Martín MA - Search Results

1

A novel RRM2B gene variant associated with Telbivudine-induced mitochondrial myopathy.

Hernández-Laín A, Guerrero AM, Domínguez-González C, Fernández-Vázquez I, Maya DG, Delmiro A, Arenas J, Morales JR, Blázquez A, Moran M, Martín MA. Hernández-Laín A, et al. Among authors: martin ma. J Neurol Sci. 2015 Nov 15;358(1-2):481-3. doi: 10.1016/j.jns.2015.08.1550. Epub 2015 Sep 2. J Neurol Sci. 2015. PMID: 26359855 No abstract available.

2

Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNA.

Campos Y, Martin MA, Lorenzo G, Aparicio M, Cabello A, Arenas J. Campos Y, et al. Among authors: martin ma. Muscle Nerve. 1996 Feb;19(2):187-90. doi: 10.1002/(SICI)1097-4598(199602)19:2<187::AID-MUS10>3.0.CO;2-S. Muscle Nerve. 1996. PMID: 8559168

3

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.

4

Multiple deletions of mitochondrial DNA in muscle from a patient with benign progressive external ophthalmoplegia.

Campos Y, Martín MA, Rubio JC, Ricard C, Cabello A, Arenas J. Campos Y, et al. Among authors: martin ma. J Inherit Metab Dis. 1996;19(3):366-7. doi: 10.1007/BF01799268. J Inherit Metab Dis. 1996. PMID: 8803781 No abstract available.

5

[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.

6

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

7

Abnormal carnitine distribution in the muscles of patients with idiopathic inflammatory myopathy.

Arenas J, Gonzalez-Crespo MR, Campos Y, Martin MA, Cabello A, Gomez-Reino JJ. Arenas J, et al. Among authors: martin ma. Arthritis Rheum. 1996 Nov;39(11):1869-74. doi: 10.1002/art.1780391113. Arthritis Rheum. 1996. PMID: 8912509

8

Cerebrospinal fluid carnitine levels in patients with Parkinson's disease.

Jiménez-Jiménez FJ, Rubio JC, Molina JA, Martín MA, Campos Y, Benito-León J, Ortí-Pareja M, Gasalla T, Arenas J. Jiménez-Jiménez FJ, et al. Among authors: martin ma. J Neurol Sci. 1997 Feb 12;145(2):183-5. doi: 10.1016/s0022-510x(96)00259-6. J Neurol Sci. 1997. PMID: 9094047 Clinical Trial.

9

Leigh syndrome associated with the T9176C mutation in the ATPase 6 gene of mitochondrial DNA.

Campos Y, Martín MA, Rubio JC, Solana LG, García-Benayas C, Terradas JL, Arenas J. Campos Y, et al. Among authors: martin ma. Neurology. 1997 Aug;49(2):595-7. doi: 10.1212/wnl.49.2.595. Neurology. 1997. PMID: 9270604

10

Bilateral striatal necrosis and MELAS associated with a new T3308C mutation in the mitochondrial ND1 gene.

Campos Y, Martín MA, Rubio JC, Gutiérrez del Olmo MC, Cabello A, Arenas J. Campos Y, et al. Among authors: martin ma. Biochem Biophys Res Commun. 1997 Sep 18;238(2):323-5. doi: 10.1006/bbrc.1997.7166. Biochem Biophys Res Commun. 1997. PMID: 9299504

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