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Felix Distelmaier

Showing results (51-60 of 151) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|June 18, 2013
A guide to diagnosis and treatment of Leigh syndromeFabian Baertling, Richard J Rodenburg, Jörg Schaper, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 4, 2009
The antioxidant Trolox restores mitochondrial membrane potential and Ca2+ -stimulated ATP production in human complex I deficiencyFelix Distelmaier, Henk-Jan Visch, Jan A M Smeitink, et al.
Pediatric Nephrology (Berlin, Germany)|July 20, 2007
Cystic renal dysplasia as a leading sign of inherited metabolic diseaseFelix Distelmaier, Markus Vogel, Ute Spiekerkötter, et al.
Plos One|November 6, 2009
C. elegans ATAD-3 is essential for mitochondrial activity and developmentMichael Hoffmann, Nadège Bellance, Rodrigue Rossignol, et al.
Nature Communications|May 13, 2022
Neuroligin-mediated neurodevelopmental defects are induced by mitochondrial dysfunction and prevented by lutein in C. elegansSilvia Maglioni, Alfonso Schiavi, Marlen Melcher, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|November 11, 2009
Clinical spectrum of the pseudotumor cerebri complex in childrenDaniel Tibussek, Dominik T Schneider, Nicola Vandemeulebroecke, et al.
Antioxidants (Basel, Switzerland)|March 29, 2023
Neuroimaging in Primary Coenzyme-Q<sub>10</sub>-Deficiency DisordersJuliane Münch, Jannik Prasuhn, Lucia Laugwitz, et al.
Cell Calcium|February 26, 2008
Mitochondrial Ca2+ homeostasis in human NADH:ubiquinone oxidoreductase deficiencyPeter H G M Willems, Federica Valsecchi, Felix Distelmaier, et al.
Mitochondrion|March 6, 2012
Identification and functional analysis of mitochondrial complex I assembly factor homologues in C. elegansDaniela van den Ecker, Mariël A van den Brand, Gerke Ariaans, et al.
European Journal of Human Genetics : EJHG|June 18, 2015
Fatal neonatal encephalopathy and lactic acidosis caused by a homozygous loss-of-function variant in COQ9Katharina Danhauser, Diran Herebian, Tobias B Haack, et al.
Pageof 16

Showing results (51-60 of 151) with videos related to

Sort By:
Pageof 16
Journal of Neurology, Neurosurgery, and Psychiatry|June 18, 2013
A guide to diagnosis and treatment of Leigh syndromeFabian Baertling, Richard J Rodenburg, Jörg Schaper, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 4, 2009
The antioxidant Trolox restores mitochondrial membrane potential and Ca2+ -stimulated ATP production in human complex I deficiencyFelix Distelmaier, Henk-Jan Visch, Jan A M Smeitink, et al.
Pediatric Nephrology (Berlin, Germany)|July 20, 2007
Cystic renal dysplasia as a leading sign of inherited metabolic diseaseFelix Distelmaier, Markus Vogel, Ute Spiekerkötter, et al.
Plos One|November 6, 2009
C. elegans ATAD-3 is essential for mitochondrial activity and developmentMichael Hoffmann, Nadège Bellance, Rodrigue Rossignol, et al.
Nature Communications|May 13, 2022
Neuroligin-mediated neurodevelopmental defects are induced by mitochondrial dysfunction and prevented by lutein in C. elegansSilvia Maglioni, Alfonso Schiavi, Marlen Melcher, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|November 11, 2009
Clinical spectrum of the pseudotumor cerebri complex in childrenDaniel Tibussek, Dominik T Schneider, Nicola Vandemeulebroecke, et al.
Antioxidants (Basel, Switzerland)|March 29, 2023
Neuroimaging in Primary Coenzyme-Q<sub>10</sub>-Deficiency DisordersJuliane Münch, Jannik Prasuhn, Lucia Laugwitz, et al.
Cell Calcium|February 26, 2008
Mitochondrial Ca2+ homeostasis in human NADH:ubiquinone oxidoreductase deficiencyPeter H G M Willems, Federica Valsecchi, Felix Distelmaier, et al.
Mitochondrion|March 6, 2012
Identification and functional analysis of mitochondrial complex I assembly factor homologues in C. elegansDaniela van den Ecker, Mariël A van den Brand, Gerke Ariaans, et al.
European Journal of Human Genetics : EJHG|June 18, 2015
Fatal neonatal encephalopathy and lactic acidosis caused by a homozygous loss-of-function variant in COQ9Katharina Danhauser, Diran Herebian, Tobias B Haack, et al.
Pageof 16