Laforêt P - 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: laforet p. Neurology. 2008 Aug 5;71(6):407-12. doi: 10.1212/01.wnl.0000324257.35759.40. Neurology. 2008. PMID: 18678823 Clinical Trial.

2

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

3

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: laforet p. Circulation. 1999 Mar 2;99(8):1041-6. doi: 10.1161/01.cir.99.8.1041. Circulation. 1999. PMID: 10051298

4

Gallium-67 scintigraphy in macrophagic myofasciitis.

Chérin P, Authier FJ, Gherardi RK, Romero N, Laforêt P, Eymard B, Herson S, Caillat-Vigneron N. Chérin P, et al. Among authors: laforet p. Arthritis Rheum. 2000 Jul;43(7):1520-6. doi: 10.1002/1529-0131(200007)43:7<1520::AID-ANR16>3.0.CO;2-Q. Arthritis Rheum. 2000. PMID: 10902755 Free article.

5

["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.

6

[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.

7

Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders.

Sternberg D, Chatzoglou E, Laforêt P, Fayet G, Jardel C, Blondy P, Fardeau M, Amselem S, Eymard B, Lombès A. Sternberg D, et al. Among authors: laforet p. Brain. 2001 May;124(Pt 5):984-94. doi: 10.1093/brain/124.5.984. Brain. 2001. PMID: 11335700

8

A non-ischemic forearm exercise test for the screening of patients with exercise intolerance.

Hogrel JY, Laforêt P, Ben Yaou R, Chevrot M, Eymard B, Lombès A. Hogrel JY, et al. Among authors: laforet p. Neurology. 2001 Jun 26;56(12):1733-8. doi: 10.1212/wnl.56.12.1733. Neurology. 2001. PMID: 11425942

9

[Metabolic myopathies in adulthood. Features and clues for diagnosis].

Eymard B, Laforêt P. Eymard B, et al. Among authors: laforet p. Rev Med Interne. 2001 Dec;22 Suppl 3:328s-337s. Rev Med Interne. 2001. PMID: 11794877 Review. French.

10

Intravenous immunoglobulin for dysphagia of inclusion body myositis.

Cherin P, Pelletier S, Teixeira A, Laforet P, Simon A, Herson S, Eymard B. Cherin P, et al. Among authors: laforet p. Neurology. 2002 Jan 22;58(2):326. doi: 10.1212/wnl.58.2.326. Neurology. 2002. PMID: 11805271 No abstract available.

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