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Journal of Inherited Metabolic Disease|April 8, 2010
Newborn screening for disorders of fatty-acid oxidation: experience and recommendations from an expert meetingMartin Lindner, Georg F Hoffmann, Dietrich Matern
European Journal of Pediatrics|August 15, 2002
Tetrahydrobiopterin monotherapy for phenylketonuria patients with common mild mutationsRobert Steinfeld, Alfried Kohlschütter, Johannes Zschocke, et al.
Orphanet Journal of Rare Diseases|October 19, 2013
Newborn screening by tandem mass spectrometry for glutaric aciduria type 1: a cost-effectiveness analysisJohannes Pfeil, Stefan Listl, Georg F Hoffmann, et al.
Deutsches Arzteblatt International|April 9, 2021
Neonatal Screening for Congenital Metabolic and Endocrine Disorders—Results From Germany for the Years 2006–2018Anja Lüders, Oliver Blankenstein, Inken Brockow, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 2010
Two inborn errors of metabolism in a newborn: glutaric aciduria type I combined with isobutyrylglycinuriaManuela Popek, Melanie Walter, Malkanthi Fernando, et al.
Journal of Inherited Metabolic Disease|August 17, 2013
Living with an inborn error of metabolism detected by newborn screening-parents' perspectives on child development and impact on family lifeGwendolyn Gramer, Gisela Haege, Esther M Glahn, et al.
Forschende Komplementarmedizin Und Klassische Naturheilkunde = Research in Complementary and Natural Classical Medicine|June 30, 2005
Integration of complementary and alternative medicine into German medical school curricula -- contradictions between the opinions of decision makers and the status quoBenno Brinkhaus, Stefanie Joos, Martin Lindner, et al.
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