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Molecular Genetics and Metabolism
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August 10, 2007
Are heterocygotes for classical homocystinuria at risk of vitamin B12 and folic acid deficiency?
Mahmoud F Elsaid, Abdulbari Bener, Martin Lindner, et al.
Plos Neglected Tropical Diseases
|
April 18, 2012
The Schistosoma mansoni tegumental-allergen-like (TAL) protein family: influence of developmental expression on human IgE responses
Colin M Fitzsimmons, Frances M Jones, Alex Stearn, et al.
Neuropediatrics
|
April 4, 2002
Congenital disorder of glycosylation IId (CDG-IId) -- a new entity: clinical presentation with Dandy-Walker malformation and myopathy
V Peters, J M Penzien, G Reiter, et al.
Pediatric Research
|
June 29, 2007
Long-term outcome in methylmalonic acidurias is influenced by the underlying defect (mut0, mut-, cblA, cblB)
Friederike Hörster, Matthias R Baumgartner, Caroline Viardot, et al.
Medical Education
|
June 5, 2009
Design principles for virtual patients: a focus group study among students
Sören Huwendiek, Friedrich Reichert, Hans-Martin Bosse, et al.
Journal of Clinical Immunology
|
September 1, 2005
No indication for a defect in toll-like receptor signaling in patients with hyper-IgE syndrome
E D Renner, I Pawlita, F Hoffmann, 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.
The Journal of Pediatrics
|
February 7, 2001
Tyrosine hydroxylase deficiency with severe clinical course: clinical and biochemical investigations and optimization of therapy
C Dionisi-Vici, G F Hoffmann, V Leuzzi, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
L-2-hydroxyglutaric acidaemia: clinical and biochemical findings in 12 patients and preliminary report on L-2-hydroxyacid dehydrogenase
P G Barth, G F Hoffmann, J Jaeken, 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.
Page
of 126
Search research articles
Search
Showing results (881-890 of 1,255) with videos related to
Sort By:
Page
of 126
Molecular Genetics and Metabolism
|
August 10, 2007
Are heterocygotes for classical homocystinuria at risk of vitamin B12 and folic acid deficiency?
Mahmoud F Elsaid, Abdulbari Bener, Martin Lindner, et al.
Plos Neglected Tropical Diseases
|
April 18, 2012
The Schistosoma mansoni tegumental-allergen-like (TAL) protein family: influence of developmental expression on human IgE responses
Colin M Fitzsimmons, Frances M Jones, Alex Stearn, et al.
Neuropediatrics
|
April 4, 2002
Congenital disorder of glycosylation IId (CDG-IId) -- a new entity: clinical presentation with Dandy-Walker malformation and myopathy
V Peters, J M Penzien, G Reiter, et al.
Pediatric Research
|
June 29, 2007
Long-term outcome in methylmalonic acidurias is influenced by the underlying defect (mut0, mut-, cblA, cblB)
Friederike Hörster, Matthias R Baumgartner, Caroline Viardot, et al.
Medical Education
|
June 5, 2009
Design principles for virtual patients: a focus group study among students
Sören Huwendiek, Friedrich Reichert, Hans-Martin Bosse, et al.
Journal of Clinical Immunology
|
September 1, 2005
No indication for a defect in toll-like receptor signaling in patients with hyper-IgE syndrome
E D Renner, I Pawlita, F Hoffmann, 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.
The Journal of Pediatrics
|
February 7, 2001
Tyrosine hydroxylase deficiency with severe clinical course: clinical and biochemical investigations and optimization of therapy
C Dionisi-Vici, G F Hoffmann, V Leuzzi, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
L-2-hydroxyglutaric acidaemia: clinical and biochemical findings in 12 patients and preliminary report on L-2-hydroxyacid dehydrogenase
P G Barth, G F Hoffmann, J Jaeken, 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.
Page
of 126