Eymard B - Search Results

1

Impaired cerebral glucose metabolism in myotonic dystrophy: a triplet-size dependent phenomenon.

Annane D, Fiorelli M, Mazoyer B, Pappata S, Eymard B, Radvanyi H, Junien C, Fardeau M, Merlet P, Gajdos P, Syrota A, Sansom Y, Duboc D. Annane D, et al. Among authors: eymard b. Neuromuscul Disord. 1998 Feb;8(1):39-45. doi: 10.1016/s0960-8966(97)00144-2. Neuromuscul Disord. 1998. PMID: 9565989

2

Decreased cerebral glucose utilization in myotonic dystrophy.

Fiorelli M, Duboc D, Mazoyer BM, Blin J, Eymard B, Fardeau M, Samson Y. Fiorelli M, et al. Among authors: eymard b. Neurology. 1992 Jan;42(1):91-4. doi: 10.1212/wnl.42.1.91. Neurology. 1992. PMID: 1734329

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. Among authors: eymard b. J Neurol Sci. 1991 Feb;101(2):168-77. doi: 10.1016/0022-510x(91)90042-6. J Neurol Sci. 1991. PMID: 1851820

4

Intracranial arachnoid cysts in myotonic dystrophy.

Fiorelli M, Duboc D, Pappatà S, Tran-Dinh S, Eymard B, Fardeau M. Fiorelli M, et al. Among authors: eymard b. Neuroradiology. 1991;33(3):258-9. doi: 10.1007/BF00588231. Neuroradiology. 1991. PMID: 1881547

5

Exercise-induced muscle modifications: study of healthy subjects and patients with metabolic myopathies with MR imaging and P-31 spectroscopy.

de Kerviler E, Leroy-Willig A, Jehenson P, Duboc D, Eymard B, Syrota A. de Kerviler E, et al. Among authors: eymard b. Radiology. 1991 Oct;181(1):259-64. doi: 10.1148/radiology.181.1.1887044. Radiology. 1991. PMID: 1887044

6

Chronic progressive external ophthalmoplegia with ragged-red fibers: clinical, morphological and genetic investigations in 43 patients.

Laforêt P, Lombès A, Eymard B, Danan C, Chevallay M, Rouche A, Frachon P, Fardeau M. Laforêt P, et al. Among authors: eymard b. Neuromuscul Disord. 1995 Sep;5(5):399-413. doi: 10.1016/0960-8966(94)00080-s. Neuromuscul Disord. 1995. PMID: 7496174

7

[Severe cardiomyopathy revealing amylopectinosis. Two cases in adolescents from the same family].

de La Blanchardière A, Vayssier C, Duboc D, Jacquemin IE, Eymard B, Fardeau M, Maire I, Dreyfus G, Guérin F. de La Blanchardière A, et al. Among authors: eymard b. Presse Med. 1994 Jun 25;23(24):1124-7. Presse Med. 1994. PMID: 7971833 Review. French.

8

Correlation between decreased myocardial glucose phosphorylation and the DNA mutation size in myotonic dystrophy.

Annane D, Duboc D, Mazoyer B, Merlet P, Fiorelli M, Eymard B, Radvanyi H, Junien C, Fardeau M, Gajdos P, et al. Annane D, et al. Among authors: eymard b. Circulation. 1994 Dec;90(6):2629-34. doi: 10.1161/01.cir.90.6.2629. Circulation. 1994. PMID: 7994802

9

[Cardiac involvement in certain muscular diseases. Apropos of 216 cases].

Monségu J, Duboc D, Freychet L, Eymard B, Fardeau M, Becane HM, Willig TN, Guérin F. Monségu J, et al. Among authors: eymard b. Arch Mal Coeur Vaiss. 1993 Oct;86(10):1421-6. Arch Mal Coeur Vaiss. 1993. PMID: 8010839 Review. French.

10

Late-onset rod myopathy associated with monoclonal gammopathy.

Eymard B, Brouet JC, Collin H, Chevallay M, Bussel A, Fardeau M. Eymard B, et al. Neuromuscul Disord. 1993 Sep-Nov;3(5-6):557-60. doi: 10.1016/0960-8966(93)90115-z. Neuromuscul Disord. 1993. PMID: 8186711

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