de Luna N - Search Results

1

[Anti-GQ1b antibodies: usefulness of its detection for the diagnosis of Miller-Fisher syndrome].

Rojas-García R, Gallardo E, Serrano-Munuera C, de Luna N, Ortiz E, Roig C, Grau-Veciana JM, Illa I. Rojas-García R, et al. Among authors: de luna n. Med Clin (Barc). 2001 Jun 2;116(20):761-4. doi: 10.1016/s0025-7753(01)71980-x. Med Clin (Barc). 2001. PMID: 11440679 Spanish.

2

Antiganglioside antibodies in acute self-limiting ataxic neuropathy: incidence and significance.

Serrano-Munuera C, Gallardo E, Rojas R, De Luna N, González-Masegosa A, Martí-Massó JF, Martínez-Matos A, Ortíz N, Reñé R, Berciano J, Grau JM, Willison HJ, Graus F, Illa I. Serrano-Munuera C, et al. Among authors: de luna n. J Neuroimmunol. 2001 Nov 1;120(1-2):78-83. doi: 10.1016/s0165-5728(01)00428-3. J Neuroimmunol. 2001. PMID: 11694322

3

Inflammation in dysferlin myopathy: immunohistochemical characterization of 13 patients.

Gallardo E, Rojas-García R, de Luna N, Pou A, Brown RH Jr, Illa I. Gallardo E, et al. Among authors: de luna n. Neurology. 2001 Dec 11;57(11):2136-8. doi: 10.1212/wnl.57.11.2136. Neurology. 2001. PMID: 11739845

4

A novel, blood-based diagnostic assay for limb girdle muscular dystrophy 2B and Miyoshi myopathy.

Ho M, Gallardo E, McKenna-Yasek D, De Luna N, Illa I, Brown RH Jr. Ho M, et al. Among authors: de luna n. Ann Neurol. 2002 Jan;51(1):129-33. doi: 10.1002/ana.10080. Ann Neurol. 2002. PMID: 11782994

5

Antidisialosyl antibodies in chronic idiopathic ataxic neuropathy.

Serrano-Munuera C, Rojas-García R, Gallardo E, De Luna N, Buenaventura I, Ferrero M, García T, García-Merino JA, González-Rodríguez C, Guerriero A, Marco M, Márquez C, Grau JM, Graus F, Illa I. Serrano-Munuera C, et al. Among authors: de luna n. J Neurol. 2002 Nov;249(11):1525-8. doi: 10.1007/s00415-002-0882-2. J Neurol. 2002. PMID: 12420092

6

Chronic neuropathy with IgM anti-ganglioside antibodies: lack of long term response to rituximab.

Rojas-García R, Gallardo E, de Andrés I, de Luna N, Juarez C, Sánchez P, Illa I. Rojas-García R, et al. Among authors: de luna n, de andres i. Neurology. 2003 Dec 23;61(12):1814-6. doi: 10.1212/01.wnl.0000098996.02934.86. Neurology. 2003. PMID: 14694058

7

In vivo and in vitro dysferlin expression in human muscle satellite cells.

De Luna N, Gallardo E, Illa I. De Luna N, et al. J Neuropathol Exp Neurol. 2004 Oct;63(10):1104-13. doi: 10.1093/jnen/63.10.1104. J Neuropathol Exp Neurol. 2004. PMID: 15535137

8

X-linked Emery-Dreifuss muscular dystrophy and vacuoles: an immunohistochemical characterization.

Paradas C, Márquez C, Gallardo E, De Luna N, Chinchón I, Recan D, Jiménez MD, Illa I. Paradas C, et al. Among authors: de luna n. Muscle Nerve. 2005 Jul;32(1):61-5. doi: 10.1002/mus.20311. Muscle Nerve. 2005. PMID: 15880484

9

Identification of a novel founder mutation in the DYSF gene causing clinical variability in the Spanish population.

Vilchez JJ, Gallano P, Gallardo E, Lasa A, Rojas-García R, Freixas A, De Luna N, Calafell F, Sevilla T, Mayordomo F, Baiget M, Illa I. Vilchez JJ, et al. Among authors: de luna n. Arch Neurol. 2005 Aug;62(8):1256-9. doi: 10.1001/archneur.62.8.1256. Arch Neurol. 2005. PMID: 16087766

10

Absence of dysferlin alters myogenin expression and delays human muscle differentiation "in vitro".

de Luna N, Gallardo E, Soriano M, Dominguez-Perles R, de la Torre C, Rojas-García R, García-Verdugo JM, Illa I. de Luna N, et al. Among authors: de la torre c. J Biol Chem. 2006 Jun 23;281(25):17092-17098. doi: 10.1074/jbc.M601885200. Epub 2006 Apr 11. J Biol Chem. 2006. PMID: 16608842 Free article.

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