IRIS
ALLEGRI, ANNA ELSA MARIA
 Distribuzione geografica
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Continente #
EU - Europa 1.966
AS - Asia 6
Totale 1.972
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Nazione #
IT - Italia 1.966
CN - Cina 5
SG - Singapore 1
Totale 1.972
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Città #
Genova 864
Genoa 753
Vado Ligure 180
Rapallo 161
Bordighera 8
Beijing 4
Singapore 1
Totale 1.971
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Nome #
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 201
Association of achondroplasia with sagittal synostosis and scaphocephaly in two patients, an underestimated condition? 185
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations. 167
Classical and non-classical causes of GH deficiency in the paediatric age 164
A novel pathogenic MYH3 mutation in a child with Sheldon–Hall syndrome and vertebral fusions 162
Management of diabetes insipidus and adipsia in the child. 156
Central adrenal insufficiency in children and adolescents 142
Posterior pituitary (PP) evaluation in patients with anterior pituitary defect associated with ectopic PP and septo-optic dysplasia. 141
Role of MRI T2-DRIVE in the assessment of pituitary stalk abnormalities without gadolinium in pituitary diseases 127
Growth factors and metabolic markers in cord blood: relationship to birth weight and length. 101
Pubertal timing in children with Silver Russell syndrome compared to those born small for gestational age 82
Clinical, Endocrine and Neuroimaging Findings in Girls with Central Precocious Puberty 64
Precocious Puberty Diagnoses Spike, COVID-19 Pandemic, and Body Mass Index: Findings From a 4-year Study 62
Reliability of clonidine testing for the diagnosis of growth hormone deficiency in children and adolescents 58
Blood Lymphocyte Subsets and Proinflammatory Cytokine Profile in ROHHAD(NET) and non-ROHHAD(NET) Obese Individuals 57
Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases 57
A novel pathogenic MYH3 mutation in a child with Sheldon-Hall syndrome and vertebral fusion 52
The clinical management of children with achondroplasia in Italy: results of clinician and parent/caregiver surveys 32
How pain affect real life of children and adults with achondroplasia: A systematic review 14
Totale 2.024
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Categoria #
all - tutte 7.600
article - articoli 7.600
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 15.200
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021129 0 0 0 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
2023/2024171 6 17 1 28 19 30 25 8 4 4 8 21
2024/2025514 14 34 16 35 48 45 48 97 17 34 67 59
2025/2026245 137 10 58 40 0 0 0 0 0 0 0 0
Totale 2.024