Nogales-Gadea G - Search Results

1

Rodent models for resolving extremes of exercise and health.

Garton FC, North KN, Koch LG, Britton SL, Nogales-Gadea G, Lucia A. Garton FC, et al. Physiol Genomics. 2016 Feb;48(2):82-92. doi: 10.1152/physiolgenomics.00077.2015. Epub 2015 Sep 22. Physiol Genomics. 2016. PMID: 26395598 Free PMC article. Review.

2

A proposed molecular diagnostic flowchart for myophosphorylase deficiency (McArdle disease) in blood samples from Spanish patients.

Rubio JC, Garcia-Consuegra I, Nogales-Gadea G, Blazquez A, Cabello A, Lucia A, Andreu AL, Arenas J, Martin MA. Rubio JC, et al. Hum Mutat. 2007 Feb;28(2):203-4. doi: 10.1002/humu.9474. Hum Mutat. 2007. PMID: 17221871

3

The 577X allele of the ACTN3 gene is associated with improved exercise capacity in women with McArdle's disease.

Lucia A, Gómez-Gallego F, Santiago C, Pérez M, Maté-Muñoz JL, Chamorro-Viña C, Nogales-Gadea G, Foster C, Rubio JC, Andreu AL, Martín MA, Arenas J. Lucia A, et al. Neuromuscul Disord. 2007 Aug;17(8):603-10. doi: 10.1016/j.nmd.2007.04.006. Epub 2007 Jun 8. Neuromuscul Disord. 2007. PMID: 17560787

4

Favorable responses to acute and chronic exercise in McArdle patients.

Maté-Muñoz JL, Moran M, Pérez M, Chamorro-Viña C, Gómez-Gallego F, Santiago C, Chicharro L, Foster C, Nogales-Gadea G, Rubio JC, Andreu AL, Martín MA, Arenas J, Lucia A. Maté-Muñoz JL, et al. Clin J Sport Med. 2007 Jul;17(4):297-303. doi: 10.1097/JSM.0b013e3180f6168c. Clin J Sport Med. 2007. PMID: 17620784

5

Expression of the muscle glycogen phosphorylase gene in patients with McArdle disease: the role of nonsense-mediated mRNA decay.

Nogales-Gadea G, Rubio JC, Fernandez-Cadenas I, Garcia-Consuegra I, Lucia A, Cabello A, Garcia-Arumi E, Arenas J, Andreu AL, Martín MA. Nogales-Gadea G, et al. Hum Mutat. 2008 Feb;29(2):277-83. doi: 10.1002/humu.20649. Hum Mutat. 2008. PMID: 17994553

6

McArdle disease: what do neurologists need to know?

Lucia A, Nogales-Gadea G, Pérez M, Martín MA, Andreu AL, Arenas J. Lucia A, et al. Nat Clin Pract Neurol. 2008 Oct;4(10):568-77. doi: 10.1038/ncpneuro0913. Nat Clin Pract Neurol. 2008. PMID: 18833216 Review.

7

Novel mutations in patients with McArdle disease by analysis of skeletal muscle mRNA.

García-Consuegra I, Rubio JC, Nogales-Gadea G, Bautista J, Jiménez S, Cabello A, Lucía A, Andreu AL, Arenas J, Martin MA. García-Consuegra I, et al. J Med Genet. 2009 Mar;46(3):198-202. doi: 10.1136/jmg.2008.059469. J Med Genet. 2009. PMID: 19251976

8

Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle disease.

Garcia-Consuegra I, Rubio JC, Nogales-Gadea G, Bautista J, Jiménez S, Cabello A, Lucía A, Andreu AL, Arenas J, Martin MA. Garcia-Consuegra I, et al. Hum Genet. 2009 Apr;125(3):342. Hum Genet. 2009. PMID: 19320015 No abstract available.

9

Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle disease.

Garcia-Consuegra I, Rubio JC, Nogales-Gadea G, Bautista J, Jiménez S, Cabello A, Lucía A, Andreu AL, Arenas J, Martin MA. Garcia-Consuegra I, et al. Hum Genet. 2009 Apr;125(3):343. Hum Genet. 2009. PMID: 19320016 No abstract available.

10

The second wind phenomenon in very young McArdle's patients.

Pérez M, Ruiz JR, Fernández Del Valle M, Nogales-Gadea G, Andreu AL, Arenas J, Lucía A. Pérez M, et al. Neuromuscul Disord. 2009 Jun;19(6):403-5. doi: 10.1016/j.nmd.2009.04.010. Epub 2009 May 27. Neuromuscul Disord. 2009. PMID: 19477644

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