Arenas J - Search Results

1

Mitochondrial diseases in children: neuroradiological and clinical features in 17 patients.

Muñoz A, Mateos F, Simón R, García-Silva MT, Cabello S, Arenas J. Muñoz A, et al. Among authors: arenas j. Neuroradiology. 1999 Dec;41(12):920-8. doi: 10.1007/s002340050868. Neuroradiology. 1999. PMID: 10639669

2

[Clinical and investigative approaches in mitochondrial diseases. A review of 15 cases].

Arpa J, Campos Y, Cruz Martínez A, Gutiérrez Molina M, Arenas J, Alonso M, Plaza I, Morales C, Palomo F, Barreiro P, et al. Arpa J, et al. Among authors: arenas j. Neurologia. 1994 Oct;9(8):324-36. Neurologia. 1994. PMID: 7803049 Spanish.

3

Encephalopathy, petechiae, and acrocyanosis with ethylmalonic aciduria associated with muscle cytochrome c oxidase deficiency.

García-Silva MT, Campos Y, Ribes A, Briones P, Cabello A, Santos Borbujo J, Arenas J, Garavaglia B. García-Silva MT, et al. Among authors: arenas j. J Pediatr. 1994 Nov;125(5 Pt 1):843-4. J Pediatr. 1994. PMID: 7965445 No abstract available.

4

Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria.

García-Silva MT, Ribes A, Campos Y, Garavaglia B, Arenas J. García-Silva MT, et al. Among authors: arenas j. Pediatr Neurol. 1997 Sep;17(2):165-70. doi: 10.1016/s0887-8994(97)00048-9. Pediatr Neurol. 1997. PMID: 9367300

5

Clinical heterogeneity associated with mitochondrial DNA depletion in muscle.

Campos Y, Martín MA, García-Silva T, del Hoyo P, Rubio JC, Castro-Gago M, García-Peñas J, Casas J, Cabello A, Ricoy JR, Arenas J. Campos Y, et al. Among authors: arenas j. Neuromuscul Disord. 1998 Dec;8(8):568-73. doi: 10.1016/s0960-8966(98)00080-7. Neuromuscul Disord. 1998. PMID: 10093063

6

Slow segregation and rapid shift to homoplasmy coexist in a family with the T8993 > G mutation.

Martín MA, Campos Y, García-Silva MT, Rubio JC, Del Hoyo P, de Bustos F, García A, Arenas J. Martín MA, et al. Among authors: arenas j. J Inherit Metab Dis. 1999 Dec;22(8):939-40. doi: 10.1023/a:1005603926730. J Inherit Metab Dis. 1999. PMID: 10604149 No abstract available.

7

Mitochondrial DNA point mutation in the COI gene in a patient with McArdle's disease.

Aguilera I, García-Lozano JR, Muñoz A, Arenas J, Campos Y, Chinchón I, Roldán AN, Bautista J. Aguilera I, et al. Among authors: arenas j. J Neurol Sci. 2001 Nov 15;192(1-2):81-4. doi: 10.1016/s0022-510x(01)00634-7. J Neurol Sci. 2001. PMID: 11701156

8

Renal pathology in children with mitochondrial diseases.

Martín-Hernández E, García-Silva MT, Vara J, Campos Y, Cabello A, Muley R, Del Hoyo P, Martín MA, Arenas J. Martín-Hernández E, et al. Among authors: arenas j. Pediatr Nephrol. 2005 Sep;20(9):1299-305. doi: 10.1007/s00467-005-1948-z. Epub 2005 Jun 24. Pediatr Nephrol. 2005. PMID: 15977024

9

Mitochondrial diseases associated with cerebral folate deficiency.

Garcia-Cazorla A, Quadros EV, Nascimento A, Garcia-Silva MT, Briones P, Montoya J, Ormazábal A, Artuch R, Sequeira JM, Blau N, Arenas J, Pineda M, Ramaekers VT. Garcia-Cazorla A, et al. Among authors: arenas j. Neurology. 2008 Apr 15;70(16):1360-2. doi: 10.1212/01.wnl.0000309223.98616.e4. Neurology. 2008. PMID: 18413591 No abstract available.

10

Pathogenic mutations in the 5' untranslated region of BCS1L mRNA in mitochondrial complex III deficiency.

Gil-Borlado MC, González-Hoyuela M, Blázquez A, García-Silva MT, Gabaldón T, Manzanares J, Vara J, Martín MA, Seneca S, Arenas J, Ugalde C. Gil-Borlado MC, et al. Among authors: arenas j. Mitochondrion. 2009 Sep;9(5):299-305. doi: 10.1016/j.mito.2009.04.001. Epub 2009 Apr 21. Mitochondrion. 2009. PMID: 19389488

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