Catalogo dei prodotti della ricerca

CASTORI, MARCO
 Distribuzione geografica
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Continente #
NA - Nord America 2.670
AS - Asia 748
EU - Europa 722
SA - Sud America 87
AF - Africa 17
Totale 4.244
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Nazione #
US - Stati Uniti d'America 2.638
SG - Singapore 452
IT - Italia 300
IN - India 130
CN - Cina 94
SE - Svezia 71
FI - Finlandia 66
BR - Brasile 63
UA - Ucraina 53
DE - Germania 47
RU - Federazione Russa 47
GB - Regno Unito 26
CA - Canada 25
HK - Hong Kong 19
NL - Olanda 17
AR - Argentina 16
FR - Francia 15
AT - Austria 14
RO - Romania 14
BE - Belgio 12
BG - Bulgaria 11
IE - Irlanda 10
ID - Indonesia 8
PK - Pakistan 8
MX - Messico 6
SA - Arabia Saudita 6
MY - Malesia 5
TG - Togo 5
BD - Bangladesh 4
PH - Filippine 4
CL - Cile 3
MA - Marocco 3
PT - Portogallo 3
CH - Svizzera 2
DK - Danimarca 2
HU - Ungheria 2
JO - Giordania 2
LT - Lituania 2
NG - Nigeria 2
PE - Perù 2
PL - Polonia 2
SC - Seychelles 2
TR - Turchia 2
TW - Taiwan 2
UZ - Uzbekistan 2
ZA - Sudafrica 2
AE - Emirati Arabi Uniti 1
AM - Armenia 1
BS - Bahamas 1
CO - Colombia 1
EC - Ecuador 1
EE - Estonia 1
EG - Egitto 1
GR - Grecia 1
HR - Croazia 1
IL - Israele 1
IQ - Iraq 1
IR - Iran 1
IS - Islanda 1
KE - Kenya 1
KR - Corea 1
KZ - Kazakistan 1
MU - Mauritius 1
NO - Norvegia 1
PS - Palestinian Territory 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
UY - Uruguay 1
VN - Vietnam 1
Totale 4.244
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Città #
Fairfield 478
Singapore 231
Woodbridge 229
Ashburn 219
Seattle 207
Houston 174
Wilmington 161
Cambridge 157
Chandler 140
Rome 111
Ann Arbor 76
Princeton 68
Beijing 67
San Paolo di Civitate 63
Plano 53
Lawrence 49
Boston 41
San Diego 39
Santa Clara 37
New York 31
Millbury 26
Des Moines 21
Jacksonville 20
Dearborn 19
Hong Kong 19
Cosenza 18
Fremont 18
Helsinki 17
Andover 14
Toronto 13
Dublin 11
Federal 11
London 11
Sofia 11
Bremen 10
Bühl 10
Norwalk 9
Peshawar 8
Council Bluffs 7
Milan 7
Nuremberg 7
Ottawa 7
Redmond 7
The Dalles 7
Bologna 6
Horia 6
Jakarta 6
Naples 6
Pittsburgh 6
Vienna 6
Waanrode 6
Boardman 5
Lomé 5
Mannheim 5
Moscow 5
Brussels 4
Buffalo 4
Dhaka 4
Falls Church 4
Los Angeles 4
Mexico City 4
Preston 4
Quezon City 4
São Paulo 4
Yubileyny 4
Belo Horizonte 3
Chennai 3
Edmonton 3
Falkenstein 3
Jeddah 3
Kuala Lumpur 3
Lauterbourg 3
Lubbock 3
Maniago 3
Padova 3
Riyadh 3
San Mateo 3
Trento 3
Amman 2
Bengaluru 2
Berlin 2
Brasília 2
Casablanca 2
Cislago 2
College Station 2
Copenhagen 2
Dallas 2
Frankfurt am Main 2
Fuzhou 2
Guangzhou 2
Hyderabad 2
Imperatriz 2
Indiana 2
Kunming 2
Lagos 2
Lappeenranta 2
Latina 2
Lima 2
Liège 2
Malang 2
Totale 3.124
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Nome #
A proposal of rehabilitative approach in the rare disease “De Barsy Syndrome”: case report 113
The use of piezosurgery in cranial surgery in children 103
Clinical and molecular characterization of a boy with intellectual disability, facial dysmorphism, minor digital anomalies and a complex IL1RAPL1 intragenic rearrangement 102
Prediction and visualization data for the interpretation of sarcomeric and non-sarcomeric DNA variants found in patients with hypertrophic cardiomyopathy 102
Exploring relationships between joint hypermobility and neurodevelopment in children (4–13 years) with hereditary connective tissue disorders and developmental coordination disorder 96
Clinical features predicting identification of CDKN2A mutations in Italian patients with familial cutaneous melanoma 92
Biallelic variants in the ciliary gene TMEM67 cause RHYNS syndrome 90
Re-writing the natural history of pain and related symptoms in the joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type 90
Oropharyngeal teratoma, oral duplication, cervical diplomyelia and anencephaly in a 22-week fetus: A review of the craniofacial teratoma syndrome 89
Clinical and genetic study of two patients with Zimmermann-Laband syndrome and literature review 88
Fast and early mandibular osteogenetic distraction in a 24-day-old female newborn with Larsen syndrome. 86
The nosology of Richieri-Costa/Guion-Almeida syndrome(s). 84
Unexpected association between joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type and obsessive-compulsive personality disorder. 83
Early ultrasound suspect of thanatophoric dysplasia followed by first trimester molecular diagnosis 81
Towards a re-thinking of the clinical significance of generalized joint hypermobility, joint hypermobiity syndrome, and Ehlers-Danlos syndrome, hypermobility type 80
Quality of Life in the Classic and Hypermobility Types of Elhers-Danlos Syndrome 79
Monozygotic twin discordance for phacomatosis cesioflammea further supports the post-zygotic mutation hypothesis 79
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 79
Evaluation of Kinesiophobia and Its Correlations with Pain and Fatigue in Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome Hypermobility Type 79
Temporomandibular joint mobility in adult females with Ehlers-Danlos syndrome, hypermobility type (also known as joint hypermobility syndrome) 78
Ehlers-Danlos syndrome hypermobility type and the excess of affected females: Possible mechanisms and perspectives 76
Evaluation of balance and improvement of proprioception by repetitive muscle vibration in a 15-year-old girl with joint hypermobility syndrome 75
Gynecologic and obstetric implications of the joint hypermobility syndrome (a.k.a. Ehlers-Danlos syndrome hypermobility type) in 82 Italian patients 75
Analysis of the miR-34a locus in 62 patients with familial cutaneous melanoma negative for CDKN2A/CDK4 screening 75
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. 73
AXIN2 germline mutations are rare in familial melanoma 73
Spectrum of mucocutaneous manifestations in 277 patients with joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type. 73
Foot type analysis based on electronic pedobarography data in individuals with joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type during upright standing. 73
Early mandibular distraction to relieve Robin severe airway obstruction in two siblings with lymphedema-distichiasis syndrome 72
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 71
Identification of a Second HOXA2 Nonsense Mutation in a Family with Autosomal Dominant Non-Syndromic Microtia and distinctive ear morphology 71
Ocular features in joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type: A clinical and in vivo confocal microscopy study 71
Heart rate, conduction and ultrasound abnormalities in adults with joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type 70
Neuropathic pain is a common feature in Ehlers-Danlos syndrome 68
Evaluation of lower limb disability in joint hypermobility syndrome 68
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 67
Identification of a second HOXA2 nonsense mutation in a family with autosomal dominant non-syndromic microtia and distinctive ear morphology 65
Screening for celiac disease in the joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type. 65
Genetic skin diseases predisposing to basal cell carcinoma 61
Whorled hairless nevus of the scalp, linear hyperpigmentation, and telangiectatic nevi of the lower limbs: a novel variant of the "phacomatosis complex". 60
Entrapment neuropathies and polyneuropathies in joint hypermobility syndrome/Ehlers-Danlos syndrome 60
Ehlers-Danlos syndrome hypermobility type: a possible unifying concept for various functional somatic syndromes 58
Late diagnosis of lateral meningocele syndrome in a 55-year-old woman with symptoms of joint instability and chronic musculoskeletal pain 57
Molecular characterization of 11 Italian patients with Darier Disease 56
null 55
Use of the Gait Profile Score for the evaluation of patients with joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type 55
null 54
Gait strategy in patients with Ehlers-Danlos syndrome hypermobility type: A kinematic and kinetic evaluation using 3D gait analysis 51
null 51
Clinical variability in DYNC2H1-related skeletal ciliopathies includes Ellis-van Creveld syndrome 51
An inherited TBX3 alteration in a prenatal case of ulnar‐mammary syndrome: Clinical assessment and functional characterization in Drosophila melanogaster 50
null 49
COL1-related overlap disorder: a novel connective tissue disorder incorporating the osteogenesis imperfecta/Ehlers-Danlos syndrome overlap 46
Use of low-molecular weight heparin, transfusion and mortality in COVID-19 patients not requiring ventilation 45
Chronic fatigue syndrome is commonly diagnosed in patients with Ehlers-Danlos syndrome hypermobility type/joint hypermobility syndrome 43
null 42
Relationship between fatigue and gait abnormality in Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome Hypermobility type 41
Copy number variation analysis implicates novel pathways in patients with oculo-auriculo-vertebral-spectrum and congenital heart defects 40
null 38
Symptom and joint mobility progression in the joint hypermobility syndrome (Ehlers-Danlos syndrome, hypermobility type) 36
Severity classes in adults with hypermobile Ehlers-Danlos syndrome/hypermobility spectrum disorders: a pilot study of 105 Italian patients 33
Loss-of-function variants in exon 4 of TAB2 cause a recognizable multisystem disorder with cardiovascular, facial, cutaneous, and musculoskeletal involvement 33
Prevalence of rare missense TTN variants in a cohort of patients with cardiomyopathy 26
Clinical and molecular description of the first Italian cohort of 33 subjects with hypophosphatasia 24
Aortic dissection and stroke in a 37-year-old woman: discovering an emerging heritable connective tissue disorder 24
Consensus based recommendations for diagnosis and medical management of Poland syndrome (sequence) 21
Reassessment of oral frenula in Ehlers-Danlos syndrome: A study of 32 patients with the hypermobility type 16
Heterozygosity for loss-of-function variants in LZTR1 is associated with isolated multiple café-au-lait macules 14
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. 12
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 8
Adapting to Adulthood: A Review of Transition Strategies for Osteogenesis Imperfecta 8
null 3
Totale 4.375
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Categoria #
all - tutte 13.218
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 13.218
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202078 0 0 0 0 0 0 0 0 0 0 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
2024/2025866 28 19 50 36 63 69 99 59 257 168 18 0
Totale 4.375