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Literature DB >> 6242259

Beta thalassemia and heart disease: three decades of gradual progress.

M A Engle, K H Ehlers, J E O'Loughlin, P J Giardina, M W Hilgartner.

Abstract

Entities: Disease

Mesh：

Substances：
Deferoxamine

Year: 1985 PMID： 6242259 PMCID： PMC2279656

Source DB: PubMed Journal: Trans Am Clin Climatol Assoc ISSN： 0065-7778

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17 in total

1. The role of splenectomy in the management of thalassemia.

Authors: C H SMITH; M E ERLANDSON; G STERN; I SCHULMAN
Journal: Blood Date: 1960-02 Impact factor: 22.113

2. Prenatal diagnosis of hemoglobinopathies. A review of 15 cases.

Authors: B P Alter; C B Modell; D Fairweather; J C Hobbins; M J Mahoney; F D Frigoletto; A S Sherman; D G Nathan
Journal: N Engl J Med Date: 1976-12-23 Impact factor: 91.245

3. Continuous subcutaenous administration of deferoxamine in patients with iron overload.

Authors: R D Propper; B Cooper; R R Rufo; A W Nienhuis; W F Anderson; H F Bunn; A Rosenthal; D G Nathan
Journal: N Engl J Med Date: 1977-08-25 Impact factor: 91.245

Review 4. Recent developments in the molecular genetics of human hemoglobin.

Authors: D J Weatherall; J B Clegg
Journal: Cell Date: 1979-03 Impact factor: 41.582

5. Marrow transplantation for thalassaemia.

Authors: E D Thomas; C D Buckner; J E Sanders; T Papayannopoulou; C Borgna-Pignatti; P De Stefano; K M Sullivan; R A Clift; R Storb
Journal: Lancet Date: 1982-07-31 Impact factor: 79.321

6. Direct gene analysis of chorionic villi: A possible technique for first-trimester antenatal diagnosis of haemoglobinopathies.

Authors: R Williamson; J Eskdale; D V Coleman; M Niazi; F E Loeffler; B M Modell
Journal: Lancet Date: 1981-11-21 Impact factor: 79.321

Beta thalassemia and heart disease: three decades of gradual progress.

1. The role of splenectomy in the management of thalassemia.

2. Prenatal diagnosis of hemoglobinopathies. A review of 15 cases.

3. Continuous subcutaenous administration of deferoxamine in patients with iron overload.

Review 4. Recent developments in the molecular genetics of human hemoglobin.

5. Marrow transplantation for thalassaemia.

6. Direct gene analysis of chorionic villi: A possible technique for first-trimester antenatal diagnosis of haemoglobinopathies.

7. Longitudinal study of cardiac function in thalassemia major.

8. Histochemical studies of the myocardium and conduction system in acquired iron-storage disease.

9. Successful application of prenatal diagnosis in a pregnancy at risk for homozygous beta-thalassemia.

Review 10. Molecular genetics of human hemoglobin synthesis.

1. Cardiac iron determines cardiac T2*, T2, and T1 in the gerbil model of iron cardiomyopathy.

2. Evidence for a novel mechanism independent of myocardial iron in β-thalassemia cardiac pathogenesis.