N B Romero - JoVE Visualize

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Genomics|April 2, 1998

Expression of genes (CAPN3, SGCA, SGCB, and TTN) involved in progressive muscular dystrophies during early human developmentF Fougerousse, M Durand, L Suel, et al.

Digestive Diseases and Sciences|March 1, 1992

Chronic intestinal pseudoobstruction with myopathy and ophthalmoplegia. A muscular biochemical study of a mitochondrial disorderV Li, J Hostein, N B Romero, et al.

Journal of Inherited Metabolic Disease|January 1, 1996

Clinical and molecular heterogeneity of cytochrome c oxidase deficiency in the newbornA Lombes, N B Romero, G Touati, et al.

Neurology|February 21, 2012

Adult cases of mitochondrial DNA depletion due to TK2 defect: an expanding spectrumA Béhin, C Jardel, K G Claeys, et al.

Neurology|May 12, 2004

Clinical and histologic findings in autosomal centronuclear myopathyP-Y Jeannet, G Bassez, B Eymard, et al.

Revue Neurologique|March 6, 2003

[Exploration of exercise intolerance by 31P NMR spectroscopy of calf muscles coupled with MRI and ergometry]P Laforêt, C Wary, S Duteil, et al.

Neuromuscular Disorders : NMD|February 3, 1998

A point mutation in the glycerol kinase gene associated with a deletion in the dystrophin gene in a familial X-linked muscular dystrophy: non-contiguous gene syndrome involving Becker muscular dystrophy and glycerol kinase lociN B Romero, D Récan, O Rigal, et al.

Journal of Inherited Metabolic Disease|January 1, 1996

Morphological studies of skeletal muscle in lactic acidosisN B Romero, A Lombès, G Touati, et al.

The Journal of Clinical Investigation|August 1, 1993

Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophinK Matsumura, F M Tomé, V Ionasescu, et al.

Neuromuscular Disorders : NMD|June 19, 2001

Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomatic carrier with 'de novo' duplication of dystrophin geneN B Romero, P De Lonlay, S Llense, et al.

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Showing results (11-20 of 37) with videos related to

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Pageof 4

Genomics|April 2, 1998

Expression of genes (CAPN3, SGCA, SGCB, and TTN) involved in progressive muscular dystrophies during early human developmentF Fougerousse, M Durand, L Suel, et al.

Digestive Diseases and Sciences|March 1, 1992

Chronic intestinal pseudoobstruction with myopathy and ophthalmoplegia. A muscular biochemical study of a mitochondrial disorderV Li, J Hostein, N B Romero, et al.

Journal of Inherited Metabolic Disease|January 1, 1996

Clinical and molecular heterogeneity of cytochrome c oxidase deficiency in the newbornA Lombes, N B Romero, G Touati, et al.

Neurology|February 21, 2012

Adult cases of mitochondrial DNA depletion due to TK2 defect: an expanding spectrumA Béhin, C Jardel, K G Claeys, et al.

Neurology|May 12, 2004

Clinical and histologic findings in autosomal centronuclear myopathyP-Y Jeannet, G Bassez, B Eymard, et al.

Revue Neurologique|March 6, 2003

[Exploration of exercise intolerance by 31P NMR spectroscopy of calf muscles coupled with MRI and ergometry]P Laforêt, C Wary, S Duteil, et al.

Neuromuscular Disorders : NMD|February 3, 1998

A point mutation in the glycerol kinase gene associated with a deletion in the dystrophin gene in a familial X-linked muscular dystrophy: non-contiguous gene syndrome involving Becker muscular dystrophy and glycerol kinase lociN B Romero, D Récan, O Rigal, et al.

Journal of Inherited Metabolic Disease|January 1, 1996

Morphological studies of skeletal muscle in lactic acidosisN B Romero, A Lombès, G Touati, et al.

The Journal of Clinical Investigation|August 1, 1993

Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophinK Matsumura, F M Tomé, V Ionasescu, et al.

Neuromuscular Disorders : NMD|June 19, 2001

Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomatic carrier with 'de novo' duplication of dystrophin geneN B Romero, P De Lonlay, S Llense, et al.

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