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Felix Distelmaier

Showing results (21-30 of 151) with videos related to

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Cerebrovascular Diseases (Basel, Switzerland)|February 23, 2013
Transient ischaemic attack in a 5-year-old girl due to focal vasculitis in neuroborreliosisMalte Kohns, Michael Karenfort, Jörg Schaper, et al.
Brain & Development|December 22, 2005
Pseudotumor cerebri as an important differential diagnosis of papilledema in childrenFelix Distelmaier, Ulrike Sengler, Martina Messing-Juenger, et al.
Stem Cell Research|November 20, 2022
Generation of an induced pluripotent stem cell line (IUFi002-A) from a Leigh syndrome patient carrying mutations in the NDUFS1 geneOnofrio Valente, Jochen Dobner, Haribaskar Ramachandran, et al.
Journal of Child Neurology|July 21, 2007
"How much brain is really necessary?" A case of complex cerebral malformation and its clinical courseFelix Distelmaier, Renate Richter-Werkle, Jörg Schaper, et al.
Pediatric Pulmonology|September 23, 2021
Laryngeal sensation and its association with aspiration and cough in children with neurological impairmentNadine Freitag, Pia Tews, Nicole Hübl, et al.
Journal of Inherited Metabolic Disease|May 4, 2018
Severe ichthyosis in MPDU1-CDGChristian Thiel, Saskia Wortmann, Korbinian Riedhammer, et al.
Stem Cell Research|November 20, 2025
CRISPR/Cas9-mediated editing of MIC13 in human induced pluripotent stem cells: A model for mitochondrial hepato-encephalopathyHaribaskar Ramachandran, Alexander Becker, Jochen Dobner, et al.
Annals of Clinical and Translational Neurology|January 4, 2018
4-Hydroxybenzoic acid restores CoQ<sub>10</sub> biosynthesis in human COQ2 deficiencyDiran Herebian, Annette Seibt, Sander H J Smits, et al.
The EMBO Journal|November 15, 2012
OXPHOS mutations and neurodegenerationWerner J H Koopman, Felix Distelmaier, Jan A M Smeitink, et al.
Brain : a Journal of Neurology|June 1, 2014
Infantile Leigh-like syndrome caused by SLC19A3 mutations is a treatable diseaseTobias B Haack, Dirk Klee, Tim M Strom, et al.
Pageof 16

Showing results (21-30 of 151) with videos related to

Sort By:
Pageof 16
Cerebrovascular Diseases (Basel, Switzerland)|February 23, 2013
Transient ischaemic attack in a 5-year-old girl due to focal vasculitis in neuroborreliosisMalte Kohns, Michael Karenfort, Jörg Schaper, et al.
Brain & Development|December 22, 2005
Pseudotumor cerebri as an important differential diagnosis of papilledema in childrenFelix Distelmaier, Ulrike Sengler, Martina Messing-Juenger, et al.
Stem Cell Research|November 20, 2022
Generation of an induced pluripotent stem cell line (IUFi002-A) from a Leigh syndrome patient carrying mutations in the NDUFS1 geneOnofrio Valente, Jochen Dobner, Haribaskar Ramachandran, et al.
Journal of Child Neurology|July 21, 2007
"How much brain is really necessary?" A case of complex cerebral malformation and its clinical courseFelix Distelmaier, Renate Richter-Werkle, Jörg Schaper, et al.
Pediatric Pulmonology|September 23, 2021
Laryngeal sensation and its association with aspiration and cough in children with neurological impairmentNadine Freitag, Pia Tews, Nicole Hübl, et al.
Journal of Inherited Metabolic Disease|May 4, 2018
Severe ichthyosis in MPDU1-CDGChristian Thiel, Saskia Wortmann, Korbinian Riedhammer, et al.
Stem Cell Research|November 20, 2025
CRISPR/Cas9-mediated editing of MIC13 in human induced pluripotent stem cells: A model for mitochondrial hepato-encephalopathyHaribaskar Ramachandran, Alexander Becker, Jochen Dobner, et al.
Annals of Clinical and Translational Neurology|January 4, 2018
4-Hydroxybenzoic acid restores CoQ<sub>10</sub> biosynthesis in human COQ2 deficiencyDiran Herebian, Annette Seibt, Sander H J Smits, et al.
The EMBO Journal|November 15, 2012
OXPHOS mutations and neurodegenerationWerner J H Koopman, Felix Distelmaier, Jan A M Smeitink, et al.
Brain : a Journal of Neurology|June 1, 2014
Infantile Leigh-like syndrome caused by SLC19A3 mutations is a treatable diseaseTobias B Haack, Dirk Klee, Tim M Strom, et al.
Pageof 16