Desnuelle C - Search Results

1

Hierarchization of myogenic and adipogenic progenitors within human skeletal muscle.

Pisani DF, Clement N, Loubat A, Plaisant M, Sacconi S, Kurzenne JY, Desnuelle C, Dani C, Dechesne CA. Pisani DF, et al. Among authors: desnuelle c. Stem Cells. 2010 Dec;28(12):2182-94. doi: 10.1002/stem.537. Stem Cells. 2010. PMID: 20936706

2

Isolation of a highly myogenic CD34-negative subset of human skeletal muscle cells free of adipogenic potential.

Pisani DF, Dechesne CA, Sacconi S, Delplace S, Belmonte N, Cochet O, Clement N, Wdziekonski B, Villageois AP, Butori C, Bagnis C, Di Santo JP, Kurzenne JY, Desnuelle C, Dani C. Pisani DF, et al. Among authors: desnuelle c. Stem Cells. 2010 Apr;28(4):753-64. doi: 10.1002/stem.317. Stem Cells. 2010. PMID: 20135684

3

Modeling Andersen's Syndrome in Human Induced Pluripotent Stem Cells.

Pini J, Rouleau M, Desnuelle C, Sacconi S, Bendahhou S. Pini J, et al. Among authors: desnuelle c. Stem Cells Dev. 2016 Jan 15;25(2):151-9. doi: 10.1089/scd.2015.0258. Epub 2015 Dec 30. Stem Cells Dev. 2016. PMID: 26573604

4

Facioscapulohumeral muscular dystrophy.

Sacconi S, Salviati L, Desnuelle C. Sacconi S, et al. Among authors: desnuelle c. Biochim Biophys Acta. 2015 Apr;1852(4):607-14. doi: 10.1016/j.bbadis.2014.05.021. Epub 2014 May 29. Biochim Biophys Acta. 2015. PMID: 24882751 Free article. Review.

5

[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. Bull Acad Natl Med. 2005 Apr;189(4):697-713; discussion 713-4. Bull Acad Natl Med. 2005. PMID: 16245686 French.

6

[Facioscapulohumeral muscular dystrophy type 2].

Sacconi S, Desnuelle C. Sacconi S, et al. Among authors: desnuelle c. Rev Neurol (Paris). 2013 Aug-Sep;169(8-9):564-72. doi: 10.1016/j.neurol.2013.02.004. Epub 2013 Aug 20. Rev Neurol (Paris). 2013. PMID: 23969240 French.

7

The inward rectifier potassium channel Kir2.1 is required for osteoblastogenesis.

Sacco S, Giuliano S, Sacconi S, Desnuelle C, Barhanin J, Amri EZ, Bendahhou S. Sacco S, et al. Among authors: desnuelle c. Hum Mol Genet. 2015 Jan 15;24(2):471-9. doi: 10.1093/hmg/ddu462. Epub 2014 Sep 8. Hum Mol Genet. 2015. PMID: 25205110

8

Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy.

Sacconi S, Trevisson E, Salviati L, Aymé S, Rigal O, Redondo AG, Mancuso M, Siciliano G, Tonin P, Angelini C, Auré K, Lombès A, Desnuelle C. Sacconi S, et al. Among authors: desnuelle c. Neuromuscul Disord. 2010 Jan;20(1):44-8. doi: 10.1016/j.nmd.2009.10.014. Epub 2009 Nov 27. Neuromuscul Disord. 2010. PMID: 19945282

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. Among authors: desnuelle c. 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

Neuromuscular electrical stimulation training: a safe and effective treatment for facioscapulohumeral muscular dystrophy patients.

Colson SS, Benchortane M, Tanant V, Faghan JP, Fournier-Mehouas M, Benaïm C, Desnuelle C, Sacconi S. Colson SS, et al. Among authors: desnuelle c. Arch Phys Med Rehabil. 2010 May;91(5):697-702. doi: 10.1016/j.apmr.2010.01.019. Arch Phys Med Rehabil. 2010. PMID: 20434605 Clinical Trial.

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