IRIS
ALLEGRI, ANNA ELSA MARIA
 Distribuzione geografica
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Continente #
EU - Europa 1.298
Totale 1.298
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Nazione #
IT - Italia 1.298
Totale 1.298
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Città #
Genova 864
Genoa 197
Rapallo 161
Vado Ligure 68
Bordighera 8
Totale 1.298
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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. 143
Association of achondroplasia with sagittal synostosis and scaphocephaly in two patients, an underestimated condition? 140
Management of diabetes insipidus and adipsia in the child. 128
Classical and non-classical causes of GH deficiency in the paediatric age 125
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 118
Posterior pituitary (PP) evaluation in patients with anterior pituitary defect associated with ectopic PP and septo-optic dysplasia. 117
A novel pathogenic MYH3 mutation in a child with Sheldon–Hall syndrome and vertebral fusions 115
Central adrenal insufficiency in children and adolescents 102
Role of MRI T2-DRIVE in the assessment of pituitary stalk abnormalities without gadolinium in pituitary diseases 98
Growth factors and metabolic markers in cord blood: relationship to birth weight and length. 74
Reliability of clonidine testing for the diagnosis of growth hormone deficiency in children and adolescents 36
Pubertal timing in children with Silver Russell syndrome compared to those born small for gestational age 32
Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases 31
Clinical, Endocrine and Neuroimaging Findings in Girls with Central Precocious Puberty 28
Accuracy of Glucagon Testing Across Transition in Young Adults with Childhood-Onset Growth Hormone Deficiency 24
Precocious Puberty Diagnoses Spike, COVID-19 Pandemic, and Body Mass Index: Findings From a 4-year Study 20
A novel pathogenic MYH3 mutation in a child with Sheldon-Hall syndrome and vertebral fusion 13
The clinical management of children with achondroplasia in Italy: results of clinician and parent/caregiver surveys 5
Totale 1.349
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Categoria #
all - tutte 5.002
article - articoli 5.002
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 10.004
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020301 0 0 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
2024/202575 18 38 19 0 0 0 0 0 0 0 0 0
Totale 1.349