Search research articles
Contact Us
Filters
Showing results (21-30 of 159) with videos related to
Page
of 16
Sort By:
Frontiers in Pediatrics
|
September 1, 2023
Case report: Variability in clinical features as a potential pitfall for the diagnosis of Barth syndrome
Nicola Tovaglieri, Silvia Russo, Emanuele Micaglio, et al.
Scientific Reports
|
November 18, 2022
Beneficial effects of SS-31 peptide on cardiac mitochondrial dysfunction in tafazzin knockdown mice
Silvia Russo, Domenico De Rasmo, Anna Signorile, et al.
Scientific Reports
|
June 13, 2024
SS-31 treatment ameliorates cardiac mitochondrial morphology and defective mitophagy in a murine model of Barth syndrome
Silvia Russo, Domenico De Rasmo, Roberta Rossi, et al.
Nursing & Health Sciences
|
July 9, 2015
Psychometric properties of the Jefferson Scale of Empathy-Health Professional Student's version: An Italian validation study with nursing students
Paola Montanari, Cristina Petrucci, Silvia Russo, et al.
Molecular and Cellular Probes
|
November 7, 2003
A fluorescent method for detecting low-grade 11patUPD mosaicism in Beckwith-Wiedemann syndrome
Silvia Russo, Monica Mencarelli, Florinda Cavalleri, et al.
European Journal of Medical Genetics
|
February 5, 2019
A novel RAD21 mutation in a boy with mild Cornelia de Lange presentation: Further delineation of the phenotype
Sarah Dorval, Maura Masciadri, Mikaël Mathot, et al.
American Journal of Medical Genetics. Part A
|
April 28, 2009
A CDKL5 mutated child with precocious puberty
Veronica Saletti, Laura Canafoglia, Paola Cambiaso, et al.
American Journal of Community Psychology
|
July 21, 2016
Social Capital and Fear of Crime in Adolescence: A Multilevel Study
Alessio Vieno, Michela Lenzi, Michele Roccato, et al.
Clinical Chemistry
|
August 23, 2007
Midtrimester amniotic fluid adiponectin in normal pregnancy
Giovanni Baviera, Francesco Corrado, Corrado Dugo, et al.
Neurogenetics
|
January 21, 2006
Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation
Marco Venturin, Silvia Moncini, Valentina Villa, et al.
Page
of 16
Search research articles
Search
Showing results (21-30 of 159) with videos related to
Sort By:
Page
of 16
Frontiers in Pediatrics
|
September 1, 2023
Case report: Variability in clinical features as a potential pitfall for the diagnosis of Barth syndrome
Nicola Tovaglieri, Silvia Russo, Emanuele Micaglio, et al.
Scientific Reports
|
November 18, 2022
Beneficial effects of SS-31 peptide on cardiac mitochondrial dysfunction in tafazzin knockdown mice
Silvia Russo, Domenico De Rasmo, Anna Signorile, et al.
Scientific Reports
|
June 13, 2024
SS-31 treatment ameliorates cardiac mitochondrial morphology and defective mitophagy in a murine model of Barth syndrome
Silvia Russo, Domenico De Rasmo, Roberta Rossi, et al.
Nursing & Health Sciences
|
July 9, 2015
Psychometric properties of the Jefferson Scale of Empathy-Health Professional Student's version: An Italian validation study with nursing students
Paola Montanari, Cristina Petrucci, Silvia Russo, et al.
Molecular and Cellular Probes
|
November 7, 2003
A fluorescent method for detecting low-grade 11patUPD mosaicism in Beckwith-Wiedemann syndrome
Silvia Russo, Monica Mencarelli, Florinda Cavalleri, et al.
European Journal of Medical Genetics
|
February 5, 2019
A novel RAD21 mutation in a boy with mild Cornelia de Lange presentation: Further delineation of the phenotype
Sarah Dorval, Maura Masciadri, Mikaël Mathot, et al.
American Journal of Medical Genetics. Part A
|
April 28, 2009
A CDKL5 mutated child with precocious puberty
Veronica Saletti, Laura Canafoglia, Paola Cambiaso, et al.
American Journal of Community Psychology
|
July 21, 2016
Social Capital and Fear of Crime in Adolescence: A Multilevel Study
Alessio Vieno, Michela Lenzi, Michele Roccato, et al.
Clinical Chemistry
|
August 23, 2007
Midtrimester amniotic fluid adiponectin in normal pregnancy
Giovanni Baviera, Francesco Corrado, Corrado Dugo, et al.
Neurogenetics
|
January 21, 2006
Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation
Marco Venturin, Silvia Moncini, Valentina Villa, et al.
Page
of 16