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Journal of Inherited Metabolic Disease|January 30, 2019
Quantitative natural history characterization in a cohort of 142 published cases of patients with galactosialidosis-A cross-sectional studyTomáš Sláma, Sven F Garbade, Stefan Kölker, et al.
Transplantation|July 1, 1987
Human immunodeficiency virus transmission by organ donation. Outcome in cornea and kidney recipientsA Schwarz, F Hoffmann, J L'age-Stehr, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 8, 2018
A cross-sectional quantitative analysis of the natural history of free sialic acid storage disease-an ultra-orphan multisystemic lysosomal storage disorderMatthias Zielonka, Sven F Garbade, Stefan Kölker, et al.
European Journal of Orthopaedic Surgery & Traumatology : Orthopedie Traumatologie|March 17, 2025
Surgical treatment of acetabular fractures: a comparative cohort study comparing orthogonal double plating to suprapectineal quadrilateral surface (QLS) plate osteosynthesisFelix Kordes, Emre Yilmaz, Matthias Königshausen, et al.
Journal of Inherited Metabolic Disease|June 22, 2019
Ultra-orphan lysosomal storage diseases: A cross-sectional quantitative analysis of the natural history of alpha-mannosidosisMatthias Zielonka, Sven F Garbade, Stefan Kölker, et al.
Molecular Genetics and Metabolism|March 1, 2011
Natural course of glutamine synthetase deficiency in a 3 year old patientJohannes Häberle, Noora Shahbeck, Khalid Ibrahim, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|July 1, 1990
[Pre- and postnatal diagnosis of organoacidopathies]G F Hoffmann, C Jakobs, D Rating, et al.
The Journal of Pediatrics|March 1, 1996
Severe hyperchloriduria-hyperkaliuria: a new congenital renal tubular abnormality?J Meyburg, E Mayatepek, G F Hoffmann, et al.
Bone|August 6, 2017
Phantomless calibration of CT scans for measurement of BMD and bone strength-Inter-operator reanalysis precisionDavid C Lee, Paul F Hoffmann, David L Kopperdahl, et al.
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