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Journal of Inherited Metabolic Disease|June 20, 2008
Newborn screening for methylmalonic acidurias--optimization by statistical parameter combinationM Lindner, S Ho, S Kölker, et al.Zeitschrift Fur Rheumatologie|July 26, 2019
Reality of care for musculoskeletal diseases at the population level : Results of the PROCLAIR collaborative projectJ Callhoff, K Albrecht, F Hoffmann, et al.Nature and Science of Sleep|April 27, 2013
The influence of emerging low mood symptoms on sleep in children: a pilot studyDeirdre A Conroy, Anameti Usoro, Robert F Hoffmann, et al.The Pediatric Infectious Disease Journal|January 22, 2000
Comparison of ritonavir plus saquinavir- and nelfinavir plus saquinavir-containing regimens as salvage therapy in children with human immunodeficiency type 1 infectionF Hoffmann, G Notheis, U Wintergerst, et al.Journal of Inherited Metabolic Disease|December 22, 1999
Sensitivity and specificity of free and total glutaric acid and 3-hydroxyglutaric acid measurements by stable-isotope dilution assays for the diagnosis of glutaric aciduria type II Baric, L Wagner, P Feyh, et al.Neuropediatrics|April 29, 1998
4-Hydroxybutyric acid and the clinical phenotype of succinic semialdehyde dehydrogenase deficiency, an inborn error of GABA metabolismK M Gibson, G F Hoffmann, A K Hodson, et al.Pediatrics|June 5, 2003
Expanded newborn screening for inborn errors of metabolism by electrospray ionization-tandem mass spectrometry: results, outcome, and implicationsAndreas Schulze, Martin Lindner, Dirk Kohlmüller, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|March 1, 1997
Ultrastructural changes in the trabecular meshwork of human eyes treated with corticosteroidsD Johnson, J Gottanka, C Flügel, et al.JASA Express Letters|September 26, 2022
Finite-difference time-domain simulations: Verification on head-related transfer functions of a rigid sphere modelJulie Meyer, Michael Smirnov, Ali Khajeh-Saeed, et al.Orphanet Journal of Rare Diseases|November 25, 2021
Potentials and current shortcomings in the cooperation between German centers for rare diseases and primary care physicians: results from the project TRANSLATE-NAMSED Druschke, F Krause, G Müller, et al.Pageof 114