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Alimentary Pharmacology & Therapeutics
|
November 22, 2016
The Endoscopic Reference Score shows modest accuracy to predict either clinical or histological activity in adult patients with eosinophilic oesophagitis
J Rodríguez-Sánchez, J Barrio-Andrés, O Nantes Castillejo, et al.
Antiviral Therapy
|
July 19, 2005
Benefit of switching from a protease inhibitor (PI) to nevirapine in PI-experienced patients suffering acquired HIV-related lipodystrophy syndrome (AHL): interim analysis at 3 months of follow-up
E Negredo, R Paredes, A Bonjoch, et al.
Journal of Medical Genetics
|
January 24, 2018
<i>FAM46A</i> mutations are responsible for autosomal recessive osteogenesis imperfecta
Mathilde Doyard, Séverine Bacrot, Céline Huber, et al.
Alimentary Pharmacology & Therapeutics
|
February 5, 2026
Safety of Immune Checkpoint Inhibitors Prior to Liver Transplantation in Hepatocellular Carcinoma
L Aceituno, C Magyar, P Tabrizian, et al.
Frontiers in Medicine
|
March 2, 2026
Correction: Case Report: Autosomal recessive palmoplantar keratoderma with additional bilateral hearing loss due to a pathogenic frameshift deletion in FAM83G
Mónica Mora-Gómez, Marta Feito, Natalia Gallego-Zazo, et al.
Geroscience
|
May 21, 2026
Impact of an online-guided physical activity intervention on cognition, resting-state brain connectivity, and the gut microbiome in healthy older adults-a randomized controlled trial
Simon J Schrenk, Corinna Bang, Lena Best, et al.
Pediatric Research
|
August 29, 2000
Glutaryl-CoA dehydrogenase deficiency in Spain: evidence of two groups of patients, genetically, and biochemically distinct
C Busquets, B Merinero, E Christensen, et al.
Molecular Genetics and Metabolism
|
January 9, 2010
Clinical experience with miglustat therapy in pediatric patients with Niemann-Pick disease type C: a case series
M Pineda, M S Perez-Poyato, M O'Callaghan, et al.
American Journal of Medical Genetics. Part A
|
March 23, 2026
A New Patient With SPOUT1-Related Neurodevelopmental Disorder Identified by Genomic Data Re-Analysis: Novel Phenotypic Features and Literature Review
Tomás Valle, Alejandra Damián, Marta Torres, et al.
Clinical Genetics
|
September 12, 2017
mTOR mutations in Smith-Kingsmore syndrome: Four additional patients and a review
G Gordo, J Tenorio, P Arias, et al.
Page
of 91
Search research articles
Search
Showing results (841-850 of 908) with videos related to
Sort By:
Page
of 91
Alimentary Pharmacology & Therapeutics
|
November 22, 2016
The Endoscopic Reference Score shows modest accuracy to predict either clinical or histological activity in adult patients with eosinophilic oesophagitis
J Rodríguez-Sánchez, J Barrio-Andrés, O Nantes Castillejo, et al.
Antiviral Therapy
|
July 19, 2005
Benefit of switching from a protease inhibitor (PI) to nevirapine in PI-experienced patients suffering acquired HIV-related lipodystrophy syndrome (AHL): interim analysis at 3 months of follow-up
E Negredo, R Paredes, A Bonjoch, et al.
Journal of Medical Genetics
|
January 24, 2018
<i>FAM46A</i> mutations are responsible for autosomal recessive osteogenesis imperfecta
Mathilde Doyard, Séverine Bacrot, Céline Huber, et al.
Alimentary Pharmacology & Therapeutics
|
February 5, 2026
Safety of Immune Checkpoint Inhibitors Prior to Liver Transplantation in Hepatocellular Carcinoma
L Aceituno, C Magyar, P Tabrizian, et al.
Frontiers in Medicine
|
March 2, 2026
Correction: Case Report: Autosomal recessive palmoplantar keratoderma with additional bilateral hearing loss due to a pathogenic frameshift deletion in FAM83G
Mónica Mora-Gómez, Marta Feito, Natalia Gallego-Zazo, et al.
Geroscience
|
May 21, 2026
Impact of an online-guided physical activity intervention on cognition, resting-state brain connectivity, and the gut microbiome in healthy older adults-a randomized controlled trial
Simon J Schrenk, Corinna Bang, Lena Best, et al.
Pediatric Research
|
August 29, 2000
Glutaryl-CoA dehydrogenase deficiency in Spain: evidence of two groups of patients, genetically, and biochemically distinct
C Busquets, B Merinero, E Christensen, et al.
Molecular Genetics and Metabolism
|
January 9, 2010
Clinical experience with miglustat therapy in pediatric patients with Niemann-Pick disease type C: a case series
M Pineda, M S Perez-Poyato, M O'Callaghan, et al.
American Journal of Medical Genetics. Part A
|
March 23, 2026
A New Patient With SPOUT1-Related Neurodevelopmental Disorder Identified by Genomic Data Re-Analysis: Novel Phenotypic Features and Literature Review
Tomás Valle, Alejandra Damián, Marta Torres, et al.
Clinical Genetics
|
September 12, 2017
mTOR mutations in Smith-Kingsmore syndrome: Four additional patients and a review
G Gordo, J Tenorio, P Arias, et al.
Page
of 91