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La ricerca find articoli where authors phrase all words ' Campos, Y' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 73 riferimenti
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    1. Campos, Y; Gamez, J; Garcia, A; Andreu, AL; Rubio, JC; Martin, MA; del Hoyo, P; Navarro, C; Cervera, C; Garesse, R; Arenas, J
      A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathy

      NEUROMUSCULAR DISORDERS
    2. Castro-Gago, M; Pintos-Martinez, E; Forteza-Vila, J; Iglesias-Diz, M; Ucieda-Somoza, R; Silva-Villar, I; Codesido-Lopez, J; Viso-Lorenzo, A; Campos, Y; Arenas, J; Eiris-Punal, J
      Congenital hydranencephalic-hydrocephalic syndrome with proliferative vasculopathy: A possible relation with mitochondrial dysfunction

      JOURNAL OF CHILD NEUROLOGY
    3. Martin, MA; Rubio, JC; Buchbinder, J; Fernandez-Hojas, R; del Hoyo, P; Teijeira, S; Gamez, J; Navarro, C; Fernandez, JM; Cabello, A; Campos, Y; Cervera, C; Culebras, JM; Andreu, AL; Fletterick, R; Arenas, J
      Molecular heterogeneity of myophosphorylase deficiency (McArdle's disease): A genotype-phenotype correlation study

      ANNALS OF NEUROLOGY
    4. Campos, Y; Garcia-Redondo, A; Fernandez-Moreno, MA; Martinez-Pardo, M; Goda, G; Rubio, JC; Martin, MA; del Hoyo, P; Cabello, A; Bornstein, B; Garesse, R; Arenas, J
      Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome c oxidase II gene

      ANNALS OF NEUROLOGY
    5. Campos, Y; Garcia, A; Eiris, J; Fuster, M; Rubio, JC; Martin, MA; del Hoyo, P; Pintos, E; Castro-Gago, M; Arenas, J
      Mitochondrial myopathy, cardiomyopathy and psychiatric illness in a Spanish family harbouring the mtDNA 3303C > T mutation

      JOURNAL OF INHERITED METABOLIC DISEASE
    6. Martinez-Fernandez, E; Gil-Peralta, A; Garcia-Lozano, R; Chinchon, I; Aguilera, I; Fernandez-Lopez, O; Arenas, J; Campos, Y; Bautista, J
      Mitochondrial disease and stroke

      STROKE
    7. de la Pena, P; Bornstein, B; del Hoyo, P; Fernandez-Moreno, MA; Martin, MA; Campos, Y; Gomez-Escalonilla, C; Molina, JA; Cabello, A; Arenas, J; Garesse, R
      Mitochondrial dysfunction associated with a mutation in the Notch3 gene ina CADASIL family

      NEUROLOGY
    8. Aguilera, I; Garcia-Lozano, JR; Munoz, A; Arenas, J; Campos, Y; Chinchon, I; Roldan, AN; Bautista, J
      Mitochondrial DNA point mutation in the COI gene in a patient with McArdle's disease

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    9. Martin, MA; Rubio, JC; Garcia, A; Fernandez, MA; Campos, Y; Krawczak, M; Cooper, DN; Arenas, J
      Resolution of a mispaired secondary structure intermediate could account for a novel micro-insertion/deletion (387 insA/del 8 bp) in the PYGM gene causing McArdle's disease

      CLINICAL GENETICS
    10. Fernandez-Moreno, MA; Bornstein, B; Campos, Y; Arenas, J; Garesse, R
      The pathogenic role of point mutations affecting the translational initiation codon of mitochondrial genes

      MOLECULAR GENETICS AND METABOLISM
    11. Campos-Roca, Y; Verweyen, L; Fernandez-Barciela, M; Sanchez, E; Curras-Francos, MC; Bronner, W; Hulsmann, A; Schlechtweg, M
      An optimized 25.5-76.5 GHz PHEMT-based coplanar frequency tripler

      IEEE MICROWAVE AND GUIDED WAVE LETTERS
    12. Curras-Francos, MC; Tasker, PJ; Fernandez-Barciela, M; Campos-Roca, Y; Sanchez, E
      Direct extraction of nonlinear FET Q-V functions from time domain large signal measurements

      IEEE MICROWAVE AND GUIDED WAVE LETTERS
    13. Campos-Roca, Y; Verweyen, L; Fernandez-Barciela, M; Bischof, W; Curras-Francos, MC; Sanchez, E; Hulsmann, A; Schlechtweg, M
      38/76 GHz PHEMT MMIC balanced frequency doublers in coplanar technology

      IEEE MICROWAVE AND GUIDED WAVE LETTERS
    14. Campos, Y; Lorenzo, G; Martin, MA; Torregrosa, A; del Hoyo, P; Rubio, JC; Garcia, A; Arenas, J
      A mitochondrial tRNA(Lys) gene mutation (T8316C) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes

      NEUROMUSCULAR DISORDERS
    15. Martin, 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

      NEUROMUSCULAR DISORDERS
    16. Rubio, JC; Martin, MA; Campos, Y; Cabello, A; Arenas, J
      A missense mutation T487N in the myophosphorylase gene in a Spanish patient with McArdle's disease

      NEUROMUSCULAR DISORDERS
    17. Campos, Y; Martin, MA; Caballero, C; Rubio, JC; de la Cruz, F; Tunon, T; Arenas, J
      Single large-scale mitochondrial DNA deletion in a patient with encephalopathy, cardiomyopathy, and prominent intestinal pseudo-obstruction

      NEUROMUSCULAR DISORDERS
    18. Martin, MA; Gomez, MA; Guillen, F; Bornstein, B; Campos, Y; Rubio, JC; de la Calzada, CS; Arenas, J
      Myocardial carnitine and carnitine palmitoyltransferase deficiencies in patients with severe heart failure

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    19. Rubio, JC; Martin, MA; Del Hoyo, P; Bautista, J; Campos, Y; Segura, D; Navarro, C; Ricoy, JR; Cabello, A; Arenas, J
      Molecular analysis of Spanish patients with AMP deaminase deficiency

      MUSCLE & NERVE
    20. Munoz-Malaga, A; Bautista, J; Salazar, JA; Aguilera, I; Garcia, R; Chinchon, I; Segura, MD; Campos, Y; Arenas, J
      Lipomatosis, proximal myopathy, and the mitochondrial 8344 mutation. A lipid storage myopathy?

      MUSCLE & NERVE
    21. Rubio, JC; Martin, 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
    22. Fernandez, J; Montemayor, T; Bautista, J; Marquez, R; Jimenez, L; Arenas, J; Campos, Y; Castillo, J
      Role of cardiopulmonary exercise test in patients with mitochondrial myopathies

      MEDICINA CLINICA
    23. Fernandez-Barciela, M; Tasker, PJ; Campos-Roca, Y; Demmler, M; Massler, H; Sanchez, E; Curras-Francos, MC; Schlechtweg, M
      A simplified broad-band large-signal nonquasi-static table-based FET model

      IEEE TRANSACTIONS ON MICROWAVE THEORY AND TECHNIQUES
    24. Campos-Roca, Y; Verweyen, L; Neumann, M; Fernandez-Barciela, M; Curras-Francos, MC; Sanchez-Sanchez, E; Hulsmann, A; Schlechtweg, M
      Coplanar pHEMT MMIC frequency multipliers for 76-GHz automotive radar

      IEEE MICROWAVE AND GUIDED WAVE LETTERS
    25. Rubio, JC; Martin, MA; Garcia, 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

      NEUROMUSCULAR DISORDERS
    26. Castro-Gago, M; Alonso, A; Pintos-Martinez, E; Beiras-Iglesias, A; Campos, Y; Arenas, J; Novo-Rodriguez, MI; Eiris-Punal, J
      Congenital hydranencephalic-hydrocephalic syndrome associated with mitochondrial dysfunction

      JOURNAL OF CHILD NEUROLOGY
    27. Gonzalez-Crespo, MR; Arenas, J; Gomez-Reino, JJ; Campos, Y; Borstein, B; Martin, MA; Cabello, A; Garcia-Ryo, R; Ricoy, JR
      Muscle dysfunction in elderly individuals with hip fracture

      JOURNAL OF RHEUMATOLOGY
    28. Martin, MA; Rubio, JC; De Bustos, F; Del Hoyo, P; Campos, Y; Garcia, A; Bornstein, B; Cabello, A; Arenas, J
      Molecular analysis in Spanish patients with muscle carnitine palmitoyltransferase deficiency

      MUSCLE & NERVE
    29. Martin, MA; Campos, Y; Garcia-Silva, MT; Rubio, JC; Del Hoyo, P; de Bustos, F; Garcia, A; Arenas, J
      Slow segregation and rapid shift to homoplasmy coexist in a family with the T8993 > G mutation

      JOURNAL OF INHERITED METABOLIC DISEASE
    30. Arenas, J; Campos, Y; Bornstein, B; Ribacoba, R; Martin, 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
    31. Curras-Francos, MC; Tasker, PJ; Fernandez-Barciela, M; Campos-Roca, Y; Sanchez, E
      Direct extraction of nonlinear FET C-V functions from time domain large signal measurements

      ELECTRONICS LETTERS
    32. Rocha, H; Flores, C; Campos, Y; Arenas, J; Vilarinho, L; Santorelli, FM; Torroni, A
      About the "pathological" role of the mtDNA T3308C mutation ...

      AMERICAN JOURNAL OF HUMAN GENETICS
    33. Campos, Y; Martin, MA; Garcia-Silva, T; del Hoyo, P; Rubio, JC; Castro-Gago, M; Garcia-Penas, J; Casas, J; Cabello, A; Ricoy, JR; Arenas, J
      Clinical heterogeneity associated with mitochondrial DNA depletion in muscle

      NEUROMUSCULAR DISORDERS
    34. BORNSTEIN B; HUERTAS R; OCHOA P; CAMPOS Y; GUILLEN F; GARESSE R; ARENAS J
      MITOCHONDRIAL GENE-EXPRESSION AND RESPIRATORY ENZYME-ACTIVITIES IN CARDIAC DISEASES

      Biochimica et biophysica acta. Molecular basis of disease
    35. PUNAL JE; RODRIGUEZ E; PINTOS E; CAMPOS Y; CASTROGAGO M
      CONGENITAL OCULAR MOTOR APRAXIA ASSOCIATED WITH MYOPATHY, EXTERNAL HYDROCEPHALUS AND NADH DEHYDROGENASE-DEFICIENCY (VOL 20, PG 175, 1998)

      Brain & development
    36. PUNAL JE; RODRIGUEZ E; PINTOS E; CAMPOS Y; CASTROGAGO M
      CONGENITAL OCULAR MOTOR APRAXIA ASSOCIATED WITH MYOPATHY, EXTERNAL HYDROCEPHALUS AND NADH DEHYDROGENASE-DEFICIENCY

      Brain & development
    37. Arenas, J; Rubio, JC; Martin, MA; Campos, Y
      Biological roles of L-carnitine in perinatal metabolism

      EARLY HUMAN DEVELOPMENT
    38. ARENAS J; CAMPOS Y; RIBACOBA R; MARTIN MA; RUBIO JC; ABLANEDO P; CABELLO A
      COMPLEX-I DEFECT IN MUSCLE FROM PATIENTS WITH HUNTINGTONS-DISEASE

      Annals of neurology
    39. PONTESUCRE A; CAMPOS Y; MENDOZALEON A; MOLL H
      EFFECT OF POTASSIUM CHANNEL BLOCKERS ON THE INTERACTION OF LEISHMANIAPARASITES WITH THE MAMMALIAN HOST-CELLS

      Naunyn-Schmiedeberg's archives of pharmacology
    40. RUBIO JC; DEBUSTOS F; MOLINA JA; JIMENEZJIMENEZ FJ; BENITOLEON J; MARTIN MA; CAMPOS Y; ORTIPAREJA M; CABRERAVALDIVIA F; ARENAS J
      CEREBROSPINAL-FLUID CARNITINE LEVELS IN PATIENTS WITH ALZHEIMERS-DISEASE

      Journal of the neurological sciences
    41. Rubio, JC; Martin, MA; Bautista, J; Campos, Y; Segura, D; Cabello, A; Chinchon, I; Arenas, J
      Myophosphorylase deficiency associated with a defect in complex I of the mitochondrial respiratory chain

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    42. PONTESUCRE A; CAMPOS Y; FERNANDEZ M; MOLL H; MENDOZALEON A
      LEISHMANIA SP - GROWTH AND SURVIVAL ARE IMPAIRED BY ION-CHANNEL BLOCKERS

      Experimental parasitology
    43. DELOSREYES B; NAVARRA JA; PEREZGARCIA R; LIRAS A; CAMPOS Y; BORNSTEIN B; ARENAS J
      EFFECTS OF L-CARNITINE ON ERYTHROCYTE ACYL-COA, FREE COA, AND GLYCEROPHOSPHOLIPID ACYLTRANSFERASE IN UREMIA

      The American journal of clinical nutrition
    44. GROSSMAN GL; CAMPOS Y; SEVERSON DW; JAMES AA
      EVIDENCE FOR 2 DISTINCT MEMBERS OF THE AMYLASE GENE FAMILY IN THE YELLOW-FEVER MOSQUITO, AEDES-AEGYPTI

      Insect biochemistry and molecular biology
    45. RUBIO JC; MARTIN MA; BAUTISTA J; CAMPOS Y; SEGURA D; ARENAS J
      ASSOCIATION OF GENETICALLY PROVEN DEFICIENCIES OF MYOPHOSPHORYLASE AND AMP-DEAMINASE - A 2ND CASE OF DOUBLE TROUBLE

      Neuromuscular disorders
    46. GARCIASILVA MT; RIBES A; CAMPOS Y; GARAVAGLIA B; ARENAS J
      SYNDROME OF ENCEPHALOPATHY, PETECHIAE, AND ETHYLMALONIC ACIDURIA

      Pediatric neurology
    47. MACHADO FJ; LOPEZ CM; GOLDWASSER J; MENDEZ B; CAMPOS Y; ESCALANTE D; TOVAR M
      SPECTROSCOPIC AND CATALYTIC EVIDENCE FOR THE INCORPORATION OF GALLIUMIN THE AEL FRAMEWORK

      Zeolites
    48. PEREZ AL; CAMPOS Y; CHINCHILLA CM; OEHLSCHLAGER AC; GRIES G; GRIES R; GIBLINDAVIS RM; CASTRILLO G; PENA JE; DUNCAN RE; GONZALEZ LM; PIERCE HD; MCDONALD R; ANDRADE R
      AGGREGATION PHEROMONES AND HOST KAIROMONES OF WEST-INDIAN SUGARCANE WEEVIL, METAMASIUS-HEMIPTERUS-SERICEUS

      Journal of chemical ecology
    49. PONTESUCRE A; CAMPOS Y; VAZQUEZ J; MOLL H; MENDOZALEON A
      SENSITIVITY OF LEISHMANIA SPP TO GLIBENCLAMIDE AND 4-AMINOPIRIDINE - A TOOL FOR THE STUDY OF DRUG-RESISTANCE DEVELOPMENT

      Memorias do Instituto Oswaldo Cruz
    50. CAMPOS Y; MARTIN MA; RUBIO JC; SOLANA LG; GARCIABENAYAS C; TERRADAS JL; ARENAS J
      LEIGH-SYNDROME ASSOCIATED WITH THE T9176C MUTATION IN THE ATPASE-6 GENE OF MITOCHONDRIAL-DNA

      Neurology
    51. MOLINA JA; DEBUSTOS F; JIMENEZJIMENEZ FJ; BENITOLEON J; GASALLA T; ORTIPAREJA M; VELA L; BERMEJO F; MARTIN MA; CAMPOS Y; ARENAS J
      RESPIRATORY-CHAIN ENZYME-ACTIVITIES IN ISOLATED-MITOCHONDRIA OF LYMPHOCYTES FROM PATIENTS WITH ALZHEIMERS-DISEASE

      Neurology
    52. JIMENEZJIMENEZ FJ; RUBIO JC; MOLINA JA; MARTIN MA; CAMPOS Y; BENITOLEON J; ORTIPAREJA M; GASALLA T; ARENAS J
      CEREBROSPINAL-FLUID CARNITINE LEVELS IN PATIENTS WITH PARKINSONS-DISEASE

      Journal of the neurological sciences
    53. CAMPOS Y; MARTIN MA; RUBIO JC; DELOLMO MCG; CABELLO A; ARENAS J
      BILATERAL STRIATAL NECROSIS AND MELAS ASSOCIATED WITH A NEW T3308C MUTATION IN THE MITOCHONDRIAL ND1 GENE

      Biochemical and biophysical research communications
    54. GONZALEZCRESPO MR; ARENAS J; CAMPOS Y; MARTINEZ MA; CABELLO A; RICOY JR; GOMEZREINO JJ
      ABNORMAL CARNITINE DISTRIBUTION AND MITOCHONDRIAL DYSFUNCTION IN MUSCLE OF ELDERLY INDIVIDUALS WITH HIP FRACTURE

      Arthritis and rheumatism
    55. ARPA J; CAMPOS Y; GUTIERREZMOLINA M; MARTINCASANUEVA MA; CRUZMARTINEZ A; PEREZCONDE MC; LOPEZPAJARES R; MORALES MC; TATAY J; LACASA T; BARREIRO P; ARENAS J
      GENE DOSAGE EFFECT IN ONE FAMILY WITH MYOCLONIC EPILEPSY AND RAGGED-RED FIBERS (MERRF)

      Acta neurologica Scandinavica
    56. CASTROGAGO M; PINTOSMARTINEZ E; BEIRASIGLESIAS A; MAROTO S; CAMPOS Y; ARENAS J; EIRISPUNAL J
      LEBERS CONGENITAL AMAUROSIS ASSOCIATED WITH MITOCHONDRIAL DYSFUNCTION

      Journal of child neurology
    57. CAMPOS Y; MARTIN 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
    58. CAMPOS Y; MARTIN MA; VAAMONDE J; CABELLO A; ESTEBAN J; ARENAS J
      CLINICAL VARIABILITY ASSOCIATED WITH THE MUTATION AT NUCLEOTIDE POSITION-8344 OF THE MITOCHONDRIAL-DNA

      Journal of inherited metabolic disease
    59. CAMPOS Y; MARTIN MA; NAVARRO C; GORDO P; ARENAS J
      SINGLE LARGE-SCALE MITOCHONDRIAL-DNA DELETION IN A PATIENT WITH MITOCHONDRIAL MYOPATHY ASSOCIATED WITH MULTIPLE SYMMETRICAL LIPOMATOSIS

      Neurology
    60. MARTIN MA; MOLINA JA; JIMENEZJIMENEZ FJ; BENITOLEON J; ORTIPAREJA M; CAMPOS Y; ARENAS J; ALVAREZCERMENO JC; ARCAYA J; AYUSOPERALTA L; BALSEIRO J; BERMEJO F; CAMINERO A; CATALAN MJ; CEBALLOS A; DOMINGO J; DUARTE J; FERNANDEZCARRIL JM; GALIANO M; GARCIARUIZ PJ; GARCIAURRA D; GIMENEZROLDAN S; GRANDAS F; LOPEZLOZANO JJ; LUENGO A; MARCO J; MARSAL C; MARTINEZMARTIN P; MATEO D; MUNOZVAZQUEZ A; NOS J; PEREZSEMPERE A; PONDALSORDO M; PUENTESGIL JM; RABASA M; RALLOGUTIERREZ B; RIVAMEANA C; RUIZEZQUERRO JJ; SANCHEZALONSO P; SANCHEZPERNAUTE R; TABERNERO C; VAAMONDE J; VAQUEZ A; VELADESOJO L; VIVANCOSMATELLANO F; DEYEBENES JG; YUSTA A
      RESPIRATORY-CHAIN ENZYME-ACTIVITIES IN ISOLATED-MITOCHONDRIA OF LYMPHOCYTES FROM UNTREATED PARKINSONS-DISEASE PATIENTS

      Neurology
    61. ARENAS J; GONZALEZCRESPO MR; CAMPOS Y; MARTIN MA; CABELLO A; GOMEZREINO JJ
      ABNORMAL CARNITINE DISTRIBUTION IN THE THE MUSCLES OF PATIENTS WITH IDIOPATHIC INFLAMMATORY MYOPATHY

      Arthritis and rheumatism
    62. CAMPOS Y; GARCIASILVA 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 FANCONIS-SYNDROME

      Pediatric neurology
    63. GONZALEZCRESPO MR; ARENAS J; CABELLO A; CAMPOS Y; GARCIABENAYAS C; GOMEZREINO JJ
      FREE CARNITINE AND CARNITINE ESTERS LEVELS IN MUSCLE OF PATIENTS WITHIDIOPATHIC INFLAMMATORY MYOSITIS

      Arthritis and rheumatism
    64. CAMPOS Y; ARENAS J; CABELLO A; GOMEZREINO JJ
      RESPIRATORY-CHAIN ENZYME DEFECTS IN PATIENTS WITH IDIOPATHIC INFLAMMATORY MYOPATHY

      Annals of the Rheumatic Diseases
    65. CAMPOS Y; BAUTISTA J; GUTIERREZRIVAS E; CHINCHON D; CABELLO A; SEGURA D; ARENAS J
      CLINICAL HETEROGENEITY IN 2 PEDIGREES WITH THE 3243-BP TRNA(LEU(UUR))MUTATION OF MITOCHONDRIAL-DNA

      Acta neurologica Scandinavica
    66. CAMPOS Y; ARENAS J
      MUSCLE CARNITINE DEFICIENCY ASSOCIATED WITH ZIDOVUDINE-INDUCED MITOCHONDRIAL MYOPATHY

      Annals of neurology
    67. CAMPOS Y; ESTEBAN J; CABELLO A; ARENAS J
      GENETIC-ANALYSIS OF ONE FAMILY WITH MYOCLONIC EPILEPSY AND RAGGED-REDFIBERS (MERRF)

      Muscle & nerve
    68. CAMPOS Y; BAUTISTA J; GUTIERREZRIVAS E; LLABRES J; LORENZO G; ARENAS J
      VARIABLE CLINICAL EXPRESSION ASSOCIATED WITH THE MUTATION 3243-NP OF MITOCHONDRIAL-DNA

      Journal of inherited metabolic disease
    69. GARCIASILVA MT; CAMPOS Y; RIBES A; BRIONES P; CABELLO A; BORBUJO JS; ARENAS J; GARAVAGLIA B
      ENCEPHALOPATHY, PETECHIAE AND ACROCYANOSIS WITH ETHYLMALONIC ACIDURIAASSOCIATED WITH MUSCLE CYTOCHROME-C-OXIDASE DEFICIENCY

      The Journal of pediatrics
    70. ARENAS J; HUERTAS R; CAMPOS Y; DIAZ AE; VILLALON JM; VILAS E
      EFFECTS OF L-CARNITINE ON THE PYRUVATE-DEHYDROGENASE COMPLEX AND CARNITINE PALMITOYL TRANSFERASE ACTIVITIES IN MUSCLE OF ENDURANCE ATHLETES

      FEBS letters
    71. ARPE J; CAMPOS Y; GUTIERREZMOLINA M; CRUZMARTINEZ A; ARENAS J; CAMINERO AB; PALOMO F; MORALES C; BARREIRO P
      BENIGN MITOCHONDRIAL MYOPATHY WITH DECREASED SUCCINATE CYTOCHROME-C REDUCTASE-ACTIVITY

      Acta neurologica Scandinavica
    72. CAMPOS Y; HUERTAS R; BAUTISTA J; GUTIERREZ E; APARICIO M; LORENZO G; SEGURA D; VILLANUEVA M; CABELLO A; ALESSO L; ARENAS J
      MUSCLE CARNITINE DEFICIENCY AND LIPID STORAGE MYOPATHY IN PATIENTS WITH MITOCHONDRIAL MYOPATHY

      Muscle & nerve
    73. BARROSO N; CAMPOS Y; HUERTAS R; ESTEBAN J; MOLINA JA; ALONSO A; GUTIERREZRIVAS E; ARENAS J
      RESPIRATORY-CHAIN ENZYME-ACTIVITIES IN LYMPHOCYTES FROM UNTREATED PATIENTS WITH PARKINSON DISEASE

      Clinical chemistry


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Documento generato il 31/05/20 alle ore 22:33:13