Publications in collaboration with researchers from 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