Bautista J - Search Results

1

[Complex I (NADH coenzyme-Q-reductase) deficiency, MELAS syndrome and hypertrophic cardiomyopathy].

Márquez C, Bautista J, Arenas J, Segura D, Chinchón I, Rafel E, Campos Y, Huerta R. Márquez C, et al. Among authors: bautista j. Neurologia. 1991 May;6(5):185-7. Neurologia. 1991. PMID: 1908255 Spanish.

2

[Adult onset mitochondrial myopathy without ophthalmoplegia. Four cases attributable to complex III and IV deficits in the respiratory chain].

Bautista J, Muñoz-Málaga A, Chinchón I, Segura D, Salazar JA, Bescansa E, Campos Y, Arenas J. Bautista J, et al. Neurologia. 1995 Oct;10(8):319-23. Neurologia. 1995. PMID: 8554781 Spanish.

3

Myophosphorylase deficiency associated with a defect in complex I of the mitochondrial respiratory chain.

Rubio JC, Martín MA, Bautista J, Campos Y, Segura D, Cabello A, Chinchón I, Arenas J. Rubio JC, et al. Among authors: bautista j. J Neurol Sci. 1998 Dec 11;161(2):110-3. doi: 10.1016/s0022-510x(98)00263-9. J Neurol Sci. 1998. PMID: 9879690

4

[Mitochondrial encephalomyopathy of late presentation with progressive ophthalmoplegia, tremor and diffuse leukoencephalopathy].

Franco E, Bautista J, Luque R, Chinchón I, García-Lozano R, Aguilera I, Campos Y, Arenas J. Franco E, et al. Among authors: bautista j. Neurologia. 1999 Nov;14(9):463-6. Neurologia. 1999. PMID: 10613022 Spanish.

5

Familial hypertrophic cardiomyopathy and muscle carnitine deficiency.

Bautista J, Rafel E, Martinez A, Sainz I, Herrera J, Segura L, Chinchon I. Bautista J, et al. Muscle Nerve. 1990 Mar;13(3):192-4. doi: 10.1002/mus.880130303. Muscle Nerve. 1990. PMID: 2320040

6

[Congenital myopathy with cores and nemaline rods in one family].

Casado JL, Arenas C, Segura D, Chinchón I, González R, Bautista J. Casado JL, et al. Among authors: bautista j. Neurologia. 1995 Mar;10(3):145-8. Neurologia. 1995. PMID: 7756014 Spanish.

7

[Recessive distal myopathies. Five cases].

Arenas C, Bautista J, Galán J, Casado JL, Salazar JA, Romero M, Segura DI, Chinchón I. Arenas C, et al. Among authors: bautista j. Neurologia. 1995 Jan;10(1):1-6. Neurologia. 1995. PMID: 7893506 Spanish.

8

Association of genetically proven deficiencies of myophosphorylase and AMP deaminase: a second case of 'double trouble'.

Rubio JC, Martín MA, Bautista J, Campos Y, Segura D, Arenas J. Rubio JC, et al. Among authors: bautista j. Neuromuscul Disord. 1997 Sep;7(6-7):387-9. doi: 10.1016/s0960-8966(97)00095-3. Neuromuscul Disord. 1997. PMID: 9327403

9

[Localized continuous muscular activity secondary to radioculopathy S1 with shin hypertrophy and focal myositis].

Pérez Errazquin F, Quesada J, Chinchón I, Segura D, Bautista J. Pérez Errazquin F, et al. Among authors: bautista j. Neurologia. 1999 Apr;14(4):193-5. Neurologia. 1999. PMID: 10363496 Spanish. No abstract available.

10

[The bent spine syndrome: a focal axial myopathy of late onset].

Redondo L, Polo MA, Rodríguez F, Aguirre J, Sánchez A, Chinchón I, Bautista J. Redondo L, et al. Among authors: bautista j. Neurologia. 1999 Oct;14(8):408-11. Neurologia. 1999. PMID: 10609465 Spanish.

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