Navarro C - Search Results

1

Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene.

Melià MJ, Kubota A, Ortolano S, Vílchez JJ, Gámez J, Tanji K, Bonilla E, Palenzuela L, Fernández-Cadenas I, Pristoupilová A, García-Arumí E, Andreu AL, Navarro C, Hirano M, Martí R. Melià MJ, et al. Among authors: navarro c. Brain. 2013 May;136(Pt 5):1508-17. doi: 10.1093/brain/awt074. Epub 2013 Mar 29. Brain. 2013. PMID: 23543484 Free PMC article.

2

Autosomal dominant limb-girdle muscular dystrophy: a large kindred with evidence for anticipation.

Gamez J, Navarro C, Andreu AL, Fernandez JM, Palenzuela L, Tejeira S, Fernandez-Hojas R, Schwartz S, Karadimas C, DiMauro S, Hirano M, Cervera C. Gamez J, et al. Among authors: navarro c. Neurology. 2001 Feb 27;56(4):450-4. doi: 10.1212/wnl.56.4.450. Neurology. 2001. PMID: 11222786

3

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

4

A new mutation in the regulatory domain of the myophosphorylase gene affecting protein dimer contact.

Gamez J, Fernandez R, Bruno C, Andreu AL, Cervera C, Navarro C, Schwartz S, Dimauro S. Gamez J, et al. Among authors: navarro c. Muscle Nerve. 1999 Aug;22(8):1136-8. doi: 10.1002/(sici)1097-4598(199908)22:8<1136::aid-mus21>3.0.co;2-2. Muscle Nerve. 1999. PMID: 10417800

5

Molecular genetic analysis of McArdle's disease in Spanish patients.

Andreu AL, Bruno C, Gamez J, Shanske S, Cervera C, Navarro C, Arbos MA, Tamburino L, Schwartz S, DiMauro S. Andreu AL, et al. Among authors: navarro c. Neurology. 1998 Jul;51(1):260-2. doi: 10.1212/wnl.51.1.260. Neurology. 1998. PMID: 9674815

6

LRP-1 and LRP-2 receptors function in the membrane neuron. Trafficking mechanisms and proteolytic processing in Alzheimer's disease.

Spuch C, Ortolano S, Navarro C. Spuch C, et al. Among authors: navarro c. Front Physiol. 2012 Jul 16;3:269. doi: 10.3389/fphys.2012.00269. eCollection 2012. Front Physiol. 2012. PMID: 22934024 Free PMC article.

7

SBF1 mutations associated with autosomal recessive axonal neuropathy with cranial nerve involvement.

Manole A, Horga A, Gamez J, Raguer N, Salvado M, San Millán B, Navarro C, Pittmann A, Reilly MM, Houlden H. Manole A, et al. Among authors: navarro c. Neurogenetics. 2017 Jan;18(1):63-67. doi: 10.1007/s10048-016-0505-1. Epub 2016 Dec 22. Neurogenetics. 2017. PMID: 28005197

8

New insights in the amyloid-Beta interaction with mitochondria.

Spuch C, Ortolano S, Navarro C. Spuch C, et al. Among authors: navarro c. J Aging Res. 2012;2012:324968. doi: 10.1155/2012/324968. Epub 2012 Mar 19. J Aging Res. 2012. PMID: 22523685 Free PMC article.

9

Lafora progressive myoclonus epilepsy: recent insights into cell degeneration.

Spuch C, Ortolano S, Navarro C. Spuch C, et al. Among authors: navarro c. Recent Pat Endocr Metab Immune Drug Discov. 2012 May;6(2):99-107. doi: 10.2174/187221412800604617. Recent Pat Endocr Metab Immune Drug Discov. 2012. PMID: 22369717 Review.

10

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

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