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Molecular Genetics and Metabolism
|
January 26, 2024
Treatment recommendations for glycogen storage disease type IB- associated neutropenia and neutrophil dysfunction with empagliflozin: Consensus from an international workshop
Sarah C Grünert, Terry G J Derks, Helen Mundy, et al.
JACC. Basic to Translational Science
|
May 4, 2023
Clustering of Cardiac Transcriptome Profiles Reveals Unique: Subgroups of Dilated Cardiomyopathy Patients
Job A J Verdonschot, Ping Wang, Kasper W J Derks, et al.
Orphanet Journal of Rare Diseases
|
May 29, 2012
Risk stratification by residual enzyme activity after newborn screening for medium-chain acyl-CoA dehyrogenase deficiency: data from a cohort study
Catharina M L Touw, G Peter A Smit, Maaike de Vries, et al.
Scientific Reports
|
September 24, 2021
Non-invasively measured brain activity and radiological progression in diffuse glioma
T Numan, S D Kulik, B Moraal, et al.
Lung Cancer (Amsterdam, Netherlands)
|
August 1, 2025
Definition of resectable stage III non-small cell lung cancer: A systematic review from EORTC lung cancer group
E Xenophontos, N Giaj Levra, V Durieux, et al.
European Heart Journal
|
November 6, 2020
Phenotypic clustering of dilated cardiomyopathy patients highlights important pathophysiological differences
Job A J Verdonschot, Marco Merlo, Fernando Dominguez, et al.
Journal of Inherited Metabolic Disease
|
March 19, 2021
Impaired Very-Low-Density Lipoprotein catabolism links hypoglycemia to hypertriglyceridemia in Glycogen Storage Disease type Ia
Joanne A Hoogerland, Fabian Peeks, Brenda S Hijmans, et al.
Orphanet Journal of Rare Diseases
|
May 19, 2016
Childhood Pompe disease: clinical spectrum and genotype in 31 patients
C I van Capelle, J C van der Meijden, J M P van den Hout, et al.
European Heart Journal
|
January 30, 2018
Titin cardiomyopathy leads to altered mitochondrial energetics, increased fibrosis and long-term life-threatening arrhythmias
Job A J Verdonschot, Mark R Hazebroek, Kasper W J Derks, et al.
Molecular Genetics and Metabolism
|
July 11, 2017
Clinical presentation and outcome in a series of 32 patients with 2-methylacetoacetyl-coenzyme A thiolase (MAT) deficiency
Sarah Catharina Grünert, Robert Niklas Schmitt, Sonja Marina Schlatter, et al.
Page
of 17
Search research articles
Search
Showing results (141-150 of 167) with videos related to
Sort By:
Page
of 17
Molecular Genetics and Metabolism
|
January 26, 2024
Treatment recommendations for glycogen storage disease type IB- associated neutropenia and neutrophil dysfunction with empagliflozin: Consensus from an international workshop
Sarah C Grünert, Terry G J Derks, Helen Mundy, et al.
JACC. Basic to Translational Science
|
May 4, 2023
Clustering of Cardiac Transcriptome Profiles Reveals Unique: Subgroups of Dilated Cardiomyopathy Patients
Job A J Verdonschot, Ping Wang, Kasper W J Derks, et al.
Orphanet Journal of Rare Diseases
|
May 29, 2012
Risk stratification by residual enzyme activity after newborn screening for medium-chain acyl-CoA dehyrogenase deficiency: data from a cohort study
Catharina M L Touw, G Peter A Smit, Maaike de Vries, et al.
Scientific Reports
|
September 24, 2021
Non-invasively measured brain activity and radiological progression in diffuse glioma
T Numan, S D Kulik, B Moraal, et al.
Lung Cancer (Amsterdam, Netherlands)
|
August 1, 2025
Definition of resectable stage III non-small cell lung cancer: A systematic review from EORTC lung cancer group
E Xenophontos, N Giaj Levra, V Durieux, et al.
European Heart Journal
|
November 6, 2020
Phenotypic clustering of dilated cardiomyopathy patients highlights important pathophysiological differences
Job A J Verdonschot, Marco Merlo, Fernando Dominguez, et al.
Journal of Inherited Metabolic Disease
|
March 19, 2021
Impaired Very-Low-Density Lipoprotein catabolism links hypoglycemia to hypertriglyceridemia in Glycogen Storage Disease type Ia
Joanne A Hoogerland, Fabian Peeks, Brenda S Hijmans, et al.
Orphanet Journal of Rare Diseases
|
May 19, 2016
Childhood Pompe disease: clinical spectrum and genotype in 31 patients
C I van Capelle, J C van der Meijden, J M P van den Hout, et al.
European Heart Journal
|
January 30, 2018
Titin cardiomyopathy leads to altered mitochondrial energetics, increased fibrosis and long-term life-threatening arrhythmias
Job A J Verdonschot, Mark R Hazebroek, Kasper W J Derks, et al.
Molecular Genetics and Metabolism
|
July 11, 2017
Clinical presentation and outcome in a series of 32 patients with 2-methylacetoacetyl-coenzyme A thiolase (MAT) deficiency
Sarah Catharina Grünert, Robert Niklas Schmitt, Sonja Marina Schlatter, et al.
Page
of 17