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PLOS Mental Health
|
March 24, 2026
Preconception mental health (Healthy Life Trajectories Initiative): Identifying factors associated with probable anxiety and depression among young women living in urban-poor South Africa
Shane A Norris, Claire Hart, Lukhanyo H Nyati, et al.
Journal of Medical Toxicology : Official Journal of the American College of Medical Toxicology
|
June 26, 2023
Correction to: A Multi-Omic Mosaic Model of Acetaminophen Induced Alanine Aminotransferase Elevation
Andrew A Monte, Alexis Vest, Julie A Reisz, et al.
Journal of Medical Toxicology : Official Journal of the American College of Medical Toxicology
|
May 25, 2023
A Multi-Omic Mosaic Model of Acetaminophen Induced Alanine Aminotransferase Elevation
Andrew A Monte, Alexis Vest, Julie A Reisz, et al.
American Journal of Medical Genetics. Part A
|
January 19, 2026
Cytosolic Phosphoenoylpyruvate Carboxykinase Deficiency: Clinical, Biochemical, and Genetic Features of Five Non-Finnish Patients
Isaac Bernhardt, Polona Le Quesne Stabej, Claire Hart, et al.
NMR in Biomedicine
|
May 23, 2007
NMR spectroscopy of aminoacylase 1 deficiency, a novel inborn error of metabolism
Udo F H Engelke, Jörn Oliver Sass, Rudy N Van Coster, et al.
Scientific Reports
|
May 22, 2026
Changes in hepatic L-carnitine levels in people with metabolic dysfunction-associated steatotic liver disease (MASLD) assessed by magnetic resonance techniques
Dragana Savic, Michael Pavlides, Mette Skalshøi Kjær, et al.
Molecular Genetics and Metabolism
|
November 2, 2024
cPMP rescue of a neonate with severe molybdenum cofactor deficiency after serendipitous early diagnosis, and characterisation of a novel MOCS1 variant
Bernd C Schwahn, Claire Hart, Louisa Ann Smith, et al.
International Journal of Neonatal Screening
|
January 22, 2024
Incidental Detection of Classical Galactosemia through Newborn Screening for Phenylketonuria: A 10-Year Retrospective Audit to Determine the Efficacy of This Approach
Nathan W P Cantley, Robert Barski, Helena Kemp, et al.
Nature Communications
|
November 3, 2019
Microenvironmental IL1β promotes breast cancer metastatic colonisation in the bone via activation of Wnt signalling
Rachel Eyre, Denis G Alférez, Angélica Santiago-Gómez, et al.
Molecular Genetics and Metabolism
|
December 3, 2014
Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: a treatable neurological disorder caused by TPK1 mutations
Siddharth Banka, Christian de Goede, Wyatt W Yue, et al.
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Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
PLOS Mental Health
|
March 24, 2026
Preconception mental health (Healthy Life Trajectories Initiative): Identifying factors associated with probable anxiety and depression among young women living in urban-poor South Africa
Shane A Norris, Claire Hart, Lukhanyo H Nyati, et al.
Journal of Medical Toxicology : Official Journal of the American College of Medical Toxicology
|
June 26, 2023
Correction to: A Multi-Omic Mosaic Model of Acetaminophen Induced Alanine Aminotransferase Elevation
Andrew A Monte, Alexis Vest, Julie A Reisz, et al.
Journal of Medical Toxicology : Official Journal of the American College of Medical Toxicology
|
May 25, 2023
A Multi-Omic Mosaic Model of Acetaminophen Induced Alanine Aminotransferase Elevation
Andrew A Monte, Alexis Vest, Julie A Reisz, et al.
American Journal of Medical Genetics. Part A
|
January 19, 2026
Cytosolic Phosphoenoylpyruvate Carboxykinase Deficiency: Clinical, Biochemical, and Genetic Features of Five Non-Finnish Patients
Isaac Bernhardt, Polona Le Quesne Stabej, Claire Hart, et al.
NMR in Biomedicine
|
May 23, 2007
NMR spectroscopy of aminoacylase 1 deficiency, a novel inborn error of metabolism
Udo F H Engelke, Jörn Oliver Sass, Rudy N Van Coster, et al.
Scientific Reports
|
May 22, 2026
Changes in hepatic L-carnitine levels in people with metabolic dysfunction-associated steatotic liver disease (MASLD) assessed by magnetic resonance techniques
Dragana Savic, Michael Pavlides, Mette Skalshøi Kjær, et al.
Molecular Genetics and Metabolism
|
November 2, 2024
cPMP rescue of a neonate with severe molybdenum cofactor deficiency after serendipitous early diagnosis, and characterisation of a novel MOCS1 variant
Bernd C Schwahn, Claire Hart, Louisa Ann Smith, et al.
International Journal of Neonatal Screening
|
January 22, 2024
Incidental Detection of Classical Galactosemia through Newborn Screening for Phenylketonuria: A 10-Year Retrospective Audit to Determine the Efficacy of This Approach
Nathan W P Cantley, Robert Barski, Helena Kemp, et al.
Nature Communications
|
November 3, 2019
Microenvironmental IL1β promotes breast cancer metastatic colonisation in the bone via activation of Wnt signalling
Rachel Eyre, Denis G Alférez, Angélica Santiago-Gómez, et al.
Molecular Genetics and Metabolism
|
December 3, 2014
Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: a treatable neurological disorder caused by TPK1 mutations
Siddharth Banka, Christian de Goede, Wyatt W Yue, et al.
Page
of 3