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Human Mutation|April 13, 1999
Two novel mutations in exon 11 of the PAH gene (V1163del TG and P362T) associated with classic phenylketonuira and mild phenylketonuria. Mutations in brief no. 143. OnlineJ Mallolas, J Campistol, N Lambruschini, et al.Human Genetics|December 22, 1999
Mutational spectrum of phenylalanine hydroxylase deficiency in the population resident in Catalonia: genotype-phenotype correlationJ Mallolas, M A Vilaseca, J Campistol, et al.Medicina Clinica|October 21, 2003
[Cytokines value as a sepsis and mortality predictor in elderly patients with fever]L Martí, A Moreno, X Filella, et al.Biochimica Et Biophysica Acta|February 25, 2016
Definition of an 18-mer Synthetic Peptide Derived from the GB virus C E1 Protein as a New HIV-1 Entry InhibitorM J Gómara, V Sánchez-Merino, A Paús, et al.Revista De Neurologia|March 14, 2001
[Clinical, biomedical , neurological and molecular study of 11 patients with new mutations in PAH gene]J Mallolas, M A Vilaseca, J Campistol, et al.Medicina Clinica|January 21, 1989
[Prospective study of 75 episodes of sepsis in hemodialysed patients]J A Martínez, J M Gatell, J Montoliu, et al.Cancer|November 1, 1982
Diagnostic value of tumoral markers in serous effusions: carcinoembryonic antigen, alpha1-acidglycoprotein, alpha-fetoprotein, phosphohexose isomerase, and beta 2-microglobulinA Martinez-Vea, J M Gatell, F Segura, et al.Annals of Oncology : Official Journal of the European Society for Medical Oncology|March 1, 1995
Granulocyte growth factors: achieving a consensusM Boogaerts, F Cavalli, H Cortés-Funes, et al.Prenatal Diagnosis|July 13, 2002
Pilot study for the neonatal screening of fragile X syndromeM Rifé, J Mallolas, C Badenas, et al.The British Journal of Dermatology|February 1, 1982
Specific cutaneous manifestations of Waldenström's macroglobulinaemia. A report of two casesJ M Mascaro, E Montserrat, T Estrach, et al.Pageof 27