Martin MA - Search Results

1

Coenzyme Q10 deficiency associated with a mitochondrial DNA depletion syndrome: a case report.

Montero R, Sánchez-Alcázar JA, Briones P, Navarro-Sastre A, Gallardo E, Bornstein B, Herrero-Martín D, Rivera H, Martin MA, Marti R, García-Cazorla A, Montoya J, Navas P, Artuch R. Montero R, et al. Among authors: martin ma. Clin Biochem. 2009 May;42(7-8):742-5. doi: 10.1016/j.clinbiochem.2008.10.027. Epub 2008 Dec 3. Clin Biochem. 2009. PMID: 19094978

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: martin ma. Neurology. 1999 Jan 15;52(2):377-82. doi: 10.1212/wnl.52.2.377. Neurology. 1999. PMID: 9932960

3

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: martin ma. Neuromuscul Disord. 1998 Dec;8(8):568-73. doi: 10.1016/s0960-8966(98)00080-7. Neuromuscul Disord. 1998. PMID: 10093063

4

Molecular analysis in Spanish patients with muscle carnitine palmitoyltransferase deficiency.

Martín MA, Rubio JC, De Bustos F, Del Hoyo P, Campos Y, García A, Börnstein B, Cabello A, Arenas J. Martín MA, et al. Muscle Nerve. 1999 Jul;22(7):941-3. doi: 10.1002/(sici)1097-4598(199907)22:7<941::aid-mus20>3.0.co;2-z. Muscle Nerve. 1999. PMID: 10398215 Clinical Trial.

5

Myocardial carnitine and carnitine palmitoyltransferase deficiencies in patients with severe heart failure.

Martín MA, Gómez MA, Guillén F, Börnstein B, Campos Y, Rubio JC, de la Calzada CS, Arenas J. Martín MA, et al. Biochim Biophys Acta. 2000 Nov 15;1502(3):330-6. doi: 10.1016/s0925-4439(00)00061-2. Biochim Biophys Acta. 2000. PMID: 11068176 Free article.

6

Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II gene.

Campos Y, García-Redondo A, Fernández-Moreno MA, Martínez-Pardo M, Goda G, Rubio JC, Martín MA, del Hoyo P, Cabello A, Bornstein B, Garesse R, Arenas J. Campos Y, et al. Among authors: martin ma. Ann Neurol. 2001 Sep;50(3):409-13. doi: 10.1002/ana.1141. Ann Neurol. 2001. PMID: 11558799

7

Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family.

de la Peña P, Bornstein B, del Hoyo P, Fernández-Moreno MA, Martín MA, Campos Y, Gómez-Escalonilla C, Molina JA, Cabello A, Arenas J, Garesse R. de la Peña P, et al. Among authors: martin ma. Neurology. 2001 Oct 9;57(7):1235-8. doi: 10.1212/wnl.57.7.1235. Neurology. 2001. PMID: 11591842

8

The A8296G mtDNA mutation associated with several mitochondrial diseases does not cause mitochondrial dysfunction in cybrid cell lines.

Bornstein B, Mas JA, Fernández-Moreno MA, Campos Y, Martín MA, del Hoyo P, Rubio JC, Arenas J, Garesse R. Bornstein B, et al. Among authors: martin ma. Hum Mutat. 2002 Mar;19(3):234-9. doi: 10.1002/humu.10050. Hum Mutat. 2002. PMID: 11857739

9

Myoglobinuria and COX deficiency in a patient taking cerivastatin and gemfibrozil.

Arenas J, Fernández-Moreno MA, Molina JA, Fernández V, del Hoyo P, Campos Y, Calvo P, Martín MA, García A, Moreno T, Martínez-Salio A, Börnstein B, Bermejo F, Cabello A, Garesse R. Arenas J, et al. Among authors: martin ma. Neurology. 2003 Jan 14;60(1):124-6. doi: 10.1212/01.wnl.0000042050.85041.fb. Neurology. 2003. PMID: 12525734

10

Lack of gastrointestinal symptoms in a 60-year-old patient with MNGIE.

Martín MA, Blázquez A, Martí R, Bautista J, Lara MC, Cabello A, Campos Y, Belda O, Andreu AL, Arenas J. Martín MA, et al. Neurology. 2004 Oct 26;63(8):1536-7. doi: 10.1212/01.wnl.0000141857.37073.97. Neurology. 2004. PMID: 15505189 No abstract available.

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