Laforet P - Search Results

1

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.

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

Macrophagic myofasciitis: an emerging entity. Groupe d'Etudes et Recherche sur les Maladies Musculaires Acquises et Dysimmunitaires (GERMMAD) de l'Association Française contre les Myopathies (AFM).

Gherardi RK, Coquet M, Chérin P, Authier FJ, Laforêt P, Bélec L, Figarella-Branger D, Mussini JM, Pellissier JF, Fardeau M. Gherardi RK, et al. Among authors: laforet p. Lancet. 1998 Aug 1;352(9125):347-52. doi: 10.1016/s0140-6736(98)02326-5. Lancet. 1998. PMID: 9717921

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

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

7

[Macrophagic myofasciitis: description and etiopathogenic hypotheses. Study and Research Group on Acquired and Dysimmunity-related Muscular Diseases (GERMMAD) of the French Association against Myopathies (AFM)].

Chérin P, Laforet P, Ghérardi RK, Authier FJ, Coquet M, Maisonobe T, Mussini JM, Pellissier JF, Herson S. Chérin P, et al. Among authors: laforet p. Rev Med Interne. 1999 Jun;20(6):483-9. doi: 10.1016/s0248-8663(99)80083-6. Rev Med Interne. 1999. PMID: 10422140 French.

8

[Macro-aspartate aminotransferase: a benign biological anomaly to consider].

Teixeira-Ribeiro A, Généreau T, Devanlay M, Laforêt P, Imbert-Bismut F, Herson S. Teixeira-Ribeiro A, et al. Among authors: laforet p. Ann Med Interne (Paris). 1999 Jun;150(4):359-60. Ann Med Interne (Paris). 1999. PMID: 10519024 French. No abstract available.

9

[Macrophagic myofasciitis. Study and Research Group on Acquired and Dysimmunity-related muscular diseases (GERMMAD)].

Chérin P, Laforêt P, Ghérardi RK, Authier FJ, Maisonobe T, Coquet M, Mussini JM, Pellissier JF, Eymard B, Herson S. Chérin P, et al. Among authors: laforet p. Presse Med. 2000 Feb 5;29(4):203-8. Presse Med. 2000. PMID: 10705901 Review. French.

10

[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.

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