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C Camaschella

Showing results (71-80 of 141) with videos related to

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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.
Molecular and Cellular Probes|December 1, 1996
Two polymorphic repeats in the candidate region for the haemochromatosis geneA Grifa, A Totaro, M Carella, 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.
Recenti Progressi in Medicina|February 1, 1987
[Thyrotropin hyperresponsiveness and antithyroid antibodies in clinically euthyroid postpubertal thalassemic patients]D Bisbocci, D Sperone, A Vignani, et al.
Haematologica|June 15, 1999
Recurrent mutations in the iron regulatory element of L-ferritin in hereditary hyperferritinemia-cataract syndromeM Cicilano, G Zecchina, A Roetto, et al.
British Journal of Haematology|August 1, 1991
Ankyrin deficiency in dominant hereditary spherocytosis: report of three casesA Iolascon, E Miraglia del Giudice, C Camaschella, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|May 30, 1979
[Biochemical and clinical studies of 2 new Italian cases of Hb G-Ferrara heterozygosis]A Guerrasio, G Saglio, C Camaschella, et al.
Pageof 15

Showing results (71-80 of 141) with videos related to

Sort By:
Pageof 15
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.
Molecular and Cellular Probes|December 1, 1996
Two polymorphic repeats in the candidate region for the haemochromatosis geneA Grifa, A Totaro, M Carella, 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.
Recenti Progressi in Medicina|February 1, 1987
[Thyrotropin hyperresponsiveness and antithyroid antibodies in clinically euthyroid postpubertal thalassemic patients]D Bisbocci, D Sperone, A Vignani, et al.
Haematologica|June 15, 1999
Recurrent mutations in the iron regulatory element of L-ferritin in hereditary hyperferritinemia-cataract syndromeM Cicilano, G Zecchina, A Roetto, et al.
British Journal of Haematology|August 1, 1991
Ankyrin deficiency in dominant hereditary spherocytosis: report of three casesA Iolascon, E Miraglia del Giudice, C Camaschella, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|May 30, 1979
[Biochemical and clinical studies of 2 new Italian cases of Hb G-Ferrara heterozygosis]A Guerrasio, G Saglio, C Camaschella, et al.
Pageof 15