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B Mousson

Showing results (41-50 of 48) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1985
Combined deficiency of xanthine oxidase and sulphite oxidase: diagnosis of a new case followed by an antenatal diagnosisP Desjacques, B Mousson, C Vianey-Liaud, et al.
Pediatrie|January 1, 1993
[Value of skin fibroblasts in culture for the diagnosis of mitochondrial cell dysfunction. Apropos of 5 cases with cytochrome c oxidase deficiency]J M Collombet, M T Zabot, M Vidailhet, et al.
Mitochondrion|May 15, 2009
Development and implementation of standardized respiratory chain spectrophotometric assays for clinical diagnosisF Medja, S Allouche, P Frachon, et al.
Annales De Biologie Clinique|January 1, 1990
[Evaluation of a technique for determining blood ethanol levels by gas chromatography. Committee for "determination of blood ethanol levels"]J M Warnet, C Boudène, J L Cluet, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 2000
Human NDUFS3 gene coding for the 30-kDa subunit of mitochondrial complex I: genomic organization and expressionV Procaccio, P Lescuyer, I Bourges, et al.
Biochimica Et Biophysica Acta|October 24, 2002
Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafnessD Perucca-Lostanlen, R W Taylor, H Narbonne, et al.
The Journal of Clinical Investigation|July 7, 1999
Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblastsV Procaccio, B Mousson, R Beugnot, et al.
Journal of the Neurological Sciences|August 20, 2016
The wide POLG-related spectrum: An integrated viewM Béreau, M Anheim, A Echaniz-Laguna, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Journal of Inherited Metabolic Disease|January 1, 1985
Combined deficiency of xanthine oxidase and sulphite oxidase: diagnosis of a new case followed by an antenatal diagnosisP Desjacques, B Mousson, C Vianey-Liaud, et al.
Pediatrie|January 1, 1993
[Value of skin fibroblasts in culture for the diagnosis of mitochondrial cell dysfunction. Apropos of 5 cases with cytochrome c oxidase deficiency]J M Collombet, M T Zabot, M Vidailhet, et al.
Mitochondrion|May 15, 2009
Development and implementation of standardized respiratory chain spectrophotometric assays for clinical diagnosisF Medja, S Allouche, P Frachon, et al.
Annales De Biologie Clinique|January 1, 1990
[Evaluation of a technique for determining blood ethanol levels by gas chromatography. Committee for "determination of blood ethanol levels"]J M Warnet, C Boudène, J L Cluet, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 2000
Human NDUFS3 gene coding for the 30-kDa subunit of mitochondrial complex I: genomic organization and expressionV Procaccio, P Lescuyer, I Bourges, et al.
Biochimica Et Biophysica Acta|October 24, 2002
Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafnessD Perucca-Lostanlen, R W Taylor, H Narbonne, et al.
The Journal of Clinical Investigation|July 7, 1999
Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblastsV Procaccio, B Mousson, R Beugnot, et al.
Journal of the Neurological Sciences|August 20, 2016
The wide POLG-related spectrum: An integrated viewM Béreau, M Anheim, A Echaniz-Laguna, et al.
Pageof 5