DI IORGI, NATASCIA
 Distribuzione geografica
Continente #
EU - Europa 10.083
AS - Asia 89
SA - Sud America 18
NA - Nord America 5
AF - Africa 3
Totale 10.198
Nazione #
IT - Italia 10.083
CN - Cina 69
BR - Brasile 12
VN - Vietnam 11
SG - Singapore 8
AR - Argentina 4
US - Stati Uniti d'America 4
AZ - Azerbaigian 1
BO - Bolivia 1
CG - Congo 1
EC - Ecuador 1
MA - Marocco 1
MX - Messico 1
ZA - Sudafrica 1
Totale 10.198
Città #
Genova 5.412
Genoa 2.917
Rapallo 873
Vado Ligure 857
Beijing 34
Bordighera 23
Ashburn 4
Ho Chi Minh City 4
Hanoi 3
Singapore 3
São Paulo 2
Baku 1
Biên Hòa 1
Brazzaville 1
Buenos Aires 1
Cabo Frio 1
Can Tho 1
Coronel Fabriciano 1
Cosmópolis 1
Fes 1
Guarulhos 1
Guayaquil 1
Haiphong 1
La Paz 1
Limeira 1
Milan 1
Passo Fundo 1
Pinamar 1
Pindoretama 1
Pretoria 1
San Antonio de Padua 1
San Juan de Sabinas 1
Santa Vitória do Palmar 1
Sorocaba 1
São José dos Pinhais 1
Totale 10.156
Nome #
A longitudinal printo study on growth and puberty in juvenile systemic lupus erythematosus. 210
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 203
Characteristics of a nationwide cohort of patients presenting with Isolated Hypogonadotropic Hypogonadism (IHH) 193
19q13 microdeletion syndrome: Further refining the critical region 187
Adult height in patients with permanent growth hormone deficiency with and without multiple pituitary hormone deficiencies 184
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 167
Small metacarpal bones of low quality in obese children. 161
Clinical Manifestations and Metabolic Outcomes of Seven Adults with Silver-Russell Syndrome 159
Idiopathic central diabetes insipidus is associated with abnormal blood supply to the posterior pituitary gland caused by vascular impairment of the inferior hypophyseal artery system. 157
Management of diabetes insipidus and adipsia in the child. 157
X-linked hypophosphatemic rickets: an Italian experts' opinion survey 154
Cut-off limits of the peak GH response to stimulation tests for the diagnosis of GH deficiency in children and adolescents: Study in patients with organic GHD 150
Primary hyperparathyroidism in pregnancy treated with cinacalcet: A case report and review of the literature 145
Central adrenal insufficiency in children and adolescents 145
Plasma total adiponectin levels in pediatrics: Reference intervals calculated as a continuous variable of age. 143
Pituitary gland imaging and outcome. 142
Posterior pituitary (PP) evaluation in patients with anterior pituitary defect associated with ectopic PP and septo-optic dysplasia. 141
Highly conserved non-coding sequences and the 18q critical region for short stature: a common mechanism of disease? 140
CNNM2 homozygous mutations cause severe refractory hypomagnesemia, epileptic encephalopathy and brain malformations 138
Growth Hormone Registry: A step forward in standard diagnostic practices in Italy. 136
Prevalence and correlates of adherence in children and adolescents treated with growth hormone: A multicenter Italian study 136
Central diabetes insipidus in children and young adults: etiological diagnosis and long-term outcome of idiopathic cases. 136
Reciprocal relation between marrow adiposity and the amount of bone in the axial and appendicular skeleton of young adults. 135
Growth Hormone Deficiency in the Transition Age 133
Midbrain-hindbrain involvement in septo-optic dysplasia. 130
Role of MRI T2-DRIVE in the assessment of pituitary stalk abnormalities without gadolinium in pituitary diseases 129
Neuroimaging in Growth hormone deficiency 126
Motor function improvement after intravenous pamidronate in osteoporosis pseudoglioma syndrome. 125
Pituitary stalk thickening on MRI: when is the best time to re-scan and how long should we continue re-scanning for? 124
Neuroendocrine late effects after tailored photon radiotherapy for children with low grade gliomas: Long term correlation with tumour and treatment parameters 123
Cross-sectional reference data for phalangeal quantitative ultrasound from early childhood to young-adulthood according to gender, age, skeletal growth, and pubertal development 123
The advantage of measuring spontaneous growth hormone (GH) secretion compared with the insulin tolerance test in the diagnosis of GH deficiency in young adults. 123
The use of neuroimaging for assessing disorders of pituitary development. 122
Update on bone density measurements and their interpretation in children and adolescents 122
Disorders of salt and water balance in children. 121
GH response to ghrelin in subjects with congenital GH deficiency: evidence that ghrelin action requires hypothalamic-pituitary connections 121
Bone acquisition in healthy young females is reciprocally related to marrow adiposity. 120
Cognitive and White Matter Microstructure Development in Congenital Hypothyroidism and Familial Thyroid Disorders 120
Evaluation of adrenal function in patients with growth hormone-deficiency and hypothalamic-pituitary disorders: comparison between insulin-induced hypoglycemia, low-dose ACTH, standard ACTH and CRH stimulation tests. 119
Recommendations for premature ovarian insufficiency surveillance for female survivors of childhood, adolescent, and young adult cancer: A report from the International Late Effects of Childhood Cancer Guideline Harmonization Group in collaboration with the PanCareSurFup consortium 118
Idiopathic central diabetes insipidus in children and young adults is commonly associated with vasopressin-cell antibodies and markers of autoimmunity 117
The Accuracy of the Glucagon Test Compared to the Insulin Tolerance Test in the Diagnosis of Adrenal Insufficiency in Young Children with Growth Hormone Deficiency. 117
The glucagon test in the diagnosis of growth hormone deficiency in children with short stature younger than 6 years. 115
Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin gene 114
New understandings of the genetic basis of isolated idiopathic central hypogonadism. 113
Quantitative ultrasound detects bone impairment after bone marrow transplantation in children and adolescents affected by hematological diseases. 113
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
Characterization of Two Novel Variants of the Steroidogenic Acute Regulatory Protein Identified in a Girl with Classic Lipoid Congenital Adrenal Hyperplasia 111
Deterioration of growth hormone (GH) response and anterior pituitary function in young adults with childhood-onset GH deficiency and ectopic posterior pituitary: a two-year prospective follow-up study 110
Serum insulin-like growth factor-I (IGF-I) reference ranges for chemiluminescence assay in childhood and adolescence. Data from a population of in- and out-patients. 105
Development of pituitary deficit after radiotherapy in pediatric patients after long follow-up 105
Differential effect of marrow adiposity and visceral and subcutaneous fat on cardiovascular risk in young, healthy adults. 103
Novel HESX1 mutations associated with a life-threatening neonatal phenotype, pituitary aplasia, but normally located posterior pituitary and no optic nerve abnormalities 103
Diabetes insipidus--diagnosis and management. 102
Growth factors and metabolic markers in cord blood: relationship to birth weight and length. 101
Case report: Acute clinical presentation and neonatal management of primary hyperparathyroidism due to a novel CaSR mutation 100
Endothelial Dysfunction in Childhood Cancer Survivors: A Narrative Review 98
Reassessment of the growth hormone status in young adults with childhood-onset growth hormone deficiency: reappraisal of insulin tolerance testing. 97
Central diabetes insipidus in children: Diagnosis and management 96
Thyroid function and structure are affected in childhood obesity 95
Quantitative Ultrasound detects Bone Changes following Bone Marrow Transplantation in Pediatric Subjects affected with Hematological Diseases: a longitudinal study. 94
Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarche. 90
Growth and puberty in juvenile dermatomyositis: a longitudinal cohort study 85
Case Report: The Emerging Role of Ring Chromosome 22 in Phelan-McDermid Syndrome With Atypical Teratoid/Rhabdoid Tumor: The First Child Treated With Growth Hormone 85
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
Developmental abnormalities of the posterior pituitary gland. 81
Approach to the Pediatric Patient: Central Diabetes Insipidus 80
cardiometabolic risk in childhood cancer survivors 78
Dyslipidemia in Children Treated with a BRAF Inhibitor for Low-Grade Gliomas: A New Side Effect? 78
Preface 75
Pediatric pituitary adenoma with mixed FSH and TSH immunostaining and FSH hypersecretion in a 6 year-old girl with precocious puberty: case report and multidisciplinary management 74
Endocrine Outcomes In Central Diabetes Insipidus: the Predictive Value of Neuroimaging "Mismatch Pattern" 71
Management of Childhood-onset Craniopharyngioma in Italy: A Multicenter, 7-Year Follow-up Study of 145 Patients 70
Sirolimus Restores Erythropoiesis and Controls Immune Dysregulation in a Child With Cartilage-Hair Hypoplasia: A Case Report 68
Sleep disturbances in craniopharyngioma: a challenging diagnosis 68
Bone mineral density surveillance for childhood, adolescent, and young adult cancer survivors: evidence-based recommendations from the International Late Effects of Childhood Cancer Guideline Harmonization Group 66
Clinical, Endocrine and Neuroimaging Findings in Girls with Central Precocious Puberty 66
Hypothalamic-Pituitary and Other Endocrine Surveillance Among Childhood Cancer Survivors 65
Correction to: Sleep disturbances in craniopharyngioma: a challenging diagnosis (Journal of Neurology, (2021), 268, 11, (4362-4369), 10.1007/s00415-021-10794-1) 63
Approach to the Child and Adolescent With Adrenal Insufficiency 60
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
Pretreatment endocrine disorders due to optic pathway gliomas in pediatric neurofibromatosis type 1: Multicenter study 56
Sleep Disturbances in Pediatric Craniopharyngioma: A Systematic Review 55
Sedentary lifestyle and precocious puberty in girls during the COVID-19 pandemic: an Italian experience 55
Abnormalities of pubertal development and gonadal function in Noonan syndrome 52
Communication and ethical considerations for fertility preservation for patients with childhood, adolescent, and young adult cancer: recommendations from the PanCareLIFE Consortium and the International Late Effects of Childhood Cancer Guideline Harmonization Group 48
Igf1 for the diagnosis of growth hormone deficiency in children and adolescents: A reappraisal 47
Expert Opinion on the Management of Growth Hormone Deficiency in Brain Tumor Survivors: Results From an Italian Survey 38
Vitamin D supplementation for children with cancer: A systematic review and consensus recommendations 36
Fertility preservation for female patients with childhood, adolescent, and young adult cancer: recommendations from the PanCareLIFE Consortium and the International Late Effects of Childhood Cancer Guideline Harmonization Group 36
null 30
Testis Development and Descent 27
Bone Health Determinants in Ambulant Prepubertal Boys With Duchenne Muscular Dystrophy Treated With Deflazacort: Findings From a 3‐Year Study 27
Hamartoma, Pituitary 24
Correction to: Case report: Acute clinical presentation and neonatal management of primary hyperparathyroidism due to a novel CaSR mutation (BMC Pediatrics (2018) 18 (340) DOI: 10.1186/s12887-018-1319-0) 13
Two-year-old girl with metabolic acidosis and hyperkalaemia 8
Totale 10.376
Categoria #
all - tutte 38.626
article - articoli 36.466
book - libri 0
conference - conferenze 395
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.765
Totale 77.252


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021535 0 0 0 0 99 50 25 72 54 106 33 96
2021/2022948 51 74 49 76 33 62 55 214 52 117 39 126
2022/20231.027 85 87 10 111 165 145 4 90 189 10 112 19
2023/2024620 31 83 11 96 43 70 54 30 34 27 35 106
2024/20252.118 56 151 50 157 294 216 187 323 99 123 233 229
2025/20261.048 458 78 267 245 0 0 0 0 0 0 0 0
Totale 10.384