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IUBMB Life|May 27, 2010
Impact of selected inborn errors of metabolism on prenatal and neonatal developmentSabine Illsinger, Anibh M DasJournal of Biomedicine & Biotechnology|July 1, 2010
Inborn errors of energy metabolism associated with myopathiesAnibh M Das, Ulrike Steuerwald, Sabine IllsingerKlinische Padiatrie|August 13, 2021
[Thrombotic Microangiopathy (TMA) after Gene Replacemant Therapy (GRT) due to Spinal Muscular Atrophy: Case Summary and Recommendations for Treatment]Damian Witte, Hans Hartmann, Jens Drube, et al.European Journal of Pediatrics|July 22, 2006
Pitfalls in paediatric gait disturbances: painless bone diseasesThomas Lücke, Sabine Illsinger, Anibh Martin Das, et al.Annals of Nutrition & Metabolism|April 2, 2010
Glycogen storage disease type 1: impact of medium-chain triglycerides on metabolic control and growthAnibh M Das, Thomas Lücke, Uta Meyer, et al.Molecular Genetics and Metabolism|April 28, 2004
Fabry disease: reduced activities of respiratory chain enzymes with decreased levels of energy-rich phosphates in fibroblastsThomas Lücke, Wiebke Höppner, Esther Schmidt, et al.Pediatric Neurology|March 23, 2004
3-methylglutaconic aciduria type I in a boy with fever-associated seizuresSabine Illsinger, Thomas Lücke, Johannes Zschocke, et al.Pediatric Neurology|May 29, 2003
BH4-sensitive hyperphenylalaninemia: new case and review of literatureThomas Lücke, Sabine Illsinger, Christa Aulehla-Scholz, et al.Orphanet Journal of Rare Diseases|December 23, 2017
Non-invasive test using palmitate in patients with suspected fatty acid oxidation defects: disease-specific acylcarnitine patterns can help to establish the diagnosisNils Janzen, Alejandro D Hofmann, Gunnar Schmidt, et al.Amino Acids|May 27, 2009
Plasma and urine amino acid pattern in preterm infants on enteral nutrition: impact of gestational ageSabine Illsinger, Karl-Heinz Schmidt, Thomas Lücke, et al.Pageof 4