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Blood|April 1, 1987
Sardinian delta beta zero-thalassemia: a further example of a C to T substitution at position -196 of the A gamma globin gene promoterS Ottolenghi, B Giglioni, A Pulazzini, et al.Hepatology (Baltimore, Md.)|April 27, 1999
Inherited HFE-unrelated hemochromatosis in Italian familiesC Camaschella, S Fargion, M Sampietro, et al.Acta Haematologica|January 1, 1979
Biosynthetic studies and gamma-chain composition in the Greek type of hereditary persistence of fetal hemoglobin and in its association with beta-thalassemiaC Camaschella, M A Ciocca-Vasino, A Guerrasio, et al.Journal of Medical Genetics|March 1, 1993
Molecular analysis of contiguous exons of the phenylalanine hydroxylase gene: identification of a new PKU mutationI Dianzani, C Camaschella, G Saglio, et al.Blood|April 1, 1988
Delineation of specific beta-thalassemia mutations in high-risk areas of Italy: a prerequisite for prenatal diagnosisM Pirastu, G Saglio, C Camaschella, et al.European Journal of Haematology|July 1, 1991
Inhibition of hexose monophosphate shunt in young erythrocytes by pyrimidine nucleotides in hereditary pyrimidine 5' nucleotidase deficiencyO David, U Ramenghi, C Camaschella, et al.Minerva Cardioangiologica|February 24, 2001
Prognostic significance of markers of thrombin generation in the acute and chronic phases of non cardioembolic ischemic strokeM Soncini, P Gasparini, M Lorena, et al.Giornale Di Clinica Medica|March 1, 1989
[Juvenile myocardial infarct. A description of 2 cases occurring before 20 years of age and a review of the literature]F Guzzini, L Banfi, R Baroffio, et al.Annales De Genetique|January 1, 1997
Assignment of ferritin L gene (FTL) to human chromosome band 19q13.3 by in situ hybridizationP Gasparini, S Calvano, E Memeo, et al.Clinical Dysmorphology|August 24, 2000
A new case of acromegaloid facial appearance (AFA) syndrome with an expanded phenotypeL Zelante, P Gasparini, A Savoia, et al.Pageof 25