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Hemoglobin
international journal for hemoglobin research
Volume 3, 1979 - Issue 1
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Original Article

β° Thalassemia Trait in Sardinia

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Pages 33-46 | Received 14 Jul 1978, Accepted 07 Feb 1979, Published online: 07 Jul 2009

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Read on this site (4)

Laura Grech, Janet Sultana, Karen Borg & Joseph Borg. (2021) Drug safety in thalassemia: lessons from the present and directions for the future. Expert Opinion on Drug Safety 20:8, pages 937-947.
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Alexandra Kolliopoulou, Stavroula Siamoglou, Anne John, Argyro Sgourou, Alexandra Kourakli, Argiris Symeonidis, Efthymia Vlachaki, Panagiota Chalkia, Stamatia Theodoridou, Bassam R. Ali, Theodora Katsila, George P. Patrinos & Adamantia Papachatzopoulou. (2019) Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in β-Thalassemia Intermedia: A Validation Cohort Study. Hemoglobin 43:1, pages 27-33.
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A. M. Gianni, E. Polli, B. Giglioni, P. Comi, S. Ottolenghi, M. Ferrari, M. Furbetta, A. Angius & A. Cao. (1981) Isoelectric Focusing of Globin Chains for Antenatal Diagnosis of β°-Thalassemia. Hemoglobin 5:4, pages 349-356.
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Renzo Galanello, Rita Ruggeri, Maria Addis, Elisabetta Paglietti & Antonio Cao. (1981) Hemoglobin A2 in Iron Deficient 8-Thalassemia Heterozygotes. Hemoglobin 5:6, pages 613-618.
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Articles from other publishers (21)

Philip M. Farrell, Elinor Langfelder-Schwind & Michael H. Farrell. (2021) Challenging the dogma of the healthy heterozygote: Implications for newborn screening policies and practices. Molecular Genetics and Metabolism 134:1-2, pages 8-19.
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Kamuran Karaman, Serdar Şahin, Hadi Geylan, Akkiz Şahin Yaşar, Mecnun Çetin, Ahmet U. Kömüroğlu & Ahmet F. Öner. (2019) Evaluation of Renal Function Disorder With Urinary Neutrophil Gelatinase–associated Lipocalin Level in Patients With β-Thalassemia Major. Journal of Pediatric Hematology/Oncology 41:7, pages 507-510.
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Zeeshan Hussain, Saqib Ansari & Tahir Shamsi. (2018) A Perspective on Thalassaemia. National Journal of Health Sciences 3:2, pages 36-40.
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A. Mangia, R. Sarli, R. Gamberini, A. Piga, G. Cenderello, V. Piazzolla, R. Santoro, V. Caruso, A. Quarta, R. Ganga, M. Copetti & G. Forni. (2017) Randomised clinical trial: sofosbuvir and ledipasvir in patients with transfusion‐dependent thalassaemia and HCV genotype 1 or 4 infection . Alimentary Pharmacology & Therapeutics 46:4, pages 424-431.
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Nasrollah Saleh-Gohari, Maryam Khademi Bami, Roya Nikbakht & Hassan Karimi-Maleh. (2015) Effects of α-thalassaemia mutations on the haematological parameters of β-thalassaemia carriers. Journal of Clinical Pathology 68:7, pages 562-566.
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Silvia Carbone. (2014) Thalassemia in Messina: A Sociological Approach to Chronic Disease. Thalassemia Reports 4:1, pages 2207.
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Stefania Satta, Lucia Perseu, Liliana Maccioni, Nicolina Giagu & Renzo Galanello. (2012) Delayed fetal hemoglobin switching in subjects with KLF1 gene mutation. Blood Cells, Molecules, and Diseases 48:1, pages 22-24.
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Ken Sin Lo, James G. Wilson, Leslie A. Lange, Aaron R. Folsom, Geneviève Galarneau, Santhi K. Ganesh, Struan F. A. Grant, Brendan J. Keating, Steven A. McCarroll, Emile R. Mohler III, Christopher J. O’Donnell, Walter Palmas, Weihong Tang, Russell P. Tracy, Alexander P. Reiner & Guillaume Lettre. (2010) Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans. Human Genetics 129:3, pages 307-317.
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Renzo Galanello & Raffaella Origa. (2010) Beta-thalassemia. Orphanet Journal of Rare Diseases 5:1.
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Antonio Cao, M. Cristina Rosatelli & Renzo Galanello. 2007. Ciba Foundation Symposium 197 ‐ Variation in the Human Genome. Ciba Foundation Symposium 197 ‐ Variation in the Human Genome 137 155 .
Chad Garner, Tracy K. Dew, Roy Sherwood, David Rees & Swee Lay Thein. (2003) Heterocellular hereditary persistence of fetal haemoglobin affects the haematological parameters of β-thalassaemia trait. British Journal of Haematology 123:2, pages 353-358.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
D. Williamson, R.W. Carrell & H. Lehmann. 1994. Scientific Foundations of Biochemistry in Clinical Practice. Scientific Foundations of Biochemistry in Clinical Practice 420 445 .
R. Galanello, M. E. Paglietti, M. Addis, M. A. Melis, T. Tuveri, M. Furbetta & A. Cao. (2008) Pitfalls in genetic counselling for β-thalassemia: an individual with 4 different thalassemia mutations. Clinical Genetics 33:3, pages 151-155.
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Giampaolo Zorcolo, Novella Landis, Elena Madeddu, Giuseppe Mandas, Elisabetta Montaldo, Sergio Perisi, Giampiero Piras, Luigi Salemi & Rosalia Sicilia. (1986) BETA-THALASSAEMIA CONTROL. The Lancet 328:8498, pages 103.
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L Maccioni & A Cao. (1985) Osmotic fragility test in heterozygotes for alpha and beta thalassaemia.. Journal of Medical Genetics 22:5, pages 374-376.
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A. Cao, L. P<sc>intus, U. Lecca, G. Oixa, P. Cossu, C. Rosatelli & R. Galanello. (2008) Control of homozygous β‐thalassemia by carrier screening and antenatal diagnosis in Sardinians. Clinical Genetics 26:1, pages 12-22.
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G. Castaldi, B. Bagni, F. Trotta, G. Menegale, A. R. Cavallini & A. Piffanelli. (2009) Folic Acid Deficiency in β‐Thalassaemia Heterozygotes. Scandinavian Journal of Haematology 30:2, pages 125-129.
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R. Galanello, M.A. Melis, R. Ruggeri & A. Cao. (1981) Prospective study of red blood cell indices, hemoglobin A2, and hemoglobin F in infants heterozygous for β-thalassemia. The Journal of Pediatrics 99:1, pages 105-108.
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R Galanello, S De Virgiliis, M Addis, E Paglietti, R Ruggeri & A Cao. (1980) Haematological characteristics of the beta 0 thalassaemia trait in Sardinian children.. Journal of Clinical Pathology 33:10, pages 946-948.
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G. Pepe, L. Lupi & L. Luzzatto. (2008) Genetic and Biochemical Heterogeneity of β‐Thalassaemia in Naples. British Journal of Haematology 45:3, pages 417-429.
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