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European Journal of Pediatrics
|
January 10, 2004
Frequencies of inherited organic acidurias and disorders of mitochondrial fatty acid transport and oxidation in Germany
Georg F Hoffmann, Rüdiger von Kries, Daniela Klose, et al.
European Journal of Human Genetics : EJHG
|
May 9, 2013
A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Document
Martina C Cornel, Tessel Rigter, Stephanie S Weinreich, et al.
Journal of Neuroscience Research
|
May 7, 2002
Chronic treatment with glutaric acid induces partial tolerance to excitotoxicity in neuronal cultures from chick embryo telencephalons
Stefan Kölker, Jürgen G Okun, Barbara Ahlemeyer, et al.
Plos One
|
March 1, 2019
Extended diagnosis of purine and pyrimidine disorders from urine: LC MS/MS assay development and clinical validation
Péter Monostori, Glynis Klinke, Jana Hauke, et al.
Endocrine
|
November 8, 2023
Exome sequencing (ES) of a pediatric cohort with chronic endocrine diseases: a single-center study (within the framework of the TRANSLATE-NAMSE project)
Sebastian Gippert, Matias Wagner, Theresa Brunet, et al.
The Journal of Biological Chemistry
|
September 16, 2003
Methylmalonic acid, a biochemical hallmark of methylmalonic acidurias but no inhibitor of mitochondrial respiratory chain
Stefan Kölker, Marina Schwab, Friederike Hörster, et al.
Patient Education and Counseling
|
February 11, 2010
Outcome of parent-physician communication skills training for pediatric residents
Christoph Nikendei, Hans Martin Bosse, Katja Hoffmann, et al.
Annals of Neurology
|
January 31, 2003
Lack of creatine in muscle and brain in an adult with GAMT deficiency
Andreas Schulze, Peter Bachert, Heinz Schlemmer, et al.
World Journal of Pediatrics : WJP
|
January 20, 2017
Newborn screening for remethylation disorders and vitamin B<sub>12</sub> deficiency-evaluation of new strategies in cohorts from Qatar and Germany
Gwendolyn Gramer, Ghassan Abdoh, Tawfeg Ben-Omran, et al.
Metabolites
|
October 22, 2021
Differences of Phenylalanine Concentrations in Dried Blood Spots and in Plasma: Erythrocytes as a Neglected Component for This Observation
Dorothea Haas, Jana Hauke, Kathrin V Schwarz, et al.
Page
of 39
Search research articles
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Showing results (181-190 of 381) with videos related to
Sort By:
Page
of 39
European Journal of Pediatrics
|
January 10, 2004
Frequencies of inherited organic acidurias and disorders of mitochondrial fatty acid transport and oxidation in Germany
Georg F Hoffmann, Rüdiger von Kries, Daniela Klose, et al.
European Journal of Human Genetics : EJHG
|
May 9, 2013
A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Document
Martina C Cornel, Tessel Rigter, Stephanie S Weinreich, et al.
Journal of Neuroscience Research
|
May 7, 2002
Chronic treatment with glutaric acid induces partial tolerance to excitotoxicity in neuronal cultures from chick embryo telencephalons
Stefan Kölker, Jürgen G Okun, Barbara Ahlemeyer, et al.
Plos One
|
March 1, 2019
Extended diagnosis of purine and pyrimidine disorders from urine: LC MS/MS assay development and clinical validation
Péter Monostori, Glynis Klinke, Jana Hauke, et al.
Endocrine
|
November 8, 2023
Exome sequencing (ES) of a pediatric cohort with chronic endocrine diseases: a single-center study (within the framework of the TRANSLATE-NAMSE project)
Sebastian Gippert, Matias Wagner, Theresa Brunet, et al.
The Journal of Biological Chemistry
|
September 16, 2003
Methylmalonic acid, a biochemical hallmark of methylmalonic acidurias but no inhibitor of mitochondrial respiratory chain
Stefan Kölker, Marina Schwab, Friederike Hörster, et al.
Patient Education and Counseling
|
February 11, 2010
Outcome of parent-physician communication skills training for pediatric residents
Christoph Nikendei, Hans Martin Bosse, Katja Hoffmann, et al.
Annals of Neurology
|
January 31, 2003
Lack of creatine in muscle and brain in an adult with GAMT deficiency
Andreas Schulze, Peter Bachert, Heinz Schlemmer, et al.
World Journal of Pediatrics : WJP
|
January 20, 2017
Newborn screening for remethylation disorders and vitamin B<sub>12</sub> deficiency-evaluation of new strategies in cohorts from Qatar and Germany
Gwendolyn Gramer, Ghassan Abdoh, Tawfeg Ben-Omran, et al.
Metabolites
|
October 22, 2021
Differences of Phenylalanine Concentrations in Dried Blood Spots and in Plasma: Erythrocytes as a Neglected Component for This Observation
Dorothea Haas, Jana Hauke, Kathrin V Schwarz, et al.
Page
of 39