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Journal of Paediatrics and Child Health|January 29, 2010
Behaviour problems of patients with Moebius sequence and parental stressWolfgang Briegel, Christina Hofmann, K Otfried SchwabZeitschrift Fur Kinder- Und Jugendpsychiatrie Und Psychotherapie|November 6, 2009
[22q11.2 deletion: handicap-related problems and coping strategies of primary caregivers]Wolfgang Briegel, Marco Schneider, K Otfried SchwabChild: Care, Health and Development|September 13, 2008
22q11.2 deletion syndrome: behaviour problems of children and adolescents and parental stressW Briegel, M Schneider, K Otfried SchwabEuropean Child & Adolescent Psychiatry|March 4, 2009
Autism spectrum disorders in children and adolescents with Moebius sequenceWolfgang Briegel, Martina Schimek, Inge Kamp-Becker, et al.Pediatric Diabetes|July 14, 2010
Characterization of 33 488 children and adolescents with type 1 diabetes based on the gender-specific increase of cardiovascular risk factorsK Otfried Schwab, Juergen Doerfer, Wolfgang Marg, et al.Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|October 10, 2021
Glycogen storage disease type I patients with hyperlipidemia have no signs of early vascular dysfunction and premature atherosclerosisJohannes Schmitt, Michael Wurm, K Otfried Schwab, et al.Journal of Diabetes and Metabolic Disorders|July 9, 2013
Ornithine transcarbamylase deficiency combined with type 1 diabetes mellitus - a challenge in clinical and dietary managementSarah C Grünert, Pablo Villavicencio-Lorini, Bendicht Wermuth, et al.European Journal of Endocrinology|November 7, 2007
Delayed pubertal onset and development in German children and adolescents with type 1 diabetes: cross-sectional analysis of recent data from the DPV diabetes documentation and quality management systemTilman Rohrer, Eva Stierkorb, Sabine Heger, et al.Orphanet Journal of Rare Diseases|January 27, 2012
Clinical and neurocognitive outcome in symptomatic isovaleric acidemiaSarah C Grünert, Udo Wendel, Martin Lindner, et al.Annals of Neurology|July 12, 2002
Clinical variability in 3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiencyRegina Ensenauer, Helmut Niederhoff, Jos P N Ruiter, et al.Pageof 3