Perfil agustiniano de Santo Tomas de Villanueva in Santo Tomas de Villanueva. V centenario de su nacimiento (1486-1986)CAMPOS Y FERNANDEZ, J.Revista agustiniana (Madrid). 1987, Vol 28, Num 86-87, pp 527-542, issn 0211-612XArticle

Vision de Santo Tomas de Villanueva en la pintura de Murillo in Santo Tomas de Villanueva. V centenario de su nacimiento (1486-1986)CAMPOS Y FERNANDEZ, J.Revista agustiniana (Madrid). 1987, Vol 28, Num 86-87, pp 587-612, issn 0211-612XArticle

Exequias en honor de Felipe III celebradas en Lima en 1621 = Funerals in honour of Philipp III celebrated in Lima in 1621 = Obsèques célébrées à Lima en 1621 en l'honneur de Philippe IIICAMPOS Y FERNANDEZ DE SEVILLA, Javier.Hispania sacra. 2001, Vol 53, Num 107, pp 327-344, issn 0018-215XConference Paper

Una Hermandad religiosa en la Ilustracion espanola : La Congregacion de Santo Tomas de Villanueva, de MadridCAMPOS Y FERNANDEZ DE SEVILLA, J.Revista agustiniana (Madrid). 1987, Vol 28, Num 85, pp 167-243, issn 0211-612XArticle

Dos historiadores jeronimos del siglo XVIII : los padres Francisco Salgado y Juan NunezCAMPOS Y FERNANDEZ DE SEVILLA, F.-J.Ciudad de Dios (1936). 1988, Vol 201, Num 1, pp 5-34, issn 0009-7756Article

La Orden de San Jeronimo en Hispanoamerica : Analisis politico, religioso y socioeconomico de unas experienciasCAMPOS Y FERNANDEZ DE SEVILLA, F. J.Studia monastica. 1988, Vol 30, Num 2, pp 305-338, issn 0039-3258Article

Bibliografia sobre Santo Tomas de VillanuevaCAMPOS Y FERNANDEZ DE SEVILLA, F.-J.Ciudad de Dios (1936). 1986, Vol 199, Num 3, pp 513-542, issn 0009-7756Article

Leishmania sp. : Growth and survival are impaired by ion channel blockersPONTE-SUCRE, A; CAMPOS, Y; FERNANDEZ, M et al.Experimental parasitology. 1998, Vol 88, Num 1, pp 11-19, issn 0014-4894Article

Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndromeCAMPOS, Y; GARCIA-SILVA, T; BARRIONUEVO, C. R et al.Pediatric neurology. 1995, Vol 13, Num 1, pp 69-72, issn 0887-8994Article

ETUDE PAR SPECTROELECTROCHIMIE DE LA REACTIVITE DES RADICAUX CATIONS. UN EXEMPLE D'ADDITION NUCLEOPHILE: L'ANISYLATION DE LA PHENOXATHIINE.GENIES M; CAMPOS Y SANSANO P.1977; J. ELECTROANAL. CHEM. INTERFACIAL ELECTROCHEM.; NETHERL.; DA. 1977; VOL. 85; NO 2; PP. 351-359; ABS. ANGL.; BIBL. 11 REF.Article

Mitochondrial disease and strokeMARTINEZ-FERNANDEZ, E; GIL-PERALTA, A; GARCIA-LOZANO, R et al.Stroke (1970). 2001, Vol 32, Num 11, pp 2507-2510, issn 0039-2499Article

Slow segregation and rapid shift to homoplasmy coexist in a family with the T8993 > G mutationMARTIN, M. A; CAMPOS, Y; GARCIA-SILVA, M. T et al.Journal of inherited metabolic disease. 1999, Vol 22, Num 8, pp 939-940, issn 0141-8955Article

Cerebrospinal fluid carnitine levels in patients with Alzheimer's diseaseRUBIO, J. C; DE BUSTOS, F; MOLINA, J. A et al.Journal of the neurological sciences. 1998, Vol 155, Num 2, pp 192-195, issn 0022-510XArticle

Congenital ocular motor apraxia associated with myopathy, external hydrocephalus and NADH dehydrogenase deficiencyPUNAL, J. E; RODRIGUEZ, E; PINTOS, E et al.Brain & development (Tokyo. 1979). 1998, Vol 20, Num 3, pp 175-178, issn 0387-7604Article

Effects of L-carnitine on erythrocyte acyl-CoA, free CoA, and glycerophospholipid acyltransferase in uremiaDE LOS REYES, B; NAVARRO, J. A; PEREZ-GARCIA, R et al.The American journal of clinical nutrition. 1998, Vol 67, Num 3, pp 386-390, issn 0002-9165Article

Respiratory chain enzyme activities in lymphocytes from untreated patients with Parkinson diseaseBARROSO, N; CAMPOS, Y; HUERTAS, R et al.Clinical chemistry (Baltimore, Md.). 1993, Vol 39, Num 4, pp 667-669, issn 0009-9147Conference Paper

Lipomatosis, proximal myopathy, and the mitochondrial 8344 mutation. A lipid storage myopathy?MUNOZ-MALAGA, A; BAUTISTA, J; SALAZAR, J. A et al.Muscle & nerve. 2000, Vol 23, Num 4, pp 538-542, issn 0148-639XArticle

Molecular analysis of Spanish patients with AMP deaminase deficiencyRUBIO, J. C; MARTIN, M. A; DEL HOYO, P et al.Muscle & nerve. 2000, Vol 23, Num 8, pp 1175-1178, issn 0148-639XArticle

Complex I defect in muscle from patients with Huntington's diseaseARENAS, J; CAMPOS, Y; RIBACOBA, R et al.Annals of neurology. 1998, Vol 43, Num 3, pp 397-400, issn 0364-5134Article

Biological roles of L-carnitine in perinatal metabolismARENAS, J; RUBIO, J. C; MARTIN, M. A et al.Early human development. 1998, Vol 53, pp S43-S50, issn 0378-3782, SUPConference Paper

Leigh syndrome associated with the T9176C mutation in the ATPase 6 gene of mitochondrial DNACAMPOS, Y; MARTIN, M. A; RUBIO, J. C et al.Neurology. 1997, Vol 49, Num 2, pp 595-597, issn 0028-3878Article

Clinical variability associated with the mutation at nucleotide position 8344 of the mitochondrial DNACAMPOS, Y; MARTIN, M. A; VAAMONDE, J et al.Journal of inherited metabolic disease. 1996, Vol 19, Num 2, pp 119-122, issn 0141-8955Article

Clinical heterogeneity in two pedigrees with the 3243 bp tRNA^LEU(UUR) mutation of mitochondrial DNACAMPOS, Y; BAUTISTA, J; GUTIERREZ-RIVAS, E et al.Acta neurologica scandinavica. 1995, Vol 91, Num 1, pp 62-65, issn 0001-6314Article

Respiratory chain enzymes in muscle of endurance athletes : effect of L-carnitineHUERTAS, R; CAMPOS, Y; DIAZ, E et al.Biochemical and biophysical research communications (Print). 1992, Vol 188, Num 1, pp 102-107, issn 0006-291XArticle

Intestinal pseudo-obstruction and urinary retention: cardinal features of a mitochondrial DNA-related diseaseGARCIA-VELASCO, A; GOMEZ-ESCALONILLA, C; GUERRA-VALES, J. M et al.Journal of internal medicine. 2003, Vol 253, Num 3, pp 381-385, issn 0954-6820, 5 p.Article