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Advances in Clinical Chemistry|November 14, 2008
Mechanisms of arterial calcification: spotlight on the inhibitorsGabriele Weissen-Plenz, Yvonne Nitschke, Frank Rutsch
Acta Paediatrica (Oslo, Norway : 1992)|February 25, 2017
Sapropterin treatment does not enhance the health-related quality of life of patients with phenylketonuria and their parentsReinhold Feldmann, Eva Wolfgart, Josef Weglage, et al.
Journal of Inherited Metabolic Disease|May 7, 2010
LMBRD1: the gene for the cblF defect of vitamin B₁₂ metabolismFrank Rutsch, Susann Gailus, Terttu Suormala, et al.
Journal of Cellular and Molecular Medicine|April 12, 2011
Npp1 promotes atherosclerosis in ApoE knockout miceYvonne Nitschke, Gabriele Weissen-Plenz, Robert Terkeltaub, et al.
Journal of Interferon & Cytokine Research : the Official Journal of the International Society for Interferon and Cytokine Research|May 6, 2017
MDA5-Associated Neuroinflammation and the Singleton-Merten Syndrome: Two Faces of the Same Type I Interferonopathy SpectrumInsa Buers, Gillian I Rice, Yanick J Crow, et al.
Journal of Cardiovascular Disease Research|May 26, 2012
Molecular diagnosis of generalized arterial calcification of infancy (GACI)Iravathy Goud Kalal, Dayakar Seetha, Anuradha Panda, et al.
International Journal of Environmental Research and Public Health|April 27, 2024
Children and Adolescents with Early Treated Phenylketonuria: Cognitive Development and Fluctuations of Blood Phenylalanine LevelsReinhold Feldmann, Ulrike Och, Lisa Sophie Beckmann, et al.
The Journal of Clinical Endocrinology and Metabolism|September 9, 2021
A Reference Range for Plasma Levels of Inorganic Pyrophosphate in Children Using the ATP Sulfurylase MethodEva Bernhard, Yvonne Nitschke, Gus Khursigara, et al.
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