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Showing results (1361-1370 of 1,983) with videos related to
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Human Mutation
|
January 12, 2008
Sedoheptulokinase deficiency due to a 57-kb deletion in cystinosis patients causes urinary accumulation of sedoheptulose: elucidation of the CARKL gene
Mirjam M C Wamelink, Eduard A Struys, Erwin E W Jansen, et al.
Journal of Inherited Metabolic Disease
|
April 8, 2006
X-linked creatine transporter defect: a report on two unrelated boys with a severe clinical phenotype
I A Anselm, I M Anselm, F S Alkuraya, et al.
International Journal of Molecular Sciences
|
April 13, 2024
Characterization of Biomarkers of Thrombo-Inflammation in Patients with First-Diagnosed Atrial Fibrillation
Julian Friebel, Max Wegner, Leon Blöbaum, et al.
Antioxidants & Redox Signaling
|
February 26, 2011
The pentose phosphate pathway is a metabolic redox sensor and regulates transcription during the antioxidant response
Antje Krüger, Nana-Maria Grüning, Mirjam M C Wamelink, et al.
International Journal of Hygiene and Environmental Health
|
June 20, 2016
Association of long-term exposure to local industry- and traffic-specific particulate matter with arterial blood pressure and incident hypertension
Kateryna B Fuks, Gudrun Weinmayr, Frauke Hennig, et al.
Annals of Neurology
|
January 13, 2000
Atypical refsum disease with pipecolic acidemia and abnormal catalase distribution
M R Baumgartner, G A Jansen, N M Verhoeven, et al.
Skeletal Radiology
|
January 31, 2012
CT fluoroscopy-guided percutaneous vertebroplasty in spinal malignancy: technical results, PMMA leakages, and complications in 202 patients
Christoph G Trumm, Anne Pahl, Thomas K Helmberger, et al.
Developmental Medicine and Child Neurology
|
July 19, 2012
Long-term outcome in pyridoxine-dependent epilepsy
Levinus A Bok, Feico J Halbertsma, Saskia Houterman, et al.
Frontiers in Immunology
|
January 8, 2025
PGM3 insufficiency: a glycosylation disorder causing a notable T cell defect
Linlin Yang, Barbara Zerbato, Alex Pessina, et al.
Neurology
|
August 18, 2006
Treatment with interferon beta-1b delays conversion to clinically definite and McDonald MS in patients with clinically isolated syndromes
L Kappos, C H Polman, M S Freedman, et al.
Page
of 199
Search research articles
Search
Showing results (1361-1370 of 1,983) with videos related to
Sort By:
Page
of 199
Human Mutation
|
January 12, 2008
Sedoheptulokinase deficiency due to a 57-kb deletion in cystinosis patients causes urinary accumulation of sedoheptulose: elucidation of the CARKL gene
Mirjam M C Wamelink, Eduard A Struys, Erwin E W Jansen, et al.
Journal of Inherited Metabolic Disease
|
April 8, 2006
X-linked creatine transporter defect: a report on two unrelated boys with a severe clinical phenotype
I A Anselm, I M Anselm, F S Alkuraya, et al.
International Journal of Molecular Sciences
|
April 13, 2024
Characterization of Biomarkers of Thrombo-Inflammation in Patients with First-Diagnosed Atrial Fibrillation
Julian Friebel, Max Wegner, Leon Blöbaum, et al.
Antioxidants & Redox Signaling
|
February 26, 2011
The pentose phosphate pathway is a metabolic redox sensor and regulates transcription during the antioxidant response
Antje Krüger, Nana-Maria Grüning, Mirjam M C Wamelink, et al.
International Journal of Hygiene and Environmental Health
|
June 20, 2016
Association of long-term exposure to local industry- and traffic-specific particulate matter with arterial blood pressure and incident hypertension
Kateryna B Fuks, Gudrun Weinmayr, Frauke Hennig, et al.
Annals of Neurology
|
January 13, 2000
Atypical refsum disease with pipecolic acidemia and abnormal catalase distribution
M R Baumgartner, G A Jansen, N M Verhoeven, et al.
Skeletal Radiology
|
January 31, 2012
CT fluoroscopy-guided percutaneous vertebroplasty in spinal malignancy: technical results, PMMA leakages, and complications in 202 patients
Christoph G Trumm, Anne Pahl, Thomas K Helmberger, et al.
Developmental Medicine and Child Neurology
|
July 19, 2012
Long-term outcome in pyridoxine-dependent epilepsy
Levinus A Bok, Feico J Halbertsma, Saskia Houterman, et al.
Frontiers in Immunology
|
January 8, 2025
PGM3 insufficiency: a glycosylation disorder causing a notable T cell defect
Linlin Yang, Barbara Zerbato, Alex Pessina, et al.
Neurology
|
August 18, 2006
Treatment with interferon beta-1b delays conversion to clinically definite and McDonald MS in patients with clinically isolated syndromes
L Kappos, C H Polman, M S Freedman, et al.
Page
of 199