IRIS
KALANTARI, SILVIA
 Distribuzione geografica
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Continente #
EU - Europa 52
NA - Nord America 35
AS - Asia 30
Totale 117
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Nazione #
US - Stati Uniti d'America 32
IT - Italia 25
SG - Singapore 22
DE - Germania 12
CN - Cina 8
IE - Irlanda 8
CA - Canada 3
FI - Finlandia 3
FR - Francia 2
GB - Regno Unito 2
Totale 117
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Città #
Boardman 19
Singapore 11
Munich 10
Dublin 8
Reggio Emilia 4
Shanghai 4
Chicago 3
Helsinki 3
Pavia 3
Ashburn 2
Azzano San Paolo 2
Beijing 2
Milan 2
New York 2
Ottawa 2
Chandler 1
Frankfurt am Main 1
Jiujiang 1
Nuremberg 1
Priocca 1
Seattle 1
Stockton-on-Tees 1
Toronto 1
Turin 1
Totale 86
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Nome #
SIMPSON-GOLABI-BEHMEL syndrome type 1: How placental immunohistochemistry can rapidly Predict the diagnosis 32
Expanding the phenotype of Brunner syndrome from childhood to adulthood: Description of the second pediatric patient and his mother 18
The Landscape of HNF1B Deficiency: A Syndrome Not Yet Fully Explored 10
De novo RANBP2 variant in a fetal demise case with cerebral intraparenchymal hemorrhage 9
Termination of pregnancy for fetal malformations and severe genetic disorders: what are the laws in Europe? 8
Advancing intercontinental collaboration in human genetics: success story of the African and European Young Investigator Forum 7
Kaposiform Hemangioendothelioma further broadens the phenotype of PIK3CA-related overgrowth spectrum 7
Gene Ontology Enrichment Analysis of Renal Agenesis: Improving Prenatal Molecular Diagnosis 6
Expanding the KIF4A-associated phenotype 5
Mosaic Williams syndrome: A case report 5
The European Society of Human Genetics—Young committee- activities and achievements between 2019–2022 5
A novel COLEC10 mutation in a child with 3MC syndrome 5
Functional evaluation of a novel nonsense variant of the calcium-sensing receptor gene leading to hypocalcemia 4
Neoplasia in Cri du Chat Syndrome from Italian and German Databases 4
New case of syncytial giant-cell variant of hepatocellular carcinoma in a pediatric patient with HNF1B deficiency: Does it fit with the syndrome? 4
Adult-onset CblC deficiency: a challenging diagnosis involving different adult clinical specialists 4
'Kinesinopathies': Emerging role of the kinesin family member genes in birth defects 3
The role of genetic testing in the diagnostic workflow of pediatric patients with kidney diseases: the experience of a single institution 3
Clinical exome sequencing is a powerful tool in the diagnostic flow of monogenic kidney diseases: an Italian experience 3
Totale 142
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Categoria #
all - tutte 1.354
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 1.354
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2022/202317 0 0 0 0 3 1 0 3 10 0 0 0
2023/202427 2 0 0 7 0 4 7 1 2 0 1 3
2024/202598 53 21 13 5 0 6 0 0 0 0 0 0
Totale 142