Gallardo E - Search Results

1

BNIP3 Is Involved in Muscle Fiber Atrophy in Late-Onset Pompe Disease Patients.

Carrasco-Rozas A, Fernández-Simón E, Suárez-Calvet X, Piñol-Jurado P, Alonso-Pérez J, de Luna N, Schoser B, Meinke P, Domínguez-González C, Hernández-Laín A, Paradas C, Rivas E, Illa I, Olivé M, Gallardo E, Díaz-Manera J. Carrasco-Rozas A, et al. Among authors: gallardo e. Am J Pathol. 2022 Aug;192(8):1151-1166. doi: 10.1016/j.ajpath.2022.05.003. Epub 2022 May 21. Am J Pathol. 2022. PMID: 35605642 Free article.

2

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: gallardo e. Ann Neurol. 2002 Jan;51(1):129-33. doi: 10.1002/ana.10080. Ann Neurol. 2002. PMID: 11782994

3

Neuromuscular dysfunction in adult growth hormone deficiency.

Webb SM, de Andrés-Aguayo I, Rojas-García R, Ortega E, Gallardo E, Mestrón A, Serrano-Munuera C, Casamitjana R, Illa I. Webb SM, et al. Among authors: gallardo e. Clin Endocrinol (Oxf). 2003 Oct;59(4):450-8. doi: 10.1046/j.1365-2265.2003.01866.x. Clin Endocrinol (Oxf). 2003. PMID: 14510907

4

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

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

5

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: gallardo e. Muscle Nerve. 2005 Jul;32(1):61-5. doi: 10.1002/mus.20311. Muscle Nerve. 2005. PMID: 15880484

6

["Seronegative" myasthenia gravis and antiMuSK positive antibodies: description of Spanish series].

Illa I, Díaz-Manera JA, Juárez C, Rojas-García R, Molina-Porcel L, Aleu A, Pradas J, Gallardo E. Illa I, et al. Among authors: gallardo e. Med Clin (Barc). 2005 Jun 18;125(3):100-2. doi: 10.1157/13076937. Med Clin (Barc). 2005. PMID: 15989843 Spanish.

7

Central nervous system involvement in hereditary neuropathy with liability to pressure palsies: description of a large family with this association.

Sanahuja J, Franco E, Rojas-García R, Gallardo E, Combarros O, Begué R, Granés P, Illa I. Sanahuja J, et al. Among authors: gallardo e. Arch Neurol. 2005 Dec;62(12):1911-4. doi: 10.1001/archneur.62.12.1911. Arch Neurol. 2005. PMID: 16344349

8

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: gallardo e. 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.

9

A novel antiganglioside specificity against terminal NeuNAc(alfa 2-3)Gal in acute bulbar palsy.

Rojas-Garcia R, Martinez-Lage M, Gallardo E, de Luna N, Marti-Vilalta JL, Diaz-Manera J, Juarez C, Blesa R, Illa I. Rojas-Garcia R, et al. Among authors: gallardo e. J Neuroimmunol. 2006 Jul;176(1-2):219-22. doi: 10.1016/j.jneuroim.2006.04.001. Epub 2006 May 16. J Neuroimmunol. 2006. PMID: 16707165

10

Antibodies to AChR, MuSK and VGKC in a patient with myasthenia gravis and Morvan's syndrome.

Díaz-Manera J, Rojas-García R, Gallardo E, Juárez C, Martínez-Domeño A, Martínez-Ramírez S, Dalmau J, Blesa R, Illa I. Díaz-Manera J, et al. Among authors: gallardo e. Nat Clin Pract Neurol. 2007 Jul;3(7):405-10. doi: 10.1038/ncpneuro0526. Nat Clin Pract Neurol. 2007. PMID: 17611489

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