Martín MA - Search Results

1

Are mitochondrial haplogroups associated with elite athletic status? A study on a Spanish cohort.

Nogales-Gadea G, Pinós T, Ruiz JR, Marzo PF, Fiuza-Luces C, López-Gallardo E, Ruiz-Pesini E, Martín MA, Arenas J, Morán M, Andreu AL, Lucia A. Nogales-Gadea G, et al. Among authors: martin ma. Mitochondrion. 2011 Nov;11(6):905-8. doi: 10.1016/j.mito.2011.08.002. Epub 2011 Aug 11. Mitochondrion. 2011. PMID: 21856449

2

Clinical variability associated with the mutation at nucleotide position 8344 of the mitochondrial DNA.

Campos Y, Martín MA, Vaamonde J, Cabello A, Esteban J, Arenas J. Campos Y, et al. Among authors: martin ma. J Inherit Metab Dis. 1996;19(2):119-22. doi: 10.1007/BF01799408. J Inherit Metab Dis. 1996. PMID: 8739944 No abstract available.

3

[Molecular genetics of mitochondrial cytopathologies].

Arenas J, Campos Y, Martín MA. Arenas J, et al. Among authors: martin ma. Neurologia. 1995 Dec;10 Suppl 1:44-9. Neurologia. 1995. PMID: 8838558 Review. Spanish.

4

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: martin ma. Neurology. 1996 Oct;47(4):1012-4. doi: 10.1212/wnl.47.4.1012. Neurology. 1996. PMID: 8857737

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

6

Biological roles of L-carnitine in perinatal metabolism.

Arenas J, Rubio JC, Martín MA, Campos Y. Arenas J, et al. Among authors: martin ma. Early Hum Dev. 1998 Dec;53 Suppl:S43-50. doi: 10.1016/s0378-3782(98)00064-4. Early Hum Dev. 1998. PMID: 10102654 Review.

7

McArdle's disease associated with homozygosity for the missense mutation Gly204Ser of the myophosphorylase gene in a Spanish patient.

Rubio JC, Martín MA, García A, Campos Y, Cabello A, Culebras JM, Arenas J. Rubio JC, et al. Among authors: martin ma. Neuromuscul Disord. 1999 May;9(3):174-5. doi: 10.1016/s0960-8966(98)00127-8. Neuromuscul Disord. 1999. PMID: 10382912

8

Single large-scale mitochondrial DNA deletion in a patient with encephalopathy, cardiomyopathy, and prominent intestinal pseudo-obstruction.

Campos Y, Martín MA, Caballero C, Rubio JC, de la Cruz F, Tuñón T, Arenas J. Campos Y, et al. Among authors: martin ma. Neuromuscul Disord. 2000 Jan;10(1):56-8. doi: 10.1016/s0960-8966(99)00072-3. Neuromuscul Disord. 2000. PMID: 10677865

9

A missense mutation T487N in the myophosphorylase gene in a Spanish patient with McArdle's disease.

Rubio JC, Martín MA, Campos Y, Cabello A, Arenas J. Rubio JC, et al. Among authors: martin ma. Neuromuscul Disord. 2000 Feb;10(2):138-40. doi: 10.1016/s0960-8966(99)00082-6. Neuromuscul Disord. 2000. PMID: 10714589

10

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: martin ma. 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

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