PATTI, GIUSEPPA
 Distribuzione geografica
Continente #
EU - Europa 3.609
AS - Asia 64
SA - Sud America 8
NA - Nord America 5
AF - Africa 1
Totale 3.687
Nazione #
IT - Italia 3.609
CN - Cina 54
VN - Vietnam 7
BR - Brasile 6
US - Stati Uniti d'America 4
SG - Singapore 3
AR - Argentina 1
EC - Ecuador 1
MA - Marocco 1
MX - Messico 1
Totale 3.687
Città #
Genoa 1.695
Genova 1.045
Vado Ligure 468
Rapallo 387
Beijing 29
Bordighera 13
Ashburn 4
Ho Chi Minh City 3
Singapore 2
Biên Hòa 1
Bắc Ninh 1
Cabo Frio 1
Can Tho 1
Ezeiza 1
Fes 1
Guarulhos 1
Guayaquil 1
Hanoi 1
Mexico City 1
Milan 1
Porto Alegre 1
Santa Vitória do Palmar 1
Sorocaba 1
São Paulo 1
Totale 3.661
Nome #
Classical and non-classical causes of GH deficiency in the paediatric age 167
Clinical Manifestations and Metabolic Outcomes of Seven Adults with Silver-Russell Syndrome 159
Central adrenal insufficiency in children and adolescents 145
Growth Hormone Deficiency in the Transition Age 133
Role of MRI T2-DRIVE in the assessment of pituitary stalk abnormalities without gadolinium in pituitary diseases 129
Sindrome di Silver Russell Correlazione genotipo-fenotipo e SNC 125
Update on bone density measurements and their interpretation in children and adolescents 122
Cognitive and White Matter Microstructure Development in Congenital Hypothyroidism and Familial Thyroid Disorders 120
Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin gene 114
Accuracy of Glucagon Testing Across Transition in Young Adults with Childhood-Onset Growth Hormone Deficiency 112
Cognitive Profiles and Brain Volume Are Affected in Patients with Silver-Russell Syndrome 112
Accuracy and limitations of the growth hormone (GH) releasing hormone-arginine retesting in young adults with childhood-onset GH deficiency 112
Characterization of Two Novel Variants of the Steroidogenic Acute Regulatory Protein Identified in a Girl with Classic Lipoid Congenital Adrenal Hyperplasia 111
Wolfram syndrome 1 in the Italian population: genotype-phenotype correlations 102
Gut Microbiota in T1DM-Onset Pediatric Patients: Machine-Learning Algorithms to Classify Microorganisms as Disease Linked 100
Central diabetes insipidus in children: Diagnosis and management 96
Gut-microbiota in children and adolescents with obesity: inferred functional analysis and machine-learning algorithms to classify microorganisms 91
Pubertal timing in children with Silver Russell syndrome compared to those born small for gestational age 84
Antibodies Against Hypothalamus and Pituitary Gland in Childhood-Onset Brain Tumors and Pituitary Dysfunction 84
Changing the diagnostic approach to diabetes insipidus: role of copeptin 80
Approach to the Pediatric Patient: Central Diabetes Insipidus 80
Infectious diseases associated with pediatric type 1 diabetes mellitus: A narrative review 73
Endocrine Outcomes In Central Diabetes Insipidus: the Predictive Value of Neuroimaging "Mismatch Pattern" 71
Sleep disorders in Prader-Willi syndrome, evidence from animal models and humans 71
Clinical, Endocrine and Neuroimaging Findings in Girls with Central Precocious Puberty 66
A case report of glucose transporter 1 deficiency syndrome with growth hormone deficiency diagnosed before starting ketogenic diet 65
Precocious Puberty Diagnoses Spike, COVID-19 Pandemic, and Body Mass Index: Findings From a 4-year Study 64
Are glucose and insulin levels at all time points during OGTT a reliable marker of diabetes mellitus risk in pediatric obesity? 64
Advances in differential diagnosis and management of growth hormone deficiency in children 61
Approach to the Child and Adolescent With Adrenal Insufficiency 60
Does the Application of Heat Gel Pack after Eutectic Mixture of Local Anesthetic Cream Improve Venipuncture or Intravenous Cannulation Success Rate in Children? A Randomized Control Trial 60
Uniparental disomy and pretreatment IGF-1 may predict elevated IGF-1 levels in Prader-Willi patients on GH treatment 59
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
Abnormalities of pubertal development and gonadal function in Noonan syndrome 52
Igf1 for the diagnosis of growth hormone deficiency in children and adolescents: A reappraisal 47
The phenotypic spectrum associated with OTX2 mutations in humans 44
Primary Adrenal Insufficiency in Childhood: Data from a Large Nationwide Cohort 43
Quality of life in children and adolescents with growth hormone deficiency and their caregivers: an Italian survey 43
Growth in Children With Noonan Syndrome and Effects of Growth Hormone Treatment on Adult Height 38
Sirolimus Therapy in Congenital Hyperinsulinism: A Successful Experience Beyond Infancy 36
Normal voiding does not exclude posterior urethral valves 35
Letter to the Editor: "Forty-One Individuals With Mutations in the AVP-NPII Gene Associated With Familial Neurohypophyseal Diabetes Insipidus." 32
null 30
Bone Health Determinants in Ambulant Prepubertal Boys With Duchenne Muscular Dystrophy Treated With Deflazacort: Findings From a 3‐Year Study 27
Cushing syndrome in paediatric population: who and how to screen. 25
Hamartoma, Pituitary 24
Clinical Course of COVID-19 in Children With Adrenal Insufficiency: Results From National Data 20
The economic burden of pediatric growth hormone deficiency in Italy: a cost of illness study 19
The Italian registry for patients with Prader-Willi syndrome 19
Hypothalamo-pituitary Disorders in Childhood and Adolescence 16
Distinguishing genetic alterations versus (epi)mutations in Silver-Russell syndrome and focus on the IGF1R gene 13
Multicentric Italian case–control study on 25OH vitamin D levels in children and adolescents with Prader-Willi syndrome 12
Correction: Cushing syndrome in paediatric population: who and how to screen 9
Two-year-old girl with metabolic acidosis and hyperkalaemia 8
Totale 3.798
Categoria #
all - tutte 17.445
article - articoli 16.520
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 603
Totale 34.568


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021209 0 0 0 0 13 11 20 43 12 65 8 37
2021/2022336 28 7 4 23 9 24 12 103 20 42 11 53
2022/2023461 37 46 7 51 58 77 4 35 79 8 50 9
2023/2024352 7 55 12 52 17 41 43 26 10 16 15 58
2024/20251.216 49 80 29 94 150 118 106 193 47 57 159 134
2025/2026660 252 56 186 165 1 0 0 0 0 0 0 0
Totale 3.798