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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 loci.
Neuromuscul Disord. 1997 Dec;7(8):499-504. doi: 10.1016/s0960-8966(97)00114-4.
Neuromuscul Disord. 1997.
PMID: 9447607
Malignant hyperthermia and central core disease: analysis of two families with heterogeneous clinical expression.
Romero NB, Nivoche Y, Lunardi J, Bruneau B, Cheval MA, Hillaire D, Fardeau M.
Romero NB, et al. Among authors: cheval ma.
Neuromuscul Disord. 1993 Sep-Nov;3(5-6):547-51. doi: 10.1016/0960-8966(93)90113-x.
Neuromuscul Disord. 1993.
PMID: 8186709
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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. Among authors: cheval ma.
J Inherit Metab Dis. 1996;19(4):528-34. doi: 10.1007/BF01799113.
J Inherit Metab Dis. 1996.
PMID: 8884576
Review.
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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. Among authors: cheval ma.
Ann Neurol. 2001 May;49(5):607-17.
Ann Neurol. 2001.
PMID: 11357951
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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: cheval ma.
J Inherit Metab Dis. 1996;19(3):286-95. doi: 10.1007/BF01799256.
J Inherit Metab Dis. 1996.
PMID: 8803770
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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: cheval ma.
Histochem Cell Biol. 1995 Jan;103(1):59-68. doi: 10.1007/BF01464476.
Histochem Cell Biol. 1995.
PMID: 7736281
Clinical Trial.
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