SEVERINO, MARIASAVINA
 Distribuzione geografica
Continente #
EU - Europa 880
AS - Asia 3
AF - Africa 1
SA - Sud America 1
Totale 885
Nazione #
IT - Italia 880
CN - Cina 3
BR - Brasile 1
ZA - Sudafrica 1
Totale 885
Città #
Genoa 710
Vado Ligure 134
Rapallo 23
Genova 10
Beijing 2
Bordighera 2
Milan 1
São Paulo 1
Totale 883
Nome #
3q29 microduplication syndrome: Description of two new cases and delineation of the minimal critical region 88
Early Extra-Uterine Growth Restriction in Very-Low-Birth-Weight Neonates with Normal or Mildly Abnormal Brain MRI: Effects on a 2-3-Year Neurodevelopmental Outcome 85
LONG-TERM OUTCOME IN CEREBRAL ARTERIA ISCHEMIC STROKE (AIS) DUE TO VARICELLA ZOSTER VIRUS (VZV) IN CHILDREN 76
Multi-view fusion of diffusion MRI microstructural models: a preterm birth study 56
Corpus callosum agenesis and interhemispheric cysts: Epileptic evaluation and long-term outcome in 9 children 53
De novo variants in DENND5B cause a neurodevelopmental disorder 51
Basal ganglia stroke in pediatric population: Single center experience 48
Vein of Galen aneurysmal malformation: does size affect outcome? 43
PRENATAL DIAGNOSIS OF CORPUS CAL­ LOSUM AGENESIS WITH ASSOCIATED INTER­ HEMISPHERIC CYSTS: LONG­TERM OUTCOME IN 23 CHILDREN 42
Imaging characteristics and neurosurgical outcome in subjects with agenesis of the corpus callosum and interhemispheric cysts 41
Intragenic Microdeletion of ULK4 and Partial Microduplication of BRWD3 in Siblings with Neuropsychiatric Features and Obesity 39
Novel KIF26A variants associated with pediatric intestinal pseudo-obstruction (PIPO) and brain developmental defects 39
Case Report: Novel biallelic moderately damaging variants in RTTN in a patient with cerebellar dysplasia 38
LOW-GRADE IVH AND LOW-GRADE CBH: WHICH INFLUENCE ON GRIFFITHS SCORE AT 2 YEARS OF AGE? 36
Expanding the phenotype of UPF3B-related disorder: Case reports and literature review 34
Expanding the Mutational Landscape and Clinical Phenotype of CHD2-Related Encephalopathy 33
Variants in the WDR44 WD40-repeat domain cause a spectrum of ciliopathy by impairing ciliogenesis initiation 31
Neonatal Perforator Stroke: Timing, Risk Factors, and Neurological Outcome from a Single-Center Experience 31
Novel loss-of-function variants expand ABCC9-related intellectual disability and myopathy syndrome 29
A hypomorphic FLVCR2 variant resulting in moderate transport deficiency causes hydranencephaly syndrome with brain calcifications 11
Arteriovenous cerebral high-flow shunts: genetic analysis of patients from a pediatric tertiary care center 9
Totale 913
Categoria #
all - tutte 3.510
article - articoli 3.510
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 7.020


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/202212 0 0 0 3 2 0 0 2 0 2 0 3
2022/202324 1 3 0 1 5 1 1 4 4 1 3 0
2023/202487 3 1 0 1 1 3 3 21 13 12 4 25
2024/2025505 33 20 8 29 20 61 38 94 35 26 75 66
2025/2026285 132 32 56 65 0 0 0 0 0 0 0 0
Totale 913