Laforêt P - Search Results

1

[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. Rev Neurol (Paris). 1997 Feb;153(1):51-8. Rev Neurol (Paris). 1997. PMID: 9296156 French.

2

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

3

[Exercise intolerance caused by muscular phosphorylase kinase deficiency. Contribution of in vivo metabolic studies].

Laforêt P, Eymard B, Lombès A, Duboc D, Jehenson P, Rocchiccioli F, Chaussain M, Chateau D, Brunet P, Fardeau M. Laforêt P, et al. Rev Neurol (Paris). 1996 Jun-Jul;152(6-7):458-64. Rev Neurol (Paris). 1996. PMID: 8944243 Review. French.

4

Exhaustive scanning approach to screen all the mitochondrial tRNA genes for mutations and its application to the investigation of 35 independent patients with mitochondrial disorders.

Sternberg D, Danan C, Lombès A, Laforêt P, Girodon E, Goossens M, Amselem S. Sternberg D, et al. Among authors: laforet p. Hum Mol Genet. 1998 Jan;7(1):33-42. doi: 10.1093/hmg/7.1.33. Hum Mol Genet. 1998. PMID: 9384601

5

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. Neurology. 1998 Nov;51(5):1454-6. doi: 10.1212/wnl.51.5.1454. Neurology. 1998. PMID: 9818880

6

[Miyoshi distal myopathy: specific signs and incidence].

Eymard B, Laforêt P, Tomé FM, Collin H, Leroy JP, Hauw JJ, Richard I, Beckmann J, Fardeau M. Eymard B, et al. Among authors: laforet p. Rev Neurol (Paris). 2000 Feb;156(2):161-8. Rev Neurol (Paris). 2000. PMID: 10743015 French.

7

Juvenile and adult-onset acid maltase deficiency in France: genotype-phenotype correlation.

Laforêt P, Nicolino M, Eymard PB, Puech JP, Caillaud C, Poenaru L, Fardeau M. Laforêt P, et al. Neurology. 2000 Oct 24;55(8):1122-8. doi: 10.1212/wnl.55.8.1122. Neurology. 2000. PMID: 11071489

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. Rev Neurol (Paris). 2000 Dec;156(12):1136-47. Rev Neurol (Paris). 2000. PMID: 11139730 French.

9

Atypical MELAS syndrome associated with a new mitochondrial tRNA glutamine point mutation.

Bataillard M, Chatzoglou E, Rumbach L, Sternberg D, Tournade A, Laforêt P, Jardel C, Maisonobe T, Lombès A. Bataillard M, et al. Among authors: laforet p. Neurology. 2001 Feb 13;56(3):405-7. doi: 10.1212/wnl.56.3.405. Neurology. 2001. PMID: 11171912

10

[Proximal myotonial myopathy (PROMM): clinical and histology study].

Bassez G, Attarian S, Laforêt P, Azulay JP, Rouche A, Ferrer X, Urtizberea JA, Pellissier JF, Duboc D, Fardeau M, Pouget J, Eymard B. Bassez G, et al. Among authors: laforet p. Rev Neurol (Paris). 2001 Feb;157(2):209-18. Rev Neurol (Paris). 2001. PMID: 11283467 French.

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