Rouche A - Search Results

1

Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophy.

Roth F, Dhiab J, Boulinguiez A, Mouigni HR, Lassche S, Negroni E, Muraine L, Marhic A, Oliver A, Lainé J, Rouche A, O'Ferrall EK, van Engelen B, Ottenheijm C, Greif H, Blumen S, Lacau St Guily J, Perie S, Butler-Browne G, Mouly V, Trollet C. Roth F, et al. Among authors: rouche a. Acta Neuropathol. 2022 Dec;144(6):1157-1170. doi: 10.1007/s00401-022-02503-7. Epub 2022 Oct 5. Acta Neuropathol. 2022. PMID: 36197469 Free PMC article.

2

Intranuclear inclusions in oculopharyngeal muscular dystrophy among Bukhara Jews.

Blumen SC, Sadeh M, Korczyn AD, Rouche A, Nisipeanu P, Asherov A, Tomé FM. Blumen SC, et al. Among authors: rouche a. Neurology. 1996 May;46(5):1324-8. doi: 10.1212/wnl.46.5.1324. Neurology. 1996. PMID: 8628475

3

Age-related morphological changes of the deltoid muscle from 50 to 79 years of age.

Fayet G, Rouche A, Hogrel JY, Tomé FM, Fardeau M. Fayet G, et al. Among authors: rouche a. Acta Neuropathol. 2001 Apr;101(4):358-66. doi: 10.1007/s004010000294. Acta Neuropathol. 2001. PMID: 11355307

4

[About a phase I gene therapy clinical trial with a full-length dystrophin gene-plasmid in Duchenne/Becker muscular dystrophy].

Fardeau M, Braun S, Romero NB, Hogrel JY, Rouche A, Ortega V, Mourot B, Squiban P, Benveniste O, Herson S. Fardeau M, et al. Among authors: rouche a. J Soc Biol. 2005;199(1):29-32. doi: 10.1051/jbio:2005004. J Soc Biol. 2005. PMID: 16114261 Clinical Trial. French.

5

Changes in surface morphology and basal lamina of cultured muscle cells from Duchenne muscular dystrophy patients.

Delaporte C, Dautreaux B, Rouche A, Fardeau M. Delaporte C, et al. Among authors: rouche a. J Neurol Sci. 1990 Jan;95(1):77-88. doi: 10.1016/0022-510x(90)90118-7. J Neurol Sci. 1990. PMID: 2338566

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: rouche a. Neuromuscul Disord. 1995 Sep;5(5):399-413. doi: 10.1016/0960-8966(94)00080-s. Neuromuscul Disord. 1995. PMID: 7496174

7

[Progressive external ophthalmoplegia of mitochondrial origin: contribution of morphological and molecular studies].

Laforêt P, Eymard B, Danan C, Chevallay M, Rouche A, Frachon P, Fardeau M, Lombès A. Laforêt P, et al. Among authors: rouche a. Rev Neurol (Paris). 1997 Feb;153(1):51-8. Rev Neurol (Paris). 1997. PMID: 9296156 French.

8

["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data].

Laforêt P, Ziegler F, Sternberg D, Rouche A, Frachon P, Fardeau M, Eymard B, Lombès A. Laforêt P, et al. Among authors: rouche a. Rev Neurol (Paris). 2000 Dec;156(12):1136-47. Rev Neurol (Paris). 2000. PMID: 11139730 French.

9

Clinical and histologic findings in autosomal centronuclear myopathy.

Jeannet PY, Bassez G, Eymard B, Laforêt P, Urtizberea JA, Rouche A, Guicheney P, Fardeau M, Romero NB. Jeannet PY, et al. Among authors: rouche a. Neurology. 2004 May 11;62(9):1484-90. doi: 10.1212/01.wnl.0000124388.67003.56. Neurology. 2004. PMID: 15136669 Review.

10

[About the technique of muscle biopsy (III). The contribution of elctron microscopy, yesterday, and at the time of the molecular genetics era. A historical overview].

Fardeau M, Rouche A, Vassilopoulos S, Romero NB; l’équipe de microscopie électronique de l’Unité Morphologie Neuromusculaire de la Division Risler (G. Brochier, M.T. Bui, C. Labasse, A. Madelaine). Fardeau M, et al. Among authors: rouche a. Med Sci (Paris). 2016 Nov;32 Hors série n°2:6-9. doi: 10.1051/medsci/201632s202. Epub 2016 Nov 21. Med Sci (Paris). 2016. PMID: 27869068 Free article. French. No abstract available.

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