ZANOBIO, MARIATERESA
 Distribuzione geografica
Continente #
EU - Europa 133
NA - Nord America 62
AS - Asia 27
SA - Sud America 2
AF - Africa 1
Totale 225
Nazione #
IT - Italia 74
US - Stati Uniti d'America 62
IE - Irlanda 37
SG - Singapore 12
DE - Germania 11
CN - Cina 6
FI - Finlandia 6
KR - Corea 6
CO - Colombia 2
IN - India 2
NL - Olanda 2
AL - Albania 1
AT - Austria 1
BJ - Benin 1
NO - Norvegia 1
TR - Turchia 1
Totale 225
Città #
Dublin 37
Santa Clara 20
Naples 17
Chandler 9
Munich 8
New York 8
Rome 8
Boardman 6
Singapore 6
Milan 5
Seoul 5
Casoria 4
Città di Castello 4
Lappeenranta 4
Wuhan 4
Agropoli 3
Porto Torres 3
San Giovanni Rotondo 3
Arquata Scrivia 2
Barranquilla 2
Cagliari 2
Ferno 2
Helsinki 2
Reggio Calabria 2
Santa Maria Capua Vetere 2
Aligarh 1
Amsterdam 1
Bacoli 1
Beijing 1
Bolzano 1
Boydton 1
Bremen 1
Cotonou 1
Delhi 1
Frankfurt am Main 1
Groningen 1
Istanbul 1
Livorno 1
Nocera Umbra 1
Nuremberg 1
Oslo 1
Sant'Anastasia 1
Tirana 1
Totale 186
Nome #
Patients with DeSanto-Shinawi syndrome: Further extension of phenotype from Italy 78
Mystery(n) Phenotypic Presentation in Europeans: Report of Three Further Novel Missense RNF213 Variants Leading to Severe Syndromic Forms of Moyamoya Angiopathy and Literature Review 34
Neurofibromatosis Type 1: Pediatric Aspects and Review of Genotype-Phenotype Correlations 31
Alu-Mediated Insertions in the DMD Gene: A Difficult Puzzle to Interpret Clinically 26
Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications 23
A new genetic cause of spastic ataxia: the p.Glu415Lys variant in TUBA4A 14
Digital health and Clinical Patient Management System (CPMS) platform utility for data sharing of neuromuscular patients: the Italian EURO-NMD experience 10
Heterozygosity for loss-of-function variants in LZTR1 is associated with isolated multiple café-au-lait macules 10
Joint contractures is a recurrent clinical feature of individuals with neurodevelopmental disorder due to FOXP1 likely gene disruptive variants 9
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses 3
Totale 238
Categoria #
all - tutte 1.347
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 1.347


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2022/202367 0 0 1 3 4 7 0 4 34 0 6 8
2023/202496 7 5 6 12 15 9 17 2 1 6 11 5
2024/202575 9 10 2 15 39 0 0 0 0 0 0 0
Totale 238