IRIS
MAGNANI, Cinzia
 Distribuzione geografica
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Continente #
NA - Nord America 1.258
EU - Europa 1.079
AS - Asia 565
Continente sconosciuto - Info sul continente non disponibili 3
AF - Africa 1
SA - Sud America 1
Totale 2.907
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Nazione #
US - Stati Uniti d'America 1.239
CN - Cina 378
IE - Irlanda 240
SE - Svezia 238
IT - Italia 148
FI - Finlandia 147
SG - Singapore 122
UA - Ucraina 98
DE - Germania 97
TR - Turchia 56
AT - Austria 38
GB - Regno Unito 27
BE - Belgio 20
CA - Canada 19
FR - Francia 14
NL - Olanda 7
EU - Europa 3
IN - India 3
CZ - Repubblica Ceca 2
VN - Vietnam 2
BR - Brasile 1
CI - Costa d'Avorio 1
CY - Cipro 1
ES - Italia 1
HK - Hong Kong 1
JP - Giappone 1
KH - Cambogia 1
PT - Portogallo 1
RO - Romania 1
Totale 2.907
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Città #
Chandler 250
Dublin 240
Jacksonville 141
Ann Arbor 94
Singapore 92
Beijing 87
Dearborn 83
Ashburn 71
Parma 71
Boardman 65
Shanghai 55
Izmir 54
Nanjing 51
Princeton 45
Vienna 38
San Mateo 31
Helsinki 25
New York 22
Wilmington 19
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
Santa Clara 9
Los Angeles 8
Munich 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
Marseille 3
Milan 3
Torino 3
Wenzhou 3
Zhengzhou 3
Ardea 2
Ariano nel Polesine 2
Auburn Hills 2
Berlin 2
Bologna 2
Borås 2
Brno 2
Caserta 2
Cervia 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
Abidjan 1
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
Totale 1.924
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Nome #
Detoxification genes polymorphisms in SIDS exposed to tobacco smoke 148
Absent ductus venosus: different perinatal outcome related to anatomy 113
Absent ductus venosus: different perinatal outcome related to anatomy 104
Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesis 93
Cystathionina Beta-Synthasec.844ins68 Gene Variant and Non-Syndromic Cleft Lip and Palate 88
Confirmed association between monoamine oxidase A molecular polymorphisms and Sudden Infant Death Syndrome. 84
Clinical and molecular characterization of Rubinstein-Taybi syndrome patients carrying distinct novel mutations of the EP300 gene 83
Universal newborn hearing screening: The experience of the University Hospital of Parma 82
3D assessment of the Umbilical Vein Deviation Angle (UVDA) for the prediction of liver herniation in Left Congenital Diaphragmatic Hernia 80
Acrofacial dysostosis syndromes: a relevant prenatal dilemma. A case report and brief literature review 78
Craniosynostosis, hydrocephalus, Chiari I malformation and radioulnar synostosis: Probably a new syndrome 76
Serotonin transporter role in identifying similarities between SIDS and Idiopathic ALTE 75
Argomenti di pediatria. 75
Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the Sudden Infant Death Syndrome 75
Evidence that polymorphic deletion of theGlutathione S-Transferase Gene, GSTM1,is associated with Esophageal Atresia. 71
Clinical and Polygraphic Improvement of Breathing Abnormalities After Valproate in a Case of Pitt-Hopkins Syndrome. 71
ALTE and smoking exposure: which role of detoxification genes polymorphisms? 71
Neonatal forearm compartment syndrome: look for cerebral stroke 67
Congenital heart defects: 15 years of experience of the Emilia-Romagna Registry (Italy) 67
Understanding demographic change in a birth defects registry : prevalence , risk factors and monitoring of an immigrant population in Emilia Romagna 65
Trisomic rescue causing reduction to homozygosity for a novel ABCA12 mutation in harlequin ichthyosis 62
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour. 61
Value of autopsy in renal malformations: Comparison of clinical diagnosis and post-mortem examination. 61
Multiple joint dislocations: an additional skeletal finding in Lowry-Wood syndrome? 58
Assistential-diagnostic guidelines: Apparent life-threatening events (ALTE) [Linee guida diagnostico-assistenziale: ALTE (Apparent Life-Threatening Events)] 57
A regional audit system for stillbirth: A way to better understand the phenomenon 56
Determinants of neonatal hypoglycemia after antenatal administration of corticosteroids (ACS) for lung maturation: Data from two referral centers and review of the literature 56
Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients 55
Unilateral ectopic parotid gland in CHARGE syndrome. 54
Insights into genotype-phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein-Taybi syndrome patients 53
Recessive bullous dermolysis of the newborn in preterm siblings with a missense mutation in type VII collagen 53
Neonatal chronic renal failure associated with maternal ingestion of an analgesic Nimesulide 52
Temporal variability in birth prevalence of congenital heart defects as recorded by a general birth defects registry 52
Early Skeletal Signs in Netherton Syndrome 49
Are there any strategies to improve neonatal outcomes associated with epidural analgesia in labor? 48
A rare case of multiple congenital epulis 47
SMC1A Codon 496 Mutations Affect the Cellular Response to Genotoxic Treatments 46
Urinary tract abnormalities (UTA) and associated malformations: Data of the Emilia-Romagna Registry 46
Il latte materno 45
DIAGNOSI DIFFERENZIALE NELLA DISTROFIA MIOTONICA: RILEVANZA OSTETRICA E PERINATALE 45
FAM111A mutations result in hypoparathyroidism and impaired skeletal development 45
Maternal obesity and congenital anomalies: Temporal change in BMI in Emilia Romagna , Italy 39
Molecular Polymorphisms of Vascular Endothelial Growth Factor Gene and Bronchopulmonary Dysplasia in Very Low Birth Weight Infants 35
Mandibular distraction in neonates: indications, technique, results 35
The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteria. 33
Limb reduction defects in Emilia Romagna, Italy: epidemiological and genetic study in 173 109 consecutive births 28
Totale 2.937
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Categoria #
all - tutte 11.178
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 11.178
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020342 0 0 0 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
2023/2024286 26 22 9 12 21 66 27 21 4 10 27 41
2024/2025174 8 49 81 36 0 0 0 0 0 0 0 0
Totale 2.937