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J Derks

Showing results (121-130 of 167) with videos related to

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BMC Biology|September 4, 2023
Personalised modelling of clinical heterogeneity between medium-chain acyl-CoA dehydrogenase patientsChristoff Odendaal, Emmalie A Jager, Anne-Claire M F Martines, et al.
Journal of Inherited Metabolic Disease|October 26, 2024
The relation between dietary polysaccharide intake and urinary excretion of tetraglucosideCandelas Gross-Valle, Tessa C Jacobs, Janneke D A Dijck-Brouwer, et al.
Journal of Inherited Metabolic Disease|April 24, 2016
Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcomeChristiaan P Sentner, Irene J Hoogeveen, David A Weinstein, et al.
Journal of Inherited Metabolic Disease|October 7, 2019
Research priorities for liver glycogen storage disease: An international priority setting partnership with the James Lind AllianceFabian Peeks, Willemijn F Boonstra, Lut de Baere, et al.
Journal of Inherited Metabolic Disease|January 12, 2008
Neonatal screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in The Netherlands: the importance of enzyme analysis to ascertain true MCAD deficiencyT G J Derks, T S Boer, A van Assen, et al.
Communications Biology|November 9, 2024
Precision-cut liver slices as an ex vivo model to assess impaired hepatic glucose productionLigia Akemi Kiyuna, Kishore Alagere Krishnamurthy, Esther B Homan, et al.
Nutrients|November 27, 2021
Glycogen Storage Disease Type Ia: Current Management Options, Burden and Unmet NeedsTerry G J Derks, David F Rodriguez-Buritica, Ayesha Ahmad, et al.
Journal of Inherited Metabolic Disease|April 12, 2021
A generic emergency protocol for patients with inborn errors of metabolism causing fasting intolerance: A retrospective, single-center study and the generation of www.emergencyprotocol.netAlessandro Rossi, Irene J Hoogeveen, Charlotte M A Lubout, et al.
Translational Stroke Research|October 14, 2020
Disruptions of Anaerobic Gut Bacteria Are Associated with Stroke and Post-stroke Infection: a Prospective Case-Control StudyBastiaan W Haak, Willeke F Westendorp, Tjitske S R van Engelen, et al.
Journal of Endocrinological Investigation|February 8, 2022
Serum sex hormone-binding globulin levels are reduced and inversely associated with intrahepatic lipid content and saturated fatty acid fraction in adult patients with glycogen storage disease type 1aP I H G Simons, O Valkenburg, I Telgenkamp, et al.
Pageof 17

Showing results (121-130 of 167) with videos related to

Sort By:
Pageof 17
BMC Biology|September 4, 2023
Personalised modelling of clinical heterogeneity between medium-chain acyl-CoA dehydrogenase patientsChristoff Odendaal, Emmalie A Jager, Anne-Claire M F Martines, et al.
Journal of Inherited Metabolic Disease|October 26, 2024
The relation between dietary polysaccharide intake and urinary excretion of tetraglucosideCandelas Gross-Valle, Tessa C Jacobs, Janneke D A Dijck-Brouwer, et al.
Journal of Inherited Metabolic Disease|April 24, 2016
Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcomeChristiaan P Sentner, Irene J Hoogeveen, David A Weinstein, et al.
Journal of Inherited Metabolic Disease|October 7, 2019
Research priorities for liver glycogen storage disease: An international priority setting partnership with the James Lind AllianceFabian Peeks, Willemijn F Boonstra, Lut de Baere, et al.
Journal of Inherited Metabolic Disease|January 12, 2008
Neonatal screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in The Netherlands: the importance of enzyme analysis to ascertain true MCAD deficiencyT G J Derks, T S Boer, A van Assen, et al.
Communications Biology|November 9, 2024
Precision-cut liver slices as an ex vivo model to assess impaired hepatic glucose productionLigia Akemi Kiyuna, Kishore Alagere Krishnamurthy, Esther B Homan, et al.
Nutrients|November 27, 2021
Glycogen Storage Disease Type Ia: Current Management Options, Burden and Unmet NeedsTerry G J Derks, David F Rodriguez-Buritica, Ayesha Ahmad, et al.
Journal of Inherited Metabolic Disease|April 12, 2021
A generic emergency protocol for patients with inborn errors of metabolism causing fasting intolerance: A retrospective, single-center study and the generation of www.emergencyprotocol.netAlessandro Rossi, Irene J Hoogeveen, Charlotte M A Lubout, et al.
Translational Stroke Research|October 14, 2020
Disruptions of Anaerobic Gut Bacteria Are Associated with Stroke and Post-stroke Infection: a Prospective Case-Control StudyBastiaan W Haak, Willeke F Westendorp, Tjitske S R van Engelen, et al.
Journal of Endocrinological Investigation|February 8, 2022
Serum sex hormone-binding globulin levels are reduced and inversely associated with intrahepatic lipid content and saturated fatty acid fraction in adult patients with glycogen storage disease type 1aP I H G Simons, O Valkenburg, I Telgenkamp, et al.
Pageof 17