Publicaciones en colaboración con investigadores/as de Universidad Autónoma de Madrid (25)

2022

  1. Prognostic markers of inflammation in endometrioid and clear cell ovarian cancer

    International Journal of Gynecological Cancer, Vol. 32, Núm. 8, pp. 1009-1016

2020

  1. Early treatment with anti-tumor necrosis factor agents improves long-term effectiveness in symptomatic stricturing Crohn’s disease

    United European Gastroenterology Journal, Vol. 8, Núm. 9, pp. 1056-1066

2008

  1. Methylmalonic acidaemia: Examination of genotype and biochemical data in 32 patients belonging to mut, cblA or cblB complementation group

    Journal of Inherited Metabolic Disease, Vol. 31, Núm. 1, pp. 55-66

2006

  1. Biweekly regimen of cisplatin, gemcitabine and vinorelbine for advanced non-small-cell lung cancer

    Cancer Chemotherapy and Pharmacology, Vol. 58, Núm. 2, pp. 266-271

2002

  1. Screening for adenylosuccinate lyase deficiency: Clinical, biochemical and molecular findings in four patients

    Neuropediatrics, Vol. 33, Núm. 4, pp. 186-189

2000

  1. Potential relationship between genotype and clinical outcome in propionic acidaemia patients

    European Journal of Human Genetics, Vol. 8, Núm. 3, pp. 187-194

1999

  1. Adolescent myopathic presentation in two sisters with very long-chain acyl-CoA dehydrogenase deficiency

    Journal of Inherited Metabolic Disease, Vol. 22, Núm. 7, pp. 802-810

  2. Genetic and phenotypic aspects of phenylalanine hydroxylase deficiency in Spain: Molecular survey by regions

    European Journal of Human Genetics, Vol. 7, Núm. 3, pp. 386-392

1998

  1. An unusual late-onset case of propionic acidaemia: Biochemical investigations, neuroradiological findings and mutation analysis

    European Journal of Pediatrics, Vol. 157, Núm. 1, pp. 50-52

  2. Correlación de las técnicas de citometría de flujo y estática; su aplicación en el estudio de los linfomas anaplásicos

    Sangre, Vol. 43, Núm. 1, pp. 25-29

  3. Reliability of biochemical parameters used in prenatal diagnosis of combined methylmalonic aciduria and homocystinuria

    Prenatal Diagnosis, Vol. 18, Núm. 9, pp. 947-952

1994

  1. Different phenotypic manifestations associated with identical phenylketonuria genotypes in two Spanish families

    Journal of Inherited Metabolic Disease, Vol. 17, Núm. 3, pp. 377-378

  2. Phenotype distribution in the Spanish phenylketonuria population and related genotypes

    Journal of Inherited Metabolic Disease, Vol. 17, Núm. 3, pp. 366-368

1993

  1. First report of prenatal diagnosis of long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency in a pregnancy at risk

    Prenatal Diagnosis, Vol. 13, Núm. 6, pp. 529-533

1992

  1. A new case of succinyl-CoA: Acetoacetate transferase deficiency

    Journal of Inherited Metabolic Disease, Vol. 15, Núm. 3, pp. 371-373

1989

  1. Successful First Trimester Diagnosis in a Pregnancy at Risk for Propionic Acidaemia

    Journal of Inherited Metabolic Disease, Vol. 12, Núm. 2, pp. 274-276

1987

  1. Results of neonatal and selective screening for biotinidase deficiency

    Journal of Inherited Metabolic Disease, Vol. 10, Núm. 2 Supplement, pp. 296-298

  2. β-Ketothiolase deficiency: Two siblings with different clinical conditions

    Journal of Inherited Metabolic Disease, Vol. 10, Núm. 2 Supplement, pp. 276-278

1984

  1. A new patient with dicarboxylic aciduria suggestive of medium-chain acyl-CoA dehydrogenase deficiency presenting as Reye's syndrome

    Journal of Inherited Metabolic Disease, Vol. 7, Núm. 2, pp. 62-64

1983

  1. ESTUDIO DE TRES PACIENTES CON LA ENFERMEDAD DE JARABE DE ARCE

    Anales Espanoles de Pediatria, Vol. 19, Núm. 5, pp. 393-400