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Expression of human cytochrome c oxidase subunits during fetal development.
Bonne G, Seibel P, Possekel S, Marsac C, Kadenbach B. Bonne G, et al. Eur J Biochem. 1993 Nov 1;217(3):1099-107. doi: 10.1111/j.1432-1033.1993.tb18342.x. Eur J Biochem. 1993. PMID: 8223633
E1 pyruvate dehydrogenase deficiency in a child with motor neuropathy.
Bonne G, Benelli C, De Meirleir L, Lissens W, Chaussain M, Diry M, Clot JP, Ponsot G, Geoffroy V, Leroux JP, et al. Bonne G, et al. Pediatr Res. 1993 Mar;33(3):284-8. doi: 10.1203/00006450-199303000-00016. Pediatr Res. 1993. PMID: 8460066
Expression of cytochrome c oxidase subunits encoded by mitochondrial or nuclear DNA in the muscle of patients with zidovudine myopathy.
Chariot P, Bonne G, Authier FJ, Marsac C, Gherardi R. Chariot P, et al. Among authors: bonne g. J Neurol Sci. 1994 Sep;125(2):190-3. doi: 10.1016/0022-510x(94)90034-5. J Neurol Sci. 1994. PMID: 7807166
Familial hypertrophic cardiomyopathy. Cardiac ultrasonic abnormalities in genetically affected subjects without echocardiographic evidence of left ventricular hypertrophy.
Hagège AA, Dubourg O, Desnos M, Mirochnik R, Isnard G, Bonne G, Carrier L, Guicheney P, Bouhour JB, Schwartz K, Komajda M. Hagège AA, et al. Among authors: bonne g. Eur Heart J. 1998 Mar;19(3):490-9. doi: 10.1053/euhj.1997.0735. Eur Heart J. 1998. PMID: 9568454
Defect in the lipoyl-bearing protein X subunit of the pyruvate dehydrogenase complex in two patients with encephalomyelopathy.
Marsac C, Stansbie D, Bonne G, Cousin J, Jehenson P, Benelli C, Leroux JP, Lindsay G. Marsac C, et al. Among authors: bonne g. J Pediatr. 1993 Dec;123(6):915-20. doi: 10.1016/s0022-3476(05)80387-7. J Pediatr. 1993. PMID: 8229524
Detection of TRIM32 deletions in LGMD patients analyzed by a combined strategy of CGH array and massively parallel sequencing.
Nectoux J, de Cid R, Baulande S, Leturcq F, Urtizberea JA, Penisson-Besnier I, Nadaj-Pakleza A, Roudaut C, Criqui A, Orhant L, Peyroulan D, Ben Yaou R, Nelson I, Cobo AM, Arné-Bes MC, Uro-Coste E, Nitschke P, Claustres M, Bonne G, Lévy N, Chelly J, Richard I, Cossée M. Nectoux J, et al. Among authors: bonne g. Eur J Hum Genet. 2015 Jul;23(7):929-34. doi: 10.1038/ejhg.2014.223. Epub 2014 Oct 29. Eur J Hum Genet. 2015. PMID: 25351777 Free PMC article.
Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy.
Carrier L, Bonne G, Bährend E, Yu B, Richard P, Niel F, Hainque B, Cruaud C, Gary F, Labeit S, Bouhour JB, Dubourg O, Desnos M, Hagège AA, Trent RJ, Komajda M, Fiszman M, Schwartz K. Carrier L, et al. Among authors: bonne g. Circ Res. 1997 Mar;80(3):427-34. Circ Res. 1997. PMID: 9048664
Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy.
Forissier JF, Carrier L, Farza H, Bonne G, Bercovici J, Richard P, Hainque B, Townsend PJ, Yacoub MH, Fauré S, Dubourg O, Millaire A, Hagège AA, Desnos M, Komajda M, Schwartz K. Forissier JF, et al. Among authors: bonne g. Circulation. 1996 Dec 15;94(12):3069-73. doi: 10.1161/01.cir.94.12.3069. Circulation. 1996. PMID: 8989109
Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped children.
Charron P, Dubourg O, Desnos M, Bouhour JB, Isnard R, Hagege A, Carrier L, Bonne G, Tesson F, Richard P, Hainque B, Schwartz K, Komajda M. Charron P, et al. Among authors: bonne g. Eur Heart J. 1998 Sep;19(9):1377-82. doi: 10.1053/euhj.1998.1049. Eur Heart J. 1998. PMID: 9792264 Clinical Trial.
Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation.
Ben Yaou R, Navarro C, Quijano-Roy S, Bertrand AT, Massart C, De Sandre-Giovannoli A, Cadiñanos J, Mamchaoui K, Butler-Browne G, Estournet B, Richard P, Barois A, Lévy N, Bonne G. Ben Yaou R, et al. Among authors: bonne g. Eur J Hum Genet. 2011 Jun;19(6):647-54. doi: 10.1038/ejhg.2010.256. Epub 2011 Jan 26. Eur J Hum Genet. 2011. PMID: 21267004 Free PMC article.
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