Romero NB - Search Results

1

Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.

Auré K, Fayet G, Leroy JP, Lacène E, Romero NB, Lombès A. Auré K, et al. Among authors: romero nb. Brain. 2006 May;129(Pt 5):1249-59. doi: 10.1093/brain/awl061. Epub 2006 Mar 14. Brain. 2006. PMID: 16537564

2

Analysis of the tissue distribution and inheritance of heteroplasmic mitochondrial DNA point mutation by denaturing gradient gel electrophoresis in MERRF syndrome.

Lombès A, Diaz C, Romero NB, Ziegler F, Fardeau M. Lombès A, et al. Among authors: romero nb. Neuromuscul Disord. 1992;2(5-6):323-30. doi: 10.1016/s0960-8966(06)80003-9. Neuromuscul Disord. 1992. PMID: 1300181

3

Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studies.

Degoul F, Nelson I, Lestienne P, Francois D, Romero N, Duboc D, Eymard B, Fardeau M, Ponsot G, Paturneau-Jouas M, et al. Degoul F, et al. J Neurol Sci. 1991 Feb;101(2):168-77. doi: 10.1016/0022-510x(91)90042-6. J Neurol Sci. 1991. PMID: 1851820

4

Immunohistochemical analysis of muscle cytochrome c oxidase deficiency in children.

Possekel S, Lombes A, Ogier de Baulny H, Cheval MA, Fardeau M, Kadenbach B, Romero NB. Possekel S, et al. Among authors: romero nb. Histochem Cell Biol. 1995 Jan;103(1):59-68. doi: 10.1007/BF01464476. Histochem Cell Biol. 1995. PMID: 7736281 Clinical Trial.

5

Clinical and molecular heterogeneity of cytochrome c oxidase deficiency in the newborn.

Lombes A, Romero NB, Touati G, Frachon P, Cheval MA, Giraud M, Simon D, Ogier de Baulny H. Lombes A, et al. Among authors: romero nb. J Inherit Metab Dis. 1996;19(3):286-95. doi: 10.1007/BF01799256. J Inherit Metab Dis. 1996. PMID: 8803770

6

Morphological studies of skeletal muscle in lactic acidosis.

Romero NB, Lombès A, Touati G, Rigal O, Frachon P, Cheval MA, Giraud M, Possekel S, Fardeau M, Ogier de Baulny H. Romero NB, et al. J Inherit Metab Dis. 1996;19(4):528-34. doi: 10.1007/BF01799113. J Inherit Metab Dis. 1996. PMID: 8884576 Review.

7

Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy.

Eymard B, Romero NB, Leturcq F, Piccolo F, Carrié A, Jeanpierre M, Collin H, Deburgrave N, Azibi K, Chaouch M, Merlini L, Thémar-Noël C, Penisson I, Mayer M, Tanguy O, Campbell KP, Kaplan JC, Tomé FM, Fardeau M. Eymard B, et al. Among authors: romero nb. Neurology. 1997 May;48(5):1227-34. doi: 10.1212/wnl.48.5.1227. Neurology. 1997. PMID: 9153448

8

Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation.

Barthélémy C, Ogier de Baulny H, Diaz J, Cheval MA, Frachon P, Romero N, Goutieres F, Fardeau M, Lombès A. Barthélémy C, et al. Ann Neurol. 2001 May;49(5):607-17. Ann Neurol. 2001. PMID: 11357951

9

[Exploration of exercise intolerance by 31P NMR spectroscopy of calf muscles coupled with MRI and ergometry].

Laforêt P, Wary C, Duteil S, de Kerviler E, Carlier PG, Lombès A, Romero NB, Fardeau M, Eymard B, Leroy-Willig A. Laforêt P, et al. Among authors: romero nb. Rev Neurol (Paris). 2003 Jan;159(1):56-67. Rev Neurol (Paris). 2003. PMID: 12618654 Clinical Trial. French.

10

Dominant and recessive central core disease associated with RYR1 mutations and fetal akinesia.

Romero NB, Monnier N, Viollet L, Cortey A, Chevallay M, Leroy JP, Lunardi J, Fardeau M. Romero NB, et al. Brain. 2003 Nov;126(Pt 11):2341-9. doi: 10.1093/brain/awg244. Epub 2003 Aug 22. Brain. 2003. PMID: 12937085

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