Gallardo E - Search Results

1

Dysferlin expression in monocytes: a source of mRNA for mutation analysis.

De Luna N, Freixas A, Gallano P, Caselles L, Rojas-García R, Paradas C, Nogales G, Dominguez-Perles R, Gonzalez-Quereda L, Vílchez JJ, Márquez C, Bautista J, Guerrero A, Salazar JA, Pou A, Illa I, Gallardo E. De Luna N, et al. Among authors: gallardo e. Neuromuscul Disord. 2007 Jan;17(1):69-76. doi: 10.1016/j.nmd.2006.09.006. Epub 2006 Oct 27. Neuromuscul Disord. 2007. PMID: 17070050

2

Distal anterior compartment myopathy: a dysferlin mutation causing a new muscular dystrophy phenotype.

Illa I, Serrano-Munuera C, Gallardo E, Lasa A, Rojas-García R, Palmer J, Gallano P, Baiget M, Matsuda C, Brown RH. Illa I, et al. Among authors: gallardo e. Ann Neurol. 2001 Jan;49(1):130-4. Ann Neurol. 2001. PMID: 11198284

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. Neurology. 2001 Dec 11;57(11):2136-8. doi: 10.1212/wnl.57.11.2136. Neurology. 2001. PMID: 11739845

4

Symptomatic dysferlin gene mutation carriers: characterization of two cases.

Illa I, De Luna N, Domínguez-Perles R, Rojas-García R, Paradas C, Palmer J, Márquez C, Gallano P, Gallardo E. Illa I, et al. Among authors: gallardo e. Neurology. 2007 Apr 17;68(16):1284-9. doi: 10.1212/01.wnl.0000256768.79353.60. Epub 2007 Feb 7. Neurology. 2007. PMID: 17287450

5

A new phenotype of dysferlinopathy with congenital onset.

Paradas C, González-Quereda L, De Luna N, Gallardo E, García-Consuegra I, Gómez H, Cabello A, Illa I, Gallano P. Paradas C, et al. Among authors: gallardo e. Neuromuscul Disord. 2009 Jan;19(1):21-5. doi: 10.1016/j.nmd.2008.09.015. Epub 2008 Dec 11. Neuromuscul Disord. 2009. PMID: 19084402

6

Redefining dysferlinopathy phenotypes based on clinical findings and muscle imaging studies.

Paradas C, Llauger J, Diaz-Manera J, Rojas-García R, De Luna N, Iturriaga C, Márquez C, Usón M, Hankiewicz K, Gallardo E, Illa I. Paradas C, et al. Among authors: gallardo e. Neurology. 2010 Jul 27;75(4):316-23. doi: 10.1212/WNL.0b013e3181ea1564. Epub 2010 Jun 23. Neurology. 2010. PMID: 20574037

7

Cathepsins are upregulated by IFN-gamma/STAT1 in human muscle culture: a possible active factor in dermatomyositis.

Gallardo E, de Andrés I, Illa I. Gallardo E, et al. J Neuropathol Exp Neurol. 2001 Sep;60(9):847-55. doi: 10.1093/jnen/60.9.847. J Neuropathol Exp Neurol. 2001. PMID: 11556541

8

Abnormal expression of dysferlin in skeletal muscle and monocytes supports primary dysferlinopathy in patients with one mutated allele.

Meznaric M, Gonzalez-Quereda L, Gallardo E, de Luna N, Gallano P, Fanin M, Angelini C, Peterlin B, Zidar J. Meznaric M, et al. Among authors: gallardo e. Eur J Neurol. 2011 Jul;18(7):1021-3. doi: 10.1111/j.1468-1331.2010.03240.x. Epub 2010 Oct 18. Eur J Neurol. 2011. PMID: 21658164

9

Identification of novel GH-regulated genes in C2C12 cells.

Resmini E, Morte B, Sorianello E, Gallardo E, de Luna N, Illa I, Zorzano A, Bernal J, Webb SM. Resmini E, et al. Among authors: gallardo e. Horm Metab Res. 2011 Dec;43(13):919-30. doi: 10.1055/s-0031-1291285. Epub 2011 Nov 9. Horm Metab Res. 2011. PMID: 22072432

10

[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: gallardo e. 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.

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