Y. Campos

发表

Molecular heterogeneity of myophosphorylase deficiency (Mcardle's disease): A genotype‐phenotype correlation study

R. Fletterick, J. Arenas, Miguel Ángel Martín, 2001, Annals of neurology.

Cerebrospinal fluid carnitine levels in patients with Alzheimer's disease

J. Benito-León, F. Jiménez-Jiménez, M. Ortı́-Pareja, 1998, Journal of the Neurological Sciences.

Letters to the editor: Letters to the Editor

N. Chu, Chin‐Chang Huang, J. Slopis, 1991 .

Plasma carnitine insufficiency and effectiveness of L‐carnitine therapy in patients with mitochondril myopathy

J. Arenas, Y. Campos, G. Lorenzo, 1993, Muscle & nerve.

Lipomatosis, proximal myopathy, and the mitochondrial 8344 mutation. A lipid storage myopathy?

J. Arenas, I. Aguilera, J. Bautista, 2000, Muscle & nerve.

Two homozygous mutations (R193W and 794/795 delAA) in the myophosphorylase gene in a patient with McArdle's disease

J. Arenas, Miguel Ángel Martín, J. Vílchez, 2000, Human mutation.

A missense mutation W797R in the myophosphorylase gene in a Spanish patient with McArdle's disease

J. Arenas, Miguel Ángel Martín, A. Cabello, 2000, Muscle & nerve.

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

J. Arenas, Miguel Ángel Martín, Y. Campos, 1996, Muscle & nerve.

Mild ocular myopathy associated with a novel mutation in mitochondrial twinkle helicase

J. Carretero, J. Arenas, Miguel Ángel Martín, 2007, Neuromuscular Disorders.

Molecular analysis in spanish patients with muscle carnitine palmitoyltransferase deficiency

J. Arenas, Miguel Ángel Martín, P. del Hoyo, 1999, Muscle & nerve.

Leber's Congenital Amaurosis Associated With Mitochondrial Dysfunction

J. Arenas, Y. Campos, Manuel Castro-Gago, 1996, Journal of child neurology.

Molecular analysis of Spanish patients with AMP deaminase deficiency

J. Arenas, Miguel Ángel Martín, C. Navarro, 2000, Muscle & nerve.

Coenzyme Q 10 Improves Lactic Acidosis, Strokelike Episodes, and Epilepsy in a Patient With MELAS (Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Strokelike episodes)

A. M. Salio, A. Cabello, A. Berbel-Garcia, 2004, Clinical neuropharmacology.

Complex I Defect in muscle from patients with Huntington's disease

J. Arenas, Miguel Ángel Martín, A. Cabello, 1998, Annals of neurology.

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

B. Bornstein, J. Arenas, Miguel Ángel Martín, 2001, Annals of neurology.

Congenital Hydranencephalic-Hydrocephalic Syndrome Associated With Mitochondrial Dysfunction

M. Castro‐Gago, J. Arenas, A. Alonso, 1999, Journal of child neurology.

Cerebrospinal fluid carnitine levels in patients with Parkinson's disease

J. Benito-León, F. Jiménez-Jiménez, M. Ortı́-Pareja, 1997, Journal of the Neurological Sciences.

Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria.

A. Ribes, J. Arenas, B. Garavaglia, 1997, Pediatric neurology.

Effects of L-carnitine on erythrocyte acyl-CoA, free CoA, and glycerophospholipid acyltransferase in uremia.

B. Bornstein, Y. Campos, R. Pérez-García, 1998, The American journal of clinical nutrition.

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

J. Terradas, J. Arenas, Y. Campos, 1997, Neurology.

Biological roles of L-carnitine in perinatal metabolism.

J. Arenas, Y. Campos, M. Martín, 1998, Early human development.

Molecular heterogeneity of myophosphorylase deficiency (Mcardle's disease): A genotype‐phenotype correlation study

R. Fletterick, J. Arenas, Miguel Ángel Martín, 2001, Annals of neurology.

Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome.

J. Arenas, Y. Campos, A. Cabello, 1995, Pediatric neurology.

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

J. Gómez-Reino, J. Arenas, M. R. Gonzalez-Crespo, 1996, Arthritis and rheumatism.

Mutation analysis in 16 patients with mtDNA depletion

E. Bertini, R. Carrozzo, N. Petit, 2003, Human mutation.

Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIE

J. Arenas, A. Andreu, R. Garesse, 2005, Neuromuscular Disorders.

Respiratory chain enzyme defects in patients with idiopathic inflammatory myopathy.

J. Gómez-Reino, J. Arenas, Y. Campos, 1995, Annals of the rheumatic diseases.