Sacconi S - Search Results

1

Dehydroepiandrosterone for myotonic dystrophy type 1.

Pénisson-Besnier I, Devillers M, Porcher R, Orlikowski D, Doppler V, Desnuelle C, Ferrer X, Bes MC, Bouhour F, Tranchant C, Lagrange E, Vershueren A, Uzenot D, Cintas P, Solé G, Hogrel JY, Laforêt P, Vial C, Vila AL, Sacconi S, Pouget J, Eymard B, Chevret S, Annane D. Pénisson-Besnier I, et al. Among authors: sacconi s. Neurology. 2008 Aug 5;71(6):407-12. doi: 10.1212/01.wnl.0000324257.35759.40. Neurology. 2008. PMID: 18678823 Clinical Trial.

2

Normal growth and regenerating ability of myoblasts from unaffected muscles of facioscapulohumeral muscular dystrophy patients.

Vilquin JT, Marolleau JP, Sacconi S, Garcin I, Lacassagne MN, Robert I, Ternaux B, Bouazza B, Larghero J, Desnuelle C. Vilquin JT, et al. Among authors: sacconi s. Gene Ther. 2005 Nov;12(22):1651-62. doi: 10.1038/sj.gt.3302565. Gene Ther. 2005. PMID: 15973444

3

[The possible place of autologus cell therapy in facioscapulohumeral muscular dystrophy].

Desnuelle C, Sacconi S, Marolleau JP, Larghero J, Vilquin JT. Desnuelle C, et al. Among authors: sacconi s. Bull Acad Natl Med. 2005 Apr;189(4):697-713; discussion 713-4. Bull Acad Natl Med. 2005. PMID: 16245686 French.

4

Diagnostic challenges in facioscapulohumeral muscular dystrophy.

Sacconi S, Salviati L, Bourget I, Figarella D, Péréon Y, Lemmers R, van der Maarel S, Desnuelle C. Sacconi S, et al. Neurology. 2006 Oct 24;67(8):1464-6. doi: 10.1212/01.wnl.0000240071.62540.6f. Neurology. 2006. PMID: 17060574

5

Alteration of expression of muscle specific isoforms of the fragile X related protein 1 (FXR1P) in facioscapulohumeral muscular dystrophy patients.

Davidovic L, Sacconi S, Bechara EG, Delplace S, Allegra M, Desnuelle C, Bardoni B. Davidovic L, et al. Among authors: sacconi s. J Med Genet. 2008 Oct;45(10):679-85. doi: 10.1136/jmg.2008.060541. Epub 2008 Jul 15. J Med Genet. 2008. PMID: 18628314

6

[McArdle disease (gycogenosis type V): analysis of clinical, biological and genetic features of five French patients].

Delmont E, Sacconi S, Berge-Lefranc JL, Aquaron R, Butori C, Desnuelle C. Delmont E, et al. Among authors: sacconi s. Rev Neurol (Paris). 2008 Nov;164(11):912-6. doi: 10.1016/j.neurol.2008.03.020. Epub 2008 Jun 3. Rev Neurol (Paris). 2008. PMID: 18808785 French.

7

[Anti-MAG paraproteinemic demyelinating polyneuropathy: a clinical, biological, electrophysiological and anatomopathological descriptive study of a 13-patients' cohort].

Launay M, Delmont E, Benaim C, Sacconi S, Butori C, Desnuelle C. Launay M, et al. Among authors: sacconi s. Rev Neurol (Paris). 2009 Dec;165(12):1071-9. doi: 10.1016/j.neurol.2009.04.008. Rev Neurol (Paris). 2009. PMID: 19487003 French.

8

[Validity of the motor function measurement scale when routinely used in the follow-up of adult outpatients in a neuromuscular center].

Benaïm C, Sacconi S, Fournier-Mehouas M, Tanant V, Desnuelle C. Benaïm C, et al. Among authors: sacconi s. Rev Neurol (Paris). 2010 Jan;166(1):49-53. doi: 10.1016/j.neurol.2009.05.005. Epub 2009 Jun 12. Rev Neurol (Paris). 2010. PMID: 19524275 Clinical Trial. French.

9

Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubes.

Sacconi S, Simkin D, Arrighi N, Chapon F, Larroque MM, Vicart S, Sternberg D, Fontaine B, Barhanin J, Desnuelle C, Bendahhou S. Sacconi S, et al. Am J Physiol Cell Physiol. 2009 Oct;297(4):C876-85. doi: 10.1152/ajpcell.00519.2008. Epub 2009 Jul 1. Am J Physiol Cell Physiol. 2009. PMID: 19570891 Free article.

10

Do patients having a decrease in SNAP amplitude during the course of MMN present with a different condition?

Delmont E, Benaïm C, Launay M, Sacconi S, Soriani MH, Desnuelle C. Delmont E, et al. Among authors: sacconi s. J Neurol. 2009 Nov;256(11):1876-80. doi: 10.1007/s00415-009-5217-0. Epub 2009 Jul 30. J Neurol. 2009. PMID: 19641982

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