CRIS Current Research Information System

COCCHI, GUIDO
 Distribuzione geografica
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Continente #
NA - Nord America 4.781
EU - Europa 4.347
AS - Asia 4.101
AF - Africa 320
SA - Sud America 245
Continente sconosciuto - Info sul continente non disponibili 20
OC - Oceania 4
Totale 13.818
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Nazione #
US - Stati Uniti d'America 4.706
IT - Italia 1.187
CN - Cina 1.135
SG - Singapore 1.084
VN - Vietnam 975
GB - Regno Unito 893
DE - Germania 460
SE - Svezia 452
HK - Hong Kong 243
UA - Ucraina 235
FR - Francia 234
IN - India 220
RU - Federazione Russa 201
NL - Olanda 164
BR - Brasile 161
KR - Corea 127
IE - Irlanda 121
CI - Costa d'Avorio 113
ZA - Sudafrica 87
JP - Giappone 68
FI - Finlandia 66
CH - Svizzera 55
EE - Estonia 44
TG - Togo 42
AR - Argentina 41
BG - Bulgaria 39
SC - Seychelles 39
CA - Canada 34
JO - Giordania 31
ES - Italia 27
TR - Turchia 26
BD - Bangladesh 25
TH - Thailandia 24
ID - Indonesia 23
MX - Messico 21
PH - Filippine 21
SK - Slovacchia (Repubblica Slovacca) 21
AT - Austria 20
DK - Danimarca 19
PL - Polonia 19
RO - Romania 19
BE - Belgio 18
A1 - Anonimo 16
EC - Ecuador 13
IQ - Iraq 12
SA - Arabia Saudita 12
HR - Croazia 11
CL - Cile 9
CZ - Repubblica Ceca 9
GR - Grecia 9
LB - Libano 9
NG - Nigeria 9
UZ - Uzbekistan 9
CO - Colombia 8
IL - Israele 8
PK - Pakistan 8
TW - Taiwan 8
DO - Repubblica Dominicana 6
IR - Iran 6
EG - Egitto 5
LT - Lituania 5
PY - Paraguay 5
AU - Australia 4
HU - Ungheria 4
MY - Malesia 4
SN - Senegal 4
TN - Tunisia 4
CY - Cipro 3
DZ - Algeria 3
EU - Europa 3
GE - Georgia 3
JM - Giamaica 3
KE - Kenya 3
KZ - Kazakistan 3
MA - Marocco 3
NI - Nicaragua 3
NP - Nepal 3
OM - Oman 3
PE - Perù 3
RS - Serbia 3
AE - Emirati Arabi Uniti 2
AL - Albania 2
AZ - Azerbaigian 2
CR - Costa Rica 2
GT - Guatemala 2
MT - Malta 2
PT - Portogallo 2
SV - El Salvador 2
TT - Trinidad e Tobago 2
UY - Uruguay 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AO - Angola 1
BF - Burkina Faso 1
BH - Bahrain 1
BJ - Benin 1
BY - Bielorussia 1
ET - Etiopia 1
GA - Gabon 1
GH - Ghana 1
GI - Gibilterra 1
Totale 13.806
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Città #
Southend 762
Singapore 761
Ashburn 531
Fairfield 459
Chandler 376
Bologna 261
San Jose 249
Woodbridge 245
Hefei 228
Hong Kong 224
Houston 201
Ho Chi Minh City 198
Seattle 187
Dong Ket 180
Wilmington 179
Ann Arbor 167
Hanoi 154
Santa Clara 152
Cambridge 149
Jacksonville 139
Princeton 134
Beijing 128
Abidjan 113
Dublin 110
Boardman 109
Nanjing 92
Seoul 92
Milan 78
Los Angeles 76
Lauterbourg 71
Frankfurt am Main 67
Westminster 59
Tokyo 58
Berlin 53
Padova 52
Helsinki 50
New York 48
Saint Petersburg 43
Lomé 42
Jinan 40
Guangzhou 39
Bern 38
Rome 38
Munich 37
Buffalo 36
Council Bluffs 36
Sofia 35
Turin 34
Hangzhou 32
Amman 31
Dallas 30
Redwood City 29
Da Nang 28
Redmond 27
Fuzhou 25
Chicago 24
Redondo Beach 24
Haiphong 22
Bratislava 21
Hebei 21
Jakarta 21
Kuban 21
Shanghai 21
Mülheim 20
Falls Church 19
San Diego 19
Changsha 18
Shenzhen 18
Brussels 17
Mahé 17
Zhengzhou 16
São Paulo 15
Chengdu 14
Orem 14
Phoenix 14
Atlanta 13
Bengaluru 13
Madrid 13
Medford 13
Shenyang 13
Mumbai 12
Tianjin 12
Dearborn 11
Düsseldorf 11
Imola 11
Istanbul 11
Jiaxing 11
Nanchang 11
Quận Bình Thạnh 11
Salt Lake City 11
Timisoara 11
Wuhan 11
Bari 10
Des Moines 10
Lappeenranta 10
London 10
Ningbo 10
Nuremberg 10
Parma 10
Pescara 10
Totale 8.467
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Nome #
International retrospective cohort study of neural tube defects in relation to folic acid recommendations:are the recommendations working? 1.082
Proton MR spectroscopy (1H-MRS) and amplitude integrated EEG (aEEG) in predicting outcome in term newborns affected by hypoxic-ischemic encephalopathy (HIE). 313
Asfissia fetale intra-partum nella Clinica Ostetrica dell'Università di Bologna: analisi critica degli ultimi 4 anni 296
Down Syndrome: how to communicate the diagnosis 274
One-carbon pathway and cognitive skills in children with Down syndrome 272
One-carbon pathway metabolites are altered in the plasma of subjects with Down syndrome: Relation to chromosomal dosage 267
Age-related changes of adaptive and neuropsychological features in persons with Down Syndrome 266
A reassessment of Jackson's checklist and identification of two Down syndrome sub-phenotypes 265
How to become an under 11 rescuer: a practical method to teach first aid to primary schoolchildren. 249
Partial trisomy 21 with or without highly restricted Down syndrome critical region (HR-DSCR): report of two new cases and reanalysis of the genotype-phenotype association 237
Human trisomy 21 fibroblasts rescue methotrexate toxic effect after treatment with 5-methyl-tetrahydrofolate and 5-formyl-tetrahydrofolate 232
Adverse pregnancy outcomes in women exposed to gabapentin and pregabalin: data from a population-based study 230
Systematic reanalysis of partial trisomy 21 cases with or without Down syndrome suggests a small region on 21q22.13 as critical to the phenotype 228
Preventing neural tube defects in Europe: A missed opportunity. 225
Cri du chat syndrome: caso clinico con cariotipo dup5p/del5p derivante da inversione pericentrica materna del cromosoma 5 223
Analysis of a nanoparticle‑enriched fraction of plasma reveals miRNA candidates for down syndrome pathogenesis 223
Identification of a DNA methylation siganture in blood cells from persons with Down Syndrome. 222
Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: An international consensus statement 221
MTHFR C677T polymorphism analysis: A simple, effective restriction enzyme-based method improving previous protocols 221
Emilia-Romagna Study on Pregnancy and Exposure to Antiepileptic drugs (ESPEA): a population-based study on prescription patterns, pregnancy outcomes and fetal health 220
Plasma metabolome and cognitive skills in Down syndrome 220
Neonatal hypoxic-ischemic encephalopathy in apparently low risk pregnancies: retrospective analysis of the last five years at the University of Bologna. 217
An integrated route to identifying new pathogenesis-based therapeutic approaches for trisomy 21 (Down Syndrome) following the thought of Jérôme Lejeune 217
Partial trisomy 21 map: Ten cases further supporting the highly restricted Down syndrome critical region (HR-DSCR) on human chromosome 21 215
Eruption delay in a 47 XXY male: a case report. 214
Oro-dental features of Pallister–Killian syndrome: Evaluation of 21 European probands 213
Integrated quantitative transcriptome maps of human trisomy 21 tissues and cells 204
Mowat-Wilson syndrome: Facial phenotype changing with age: Study of 19 Italian patients and review of the literature 200
Plasma and urinary metabolomic profiles of Down syndrome correlate with alteration of mitochondrial metabolism 199
The transcriptome profile of human trisomy 21 blood cells 199
Bullous recurrent eruption of incontinentia pigmenti. 198
A regional audit system for stillbirth: A way to better understand the phenomenon 196
Clinical features and follow-up in patients with 22q11.2 deletion syndrome 195
Myoclonic epilepsy with photosensitivity in infants with Pallister-Killian Syndrome 194
Disseminate Recurrent Folliculitis and Hidradenitis Suppurativa Are Associated Conditions: Results From a Retrospective Study of 131 Patients With Down Syndrome and a Cohort of 12,351 Pediatric Controls 189
Diagnosis and Successful Intrauterine Treatment of Fetal Goiter: A Case Report 188
Is the age of developmental milestones a predictor for future development in down syndrome? 188
INTERNATIONAL TRENDS OF DOWN SYNDROME 1993-2004: BIRTHS IN RELATION TO MATERNAL AGE AND TERMINATIONS OF PREGNANCIES. 186
Prenatal diagnosis of open spina bifida in Emilia-Romagna 184
Prenatal diagnosis of open and closed spina bifida 184
Abstracts from the 13th EUROCAT SCIENTIFIC SYMPOSIUM: Advancing congenital anomaly research through collaboration, 16-17 June 2016, Milan, Italy 184
HOW VALID ARE THE RATES OF DOWN SYNDROME INTERNATIONALLY? FINDINGS FROM THE INTERNATIONAL CLEARINGHOUSE FOR BIRTH DEFECTS SURVEILLANCE AND RESEARCH. 180
Eating and Lifestyle Habits in Youth With Down Syndrome Attending a Care Program: An Exploratory Lesson for Future Improvements 180
CD64 as a diagnostic marker for neonatal infection 176
Neonatal Outcome in Operative Vaginal Delivery 176
Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care 173
Down Syndrome and thyroid dysfunction: longitudinal follow-up 0-10 years 173
Proton MR Spectroscopy (1H-MRS) and ampltude integrated EEG on predicting outcome in newborns affected by Hypoxic-Ischemic Encephalopathy (HIE) 166
Bladder exstrophy: An epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research, and an overview of the literature 165
Amelia: A multi-center descriptive epidemiologic study in a large dataset from the International Clearinghouse for Birth Defects Surveillance and Research, and overview of the literature 164
Neuroimaging findings in Mowat-Wilson syndrome: A study of 54 patients 160
Quanto il ritardo di crescita intrauterino influenza le malformazioni congenite? 158
Comparison of two different neonatal skin care practices and their influence on transepidermal water loss in healthy newborns within first 10 days of life. 156
Silver-Russell syndrome due to paternal H19/IGF2 hypomethylation in a twin girl born after in vitro fertilization 154
Starch thickening of human milk is ineffective in reducing the gastroesophageal reflux in preterm infants: a crossover study using intraluminal impedance. 151
Prenatal profile of Pallister-Killian syndrome: Retrospective analysis of 114 pregnancies, literature review and approach to prenatal diagnosis 151
CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases 146
Recommendations of the Scientific Committee of the Italian Beckwith-Wiedemann Syndrome Association on the diagnosis, Management and follow-up of the syndrome 146
Hair in newborns and infants: clinical and dermoscopic evaluation of 45 cases 137
Short distal limbs, polydactyly and nail hypoplasia 136
PREFERENTIAL ASSOCIATIONS BETWEEN ORAL CLEFTS AND OTHER MAJOR CONGENITAL ANOMALIES 136
Hay-Wells syndrome: a case report. 135
Genotype-phenotype correlation for congenital heart disease in Down syndrome through analysis of partial trisomy 21 cases 134
Highly restricted Down syndrome critical region identified on human chromosome 21. 126
Ritardo di crescita e malformazioni congenite 121
null 112
IMMUNOLOGICAL PATTERNS IN CHILDREN WITH DOWN SYNDROME: IS THERE A TEMPORAL TREND? 108
FAMILIAL OCCURRENCE OF MULTIPLE PTERYGIUM SYNDROME: EXPRESSION IN A HETEROZYGOTE OF THE RECESSSIVE FORM OR VARIABILITY OF THE DOMINANT FORM 104
Proton mr spectroscopy (1h-mrs) and amplitude integrated eeg in predicting outcome in newborns affected by hypoxic-ischemic encephalopathy (hie): 356 89
null 77
Functional Dysregulation of CDC42 Causes Diverse Developmental Phenotypes 66
Totale 14.206
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Categoria #
all - tutte 33.856
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 33.856
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021767 0 0 0 0 0 0 0 0 0 164 182 421
2021/20222.140 179 136 242 170 192 125 108 188 160 121 300 219
2022/20231.632 169 250 83 181 78 139 62 84 284 55 149 98
2023/2024613 23 91 42 55 46 102 60 52 25 38 36 43
2024/20251.834 99 235 149 125 241 73 144 65 61 220 82 340
2025/20263.876 364 459 375 346 440 231 393 204 804 260 0 0
Totale 14.206