ALLEGRI, ANNA ELSA MARIA
 Distribuzione geografica
Continente #
EU - Europa 17
Totale 17
Nazione #
IT - Italia 17
Totale 17
Città #
Genova 12
Genoa 2
Rapallo 2
Bordighera 1
Totale 17
Nome #
Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases, file e268c4ce-452d-a6b7-e053-3a05fe0adea1 5
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations., file e268c4cb-b405-a6b7-e053-3a05fe0adea1 3
Management of diabetes insipidus and adipsia in the child., file e268c4cb-d941-a6b7-e053-3a05fe0adea1 2
Role of MRI T2-DRIVE in the assessment of pituitary stalk abnormalities without gadolinium in pituitary diseases, file e268c4cb-ec91-a6b7-e053-3a05fe0adea1 2
A novel pathogenic MYH3 mutation in a child with Sheldon–Hall syndrome and vertebral fusions, file e268c4cb-9411-a6b7-e053-3a05fe0adea1 1
Classical and non-classical causes of GH deficiency in the paediatric age, file e268c4cb-d943-a6b7-e053-3a05fe0adea1 1
Central adrenal insufficiency in children and adolescents, file e268c4cb-d949-a6b7-e053-3a05fe0adea1 1
Association of achondroplasia with sagittal synostosis and scaphocephaly in two patients, an underestimated condition?, file e268c4cc-0c27-a6b7-e053-3a05fe0adea1 1
Reliability of clonidine testing for the diagnosis of growth hormone deficiency in children and adolescents, file e268c4cd-0122-a6b7-e053-3a05fe0adea1 1
Totale 17
Categoria #
all - tutte 59
article - articoli 59
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 118


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20204 0 0 0 0 0 0 0 0 1 1 2 0
2020/20217 0 0 0 0 0 0 0 1 3 0 1 2
2021/20221 0 0 0 0 0 0 0 0 1 0 0 0
2022/20232 0 0 0 0 1 0 0 0 0 1 0 0
2023/20243 0 0 0 0 0 1 1 1 0 0 0 0
Totale 17