Search research articles
Contact Us
Filters
Showing results (821-830 of 1,255) with videos related to
Page
of 126
Sort By:
Frontiers in Oncology
|
June 9, 2020
Mitochondrial Dysfunction Inhibits Hypoxia-Induced HIF-1α Stabilization and Expression of Its Downstream Targets
Marike W van Gisbergen, Kelly Offermans, An M Voets, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
May 26, 2007
Atypical case of Aicardi-Goutières syndrome with late-onset myoclonic status
Andrea Berger, Christiane Schroeter, Adelheid Wiemer-Kruel, et al.
Child Psychiatry and Human Development
|
May 20, 2014
Health-related quality of life in adolescents with inflammatory bowel disease depends on disease activity and psychiatric comorbidity
G Engelmann, D Erhard, M Petersen, et al.
Neuropediatrics
|
August 30, 2000
Combined D-2- and L-2-hydroxyglutaric aciduria with neonatal onset encephalopathy: a third biochemical variant of 2-hydroxyglutaric aciduria?
A C Muntau, W Röschinger, A Merkenschlager, et al.
Bone Marrow Transplantation
|
August 11, 2001
Successful HLA-identical bone marrow transplantation in a patient with PNP deficiency using busulfan and fludarabine for conditioning
C F Classen, A S Schulz, M Sigl-Kraetzig, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
November 1, 1991
[Macrocephaly as the initial manifestation of glutaryl-CoA-dehydrogenase deficiency (glutaric aciduria type I)]
F K Trefz, G F Hoffmann, E Mayatepek, et al.
Journal of Inherited Metabolic Disease
|
September 13, 2014
Understanding cerebral L-lysine metabolism: the role of L-pipecolate metabolism in Gcdh-deficient mice as a model for glutaric aciduria type I
Roland Posset, Silvana Opp, Eduard A Struys, et al.
Autophagy
|
November 24, 2021
Quantitative retrospective natural history modeling of <i>WDR45</i>-related developmental and epileptic encephalopathy - a systematic cross-sectional analysis of 160 published cases
Afshin Saffari, Julian Schröter, Sven F Garbade, et al.
European Journal of Pediatrics
|
March 16, 2022
Sudden neonatal death in individuals with medium-chain acyl-coenzyme A dehydrogenase deficiency: limit of newborn screening
Ulrike Mütze, Uta Nennstiel, Birgit Odenwald, et al.
Der Nervenarzt
|
January 22, 2015
[Tryptophan immunoadsorption for multiple sclerosis and neuromyelitis optica: therapy option for acute relapses during pregnancy and breastfeeding]
F Hoffmann, A Kraft, F Heigl, et al.
Page
of 126
Search research articles
Search
Showing results (821-830 of 1,255) with videos related to
Sort By:
Page
of 126
Frontiers in Oncology
|
June 9, 2020
Mitochondrial Dysfunction Inhibits Hypoxia-Induced HIF-1α Stabilization and Expression of Its Downstream Targets
Marike W van Gisbergen, Kelly Offermans, An M Voets, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
May 26, 2007
Atypical case of Aicardi-Goutières syndrome with late-onset myoclonic status
Andrea Berger, Christiane Schroeter, Adelheid Wiemer-Kruel, et al.
Child Psychiatry and Human Development
|
May 20, 2014
Health-related quality of life in adolescents with inflammatory bowel disease depends on disease activity and psychiatric comorbidity
G Engelmann, D Erhard, M Petersen, et al.
Neuropediatrics
|
August 30, 2000
Combined D-2- and L-2-hydroxyglutaric aciduria with neonatal onset encephalopathy: a third biochemical variant of 2-hydroxyglutaric aciduria?
A C Muntau, W Röschinger, A Merkenschlager, et al.
Bone Marrow Transplantation
|
August 11, 2001
Successful HLA-identical bone marrow transplantation in a patient with PNP deficiency using busulfan and fludarabine for conditioning
C F Classen, A S Schulz, M Sigl-Kraetzig, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
November 1, 1991
[Macrocephaly as the initial manifestation of glutaryl-CoA-dehydrogenase deficiency (glutaric aciduria type I)]
F K Trefz, G F Hoffmann, E Mayatepek, et al.
Journal of Inherited Metabolic Disease
|
September 13, 2014
Understanding cerebral L-lysine metabolism: the role of L-pipecolate metabolism in Gcdh-deficient mice as a model for glutaric aciduria type I
Roland Posset, Silvana Opp, Eduard A Struys, et al.
Autophagy
|
November 24, 2021
Quantitative retrospective natural history modeling of <i>WDR45</i>-related developmental and epileptic encephalopathy - a systematic cross-sectional analysis of 160 published cases
Afshin Saffari, Julian Schröter, Sven F Garbade, et al.
European Journal of Pediatrics
|
March 16, 2022
Sudden neonatal death in individuals with medium-chain acyl-coenzyme A dehydrogenase deficiency: limit of newborn screening
Ulrike Mütze, Uta Nennstiel, Birgit Odenwald, et al.
Der Nervenarzt
|
January 22, 2015
[Tryptophan immunoadsorption for multiple sclerosis and neuromyelitis optica: therapy option for acute relapses during pregnancy and breastfeeding]
F Hoffmann, A Kraft, F Heigl, et al.
Page
of 126