Search research articles
Contact Us
Filters
Showing results (31-40 of 48) with videos related to
Page
of 5
Sort By:
Biomaterials
|
June 15, 2021
A novel organ-chip system emulates three-dimensional architecture of the human epithelia and the mechanical forces acting on it
Antonio Varone, Justin Ke Nguyen, Lian Leng, et al.
Minerva Pediatrics
|
April 6, 2021
A complicated association between two different genetic rare disorders: cystic fibrosis and spinal muscular atrophy
Marta Palma, Simona Spadarella, Bernadette Donnarumma, et al.
International Journal of Molecular Sciences
|
September 13, 2025
Early Diagnosis and Follow-Up of a Novel Homozygous Mutation in <i>SOST</i> Gene in a Child with Recurrent Facial Palsy: A Case Report and Review of the Literature
Fabio Acquaviva, Giorgia Bruno, Federica Palladino, et al.
International Journal of Cancer
|
May 28, 2014
Noninvasive assessment of mitochondrial organization in three-dimensional tissues reveals changes associated with cancer development
Joanna Xylas, Antonio Varone, Kyle P Quinn, et al.
American Journal of Respiratory Cell and Molecular Biology
|
July 25, 2020
A Microengineered Airway Lung Chip Models Key Features of Viral-induced Exacerbation of Asthma
Janna C Nawroth, Carolina Lucchesi, Deion Cheng, et al.
Nature Methods
|
December 23, 2015
Small airway-on-a-chip enables analysis of human lung inflammation and drug responses in vitro
Kambez H Benam, Remi Villenave, Carolina Lucchesi, et al.
Journal of Clinical Medicine
|
November 13, 2025
Cortical Tubers' Transformation in Pediatric Patients Diagnosed with Tuberous Sclerosis Complex: A Retrospective Longitudinal MRI Analysis
Camilla Russo, Simone Coluccino, Maria Fulvia De Leva, et al.
Circulation. Genomic and Precision Medicine
|
May 17, 2023
Combined Clinical, Molecular, and Muscle Biopsy Approach to Unveil Prevalence and Clinical Features of Rare Neuromuscular and Mitochondrial Diseases in Patients With Cardiomyopathies
Michele Lioncino, Emanuele Monda, Martina Caiazza, et al.
International Journal of Molecular Sciences
|
May 27, 2023
Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy Phenotypes
Emanuele Monda, Michele Lioncino, Martina Caiazza, et al.
Expert Review of Neurotherapeutics
|
January 17, 2024
A proposal for a shared therapeutic algorithm in children with prolonged convulsive seizures and status epilepticus
Roberta Roberti, Antonella Riva, Gianluca D'Onofrio, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 48) with videos related to
Sort By:
Page
of 5
Biomaterials
|
June 15, 2021
A novel organ-chip system emulates three-dimensional architecture of the human epithelia and the mechanical forces acting on it
Antonio Varone, Justin Ke Nguyen, Lian Leng, et al.
Minerva Pediatrics
|
April 6, 2021
A complicated association between two different genetic rare disorders: cystic fibrosis and spinal muscular atrophy
Marta Palma, Simona Spadarella, Bernadette Donnarumma, et al.
International Journal of Molecular Sciences
|
September 13, 2025
Early Diagnosis and Follow-Up of a Novel Homozygous Mutation in <i>SOST</i> Gene in a Child with Recurrent Facial Palsy: A Case Report and Review of the Literature
Fabio Acquaviva, Giorgia Bruno, Federica Palladino, et al.
International Journal of Cancer
|
May 28, 2014
Noninvasive assessment of mitochondrial organization in three-dimensional tissues reveals changes associated with cancer development
Joanna Xylas, Antonio Varone, Kyle P Quinn, et al.
American Journal of Respiratory Cell and Molecular Biology
|
July 25, 2020
A Microengineered Airway Lung Chip Models Key Features of Viral-induced Exacerbation of Asthma
Janna C Nawroth, Carolina Lucchesi, Deion Cheng, et al.
Nature Methods
|
December 23, 2015
Small airway-on-a-chip enables analysis of human lung inflammation and drug responses in vitro
Kambez H Benam, Remi Villenave, Carolina Lucchesi, et al.
Journal of Clinical Medicine
|
November 13, 2025
Cortical Tubers' Transformation in Pediatric Patients Diagnosed with Tuberous Sclerosis Complex: A Retrospective Longitudinal MRI Analysis
Camilla Russo, Simone Coluccino, Maria Fulvia De Leva, et al.
Circulation. Genomic and Precision Medicine
|
May 17, 2023
Combined Clinical, Molecular, and Muscle Biopsy Approach to Unveil Prevalence and Clinical Features of Rare Neuromuscular and Mitochondrial Diseases in Patients With Cardiomyopathies
Michele Lioncino, Emanuele Monda, Martina Caiazza, et al.
International Journal of Molecular Sciences
|
May 27, 2023
Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy Phenotypes
Emanuele Monda, Michele Lioncino, Martina Caiazza, et al.
Expert Review of Neurotherapeutics
|
January 17, 2024
A proposal for a shared therapeutic algorithm in children with prolonged convulsive seizures and status epilepticus
Roberta Roberti, Antonella Riva, Gianluca D'Onofrio, et al.
Page
of 5