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Journal of Inherited Metabolic Disease
|
April 9, 2008
Pathogenesis of CNS involvement in disorders of amino and organic acid metabolism
S Kölker, S W Sauer, G F Hoffmann, et al.
World Journal of Pediatrics : WJP
|
June 28, 2018
High incidence of maternal vitamin B<sub>12</sub> deficiency detected by newborn screening: first results from a study for the evaluation of 26 additional target disorders for the German newborn screening panel
Gwendolyn Gramer, Junmin Fang-Hoffmann, Patrik Feyh, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2004
Challenges for basic research in glutaryl-CoA dehydrogenase deficiency
S Kölker, K A Strauss, S I Goodman, et al.
Biochimica Et Biophysica Acta
|
September 17, 2011
Severe dysfunction of respiratory chain and cholesterol metabolism in Atp7b(-/-) mice as a model for Wilson disease
Sven W Sauer, Uta Merle, Silvana Opp, et al.
Archives of Gynecology and Obstetrics
|
March 14, 2022
Potential of blood-based biomarker approaches in endometrium and breast cancer: a case-control comparison study
Anne Schuhn, Tania Witte Tobar, Aoife Ward Gahlawat, et al.
International Journal of Cardiology. Heart & Vasculature
|
September 5, 2020
Trimethylamine N-oxide in atrial fibrillation progression
Petra Büttner, Jürgen G Okun, Jana Hauke, et al.
Acta Diabetologica
|
March 17, 2018
Urine levels of 5-aminoimidazole-4-carboxamide riboside (AICAR) in patients with type 2 diabetes
Michael Mendler, Stefan Kopf, Jan B Groener, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme
|
November 26, 2005
Massive insulin secretion in response to anaerobic exercise in exercise-induced hyperinsulinism
T Meissner, B Friedmann, J G Okun, et al.
Human Molecular Genetics
|
October 1, 2015
Molecular and biochemical alterations in tubular epithelial cells of patients with isolated methylmalonic aciduria
T Ruppert, A Schumann, H J Gröne, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2004
Looking forward--an evidence-based approach to glutaryl-CoA dehydrogenase deficiency
S Kölker, P Burgard, J G Okun, et al.
Page
of 17
Search research articles
Search
Showing results (31-40 of 165) with videos related to
Sort By:
Page
of 17
Journal of Inherited Metabolic Disease
|
April 9, 2008
Pathogenesis of CNS involvement in disorders of amino and organic acid metabolism
S Kölker, S W Sauer, G F Hoffmann, et al.
World Journal of Pediatrics : WJP
|
June 28, 2018
High incidence of maternal vitamin B<sub>12</sub> deficiency detected by newborn screening: first results from a study for the evaluation of 26 additional target disorders for the German newborn screening panel
Gwendolyn Gramer, Junmin Fang-Hoffmann, Patrik Feyh, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2004
Challenges for basic research in glutaryl-CoA dehydrogenase deficiency
S Kölker, K A Strauss, S I Goodman, et al.
Biochimica Et Biophysica Acta
|
September 17, 2011
Severe dysfunction of respiratory chain and cholesterol metabolism in Atp7b(-/-) mice as a model for Wilson disease
Sven W Sauer, Uta Merle, Silvana Opp, et al.
Archives of Gynecology and Obstetrics
|
March 14, 2022
Potential of blood-based biomarker approaches in endometrium and breast cancer: a case-control comparison study
Anne Schuhn, Tania Witte Tobar, Aoife Ward Gahlawat, et al.
International Journal of Cardiology. Heart & Vasculature
|
September 5, 2020
Trimethylamine N-oxide in atrial fibrillation progression
Petra Büttner, Jürgen G Okun, Jana Hauke, et al.
Acta Diabetologica
|
March 17, 2018
Urine levels of 5-aminoimidazole-4-carboxamide riboside (AICAR) in patients with type 2 diabetes
Michael Mendler, Stefan Kopf, Jan B Groener, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme
|
November 26, 2005
Massive insulin secretion in response to anaerobic exercise in exercise-induced hyperinsulinism
T Meissner, B Friedmann, J G Okun, et al.
Human Molecular Genetics
|
October 1, 2015
Molecular and biochemical alterations in tubular epithelial cells of patients with isolated methylmalonic aciduria
T Ruppert, A Schumann, H J Gröne, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2004
Looking forward--an evidence-based approach to glutaryl-CoA dehydrogenase deficiency
S Kölker, P Burgard, J G Okun, et al.
Page
of 17