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Ron A Wevers

Showing results (111-120 of 266) with videos related to

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Journal of Inherited Metabolic Disease|August 24, 2022
Abnormal concentrations of acetylated amino acids in cerebrospinal fluid in acetyl-CoA transporter deficiencyKatarina Šikić, Tessa M A Peters, Eugenija Marušić, et al.
Molecular Genetics and Metabolism Reports|December 7, 2023
CYP2U1: An emerging treatable neurometabolic disease with cerebral folate deficiency in 2 Chinese brothersSheila Suet-Na Wong, Liz Yuet-Ping Yuen, Elaine Kan, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 17, 2009
Expression of sialidase and dystroglycan in human glomerular diseasesNils P J Vogtländer, Johan van der Vlag, Marinka A H Bakker, et al.
Journal of Child Neurology|May 23, 2009
[(1)H] magnetic resonance spectroscopy of urine: diagnosis of a guanidinoacetate methyl transferase deficiency caseMaria Tassini, Raffaella Zannolli, Sabrina Buoni, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids|July 7, 2020
Evaluation of cyclooxygenase oxylipins as potential biomarker for obesity-associated adipose tissue inflammation and type 2 diabetes using targeted multiple reaction monitoring mass spectrometryRoel Tans, Rieke Bande, Arno van Rooij, et al.
Plos One|August 13, 2013
Optimized metabolomic approach to identify uremic solutes in plasma of stage 3-4 chronic kidney disease patientsHenricus A M Mutsaers, Udo F H Engelke, Martijn J G Wilmer, et al.
European Journal of Human Genetics : EJHG|December 13, 2012
Symptomatic lipid storage in carriers for the PNPLA2 geneMirian C H Janssen, Baziel van Engelen, Livia Kapusta, et al.
Annals of Neurology|November 10, 2010
Mucopolysaccharidosis type IIIA: clinical spectrum and genotype-phenotype correlationsMarlies J Valstar, Sanne Neijs, Hennie T Bruggenwirth, et al.
Molecular Genetics and Metabolism|December 4, 2014
Cerebral lipid accumulation in Chanarin-Dorfman SyndromeMarleen C D G Huigen, Marinette van der Graaf, Eva Morava, et al.
Annals of Neurology|August 2, 2003
Tyrosine hydroxylase deficiency causes progressive encephalopathy and dopa-nonresponsive dystoniaGeorg F Hoffmann, Birgit Assmann, Christa Bräutigam, et al.
Pageof 27

Showing results (111-120 of 266) with videos related to

Sort By:
Pageof 27
Journal of Inherited Metabolic Disease|August 24, 2022
Abnormal concentrations of acetylated amino acids in cerebrospinal fluid in acetyl-CoA transporter deficiencyKatarina Šikić, Tessa M A Peters, Eugenija Marušić, et al.
Molecular Genetics and Metabolism Reports|December 7, 2023
CYP2U1: An emerging treatable neurometabolic disease with cerebral folate deficiency in 2 Chinese brothersSheila Suet-Na Wong, Liz Yuet-Ping Yuen, Elaine Kan, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 17, 2009
Expression of sialidase and dystroglycan in human glomerular diseasesNils P J Vogtländer, Johan van der Vlag, Marinka A H Bakker, et al.
Journal of Child Neurology|May 23, 2009
[(1)H] magnetic resonance spectroscopy of urine: diagnosis of a guanidinoacetate methyl transferase deficiency caseMaria Tassini, Raffaella Zannolli, Sabrina Buoni, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids|July 7, 2020
Evaluation of cyclooxygenase oxylipins as potential biomarker for obesity-associated adipose tissue inflammation and type 2 diabetes using targeted multiple reaction monitoring mass spectrometryRoel Tans, Rieke Bande, Arno van Rooij, et al.
Plos One|August 13, 2013
Optimized metabolomic approach to identify uremic solutes in plasma of stage 3-4 chronic kidney disease patientsHenricus A M Mutsaers, Udo F H Engelke, Martijn J G Wilmer, et al.
European Journal of Human Genetics : EJHG|December 13, 2012
Symptomatic lipid storage in carriers for the PNPLA2 geneMirian C H Janssen, Baziel van Engelen, Livia Kapusta, et al.
Annals of Neurology|November 10, 2010
Mucopolysaccharidosis type IIIA: clinical spectrum and genotype-phenotype correlationsMarlies J Valstar, Sanne Neijs, Hennie T Bruggenwirth, et al.
Molecular Genetics and Metabolism|December 4, 2014
Cerebral lipid accumulation in Chanarin-Dorfman SyndromeMarleen C D G Huigen, Marinette van der Graaf, Eva Morava, et al.
Annals of Neurology|August 2, 2003
Tyrosine hydroxylase deficiency causes progressive encephalopathy and dopa-nonresponsive dystoniaGeorg F Hoffmann, Birgit Assmann, Christa Bräutigam, et al.
Pageof 27