Ribacoba R - Search Results

1

Complex I defect in muscle from patients with Huntington's disease.

Arenas J, Campos Y, Ribacoba R, Martín MA, Rubio JC, Ablanedo P, Cabello A. Arenas J, et al. Among authors: ribacoba r. Ann Neurol. 1998 Mar;43(3):397-400. doi: 10.1002/ana.410430321. Ann Neurol. 1998. PMID: 9506560

2

A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibers.

Arenas J, Campos Y, Bornstein B, Ribacoba R, Martín MA, Rubio JC, Santorelli FM, Zeviani M, DiMauro S, Garesse R. Arenas J, et al. Among authors: ribacoba r. Neurology. 1999 Jan 15;52(2):377-82. doi: 10.1212/wnl.52.2.377. Neurology. 1999. PMID: 9932960

3

Two pathogenic mutations in the mitochondrial DNA tRNA Leu(UUR) gene (T3258C and A3280G) resulting in variable clinical phenotypes.

Campos Y, García A, del Hoyo P, Jara P, Martín MA, Rubio JC, Berbel A, Barberá JR, Ribacoba R, Astudillo A, Cabello A, Ricoy JR, Arenas J. Campos Y, et al. Among authors: ribacoba r. Neuromuscul Disord. 2003 Jun;13(5):416-20. doi: 10.1016/s0960-8966(03)00039-7. Neuromuscul Disord. 2003. PMID: 12798797

4

Clinical manifestations of intermediate allele carriers in Huntington disease.

Cubo E, Ramos-Arroyo MA, Martinez-Horta S, Martínez-Descalls A, Calvo S, Gil-Polo C; European HD Network. Cubo E, et al. Neurology. 2016 Aug 9;87(6):571-8. doi: 10.1212/WNL.0000000000002944. Epub 2016 Jul 8. Neurology. 2016. PMID: 27402890

5

Circulating microRNAs in Huntington's disease: Emerging mediators in metabolic impairment.

Díez-Planelles C, Sánchez-Lozano P, Crespo MC, Gil-Zamorano J, Ribacoba R, González N, Suárez E, Martínez-Descals A, Martínez-Camblor P, Álvarez V, Martín-Hernández R, Huerta-Ruíz I, González-García I, Cosgaya JM, Visioli F, Dávalos A, Iglesias-Gutiérrez E, Tomás-Zapico C. Díez-Planelles C, et al. Among authors: ribacoba r. Pharmacol Res. 2016 Jun;108:102-110. doi: 10.1016/j.phrs.2016.05.005. Epub 2016 May 4. Pharmacol Res. 2016. PMID: 27155059

6

Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study.

McNulty P, Pilcher R, Ramesh R, Necuiniate R, Hughes A, Farewell D, Holmans P, Jones L; REGISTRY Investigators of the European Huntington's Disease Network. McNulty P, et al. J Huntingtons Dis. 2018;7(3):209-222. doi: 10.3233/JHD-170263. J Huntingtons Dis. 2018. PMID: 30103338

7

MiRNA profile in the substantia nigra of Parkinson's disease and healthy subjects.

Cardo LF, Coto E, Ribacoba R, Menéndez M, Moris G, Suárez E, Alvarez V. Cardo LF, et al. Among authors: ribacoba r. J Mol Neurosci. 2014 Dec;54(4):830-6. doi: 10.1007/s12031-014-0428-y. Epub 2014 Oct 5. J Mol Neurosci. 2014. PMID: 25284245

8

Analysis of the Micro-RNA-133 and PITX3 genes in Parkinson's disease.

de Mena L, Coto E, Cardo LF, Díaz M, Blázquez M, Ribacoba R, Salvador C, Pastor P, Samaranch L, Moris G, Menéndez M, Corao AI, Alvarez V. de Mena L, et al. Among authors: ribacoba r. Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1234-9. doi: 10.1002/ajmg.b.31086. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20468068

9

Mutational screening of the mitochondrial transcription factors B1 and B2 (TFB1M and TFB2M) in Parkinson's disease.

Sánchez-Ferrero E, Coto E, Blázquez M, Ribacoba R, Guisasola LM, Salvador C, Alvarez V. Sánchez-Ferrero E, et al. Among authors: ribacoba r. Parkinsonism Relat Disord. 2009 Jul;15(6):468-70. doi: 10.1016/j.parkreldis.2008.09.004. Epub 2008 Nov 5. Parkinsonism Relat Disord. 2009. PMID: 18980857

10

Mitochondrial transcription factor A (TFAM) gene variation in Parkinson's disease.

Alvarez V, Corao AI, Sánchez-Ferrero E, De Mena L, Alonso-Montes C, Huerta C, Blázquez M, Ribacoba R, Guisasola LM, Salvador C, García-Castro M, Coto E. Alvarez V, et al. Among authors: ribacoba r. Neurosci Lett. 2008 Feb 13;432(1):79-82. doi: 10.1016/j.neulet.2007.12.010. Epub 2007 Dec 15. Neurosci Lett. 2008. PMID: 18248889

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