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Saskia B Wortmann

Showing results (11-20 of 178) with videos related to

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Neuropediatrics|June 10, 2017
A Guideline for the Diagnosis of Pediatric Mitochondrial Disease: The Value of Muscle and Skin Biopsies in the Genetics EraSaskia B Wortmann, Johannes A Mayr, Jean Marc Nuoffer, et al.
Genes|June 28, 2023
Case Report-An Inherited Loss-of-Function <i>NRXN3</i> Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 DeletionsRené G Feichtinger, Martin Preisel, Karin Brugger, et al.
Brain : a Journal of Neurology|December 21, 2016
Treatable mitochondrial diseases: cofactor metabolism and beyondFelix Distelmaier, Tobias B Haack, Saskia B Wortmann, et al.
Diagnostics (Basel, Switzerland)|May 27, 2023
Treatment of the Neutropenia Associated with GSD1b and G6PC3 Deficiency with SGLT2 InhibitorsMaria Veiga-da-Cunha, Saskia B Wortmann, Sarah C Grünert, et al.
JIMD Reports|April 24, 2014
Leucine Loading Test is Only Discriminative for 3-Methylglutaconic Aciduria Due to AUH DefectSaskia B Wortmann, Leo A J Kluijtmans, Silvia Sequeira, et al.
Orphanet Journal of Rare Diseases|July 4, 2021
Ketogenic diet for mitochondrial disease: a systematic review on efficacy and safetyHeidi Zweers, Annemiek M J van Wegberg, Mirian C H Janssen, et al.
Orphanet Journal of Rare Diseases|September 28, 2021
Correction to: Ketogenic diet for mitochondrial disease: a systematic review on efficacy and safetyHeidi Zweers, Annemiek M J van Wegberg, Mirian C H Janssen, et al.
Journal of Inherited Metabolic Disease|October 1, 2010
The 3-methylglutaconic acidurias: what's new?Saskia B Wortmann, Leo A Kluijtmans, Udo F H Engelke, et al.
Journal of Inherited Metabolic Disease|March 5, 2015
Whole exome sequencing of suspected mitochondrial patients in clinical practiceSaskia B Wortmann, David A Koolen, Jan A Smeitink, et al.
JIMD Reports|December 9, 2016
Previously Unreported Biallelic Mutation in DNAJC19: Are Sensorineural Hearing Loss and Basal Ganglia Lesions Additional Features of Dilated Cardiomyopathy and Ataxia (DCMA) Syndrome?Sema Kalkan Ucar, Johannes A Mayr, René G Feichtinger, et al.
Pageof 18

Showing results (11-20 of 178) with videos related to

Sort By:
Pageof 18
Neuropediatrics|June 10, 2017
A Guideline for the Diagnosis of Pediatric Mitochondrial Disease: The Value of Muscle and Skin Biopsies in the Genetics EraSaskia B Wortmann, Johannes A Mayr, Jean Marc Nuoffer, et al.
Genes|June 28, 2023
Case Report-An Inherited Loss-of-Function <i>NRXN3</i> Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 DeletionsRené G Feichtinger, Martin Preisel, Karin Brugger, et al.
Brain : a Journal of Neurology|December 21, 2016
Treatable mitochondrial diseases: cofactor metabolism and beyondFelix Distelmaier, Tobias B Haack, Saskia B Wortmann, et al.
Diagnostics (Basel, Switzerland)|May 27, 2023
Treatment of the Neutropenia Associated with GSD1b and G6PC3 Deficiency with SGLT2 InhibitorsMaria Veiga-da-Cunha, Saskia B Wortmann, Sarah C Grünert, et al.
JIMD Reports|April 24, 2014
Leucine Loading Test is Only Discriminative for 3-Methylglutaconic Aciduria Due to AUH DefectSaskia B Wortmann, Leo A J Kluijtmans, Silvia Sequeira, et al.
Orphanet Journal of Rare Diseases|July 4, 2021
Ketogenic diet for mitochondrial disease: a systematic review on efficacy and safetyHeidi Zweers, Annemiek M J van Wegberg, Mirian C H Janssen, et al.
Orphanet Journal of Rare Diseases|September 28, 2021
Correction to: Ketogenic diet for mitochondrial disease: a systematic review on efficacy and safetyHeidi Zweers, Annemiek M J van Wegberg, Mirian C H Janssen, et al.
Journal of Inherited Metabolic Disease|October 1, 2010
The 3-methylglutaconic acidurias: what's new?Saskia B Wortmann, Leo A Kluijtmans, Udo F H Engelke, et al.
Journal of Inherited Metabolic Disease|March 5, 2015
Whole exome sequencing of suspected mitochondrial patients in clinical practiceSaskia B Wortmann, David A Koolen, Jan A Smeitink, et al.
JIMD Reports|December 9, 2016
Previously Unreported Biallelic Mutation in DNAJC19: Are Sensorineural Hearing Loss and Basal Ganglia Lesions Additional Features of Dilated Cardiomyopathy and Ataxia (DCMA) Syndrome?Sema Kalkan Ucar, Johannes A Mayr, René G Feichtinger, et al.
Pageof 18