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International Journal of Environmental Research and Public Health|May 28, 2022
Towards Understanding Behaviour and Emotions of Children with CLN3 Disease (Batten Disease): Patterns, Problems and Support for Child and FamilyAline K Honingh, Yvonne L Kruithof, Willemijn F E Kuper, et al.Pediatric Neurology|March 13, 2026
Mitochondrial Dysfunction in Monogenic Developmental and Epileptic EncephalopathiesCrista A Minderhoud, Eva H Brilstra, Floor E Jansen, et al.Pharmaceutical Research|June 2, 2016
A Mixed Micelle Formulation for Oral Delivery of Vitamin KFeilong Sun, Tessa C C Jaspers, Peter M van Hasselt, et al.Intensive Care Medicine|March 12, 2011
Intracranial bleeding due to vitamin K deficiency: advantages of using a pediatric intensive care registryDésirée Y Visser, Nicolaas J Jansen, Marloes M Ijland, et al.Journal of Inherited Metabolic Disease|May 24, 2019
Pathophysiology of propionic and methylmalonic acidemias. Part 1: ComplicationsHanneke A Haijes, Judith J M Jans, Simone Y Tas, et al.JAMA Neurology|December 11, 2013
Survival and psychomotor development with early betaine treatment in patients with severe methylenetetrahydrofolate reductase deficiencyEugene F Diekman, Tom J de Koning, Nanda M Verhoeven-Duif, et al.Metallomics : Integrated Biometal Science|May 5, 2012
Application of exome sequencing in the search for genetic causes of rare disorders of copper metabolismSabine A Fuchs, Magdalena Harakalova, Gijs van Haaften, et al.Colloids and Surfaces. B, Biointerfaces|July 4, 2018
Mixed micellar system stabilized with saponins for oral delivery of vitamin KFeilong Sun, Chengpei Ye, Kaushik Thanki, et al.European Journal of Medical Genetics|December 5, 2020
Deep intronic TIMMDC1 variant delays diagnosis of rapidly progressive complex I deficiencyMyrthe Naber, Debby Hellebrekers, Rutger A J Nievelstein, et al.Journal of Inherited Metabolic Disease|October 12, 2019
Inborn errors of enzymes in glutamate metabolismLynne Rumping, Esmee Vringer, Roderick H J Houwen, et al.Pageof 13