Eymard B - Search Results

1

Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy.

van der Kooi AJ, Bonne G, Eymard B, Duboc D, Talim B, Van der Valk M, Reiss P, Richard P, Demay L, Merlini L, Schwartz K, Busch HF, de Visser M. van der Kooi AJ, et al. Among authors: eymard b. Neurology. 2002 Aug 27;59(4):620-3. doi: 10.1212/wnl.59.4.620. Neurology. 2002. PMID: 12196663

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

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

4

[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.

5

Blunted coronary reserve in myotonic dystrophy. An early and gene-related phenomenon.

Annane D, Merlet P, Radvanyi H, Mazoyer B, Eymard B, Fiorelli M, Junien C, Fardeau M, Ounnoughene Z, Gajdos P, Syrota A, Duboc D. Annane D, et al. Among authors: eymard b. Circulation. 1996 Sep 1;94(5):973-7. doi: 10.1161/01.cir.94.5.973. Circulation. 1996. PMID: 8790034

6

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. Neurology. 1997 May;48(5):1227-34. doi: 10.1212/wnl.48.5.1227. Neurology. 1997. PMID: 9153448

7

Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophy.

Laforêt P, de Toma C, Eymard B, Becane HM, Jeanpierre M, Fardeau M, Duboc D. Laforêt P, et al. Among authors: eymard b. Neurology. 1998 Nov;51(5):1454-6. doi: 10.1212/wnl.51.5.1454. Neurology. 1998. PMID: 9818880

8

Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophy.

Lazarus A, Varin J, Ounnoughene Z, Radvanyi H, Junien C, Coste J, Laforet P, Eymard B, Becane HM, Weber S, Duboc D. Lazarus A, et al. Among authors: eymard b. Circulation. 1999 Mar 2;99(8):1041-6. doi: 10.1161/01.cir.99.8.1041. Circulation. 1999. PMID: 10051298

9

Calpainopathy-a survey of mutations and polymorphisms.

Richard I, Roudaut C, Saenz A, Pogue R, Grimbergen JE, Anderson LV, Beley C, Cobo AM, de Diego C, Eymard B, Gallano P, Ginjaar HB, Lasa A, Pollitt C, Topaloglu H, Urtizberea JA, de Visser M, van der Kooi A, Bushby K, Bakker E, Lopez de Munain A, Fardeau M, Beckmann JS. Richard I, et al. Among authors: eymard b. Am J Hum Genet. 1999 Jun;64(6):1524-40. doi: 10.1086/302426. Am J Hum Genet. 1999. PMID: 10330340 Free PMC article.

10

A diagnostic fluorescent marker kit for six limb girdle muscular dystrophies.

Richard I, Bourg N, Marchand S, Alibert O, Eymard B, van der Kooi AJ, Jackson CE, Garcia C, Burgunder JM, Legum C, de Visser M, Fardeau M, Beckmann JS. Richard I, et al. Among authors: eymard b. Neuromuscul Disord. 1999 Dec;9(8):555-63. doi: 10.1016/s0960-8966(99)00037-1. Neuromuscul Disord. 1999. PMID: 10619713

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