Claudia Dimatteo
Foggia, Italy
Last Updated: 09/26/2026
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Found 9 publications
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability.
Journal: Thrombosis research
Published: June 29, 2016
Pharmacogenetics of dabigatran etexilate interindividual variability.
Journal: Thrombosis research
Published: March 10, 2016
Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: May 28, 2015
Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: March 30, 2014
Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia.
Journal: Blood
Published: December 21, 2013
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees.
Journal: Clinical biochemistry
Published: September 21, 2013
Mutation analysis in hyperphenylalaninemia patients from South Italy.
Journal: Clinical biochemistry
Published: March 21, 2013
Role of GALNT2 in the modulation of ENPP1 expression, and insulin signaling and action: GALNT2: a novel modulator of insulin signaling.
Journal: Biochimica et biophysica acta
Published: October 18, 2012
Role of somatomedin-B-like domains on ENPP1 inhibition of insulin signaling.
Journal: Biochimica et biophysica acta
Published: June 11, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026