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Molecular Genetics and Metabolism
|
January 3, 2026
Use of untargeted metabolomics for the study of pediatric neurometabolic disorders: A review
Cathrin Lytomt Salvador, Paula Juliana Rodríguez-Soler, Cristian Irela Aranda, et al.
Transplantation
|
January 15, 2008
Expression of IMPDH1 and IMPDH2 after transplantation and initiation of immunosuppression
Sara Bremer, Randeep Mandla, Nils T Vethe, et al.
Journal of Translational Medicine
|
July 29, 2009
Mycophenolate pharmacokinetics and pharmacodynamics in belatacept treated renal allograft recipients - a pilot study
Sara Bremer, Nils T Vethe, Helge Rootwelt, et al.
Acta Ophthalmologica
|
April 11, 2026
Dry eye disease symptoms and associated risk factors in a Norwegian clinical cohort
Mazyar Yazdani, Fredrik A Fineide, Reza A Badian, et al.
JIMD Reports
|
April 13, 2013
Novel Deletion Mutation Identified in a Patient with Late-Onset Combined Methylmalonic Acidemia and Homocystinuria, cblC Type
Paul Hoff Backe, Mari Ytre-Arne, Asmund Kjendseth Røhr, et al.
Mechanisms of Ageing and Development
|
September 3, 2011
DNA base excision repair gene polymorphisms modulate human cognitive performance and decline during normal life span
Meryl S Lillenes, Thomas Espeseth, Mari Støen, et al.
Cells
|
February 15, 2022
Saliva Metabolomics in Dry Mouth Patients with Head and Neck Cancer or Sjögren's Syndrome
Håvard Hynne, Elise Mørk Sandås, Katja Benedikte Prestø Elgstøen, et al.
Acta Ophthalmologica
|
May 24, 2008
Apolipoprotein E genotype and risk for development of cataract and age-related macular degeneration
Øygunn A Utheim, Jon Ståle Ritland, Tor P Utheim, et al.
Acta Ophthalmologica Scandinavica
|
May 10, 2007
Effects of APOE and CHRNA4 genotypes on retinal nerve fibre layer thickness at the optic disc and on risk for developing exfoliation syndrome
Jon Ståle Ritland, Tor Paaske Utheim, Oygunn Aass Utheim, et al.
Molecular Genetics and Metabolism
|
June 24, 2010
Four novel mutations identified in Norwegian patients result in intermittent maple syrup urine disease when combined with the R301C mutation
Else Brodtkorb, Janne Strand, Paul Hoff Backe, et al.
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of 7
Search research articles
Search
Showing results (31-40 of 62) with videos related to
Sort By:
Page
of 7
Molecular Genetics and Metabolism
|
January 3, 2026
Use of untargeted metabolomics for the study of pediatric neurometabolic disorders: A review
Cathrin Lytomt Salvador, Paula Juliana Rodríguez-Soler, Cristian Irela Aranda, et al.
Transplantation
|
January 15, 2008
Expression of IMPDH1 and IMPDH2 after transplantation and initiation of immunosuppression
Sara Bremer, Randeep Mandla, Nils T Vethe, et al.
Journal of Translational Medicine
|
July 29, 2009
Mycophenolate pharmacokinetics and pharmacodynamics in belatacept treated renal allograft recipients - a pilot study
Sara Bremer, Nils T Vethe, Helge Rootwelt, et al.
Acta Ophthalmologica
|
April 11, 2026
Dry eye disease symptoms and associated risk factors in a Norwegian clinical cohort
Mazyar Yazdani, Fredrik A Fineide, Reza A Badian, et al.
JIMD Reports
|
April 13, 2013
Novel Deletion Mutation Identified in a Patient with Late-Onset Combined Methylmalonic Acidemia and Homocystinuria, cblC Type
Paul Hoff Backe, Mari Ytre-Arne, Asmund Kjendseth Røhr, et al.
Mechanisms of Ageing and Development
|
September 3, 2011
DNA base excision repair gene polymorphisms modulate human cognitive performance and decline during normal life span
Meryl S Lillenes, Thomas Espeseth, Mari Støen, et al.
Cells
|
February 15, 2022
Saliva Metabolomics in Dry Mouth Patients with Head and Neck Cancer or Sjögren's Syndrome
Håvard Hynne, Elise Mørk Sandås, Katja Benedikte Prestø Elgstøen, et al.
Acta Ophthalmologica
|
May 24, 2008
Apolipoprotein E genotype and risk for development of cataract and age-related macular degeneration
Øygunn A Utheim, Jon Ståle Ritland, Tor P Utheim, et al.
Acta Ophthalmologica Scandinavica
|
May 10, 2007
Effects of APOE and CHRNA4 genotypes on retinal nerve fibre layer thickness at the optic disc and on risk for developing exfoliation syndrome
Jon Ståle Ritland, Tor Paaske Utheim, Oygunn Aass Utheim, et al.
Molecular Genetics and Metabolism
|
June 24, 2010
Four novel mutations identified in Norwegian patients result in intermittent maple syrup urine disease when combined with the R301C mutation
Else Brodtkorb, Janne Strand, Paul Hoff Backe, et al.
Page
of 7