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Pediatric Radiology
|
February 13, 2010
Pericallosal lipoma and middle cerebral artery aneurysm: a coincidence?
Julie Sommet, Manuel Schiff, Philippe Evrard, et al.
Trends in Molecular Medicine
|
April 13, 2010
Genetic background influences mitochondrial function: modeling mitochondrial disease for therapeutic development
Paule Bénit, Riyad El-Khoury, Manuel Schiff, et al.
Journal of Inherited Metabolic Disease
|
September 28, 2017
Metabolic pathways at the crossroads of diabetes and inborn errors
Eric S Goetzman, Zhenwei Gong, Manuel Schiff, et al.
Molecular Genetics and Metabolism
|
March 3, 2006
Electron transfer flavoprotein deficiency: functional and molecular aspects
Manuel Schiff, Roseline Froissart, Rikke K J Olsen, et al.
Molecular Genetics and Metabolism
|
March 14, 2013
Molecular and cellular pathology of very-long-chain acyl-CoA dehydrogenase deficiency
Manuel Schiff, Al-Walid Mohsen, Anuradha Karunanidhi, et al.
The Journal of Pediatrics
|
August 30, 2005
Neonatal hyperammonemia: the N-carbamoyl-L-glutamic acid test
Nathalie Guffon, Manuel Schiff, David Cheillan, et al.
Nutrition Reviews
|
February 8, 2011
Mitochondrial response to controlled nutrition in health and disease
Manuel Schiff, Paule Bénit, Assetou Coulibaly, et al.
Molecular Genetics and Metabolism
|
February 21, 2021
Clinical outcomes in a series of 18 patients with long chain fatty acids oxidation disorders treated with triheptanoin for a median duration of 22 months
Nathalie Guffon, Fanny Mochel, Manuel Schiff, et al.
Journal of Inherited Metabolic Disease
|
June 3, 2026
Vitamin-Responsive Disorders: From Molecular Basis to Clinical Presentation and Therapy
Cécile Acquaviva, Yann Nadjar, Manuel Schiff, et al.
Plos One
|
December 17, 2011
Mouse studies to shape clinical trials for mitochondrial diseases: high fat diet in Harlequin mice
Manuel Schiff, Paule Bénit, Riyad El-Khoury, et al.
Page
of 16
Search research articles
Search
Showing results (11-20 of 159) with videos related to
Sort By:
Page
of 16
Pediatric Radiology
|
February 13, 2010
Pericallosal lipoma and middle cerebral artery aneurysm: a coincidence?
Julie Sommet, Manuel Schiff, Philippe Evrard, et al.
Trends in Molecular Medicine
|
April 13, 2010
Genetic background influences mitochondrial function: modeling mitochondrial disease for therapeutic development
Paule Bénit, Riyad El-Khoury, Manuel Schiff, et al.
Journal of Inherited Metabolic Disease
|
September 28, 2017
Metabolic pathways at the crossroads of diabetes and inborn errors
Eric S Goetzman, Zhenwei Gong, Manuel Schiff, et al.
Molecular Genetics and Metabolism
|
March 3, 2006
Electron transfer flavoprotein deficiency: functional and molecular aspects
Manuel Schiff, Roseline Froissart, Rikke K J Olsen, et al.
Molecular Genetics and Metabolism
|
March 14, 2013
Molecular and cellular pathology of very-long-chain acyl-CoA dehydrogenase deficiency
Manuel Schiff, Al-Walid Mohsen, Anuradha Karunanidhi, et al.
The Journal of Pediatrics
|
August 30, 2005
Neonatal hyperammonemia: the N-carbamoyl-L-glutamic acid test
Nathalie Guffon, Manuel Schiff, David Cheillan, et al.
Nutrition Reviews
|
February 8, 2011
Mitochondrial response to controlled nutrition in health and disease
Manuel Schiff, Paule Bénit, Assetou Coulibaly, et al.
Molecular Genetics and Metabolism
|
February 21, 2021
Clinical outcomes in a series of 18 patients with long chain fatty acids oxidation disorders treated with triheptanoin for a median duration of 22 months
Nathalie Guffon, Fanny Mochel, Manuel Schiff, et al.
Journal of Inherited Metabolic Disease
|
June 3, 2026
Vitamin-Responsive Disorders: From Molecular Basis to Clinical Presentation and Therapy
Cécile Acquaviva, Yann Nadjar, Manuel Schiff, et al.
Plos One
|
December 17, 2011
Mouse studies to shape clinical trials for mitochondrial diseases: high fat diet in Harlequin mice
Manuel Schiff, Paule Bénit, Riyad El-Khoury, et al.
Page
of 16