INVESTIGACIÓN

1991

Artículos

Alberquilla Menéndez-Asenjo A, Ugalde Diez M, Pérez Arévalo JM, Rivera Guzmán JM. El libro de registro de enfermos. Un instrumento útil como fuente de información sanitaria? Rev Sanid Hig Publica (Madr). 1991 Mar-Apr;65(2):147-54 [PubMed]

Arenas J, Ricoy JR, Encinas AR, Pola P, D’Iddio S, Zeviani M, et al. Carnitine in muscle, serum, and urine of nonprofessional athletes: effects of physical exercise, training, and L-carnitine administration. Muscle Nerve. 1991;14(7):598-604

Fernández B, Balsinde J. Receptor-mediated activation of arachidonic acid release in mouse peritoneal macrophages is linked to extracellular calcium influx. Biochem Biophys Res Commun. 1991;180(2):1036-40

Landa García I, Arias Díaz J, Gómez Gutiérrez M, Ortega Medina L, Llanos K, Martos A, et al. -Efecto de la somatostatina sobre la supervivencia y los niveles de PGE:2) en un modelo de pancreatitis aguda necrohemorragica en el perro. Gastroenterol Hepatol. 1991;14(9):481-7

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1992

Artículos

Arenas J, Huertas RA, Campos Y, Cabello A, Gutiérrez E, Bautista J, et al. Oculopharyngeal muscular dystrophy and mitochondrial abnormalities. Muscle Nerve. 1992 Sep;15(9):1055-6 [PubMed]

Balsinde J, Fernández B, Solís Herruzo JA, Diez E. Pathways for arachidonic acid mobilization in zymosan-stimulated mouse peritoneal macrophages. Biochim Biophys Acta. 1992;1136(1):75-82.

Fernández B, Solís Herruzo JA, Balsinde J. Mouse peritoneal macrophages contain an acylating system specific for twenty-carbon polyunsaturated fatty acids. A study with intact cells. Eicosanoids. 1992;5(2):115-20 [PubMed]

Huertas R, Campos Y, Díaz E, Esteban J, Vechietti L, Montanari G, et al. Respiratory chain enzymes in muscle of endurance athletes: effect of L-carnitine. Biochem Biophys Res Commun. 1992;188(1):102-7.

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1993

Artículos

Alcamí J, Paya CV, Virelizier JL, Michelson S. Antagonistic modulation of human cytomegalovirus replication by transforming growth factor beta and basic fibroblastic growth factor. J Gen Virol. 1993 Feb;74 ( Pt 2):269-74 [PubMed]

Balsinde J. Mechanism of arachidonic acid liberation in ethanol-treated mouse peritoneal macrophages. Biochim Biophys Acta. 1993 21;1169(1):54-8.

Campos Y, Huertas R, Bautista J, Gutiérrez E, Aparicio M, Lorenzo G, et al. Muscle carnitine deficiency and lipid storage myopathy in patients with mitochondrial myopathy. Muscle Nerve. 1993;16(7):778-81.

Campos Y, Huertas R, Lorenzo G, Bautista J, Gutiérrez E, Aparicio M, et al. Plasma carnitine insufficiency and effectiveness of L-carnitine therapy in patients with mitochondrial myopathy. Muscle Nerve. 1993;16(2):150-3.

Fernández B, Balsinde J. Calcium- and G-protein-dependent activation of arachidonic acid release by concanavalin-A-stimulated mouse macrophages. Biochim Biophys Acta. 1993;1176(1-2):169-74

Muñoz JJ, Roca C, Santos JL, Arroyo M, Enríquez de Salamanca R. Effect of zinc or S-adenosyl-l-methionine on long term administration of low doses of lead to rats. Pharmacol Toxicol. 1993 Oct;73(4):189-91 [PubMed]

Solís Herruzo JA, Fernández B, Vilalta Castell E, Muñoz Yagüe MT, Hernández Muñoz I, De la Torre Merino MP, et al. Diminished cytochrome b content and toxic oxygen metabolite production in circulating neutrophils from patients with Crohn’s disease. Dig Dis Sci. 1993 Sep;38(9):1631-7 [PubMed]

Trueba JL, Gutiérrez Rivas E, Arenas J, Cabello A. Miopatías mitocondriales. An Med Interna. 1993;10 Suppl:21-7 [PubMed]

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1994

Artículos

Arenas J, Huertas R, Campos Y, Díaz AE, Villalón JM, Vilas E. Effects of L-carnitine on the pyruvate dehydrogenase complex and carnitine palmitoyl transferase activities in muscle of endurance athletes. FEBS Lett. 1994;341(1):91-3

Arpa J, Campos Y, Gutiérrez-Molina M, Cruz Martínez A, Arenas J, Caminero AB, et al. Benign mitochondrial myopathy with decreased succinate cytochrome C reductase activity. Acta Neurol Scand. 1994 Oct;90(4):281-4 [PubMed]

Balsinde J, Fernández B, Solís Herruzo JA. Increased incorporation of arachidonic acid into phospholipids in zymosan-stimulated mouse peritoneal macrophages. Eur J Biochem. 1994;221(3):1013-8.

Balsinde J, Fernández B, Solís Herruzo JA. Ethanol inhibits zymosan-stimulated eicosanoid production in mouse peritoneal macrophages. Biochim Biophys Acta. 1994;1210(2):195-201

Campos Y, Arenas J. Muscle carnitine deficiency associated with zidovudine-induced mitochondrial myopathy. Ann Neurol. 1994 Oct;36(4):680-1 [PubMed]

Campos Y, Arenas J. Muscle carnitine deficiency associated with zidovudine-induced mitochondrial myopathy. Ann Neurol. 1994 Oct;36(4):680-1 [PubMed]

Campos Y, Bautista J, Gutiérrez Rivas E, Llabrés J, Lorenzo G, Arenas J. Variable clinical expression associated with the mutation 3243 np of mitochondrial DNA. J Inherit Metab Dis. 1994;17(5):634-5

Fernández B, Balboa MA, Solís Herruzo JA, Balsinde J. Phosphatidate-induced arachidonic acid mobilization in mouse peritoneal macrophages. J Biol Chem. 1994;269(43):26711-6

Gómez Reino JJ, Aznar JJ, Pablos JL, Díaz González F, Laffón A. Nontropical pyomyositis in adults. Semin Arthritis Rheum. 1994;23(6):396-405

Hernández Muñoz I, De la Torre MP, Pedraza MA, Sánchez Alcázar JA, Muñoz Yagüe MT, Solís Herruzo JA. Toxic oil stimulates collagen synthesis acting at a pretranslational level in cultured fat-storing cells. Gastroenterology. 1994;106(3):691-701

Peces R, Enríquez de Salamanca R, Fontanellas A, Sánchez A, De la Torre M, Caparrós G, et al. Successful treatment of haemodialysis-related porphyria cutanea tarda with erythropoietin. Nephrol Dial Transplant. 1994;9(4):433-5 [PubMed]

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1995

Artículos

Alcamí J, Laín de Lera T, Folgueira L, Pedraza MA, Jacqué JM, Bachelerie F, et al. Absolute dependence on kappa B responsive elements for initiation and Tat-mediated amplification of HIV transcription in blood CD4 T lymphocytes. EMBO J. 1995 Apr 3;14(7):1552-60 [PubMed]

Arenas J, Campos Y, Martín MA. Genética molecular de las citopatías mitocondriales. Neurologia. 1995 Dec;10 Suppl 1:44-9 [PubMed]

Campos Y, Arenas J, Cabello A, Gómez-Reino JJ. Respiratory chain enzyme defects in patients with idiopathic inflammatory myopathy. Ann Rheum Dis. 1995 Jun;54(6):491-3 [PubMed]

Campos Y, Bautista J, Gutiérrez Rivas E, Chinchón D, Cabello A, Segura D, et al. Clinical heterogeneity in two pedigrees with the 3243 bp tRNA(Leu(UUR)) mutation of mitochondrial DNA. Acta Neurol Scand. 1995;91(1):62-5

Campos Y, García Silva T, Barrionuevo CR, Cabello A, Muley R, Arenas J. Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi’s syndrome. Pediatr Neurol. 1995 Jul;13(1):69-72 [doi]

De La Mata J, Blanco FJ, Gómez-Reino JJ. Survival analysis of disease modifying antirheumatic drugs in Spanish rheumatoid arthritis patients. Ann Rheum Dis. 1995 Nov;54(11):881-5 [PubMed]

González Crespo MR, Blanco FJ, Ramos A, Ciruelo E, Mateo I, López Pino MA, et al. Magnetic resonance imaging of the brain in systemic lupus erythematosus. Br J Rheumatol. 1995 Nov;34(11):1055-60 [PubMed]

González Crespo MR, Gómez-Reino JJ. Invasive aspergillosis in systemic lupus erythematosus. Semin Arthritis Rheum. 1995 Apr;24(5):304-14 [PubMed]

Landa JI, Alvarez Sánchez J, Grau M, Sánchez JA, Balibrea JL. Somatostatin reduces the levels of tumor necrosis factor alpha in a rat model of endotoxemia induced by lipopolysaccharide. Res Exp Med (Berl). 1995;195(5):317-25 [doi]

Pablos JL, Carreira PE, Gómez-Reino JJ. Lack of association between the MHC linked OTF3 gene and systemic lupus erythematosus. Lupus. 1995 Oct;4(5):390-2 [PubMed]

Pablos JL, Carreira PE, Martín Villa JM, Montalvo G, Arnaiz Villena A, Gómez-Reino JJ. Polymorphism of the heat-shock protein gene HSP70-2 in systemic lupus erythematosus. Br J Rheumatol. 1995 Aug;34(8):721-3 [PubMed]

Sánchez Alcázar JA, Hernández I, De la Torre MP, García I, Santiago E, Muñoz-Yagüe MT, et al. Down-regulation of tumor necrosis factor receptors by blockade of mitochondrial respiration. J Biol Chem. 1995 Oct 13;270(41):23944-50 [doi] 

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1996

Artículos

Arenas J, González Crespo MR, Campos Y, Martín MA, Cabello A, Gómez Reino JJ. Abnormal carnitine distribution in the muscles of patients with idiopathic inflammatory myopathy. Arthritis Rheum. 1996;39(11):1869-74.

Campos Y, Martín MA, Lorenzo G, Aparicio M, Cabello A, Arenas J. Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNA. Muscle Nerve. 1996;19(2):187-90.

Campos Y, Martín MA, Navarro C, Gordo P, Arenas J. Single large-scale mitochondrial DNA deletion in a patient with mitochondrial myopathy associated with multiple symmetric lipomatosis. Neurology. 1996;47(4):1012-4.

Campos Y, Martín MA, Rubio JC, Ricard C, Cabello A, Arenas J. Multiple deletions of mitochondrial DNA in muscle from a patient with benign progressive external ophthalmoplegia. J Inherit Metab Dis. 1996;19(3):366-7.

Campos Y, Martín MA, Vaamonde J, Cabello A, Esteban J, Arenas J. Clinical variability associated with the mutation at nucleotide position 8344 of the mitochondrial DNA. J Inherit Metab Dis. 1996;19(2):119-22

Castro Gago M, Pintos Martínez E, Beiras Iglesias A, Maroto S, Campos Y, Arenas J, et al. Leber’s congenital amaurosis associated with mitochondrial dysfunction. J Child Neurol. 1996 Mar;11(2):108-11 [PubMed]

De los Reyes B, Pérez García R, Liras A, Arenas J. Reduced carnitine palmitoyl transferase activity and altered acyl-trafficking in red blood cells from hemodialysis patients. Biochim Biophys Acta. 1996;1315(1):37-9.

Gabriel Sánchez R, Gómez de la Cámara A. Métodos de investigación en cardiología clínica (I): Tipos de diseños básicos. Estudios observacionales en cardiología clínica (I). Rev Esp Cardiol. 1996;49(11):837-51

Gómez PA, Díez Lobato R, Ortega JM, De la Cruz J. Mild head injury: differences in prognosis among patients with a Glasgow Coma Scale score of 13 to 15 and analysis of factors associated with abnormal CT findings. Br J Neurosurg. 1996;10(5):453-60

Gómez de la Cámara A. Cómo y para qué hacer un protocolo. Med Clin (Barc). 1996;107(13):518-9 [PubMed]

Verdú A, Alonso LA, Arenas J. Respiratory chain complex I deficiency in an infant with infantile spasms. J Neurol Neurosurg Psychiatry. 1996 Mar;60(3):349 [PubMed]

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1997

Artículos

Arpa J, Campos Y, Gutiérrez Molina M, Martín Casanueva MA, Cruz Martínez A, Pérez Conde MC, et al. Gene dosage effect in one family with myoclonic epilepsy and ragged-red fibers (MERRF). Acta Neurol Scand. 1997 Aug;96(2):65-71 [PubMed]

Cabello López JB, Pozo Rodríguez P. Métodos de investigación en cardiología clínica (X): Estudios de evaluación de las pruebas diagnósticas en cardiología. Rev Esp Cardiol. 1997;50(7):507-19.

Campos Y, Martín MA, Rubio JC, Gutiérrez del Olmo MC, Cabello A, Arenas J. Bilateral striatal necrosis and MELAS associated with a new T3308C mutation in the mitochondrial ND1 gene. Biochem Biophys Res Commun. 1997;238(2):323-5

Campos Y, Martín MA, Rubio JC, Solana LG, García Benayas C, Terradas JL, et al. Leigh syndrome associated with the T9176C mutation in the ATPase 6 gene of mitochondrial DNA. Neurology. 1997 Aug;49(2):595-7 [PubMed]

De los Reyes B, Pérez Garcia R, Liras A, Valderrabano F, Arenas J. L-carnitine normalizes the reduced carnitine palmitoyl transferase activity in red cells from haemodialysis patients. Nephrol Dial Transplant. 1997 Jun;12(6):1300-1 [PubMed]

Ebeling P, Tuominen JA, Arenas J, Garcia Benayas C, Koivisto VA. The association of acetyl-L-carnitine with glucose and lipid metabolism in human muscle in vivo: the effect of hyperinsulinemia. Metabolism. 1997 Dec;46(12):1454-7 [PubMed]

Fernández I, Castellano G, Domingo MJ, Fuertes A, Colina F, Canga F, et al. Influence of viral genotype and level of viremia on the severity of liver injury and the response to interferon therapy inSpanish patients with chronic C infection. Scand J Gastroenterol. 1997;32(1):70-6

Frade JM, Llorente M, Mellado M, Alcamí J, Gutiérrez Ramos JC, Zaballos A, et al. The amino-terminal domain of the CCR2 chemokine receptor acts as coreceptor for HIV-1 infection. J Clin Invest. 1997 Aug 1;100(3):497-502 [PubMed]

García Pascual J, Urbina Fuentes J. Hipertiroidismo e insuficiencia tricúspide. Rev Esp Cardiol. 1997;50(7):539

Gómez de la Cámara A, Ciruelo Monge E, De la Cruz Bértolo J, Serrano Díaz JM, Pato Cour E, Gómez-Reino Carnota JJ. Pérdida de fiabilidad en la extracción de datos de las historias clínicas: origen de los defectos y utilidad del adiestramiento. Med Clin (Barc). 1997;108(10):377-81 [PubMed]

Gómez de la Cámara A, Cruz Martos E, De la Cruz Bértolo J, Landa Goñi J, Guillomía Contreras S, Aurrecoechea R. Análisis de la fiabilidad de tres dosímetros portátiles de glucemia. Comparación de diferentes métodos para el estudio de la fiabilidad de las observaciones clínicas. Med Clin (Barc). 1997;108(11):410-3

González CI, Thomas MC, Martín F, Alcami J, Alonso C, López MC. Reverse transcriptase-like activity in Trypanosoma cruzi. Acta Trop. 1997 Feb;63(2-3):117-26 [PubMed]

Hernández Muñoz I, De la Torre P, Sánchez Alcázar JA, García I, Santiago E, Muñoz Yagüe MT, et al. Tumor necrosis factor alpha inhibits collagen alpha 1(I) gene expression in rat hepatic stellate cells through a G protein. Gastroenterology. 1997;113(2):625-40

Pablos JL, Carreira PE, Serrano L, Del Castillo P, Gómez Reino JJ. Apoptosis and proliferation of fibroblasts during postnatal skin development and scleroderma in the tight-skin mouse. J Histochem Cytochem. 1997 May;45(5):711-9 [doi]

Rubio JC, Martín MA, Bautista J, Campos Y, Segura D, Arenas J. Association of genetically proven deficiencies of myophosphorylase and AMP deaminase: a second case of ‘double trouble’. Neuromuscul Disord. 1997;7(6-7):387-9.

Sánchez Alcázar JA, Ruíz Cabello J, Hernández Muñoz I, Pobre PS, De la Torre P, Siles-Rivas E, et al. Tumor necrosis factor-alpha increases ATP content in metabolically inhibited L929 cells preceding cell death. J Biol Chem. 1997;272(48):30167-77.

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1998

Artículos

Arenas J, Campos Y, Ribacoba R, Martín MA, Rubio JC, Ablanedo P, et al. Complex I defect in muscle from patients with Huntington’s disease. Ann Neurol. 1998;43(3):397-400.

Arenas J, Rubio JC, Martín MA, Campos Y. Biological roles of L-carnitine in perinatal metabolism. Early Hum Dev. 1998;53 Suppl:S43-50

Bermejo M, Martín Serrano J, Oberlin E, Pedraza MA, Serrano A, Santiago B, et al. Activation of blood T lymphocytes down-regulates CXCR4 expression and interferes with propagation of X4 HIV strains. Eur J Immunol. 1998;28(10):3192-204

Blanco FJ, Gómez Reino JJ, De la Mata J, Corrales A, Rodríguez Valverde V, Rosas JC, et al. Survival analysis of 306 European Spanish patients with systemic lupus erythematosus. Lupus. 1998;7(3):159-63 [PubMed]

Bornstein B, Huertas R, Ochoa P, Campos Y, Guillén F, Garesse R, et al. Mitochondrial gene expression and respiratory enzyme activities in cardiac diseases. Biochim Biophys Acta. 1998 Feb 27;1406(1):85-90 [PubMed]

Calandre L, Grau M, Álvarez J, Rabasa M, Ruiz J, Hernández Lain A. Early complete recanalization in internal carotid artery embolism treated with high-dose t-PA: a sequential angiographic study in a novel model of embolism in rats. J Neurol Sci. 1998;157(1):19-24

Calandre L, Grau M, Cabello A. Lysis rates with rt-PA vary between different human emboli in a rat model of cerebral embolism. Fibrinolysis Proteolysis. 1998;12(2):107-11

Campos Y, Martín MA, García Silva T, Del Hoyo P, Rubio JC, Castro Gago M, et al. Clinical heterogeneity associated with mitochondrial DNA depletion in muscle. Neuromuscul Disord. 1998;8(8):568-73 [PubMed]

Caruz A, Samsom M, Alonso JM, Alcami J, Baleux F, Virelizier JL, et al. Genomic organization and promoter characterization of human CXCR4 gene. FEBS Lett. 1998 Apr 17;426(2):271-8 [PubMed]

De los Reyes B, Navarro JA, Pérez García R, Liras A, Campos Y, Bornstein B, et al. Effects of L-carnitine on erythrocyte acyl-CoA, free CoA, and glycerophospholipid acyltransferase in uremia. Am J Clin Nutr. 1998;67(3):386-90

González Crespo MR, Navarro JA, Arenas J, Martín Mola E, De la Cruz J, Gómez-Reino JJ. Prospective study of serum and urinary nitrate levels in patients with systemic lupus erythematosus. Br J Rheumatol. 1998 Sep;37(9):972-7 [PubMed]

Íñiguez MA, Pablos JL, Carreira PE, Cabré F, Gómez Reino JJ. Detection of COX-1 and COX-2 isoforms in synovial fluid cells from inflammatory joint diseases. Br J Rheumatol. 1998;37(7):773-8.

Martín MA, Campos Y, De Bustos F, Del Hoyo P, Rubio JC, Arenas J. Genética molecular de las alteraciones de la cadena respiratoria mitocondrial. Rev Neurol. 1998;26 Suppl 1:S27-35.

Martín Serrano J, Folgueira L, Laín de Lera T, Pedraza MA, Lemichez E, Sánchez Palomino S, et al. In vitro selective elimination of HIV-infected cells from peripheral blood in AIDS patients by the immunotoxin DAB389CD4. AIDS. 1998;12(8):859-63.

Moreira Andrés MN, Cañizo FJ, De la Cruz FJ, Gómez de la Cámara A, Hawkins FG. Bone mineral status in prepubertal children with constitutional delay of growth and puberty. Eur J Endocrinol. 1998;139(3):271-5

Ortiz de Frutos FJ, Guerra Tapia A, Gómez de la Cámara A, De la Cruz Bertolo J, Álvarez Fernández JG, De la Mano Orejón D. Validación de la versión española del cuestionario diagnóstico del Grupo de Trabajo sobre la Dermatitis Atópica del Reino Unido. Rev Clin Esp. 1998;198(7):424-8

Pablos J, Gómez-Reino J. Defective phagocytosis in systemic lupus erythematosus. Eur J Clin Investig. 1998 Oct;28(10):864-5

Puñal JE, Rodríguez E, Pintos E, Campos Y, Castro Gago M. Congenital ocular motor apraxia associated with myopathy, external hydrocephalus and NADH dehydrogenase deficiency. Brain Dev. 1998 Apr;20(3):175-8 [PubMed]. Erratum in: Brain Dev 1998 Oct;20(7):547

Quiñones Mateu ME, Mas A, Laín de Lera T, Soriano V, Alcamí J, Lederman MM, et al. LTR and tat variability of HIV-1 isolates from patients with divergent rates of disease progression. Virus Res. 1998 Sep;57(1):11-20 [PubMed]

Ricoy JR, Encinas AR, Cabello A, Madero S, Arenas J. Histochemical study of the vastus lateralis muscle fibre types of athletes. J Physiol Biochem. 1998 Mar;54(1):41-7 [PubMed]

Rubio JC, Martín MA, Bautista J, Campos Y, Segura D, Cabello A, et al. Myophosphorylase deficiency associated with a defect in complex I of the mitochondrial respiratory chain. J Neurol Sci. 1998;161(2):110-3.

Rubio JC, Martín MA, Del Hoyo P, De Bustos F, Campos Y, Arenas J. Déficits de los complejos enzimáticos de la cadena respiratoria mitocondrial. Rev Neurol. 1998;26 Suppl 1:S15-20.

Ruiz Pesini E, Díez C, Lapeña AC, Pérez Martos A, Montoya J, Álvarez E, et al. Correlation of sperm motility with mitocondrial enzymatic activities. Clin Chem. 1998;44(8 Pt 1):1616-20.

Solís Herruzo JA, Hernández I, De la Torre P, García I, Sánchez JA, Fernández I, et al. G proteins are involved in the suppression of collagen alpha 1 (I) gene expression in cultured rat hepatic stellate cells. Cell Signal. 1998;10(3):173-83

Valdezate S, Mesa F, Otero JR. Meningitis por enterovirus en un hospital pediátrico: experiencia en 1996. Enferm Infecc Microbiol Clin. 1998 Mar;16(3):135-7 [PubMed]

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1999

Artículos

Arenas J, Campos Y, Bornstein B, Ribacoba R, Martín MA, Rubio JC, Santorelli FM, Zeviani M, DiMauro S, Garesse R. A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibers. Neurology. 1999;52(2):377-82

Ayerbe J, Díez Lobato R, De la Cruz J, Alday R, Rivas JJ, Gómez PA, Cabrera A. Risk factors predicting recurrence in patients operated on for intracranial meningioma. A multivariate analysis. Acta Neurochir (Wien). 1999;141(9):921-32

Castro Gago M, Alonso A, Pintos Martínez E, Beiras Iglesias A, Campos Y, Arenas J, et al. Congenital hydranencephalic-hydrocephalic syndrome associated with mitochondrial dysfunction. J Child Neurol. 1999 Feb;14(2):131-5 [PubMed]

Castro Gago M, González Conde V, Fernández Seara MJ, Rodrigo Sáez E, Fernández Cebrián S, Alonso Martín A, et al. Encefalomiopatía mitocondrial precoz por deficiencia aislada del complejo IV compatible con el síndrome de Alpers-Huttenlocher: a propósito de dos observaciones. Rev Neurol. 1999 Nov 16-30;29(10):912-7 [PubMed]

De la Cruz Bértolo FJ, Pallás Alonso CR, Tejada Palacios P. Cribado para la retinopatía de la prematuridad: ni son todos los que están, ni están todos los que son. An Esp Pediatr. 1999;50(2):156-60

Fernández Miranda C, Aranda JL, Gómez González P, Díaz Rubio P, Estenoz J, Gómez de la Cámara A. La hiperhomocisteinemia es frecuente en pacientes con enfermedad coronaria. Estudio de 202 enfermos. Med Clin (Barc). 1999;113(11):407-10

Gil J, Alcamí J, Esteban M. Induction of apoptosis by double-stranded-RNA-dependent protein kinase (PKR) involves the alpha subunit of eukaryotic translation initiation factor 2 and NF-kappaB. Mol Cell Biol. 1999 Jul;19(7):4653-63 [PubMed]

Gómez de la Cámara A. Tipos de estudios de investigación clínica: errores más importantes en su diseño e interpretación. Arch Bronconeumol. 1999;35 Suppl 1:9-13

Gómez PA, Díez Lobato R, González P, Boto GR, De la Lama A, De la Cruz FJ.  Trauma craneal grave. Base datos Hospital 12 de Octubre. I descripción base datos. Evolución final. Neurocirugía. 1999;10(4):297-308

Laín de Lera T, Folgueira L, Martín AG, Dargemont C, Pedraza MA, Bermejo M, Bonay P, Fresno M, Alcami J. Expression of IkappaBalpha in the nucleus of human peripheral blood T lymphocytes. Oncogene. 1999;18(8):1581-8

Lassaletta L, Brandáriz JA, Benito A, De la Cruz J, Gómez C, Ballestín C, et al. p53 expression in locally advanced pharyngeal squamous cell carcinoma. Arch Otolaryngol Head Neck Surg. 1999 Dec;125(12):1356-9 [PubMed]

Martín MA, Campos Y, García Silva MT, Rubio JC, Del Hoyo P, De Bustos F, García A, Arenas J. Slow segregation and rapid shift to homoplasmy coexist in a family with the T8993 > G mutation. J Inherit Metab Dis. 1999;22(8):939-40

Martín MA, Rubio JC, De Bustos F, Del Hoyo P, Campos Y, García A, Börnstein B, Cabello A, Arenas J. Molecular analysis in Spanish patients with muscle carnitine palmitoyltransferase deficiency. Muscle Nerve. 1999;22(7):941-3

Mas A, Español T, Heredia A, Pedraza MA, Hernández M, Caragol I, et al. CCR5 genotype and HIV-1 infection in perinatally-exposed infants. J Infect. 1999 Jan;38(1):9-11 [PubMed]

Molina Arjona JA, De Bustos F, Benito León J, Jiménez Jiménez FJ, Rodríguez J, Trincado R, et al. Plasma prooxidant and antioxidant factors and risk of Parkinson’s disease: A population study. Rev Neurologia. 1999;29(1):12–5

Morales Gutiérrez C, Vegh I, Colina F, Gómez Cámara A, Ignacio Landa J, Ballesteros D, Carreira PE, Enríquez de Salamanca R. Survival of patients with colorectal carcinoma: possible prognostic value of tissular carbohydrate antigen 19.9 determination. Cancer. 1999;86(9):1675-81

Pablos JL, Amara A, Bouloc A, Santiago B, Caruz A, Galindo M, Delaunay T, Virelizier JL, Arenzana Seisdedos F. Stromal-cell derived factor is expressed by dendritic cells and endothelium in human skin. Am J Pathol. 1999;155(5):1577-86

Pedraza MA, Del Romero J, Roldán F, García S, Ayerbe MC, Noriega AR, Alcamí J. Heterosexual transmission of HIV-1 is associated with high plasma viral load levels and a positive viral isolation in the infected partner. J Acquir Immune Defic Syndr. 1999;21(2):120-5

Rocha H, Flores C, Campos Y, Arenas J, Vilarinho L, Santorelli FM, et al. About the «Pathological» role of the mtDNA T3308C mutationellipsis. Am J Hum Genet. 1999 Nov;65(5):1457-9 [PubMed]

Rubio JC, Martín MA, García A, Campos Y, Cabello A, Culebras JM, Arenas J. McArdle’s disease associated with homozygosity for the missense mutation Gly204Ser of the myophosphorylase gene in a Spanish patient. Neuromuscul Disord. 1999;9(3):174-5

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2000

Artículos

Agace WW, Amara A, Roberts AI, Pablos JL, Thelen S, Uguccioni M, et al. Constitutive expression of stromal derived factor-1 by mucosal epithelia and its role in HIV transmission and propagation. Curr Biol. 2000;10(6):325-8 [doi]

Ballesteros Pomar MD, Rubio Herrera MA, Gutiérrez Fuentes JA, Gómez Gerique JA, Gómez de la Cámara A, Pascual O, et al. Dietary habits and cardiovascular risk in the Spanish population: the DRECE study (I). Diet and Cardiovascular Events Risk in Spain. Ann Nutr Metab. 2000;44(3):108-14 [doi] 

Ballesteros Pomar MD, Rubio Herrera MA, Gutiérrez Fuentes JA, Gómez Gerique JA, Gómez de la Cámara A, Pascual O, et al. Dietary habits and cardiovascular risk in the Spanish population: The DRECE study (II) micronutrient intake. Ann Nutr Metab. 2000 Aug;44(4):177–82

Campos Y, Lorenzo G, Martín MA, Torregrosa A, Del Hoyo P, Rubio JC, García A, Arenas J. A mitochondrial tRNA(Lys) gene mutation (T8316C) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes. Neuromuscul Disord. 2000;10(7):493-6 [doi]

Campos Y, Martín MA, Caballero C, Rubio JC, De la Cruz F, Tuñón T, Arenas J. Single large-scale mitochondrial DNA deletion in a patient with encephalopathy, cardiomyopathy, and prominent intestinal pseudo-obstruction. Neuromuscul Disord. 2000;10(1):56-8

Castro Gago M, Eiris J, Pintos E, Blanco Barca O, Campos Y, Arenas J. Benign congenital myopathy associated with partial deficiency of complexes I and III of respiratory chain. Rev Neurologia. 2000;31(9):838–41

Castro Gago M, Novo Rodríguez MI, Pintos Martínez E, Campos Y, Arenas J, Eirís-Puñal J. Encefalomiopatías mitocondriales. Rev Neurol. 2000 Aug 1-15;31(3):263-82 [PubMed]

Del Palacio A, Sanz F, Sánchez Alor G, Garau M, Calvo MT, Boncompte E, Algueró M, Pontes C, Gómez de la Cámara A. Double-blind randomized dose-finding study in acute vulvovaginal candidosis. Comparison of flutrimazole site-release cream (1, 2 and 4%) with placebo site-release vaginal cream. Mycoses. 2000;43(9-10):355-65

Fernández Moreno MA, Bornstein B, Campos Y, Arenas J, Garesse R. The pathogenic role of point mutations affecting the translational initiation codon of mitochondrial genes. Mol Genet Metab. 2000 Jul;70(3):238–40

Fontanellas A, Mazurier F, Landry M, Taine L, Morel C, Larou M, et al. Reversion of hepatobiliary alterations By bone marrow transplantation in a murine model of erythropoietic protoporphyria. Hepatology. 2000;32(1):73-81 [doi]

Gil J, Alcamí J, Esteban M. Activation of NF-kappa B by the dsRNA-dependent protein kinase, PKR involves the I kappa B kinase complex. Oncogene. 2000;19(11):1369-78 [doi] 

Gómez de la Cámara A, Navarro Gil P, Grandes Velasco S, Ortega Fraile MA, Jurado Valenzuela C, Gómez Medina MA. Intervenciones médicas no farmacológicas basadas en la evidencia. Estudio exploratorio. Med Clin (Barc). 2000;114 Suppl 2:85-7

Gómez de la Cámara A, Nemery B. Epidemias, histeria colectiva y desinformación. Rev Med Fam Comunitaria. 2000;10(6):331-3

Gutiérrez Fuentes JA, Gómez Jerique J, Gómez de la Cámara A, Rubio MA, García Hernández A, Arístegui I; Diet and Cardiovascular Risk in Spain Study (DRECE II). Dieta y riesgo cardiovascular en España (DRECE II). Descripción de la evolución del perfil cardiovascular. Med Clin (Barc). 2000;115(19):726-9 [PubMed]

Haynes RB, Sánchez RG, Jadad AR, Browman GP, De la Cámara AG. Tools for the practice of evidence based medicine (I). Update in evidence based information resources for clinical practice. Med Clin (Barc). 2000 Sep 9;115(7):258–60

Hernández I, De la Torre P, Rey Campos J, García I, Sánchez JA, Muñoz R, Rippe RA, Muñoz Yagüe T, Solís Herruzo JA. Collagen alpha1(I) gene contains an element responsive to tumor necrosis factor-alpha located in the 5′ untranslated region of its first exon. DNA Cell Biol. 2000;19(6):341-52.

Lagartera L, Fontanellas A, Muñoz Ribero MC, Navarro S, Enríquez de Salamanca R. Aproximación de laboratorio al diagnóstico y tipificación de una porfiria. An Med Interna. 2000;17(11):609-13

López Valdés E, Hernández Laín A, Calandre L, Grau M, Cabello A, Gómez Escalonilla C. Time window for clinical effectiveness of mass evacuation in a rat balloon model mimicking an intraparenchymatous hematoma. J Neurol Sci. 2000;174(1):40-6 [doi] 

Martín MA, Gómez MA, Guillén F, Börnstein B, Campos Y, Rubio JC, De la Calzada CS, Arenas J. Myocardial carnitine and carnitine palmitoyltransferase deficiencies in patients with severe heart failure. Biochim Biophys Acta. 2000;1502(3):330-6.

Martín MA, Rubio JC, Campos Y, Ricoy JR, Cabello A, Arenas J. A homozygous missense mutation (A659D) in the myophosphorylase gene in a Spanish patient with McArdle’s disease. Neuromuscul Disord. 2000;10(6):447-9.

Martín MA, Rubio JC, Campos Y, Vílchez J, Cabello A, Arenas J. Two homozygous mutations (R193W and 794/795 delAA) in the myophosphorylase gene in a patient with McArdle’s disease. Hum Mutat. 2000;15(3):294.

Martín MA, Rubio JC, Del Hoyo P, García A, Bustos F, Campos Y, Cabello A, Culebras JM, Arenas J. Identification of novel mutations in Spanish patients with muscle carnitine palmitoyltransferase II deficiency. Hum Mutat. 2000;15(6):579-80

Moreira Andrés MN, Cañizo FJ, De la Cruz FJ, Gómez de la Cámara A, Hawkins FG. Evaluation of radial bone mineral content in prepubertal children with constitutional delay of growth. J Pediatr Endocrinol Metab. 2000;13(6):591-7

Muñoz DG, Ganapathy GR, Eliasziw M, Hachinski V. Educational attainment and socioeconomic status of patients with autopsy-confirmed Alzheimer disease. Arch Neurol. 2000;57(1):85-9 [doi] 

Rodríguez J, Fernández Crespo J, Lopez Rubio A, De La Cruz Bértolo J, Ferrando Vivas P, Vives R, et al. Clinical cross-reactivity among foods of the Rosaceae family. J Allergy Clin Immunol. 2000;106(1 Pt 1):183-9 [doi]

Rubio JC, Martín MA, Campos Y, Auciello R, Cabello A, Arenas J. A missense mutation W797R in the myophosphorylase gene in a Spanish patient with McArdle’s disease. Muscle Nerve. 2000;23(1):129-31

Rubio JC, Martín MA, Campos Y, Cabello A, Arenas J. A missense mutation T487N in the myophosphorylase gene in a Spanish patient with McArdle’s disease. Neuromuscul Disord. 2000;10(2):138-40

Rubio JC, Martín MA, Del Hoyo P, Bautista J, Campos Y, Segura D, et al. Molecular analysis of Spanish patients with AMP deaminase deficiency. Muscle Nerve. 2000;23(8):1175-8 [doi] 

Ruiz Solís S, Mingote C, Gozalo A, Fernández Salas MJ, Varela P, Gómez de la Cámara A. Aproximación neurobiológica al trastorno de estrés postraumático. Arch Psiquiatr. 2000;63(3):221-40

Sánchez Alcázar JA, Schneider E, Martínez MA, Carmona P, Hernández Muñoz I, Siles E, De la Torre P, Ruiz Cabello J, García I, Solís Herruzo JA. Tumor necrosis factor-alpha increases the steady-state reduction of cytochrome b of the mitochondrial respiratory chain in metabolically inhibited L929 cells. J Biol Chem. 2000;275(18):13353-61

Woulfe J, Muñoz D. Tubulin immunoreactive neuronal intranuclear inclusions in the human brain. Neuropathol Appl Neurobiol. 2000;26(2):161-71 [doi]