Leturcq F - Search Results

1

Diagnosis and management of Becker muscular dystrophy: the French guidelines.

Magot A, Wahbi K, Leturcq F, Jaffre S, Péréon Y, Sole G; French BMD working group. Magot A, et al. Among authors: leturcq f. J Neurol. 2023 Oct;270(10):4763-4781. doi: 10.1007/s00415-023-11837-5. Epub 2023 Jul 9. J Neurol. 2023. PMID: 37422773 Free article. Review.

2

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy.

Roberds SL, Leturcq F, Allamand V, Piccolo F, Jeanpierre M, Anderson RD, Lim LE, Lee JC, Tomé FM, Romero NB, et al. Roberds SL, et al. Among authors: leturcq f. Cell. 1994 Aug 26;78(4):625-33. doi: 10.1016/0092-8674(94)90527-4. Cell. 1994. PMID: 8069911

3

[Molecular analysis and prenatal diagnosis of beta-thalassemia: about our experience in central Tunisia].

Laradi S, Haj Khelil A, Omri H, Chaieb A, Mahjoub T, Benlimam H, Amri F, Saad A, Miled A, Leturcq F, Ben Chibani J, Beldjord C. Laradi S, et al. Among authors: leturcq f. Ann Biol Clin (Paris). 2000 Jul-Aug;58(4):453-60. Ann Biol Clin (Paris). 2000. PMID: 10932046 Free article. French.

4

Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophy.

Matsumura K, Tomé FM, Collin H, Leturcq F, Jeanpierre M, Kaplan JC, Fardeau M, Campbell KP. Matsumura K, et al. Among authors: leturcq f. Neuromuscul Disord. 1994 Mar;4(2):115-20. doi: 10.1016/0960-8966(94)90002-7. Neuromuscul Disord. 1994. PMID: 7516752

5

[Phenotypic heterogeneity of Duchenne myopathy and prognosis criteria].

Desguerre I, Mayer M, Christov C, Leturcq F, Chelly J, Gherardi RK. Desguerre I, et al. Among authors: leturcq f. Arch Pediatr. 2009 Jun;16(6):681-3. doi: 10.1016/S0929-693X(09)74110-7. Arch Pediatr. 2009. PMID: 19541128 French. No abstract available.

6

Beta-sarcoglycanopathy (LGMD 2E) in a Spanish family.

Rivas E, Teijeira S, dos Santos MR, Porrit I, Leturcq F, Fernandez JM, Navarro C. Rivas E, et al. Among authors: leturcq f. Acta Myol. 2004 Dec;23(3):159-62. Acta Myol. 2004. PMID: 15938574

7

Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12.

Jung D, Leturcq F, Sunada Y, Duclos F, Tomé FM, Moomaw C, Merlini L, Azibi K, Chaouch M, Slaughter C, Fardeau M, Kaplan JC, Campbell KP. Jung D, et al. Among authors: leturcq f. FEBS Lett. 1996 Feb 26;381(1-2):15-20. doi: 10.1016/0014-5793(96)00056-7. FEBS Lett. 1996. PMID: 8641426 Free article.

8

Neurosensory hearing loss in secondary adhalinopathy.

Oexle K, Herrmann R, Dodé C, Leturcq F, Hübner C, Kaplan JC, Mizuno Y, Ozawa E, Campbell KP, Voit T. Oexle K, et al. Among authors: leturcq f. Neuropediatrics. 1996 Feb;27(1):32-6. doi: 10.1055/s-2007-973744. Neuropediatrics. 1996. PMID: 8677023

9

Are cysteine-rich and COOH-terminal domains of dystrophin critical for sarcolemmal localization?

Récan D, Chafey P, Leturcq F, Hugnot JP, Vincent N, Tomé F, Collin H, Simon D, Czernichow P, Nicholson LV, et al. Récan D, et al. Among authors: leturcq f. J Clin Invest. 1992 Feb;89(2):712-6. doi: 10.1172/JCI115640. J Clin Invest. 1992. PMID: 1737859 Free PMC article.

10

Eosinophilic infiltration related to CAPN3 mutations: a pathophysiological component of primary calpainopathy?

Krahn M, Goicoechea M, Hanisch F, Groen E, Bartoli M, Pécheux C, Garcia-Bragado F, Leturcq F, Jeannet PY, Lobrinus JA, Jacquemont S, Strober J, Urtizberea JA, Saenz A, Bushby K, Lévy N, Lopez de Munain A. Krahn M, et al. Among authors: leturcq f. Clin Genet. 2011 Oct;80(4):398-402. doi: 10.1111/j.1399-0004.2010.01620.x. Clin Genet. 2011. PMID: 21204801 No abstract available.

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