1411+1G>A mutation in the SLC2A10 gene. 62
Heart rate, conduction and ultrasound abnormalities in adults with joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type 62
Analysis of the miR-34a locus in 62 patients with familial cutaneous melanoma negative for CDKN2A/CDK4 screening 62
Neuropathic pain is a common feature in Ehlers-Danlos syndrome 61
Evaluation of lower limb disability in joint hypermobility syndrome 60
Management of pain and fatigue in the joint hypermobility syndrome (a.k.a. Ehlers-Danlos syndrome, hypermobility type): Principles and proposal for a multidisciplinary approach 60
Ocular features in joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type: A clinical and in vivo confocal microscopy study 58
The "Old Theme" of Variability Versus Transitory Phenotypes in Thanatophoric Dysplasia Type 1: Two 19-Week-Old Fetuses With ("San Diego" Variant) and Without Ragged Metaphyses Due to the Same FGFR3 Mutation 57
Screening for celiac disease in the joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type. 56
Spectrum of mucocutaneous manifestations in 277 patients with joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type. 56
null 55
Identification of a second HOXA2 nonsense mutation in a family with autosomal dominant non-syndromic microtia and distinctive ear morphology 55
Entrapment neuropathies and polyneuropathies in joint hypermobility syndrome/Ehlers-Danlos syndrome 55
null 54
Ehlers-Danlos syndrome hypermobility type: a possible unifying concept for various functional somatic syndromes 53
Genetic skin diseases predisposing to basal cell carcinoma 53
Whorled hairless nevus of the scalp, linear hyperpigmentation, and telangiectatic nevi of the lower limbs: a novel variant of the "phacomatosis complex". 52
Use of the Gait Profile Score for the evaluation of patients with joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type 52
null 51
Identification of a Second HOXA2 Nonsense Mutation in a Family with Autosomal Dominant Non-Syndromic Microtia and distinctive ear morphology 51
Late diagnosis of lateral meningocele syndrome in a 55-year-old woman with symptoms of joint instability and chronic musculoskeletal pain 49
null 49
Gait strategy in patients with Ehlers-Danlos syndrome hypermobility type: A kinematic and kinetic evaluation using 3D gait analysis 48
Molecular characterization of 11 Italian patients with Darier Disease 47
null 42
Relationship between fatigue and gait abnormality in Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome Hypermobility type 38
null 38
Chronic fatigue syndrome is commonly diagnosed in patients with Ehlers-Danlos syndrome hypermobility type/joint hypermobility syndrome 37
COL1-related overlap disorder: a novel connective tissue disorder incorporating the osteogenesis imperfecta/Ehlers-Danlos syndrome overlap 32
Use of low-molecular weight heparin, transfusion and mortality in COVID-19 patients not requiring ventilation 32
Symptom and joint mobility progression in the joint hypermobility syndrome (Ehlers-Danlos syndrome, hypermobility type) 26
Clinical variability in DYNC2H1-related skeletal ciliopathies includes Ellis-van Creveld syndrome 26
Copy number variation analysis implicates novel pathways in patients with oculo-auriculo-vertebral-spectrum and congenital heart defects 20
Loss-of-function variants in exon 4 of TAB2 cause a recognizable multisystem disorder with cardiovascular, facial, cutaneous, and musculoskeletal involvement 20
Consensus based recommendations for diagnosis and medical management of Poland syndrome (sequence) 14
Severity classes in adults with hypermobile Ehlers-Danlos syndrome/hypermobility spectrum disorders: a pilot study of 105 Italian patients 14
Aortic dissection and stroke in a 37-year-old woman: discovering an emerging heritable connective tissue disorder 12
Reassessment of oral frenula in Ehlers-Danlos syndrome: A study of 32 patients with the hypermobility type 9
Clinical and molecular description of the first Italian cohort of 33 subjects with hypophosphatasia 6
An inherited TBX3 alteration in a prenatal case of ulnar‐mammary syndrome: Clinical assessment and functional characterization in Drosophila melanogaster 2
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. 2
Variability in a three-generation family with pierre robin sequence, acampomelic campomelic dysplasia, and intellectual disability due to a novel ∼1 Mb deletion upstream of SOX9, and including KCNJ2 and KCNJ16 1
Totale 3.607
Categoria #
all - tutte 9.950
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 9.950


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020781 0 0 0 52 101 109 133 118 106 84 53 25
2020/2021306 36 40 37 35 7 31 7 42 32 12 12 15
2021/2022621 11 45 57 14 87 19 18 76 42 51 70 131
2022/2023584 122 139 29 52 46 70 6 21 45 8 32 14
2023/2024322 20 39 11 40 32 53 16 6 4 26 24 51
2024/202598 28 19 50 1 0 0 0 0 0 0 0 0
Totale 3.607