IRIS
ALLEGRI, ANNA ELSA MARIA
 Distribuzione geografica
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Continente #
EU - Europa 1.229
Totale 1.229
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Nazione #
IT - Italia 1.229
Totale 1.229
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Città #
Genova 864
Genoa 196
Rapallo 161
Bordighera 8
Totale 1.229
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Nome #
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations. 142
Association of achondroplasia with sagittal synostosis and scaphocephaly in two patients, an underestimated condition? 136
Management of diabetes insipidus and adipsia in the child. 125
Classical and non-classical causes of GH deficiency in the paediatric age 121
Posterior pituitary (PP) evaluation in patients with anterior pituitary defect associated with ectopic PP and septo-optic dysplasia. 116
A novel pathogenic MYH3 mutation in a child with Sheldon–Hall syndrome and vertebral fusions 113
Age- and sex-matched reference curves for serum collagen type I C-telopeptides and bone alkaline phosphatase in children and adolescents: An alternative multivariate statistical analysis approach 112
Central adrenal insufficiency in children and adolescents 96
Role of MRI T2-DRIVE in the assessment of pituitary stalk abnormalities without gadolinium in pituitary diseases 93
Growth factors and metabolic markers in cord blood: relationship to birth weight and length. 72
Reliability of clonidine testing for the diagnosis of growth hormone deficiency in children and adolescents 35
Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases 29
Pubertal timing in children with Silver Russell syndrome compared to those born small for gestational age 25
Clinical, Endocrine and Neuroimaging Findings in Girls with Central Precocious Puberty 24
Precocious Puberty Diagnoses Spike, COVID-19 Pandemic, and Body Mass Index: Findings From a 4-year Study 14
Accuracy of Glucagon Testing Across Transition in Young Adults with Childhood-Onset Growth Hormone Deficiency 13
A novel pathogenic MYH3 mutation in a child with Sheldon-Hall syndrome and vertebral fusion 12
The clinical management of children with achondroplasia in Italy: results of clinician and parent/caregiver surveys 2
Totale 1.280
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Categoria #
all - tutte 4.506
article - articoli 4.506
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 9.012
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020326 14 11 12 20 23 39 42 34 40 48 35 8
2020/2021163 9 10 15 14 9 10 6 14 7 17 8 44
2021/2022153 14 1 5 16 8 20 2 30 15 20 4 18
2022/2023185 14 15 3 21 25 24 3 13 34 3 30 0
2023/2024180 6 17 1 28 19 30 25 8 4 4 8 30
2024/20256 6 0 0 0 0 0 0 0 0 0 0 0
Totale 1.280