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Journal of Clinical Medicine
|
August 12, 2023
Telemedicine in Patients Affected by Chronic Liver Disease: A Scoping Review of Clinical Outcomes and the Devices Evaluated
Paolo Capuano, Bethany Hileman, Stefano Tigano, et al.
Nutrients
|
March 2, 2018
Galacto-Oligosaccharide/Polidextrose Enriched Formula Protects against Respiratory Infections in Infants at High Risk of Atopy: A Randomized Clinical Trial
Giusy Ranucci, Vittoria Buccigrossi, Eleonora Borgia, et al.
Journal of Inherited Metabolic Disease
|
July 2, 2019
Chronic liver involvement in urea cycle disorders
Giusy Ranucci, Miriam Rigoldi, Giovanna Cotugno, et al.
International Journal of Molecular Sciences
|
August 26, 2022
Mystery(n) Phenotypic Presentation in Europeans: Report of Three Further Novel Missense <i>RNF213</i> Variants Leading to Severe Syndromic Forms of Moyamoya Angiopathy and Literature Review
Claudia Santoro, Giuseppe Mirone, Mariateresa Zanobio, et al.
Journal of Hepatology
|
January 3, 2009
Genotype-phenotype correlation in Italian children with Wilson's disease
Emanuele Nicastro, Georgios Loudianos, Lucia Zancan, et al.
European Journal of Pediatrics
|
November 14, 2022
Congenital syphilis in the twenty-first century: an area-based study
Serena Salomè, Maria Donata Cambriglia, Sara Maria Scarano, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
July 25, 2023
Thrombotic Features as the Primary Cause of SARS-CoV-2 Related Acute Abdomen in Children
Angela Amoroso, Fabiana Di Stasio, Giusy Ranucci, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 9, 2018
SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN)
Dominic Lenz, Patricia McClean, Aydan Kansu, et al.
Human Genetics
|
August 21, 2021
ASL expression in ALDH1A1<sup>+</sup> neurons in the substantia nigra metabolically contributes to neurodegenerative phenotype
Shaul Lerner, Raya Eilam, Lital Adler, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
July 13, 2026
The Italian biliary atresia registry: Insights and lessons from the retrospective analysis of a 10-year period cohort
Giovanni Boroni, Daniela Liccardo, Daniele Alberti, et al.
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Search research articles
Search
Showing results (31-40 of 44) with videos related to
Sort By:
Page
of 5
Journal of Clinical Medicine
|
August 12, 2023
Telemedicine in Patients Affected by Chronic Liver Disease: A Scoping Review of Clinical Outcomes and the Devices Evaluated
Paolo Capuano, Bethany Hileman, Stefano Tigano, et al.
Nutrients
|
March 2, 2018
Galacto-Oligosaccharide/Polidextrose Enriched Formula Protects against Respiratory Infections in Infants at High Risk of Atopy: A Randomized Clinical Trial
Giusy Ranucci, Vittoria Buccigrossi, Eleonora Borgia, et al.
Journal of Inherited Metabolic Disease
|
July 2, 2019
Chronic liver involvement in urea cycle disorders
Giusy Ranucci, Miriam Rigoldi, Giovanna Cotugno, et al.
International Journal of Molecular Sciences
|
August 26, 2022
Mystery(n) Phenotypic Presentation in Europeans: Report of Three Further Novel Missense <i>RNF213</i> Variants Leading to Severe Syndromic Forms of Moyamoya Angiopathy and Literature Review
Claudia Santoro, Giuseppe Mirone, Mariateresa Zanobio, et al.
Journal of Hepatology
|
January 3, 2009
Genotype-phenotype correlation in Italian children with Wilson's disease
Emanuele Nicastro, Georgios Loudianos, Lucia Zancan, et al.
European Journal of Pediatrics
|
November 14, 2022
Congenital syphilis in the twenty-first century: an area-based study
Serena Salomè, Maria Donata Cambriglia, Sara Maria Scarano, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
July 25, 2023
Thrombotic Features as the Primary Cause of SARS-CoV-2 Related Acute Abdomen in Children
Angela Amoroso, Fabiana Di Stasio, Giusy Ranucci, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 9, 2018
SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN)
Dominic Lenz, Patricia McClean, Aydan Kansu, et al.
Human Genetics
|
August 21, 2021
ASL expression in ALDH1A1<sup>+</sup> neurons in the substantia nigra metabolically contributes to neurodegenerative phenotype
Shaul Lerner, Raya Eilam, Lital Adler, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
July 13, 2026
The Italian biliary atresia registry: Insights and lessons from the retrospective analysis of a 10-year period cohort
Giovanni Boroni, Daniela Liccardo, Daniele Alberti, et al.
Page
of 5