Navarro C - Search Results

1

Single large-scale mitochondrial DNA deletion in a patient with mitochondrial myopathy associated with multiple symmetric lipomatosis.

Campos Y, Martín MA, Navarro C, Gordo P, Arenas J. Campos Y, et al. Among authors: navarro c. Neurology. 1996 Oct;47(4):1012-4. doi: 10.1212/wnl.47.4.1012. Neurology. 1996. PMID: 8857737

2

Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population.

González-Vioque E, Blázquez A, Fernández-Moreira D, Bornstein B, Bautista J, Arpa J, Navarro C, Campos Y, Fernández-Moreno MA, Garesse R, Arenas J, Martín MA. González-Vioque E, et al. Among authors: navarro c. Arch Neurol. 2006 Jan;63(1):107-11. doi: 10.1001/archneur.63.1.107. Arch Neurol. 2006. PMID: 16401742

3

Molecular analysis of Spanish patients with AMP deaminase deficiency.

Rubio JC, Martín MA, Del Hoyo P, Bautista J, Campos Y, Segura D, Navarro C, Ricoy JR, Cabello A, Arenas J. Rubio JC, et al. Among authors: navarro c. Muscle Nerve. 2000 Aug;23(8):1175-8. doi: 10.1002/1097-4598(200008)23:8<1175::aid-mus3>3.0.co;2-m. Muscle Nerve. 2000. PMID: 10918252

4

A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathy.

Campos Y, Gámez J, García A, Andreu AL, Rubio JC, Martín MA, del Hoyo P, Navarro C, Cervera C, Garesse R, Arenas J. Campos Y, et al. Among authors: navarro c. Neuromuscul Disord. 2001 Jul;11(5):477-80. doi: 10.1016/s0960-8966(00)00223-6. Neuromuscul Disord. 2001. PMID: 11404120

5

Molecular heterogeneity of myophosphorylase deficiency (McArdle's disease): a genotype-phenotype correlation study.

Martín MA, Rubio JC, Buchbinder J, Fernández-Hojas R, del Hoyo P, Teijeira S, Gámez J, Navarro C, Fernández JM, Cabello A, Campos Y, Cervera C, Culebras JM, Andreu AL, Fletterick R, Arenas J. Martín MA, et al. Among authors: navarro c. Ann Neurol. 2001 Nov;50(5):574-81. Ann Neurol. 2001. PMID: 11706962

6

Genotypic and phenotypic features of McArdle disease: insights from the Spanish national registry.

Lucia A, Ruiz JR, Santalla A, Nogales-Gadea G, Rubio JC, García-Consuegra I, Cabello A, Pérez M, Teijeira S, Vieitez I, Navarro C, Arenas J, Martin MA, Andreu AL. Lucia A, et al. Among authors: navarro c. J Neurol Neurosurg Psychiatry. 2012 Mar;83(3):322-8. doi: 10.1136/jnnp-2011-301593. Epub 2012 Jan 16. J Neurol Neurosurg Psychiatry. 2012. PMID: 22250184

7

Familial multiple symmetric lipomatosis associated with the A8344G mutation of mitochondrial DNA.

Gámez J, Playán A, Andreu AL, Bruno C, Navarro C, Cervera C, Arbós MA, Schwartz S, Enriquez JA, Montoya J. Gámez J, et al. Among authors: navarro c. Neurology. 1998 Jul;51(1):258-60. doi: 10.1212/wnl.51.1.258. Neurology. 1998. PMID: 9674814

8

Unusual clinical findings and Complex III deficiency in a family with myotonic dystrophy.

Seijo-Martínez M, Castro del Río M, Campos Y, Palau F, Arenas J, Teijeira S, Fernández Hojas R, Navarro C. Seijo-Martínez M, et al. Among authors: navarro c. J Neurol Sci. 2003 Apr 15;208(1-2):87-91. doi: 10.1016/s0022-510x(02)00442-2. J Neurol Sci. 2003. PMID: 12639730

9

Quantitative analysis of proteins of metabolism by reverse phase protein microarrays identifies potential biomarkers of rare neuromuscular diseases.

Santacatterina F, Chamorro M, de Arenas CN, Navarro C, Martín MA, Cuezva JM, Sánchez-Aragó M. Santacatterina F, et al. Among authors: navarro c. J Transl Med. 2015 Feb 18;13:65. doi: 10.1186/s12967-015-0424-1. J Transl Med. 2015. PMID: 25880557 Free PMC article.

10

[Morphological changes of mitochondrial myopathies].

Cabello A, Navarro C, Ricoy JR. Cabello A, et al. Among authors: navarro c. Rev Neurol. 1998 Apr;26 Suppl 1:S44-9. Rev Neurol. 1998. PMID: 9810590 Review. Spanish.

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