IRIS
MAGNANI, Cinzia
 Distribuzione geografica
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Continente #
NA - Nord America 1.181
EU - Europa 1.059
AS - Asia 423
Continente sconosciuto - Info sul continente non disponibili 3
SA - Sud America 1
Totale 2.667
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Nazione #
US - Stati Uniti d'America 1.162
CN - Cina 348
IE - Irlanda 240
SE - Svezia 238
IT - Italia 146
FI - Finlandia 142
UA - Ucraina 98
DE - Germania 89
TR - Turchia 56
AT - Austria 38
GB - Regno Unito 27
BE - Belgio 20
CA - Canada 19
FR - Francia 11
SG - Singapore 10
NL - Olanda 7
EU - Europa 3
IN - India 3
VN - Vietnam 2
BR - Brasile 1
CY - Cipro 1
ES - Italia 1
HK - Hong Kong 1
JP - Giappone 1
KH - Cambogia 1
PT - Portogallo 1
RO - Romania 1
Totale 2.667
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Città #
Chandler 250
Dublin 240
Jacksonville 141
Ann Arbor 94
Beijing 87
Dearborn 83
Ashburn 71
Parma 71
Izmir 54
Nanjing 51
Princeton 45
Vienna 38
Shanghai 33
San Mateo 31
New York 22
Helsinki 20
Wilmington 19
Boardman 18
Shenyang 18
Des Moines 17
Brussels 16
Hebei 16
Nanchang 16
Toronto 16
Hefei 15
Jiaxing 15
Rio Saliceto 15
Tianjin 14
Bremen 13
Kunming 13
Woodbridge 10
Jinan 9
Norwalk 9
Los Angeles 8
Guangzhou 7
Seattle 7
Tulsa 7
Ningbo 6
Falls Church 5
Hangzhou 5
Reggio Emilia 5
Taiyuan 5
Chengdu 4
Haikou 4
Taizhou 4
Waanrode 4
Changsha 3
Fuzhou 3
Milan 3
Torino 3
Wenzhou 3
Zhengzhou 3
Ardea 2
Ariano nel Polesine 2
Auburn Hills 2
Berlin 2
Bologna 2
Borås 2
Caserta 2
Chicago 2
Chongqing 2
Dong Ket 2
Düsseldorf 2
Fairfield 2
Fremont 2
Genova 2
Heidelberg 2
Kocaeli 2
Modena 2
Oakland 2
Paris 2
Pittsburgh 2
Pune 2
Rockville 2
Tappahannock 2
Amsterdam 1
Augusta 1
Cambridge 1
Central 1
Chaoyang 1
Elk Grove Village 1
Frankfurt am Main 1
Huizen 1
Iasi 1
Lanzhou 1
Leawood 1
Leiden 1
Lisbon 1
Madrid 1
Mainz 1
Monmouth Junction 1
Monopoli 1
Napoli 1
Nicosia 1
Phnom Penh 1
Piacenza 1
Pomezia 1
Povegliano Veronese 1
Quzhou 1
San Jose 1
Totale 1.740
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Nome #
Detoxification genes polymorphisms in SIDS exposed to tobacco smoke 141
Absent ductus venosus: different perinatal outcome related to anatomy 106
Absent ductus venosus: different perinatal outcome related to anatomy 97
Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesis 87
Cystathionina Beta-Synthasec.844ins68 Gene Variant and Non-Syndromic Cleft Lip and Palate 82
Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 gene 78
Universal newborn hearing screening: The experience of the University Hospital of Parma 77
Confirmed association between monoamine oxidase A molecular polymorphisms and Sudden Infant Death Syndrome. 77
Acrofacial dysostosis syndromes: a relevant prenatal dilemma. A case report and brief literature review 72
Craniosynostosis, hydrocephalus, Chiari I malformation and radioulnar synostosis: Probably a new syndrome 70
Serotonin transporter role in identifying similarities between SIDS and Idiopathic ALTE 70
3D assessment of the Umbilical Vein Deviation Angle (UVDA) for the prediction of liver herniation in Left Congenital Diaphragmatic Hernia 69
Argomenti di pediatria. 68
Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the Sudden Infant Death Syndrome 68
Evidence that polymorphic deletion of theGlutathione S-Transferase Gene, GSTM1,is associated with Esophageal Atresia. 66
ALTE and smoking exposure: which role of detoxification genes polymorphisms? 64
Clinical and Polygraphic Improvement of Breathing Abnormalities After Valproate in a Case of Pitt-Hopkins Syndrome. 63
Neonatal forearm compartment syndrome: look for cerebral stroke 62
Understanding demographic change in a birth defects registry : prevalence , risk factors and monitoring of an immigrant population in Emilia Romagna 61
Trisomic rescue causing reduction to homozygosity for a novel ABCA12 mutation in harlequin ichthyosis 59
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour. 58
Value of autopsy in renal malformations: Comparison of clinical diagnosis and post-mortem examination. 57
Congenital heart defects: 15 years of experience of the Emilia-Romagna Registry (Italy) 57
Multiple joint dislocations: an additional skeletal finding in Lowry-Wood syndrome? 53
Assistential-diagnostic guidelines: Apparent life-threatening events (ALTE) [Linee guida diagnostico-assistenziale: ALTE (Apparent Life-Threatening Events)] 51
Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients 50
Insights into genotype-phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein-Taybi syndrome patients 50
A regional audit system for stillbirth: A way to better understand the phenomenon 50
Determinants of neonatal hypoglycemia after antenatal administration of corticosteroids (ACS) for lung maturation: Data from two referral centers and review of the literature 50
Unilateral ectopic parotid gland in CHARGE syndrome. 49
Neonatal chronic renal failure associated with maternal ingestion of an analgesic Nimesulide 49
Recessive bullous dermolysis of the newborn in preterm siblings with a missense mutation in type VII collagen 48
Temporal variability in birth prevalence of congenital heart defects as recorded by a general birth defects registry 47
Early Skeletal Signs in Netherton Syndrome 46
A rare case of multiple congenital epulis 43
Are there any strategies to improve neonatal outcomes associated with epidural analgesia in labor? 43
Il latte materno 42
SMC1A Codon 496 Mutations Affect the Cellular Response to Genotoxic Treatments 42
FAM111A mutations result in hypoparathyroidism and impaired skeletal development 42
Urinary tract abnormalities (UTA) and associated malformations: Data of the Emilia-Romagna Registry 41
DIAGNOSI DIFFERENZIALE NELLA DISTROFIA MIOTONICA: RILEVANZA OSTETRICA E PERINATALE 39
Maternal obesity and congenital anomalies: Temporal change in BMI in Emilia Romagna , Italy 36
Molecular Polymorphisms of Vascular Endothelial Growth Factor Gene and Bronchopulmonary Dysplasia in Very Low Birth Weight Infants 32
Mandibular distraction in neonates: indications, technique, results 32
The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteria. 29
Limb reduction defects in Emilia Romagna, Italy: epidemiological and genetic study in 173 109 consecutive births 24
Totale 2.697
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Categoria #
all - tutte 8.865
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 8.865
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201977 0 0 0 0 0 0 0 0 0 0 72 5
2019/2020578 96 103 37 3 44 75 68 13 48 41 13 37
2020/2021297 8 28 26 8 39 13 25 5 71 17 44 13
2021/2022195 12 2 2 6 6 2 22 23 11 20 12 77
2022/2023953 88 102 69 78 97 114 5 57 291 2 34 16
2023/2024220 26 22 9 12 21 66 27 21 4 10 2 0
Totale 2.697