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Georg F Hoffmann

Showing results (51-60 of 381) with videos related to

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Journal of Inherited Metabolic Disease|December 5, 2015
Neonatal mortality and outcome at the end of the first year of life in early onset urea cycle disorders--review and meta-analysis of observational studies published over more than 35 yearsPeter Burgard, Stefan Kölker, Gisela Haege, et al.
Pediatric Research|June 27, 2002
Selective decrease in central nervous system serotonin turnover in children with dopa-nonresponsive dystoniaBirgit Assmann, Martin Köhler, Georg F Hoffmann, et al.
Biofactors (Oxford, England)|December 20, 2008
Plasma and thrombocyte levels of coenzyme Q10 in children with Smith-Lemli-Opitz syndrome (SLOS) and the influence of HMG-CoA reductase inhibitorsDorothea Haas, Petra Niklowitz, Georg F Hoffmann, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 7, 2006
The pattern of Down syndrome among children in Qatar: a population-based studyAtqah Abdul Wahab, Abdulbari Bener, Amy L Sandridge, et al.
Neuropediatrics|March 11, 2015
Hereditary orotic aciduria with epilepsy and without megaloblastic anemiaKarina Grohmann, Heinz Lauffer, Peter Lauenstein, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 11, 2018
Corrigendum: Quantitative clinical characteristics of 53 patients with MPS VII: a cross-sectional analysisMatthias Zielonka, Sven F Garbade, Stefan Kölker, 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.
Brain : a Journal of Neurology|April 17, 2018
ATAD1 encephalopathy and stiff baby syndrome: a recognizable clinical presentationNicole I Wolf, Johannes Zschocke, Cornelis Jakobs, 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.
Zeitschrift Fur Evidenz, Fortbildung Und Qualitat Im Gesundheitswesen|October 23, 2018
Pediatric communication training: A project report on an innovative approach and its effects on student acceptanceAstrid Helling-Bakki, Thomas Lutz, Bettina Kraft, et al.
Pageof 39

Showing results (51-60 of 381) with videos related to

Sort By:
Pageof 39
Journal of Inherited Metabolic Disease|December 5, 2015
Neonatal mortality and outcome at the end of the first year of life in early onset urea cycle disorders--review and meta-analysis of observational studies published over more than 35 yearsPeter Burgard, Stefan Kölker, Gisela Haege, et al.
Pediatric Research|June 27, 2002
Selective decrease in central nervous system serotonin turnover in children with dopa-nonresponsive dystoniaBirgit Assmann, Martin Köhler, Georg F Hoffmann, et al.
Biofactors (Oxford, England)|December 20, 2008
Plasma and thrombocyte levels of coenzyme Q10 in children with Smith-Lemli-Opitz syndrome (SLOS) and the influence of HMG-CoA reductase inhibitorsDorothea Haas, Petra Niklowitz, Georg F Hoffmann, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 7, 2006
The pattern of Down syndrome among children in Qatar: a population-based studyAtqah Abdul Wahab, Abdulbari Bener, Amy L Sandridge, et al.
Neuropediatrics|March 11, 2015
Hereditary orotic aciduria with epilepsy and without megaloblastic anemiaKarina Grohmann, Heinz Lauffer, Peter Lauenstein, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 11, 2018
Corrigendum: Quantitative clinical characteristics of 53 patients with MPS VII: a cross-sectional analysisMatthias Zielonka, Sven F Garbade, Stefan Kölker, 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.
Brain : a Journal of Neurology|April 17, 2018
ATAD1 encephalopathy and stiff baby syndrome: a recognizable clinical presentationNicole I Wolf, Johannes Zschocke, Cornelis Jakobs, 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.
Zeitschrift Fur Evidenz, Fortbildung Und Qualitat Im Gesundheitswesen|October 23, 2018
Pediatric communication training: A project report on an innovative approach and its effects on student acceptanceAstrid Helling-Bakki, Thomas Lutz, Bettina Kraft, et al.
Pageof 39