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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 years
Peter 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 dystonia
Birgit 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 inhibitors
Dorothea 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 study
Atqah Abdul Wahab, Abdulbari Bener, Amy L Sandridge, et al.
Neuropediatrics
|
March 11, 2015
Hereditary orotic aciduria with epilepsy and without megaloblastic anemia
Karina 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 analysis
Matthias 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-mannosidosis
Matthias 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 presentation
Nicole 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 patient
Johannes 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 acceptance
Astrid Helling-Bakki, Thomas Lutz, Bettina Kraft, et al.
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of 39
Search research articles
Search
Showing results (51-60 of 381) with videos related to
Sort By:
Page
of 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 years
Peter 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 dystonia
Birgit 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 inhibitors
Dorothea 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 study
Atqah Abdul Wahab, Abdulbari Bener, Amy L Sandridge, et al.
Neuropediatrics
|
March 11, 2015
Hereditary orotic aciduria with epilepsy and without megaloblastic anemia
Karina 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 analysis
Matthias 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-mannosidosis
Matthias 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 presentation
Nicole 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 patient
Johannes 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 acceptance
Astrid Helling-Bakki, Thomas Lutz, Bettina Kraft, et al.
Page
of 39