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Best Practice & Research. Clinical Endocrinology & Metabolism
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December 16, 2016
Classical and non-classical causes of GH deficiency in the paediatric age
Natascia Di Iorgi, Giovanni Morana, Anna Elsa Maria Allegri, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 22, 2020
Gut Microbiota in T1DM-Onset Pediatric Patients: Machine-Learning Algorithms to Classify Microorganisms as Disease Linked
Roberto Biassoni, Eddi Di Marco, Margherita Squillario, et al.
Pediatric Research
|
July 3, 2019
Wolfram syndrome 1 in the Italian population: genotype-phenotype correlations
Luciana Rigoli, Concetta Aloi, Alessandro Salina, et al.
Endocrine Connections
|
October 28, 2020
IGF1 for the diagnosis of growth hormone deficiency in children and adolescents: a reappraisal
Anastasia Ibba, Francesca Corrias, Chiara Guzzetti, et al.
Scientific Reports
|
December 22, 2025
PEG10 loss of function causes Silver-Russell syndrome: a familial case with paternal deletion
Alessandro Vimercati, Giuseppa Patti, Pierpaola Tannorella, et al.
Scientific Reports
|
July 12, 2023
Gut-microbiota in children and adolescents with obesity: inferred functional analysis and machine-learning algorithms to classify microorganisms
Margherita Squillario, Carola Bonaretti, Alberto La Valle, et al.
International Journal of Molecular Sciences
|
September 2, 2020
Characterization of Two Novel Variants of the Steroidogenic Acute Regulatory Protein Identified in a Girl with Classic Lipoid Congenital Adrenal Hyperplasia
Efstathios Katharopoulos, Natascia Di Iorgi, Paula Fernandez-Alvarez, et al.
Frontiers in Endocrinology
|
August 14, 2023
Abnormalities of pubertal development and gonadal function in Noonan syndrome
Giuseppa Patti, Marco Scaglione, Nadia Gabriella Maiorano, et al.
Genes
|
April 30, 2021
Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases
Pierpaola Tannorella, Daniele Minervino, Sara Guzzetti, et al.
Journal of the Endocrine Society
|
August 11, 2023
Blood Lymphocyte Subsets and Proinflammatory Cytokine Profile in ROHHAD(NET) and non-ROHHAD(NET) Obese Individuals
Daniela Fava, Fabio Morandi, Ignazia Prigione, et al.
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of 6
Search research articles
Search
Showing results (21-30 of 55) with videos related to
Sort By:
Page
of 6
Best Practice & Research. Clinical Endocrinology & Metabolism
|
December 16, 2016
Classical and non-classical causes of GH deficiency in the paediatric age
Natascia Di Iorgi, Giovanni Morana, Anna Elsa Maria Allegri, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 22, 2020
Gut Microbiota in T1DM-Onset Pediatric Patients: Machine-Learning Algorithms to Classify Microorganisms as Disease Linked
Roberto Biassoni, Eddi Di Marco, Margherita Squillario, et al.
Pediatric Research
|
July 3, 2019
Wolfram syndrome 1 in the Italian population: genotype-phenotype correlations
Luciana Rigoli, Concetta Aloi, Alessandro Salina, et al.
Endocrine Connections
|
October 28, 2020
IGF1 for the diagnosis of growth hormone deficiency in children and adolescents: a reappraisal
Anastasia Ibba, Francesca Corrias, Chiara Guzzetti, et al.
Scientific Reports
|
December 22, 2025
PEG10 loss of function causes Silver-Russell syndrome: a familial case with paternal deletion
Alessandro Vimercati, Giuseppa Patti, Pierpaola Tannorella, et al.
Scientific Reports
|
July 12, 2023
Gut-microbiota in children and adolescents with obesity: inferred functional analysis and machine-learning algorithms to classify microorganisms
Margherita Squillario, Carola Bonaretti, Alberto La Valle, et al.
International Journal of Molecular Sciences
|
September 2, 2020
Characterization of Two Novel Variants of the Steroidogenic Acute Regulatory Protein Identified in a Girl with Classic Lipoid Congenital Adrenal Hyperplasia
Efstathios Katharopoulos, Natascia Di Iorgi, Paula Fernandez-Alvarez, et al.
Frontiers in Endocrinology
|
August 14, 2023
Abnormalities of pubertal development and gonadal function in Noonan syndrome
Giuseppa Patti, Marco Scaglione, Nadia Gabriella Maiorano, et al.
Genes
|
April 30, 2021
Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases
Pierpaola Tannorella, Daniele Minervino, Sara Guzzetti, et al.
Journal of the Endocrine Society
|
August 11, 2023
Blood Lymphocyte Subsets and Proinflammatory Cytokine Profile in ROHHAD(NET) and non-ROHHAD(NET) Obese Individuals
Daniela Fava, Fabio Morandi, Ignazia Prigione, et al.
Page
of 6