Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Total management of thalassaemia major.

Literature DB >> 879834

Total management of thalassaemia major.

B Modell.

Abstract

Mesh：

Substances：

Year: 1977 PMID： 879834 PMCID： PMC1544709 DOI： 10.1136/adc.52.6.489

Source DB: PubMed Journal: Arch Dis Child ISSN： 0003-9888 Impact factor: 3.791

× No keyword cloud information.

27 in total

1. COMPARISON OF SIXTY-SIX PATIENTS WITH THALASSEMIA MAJOR AND THIRTEEN PATIENTS WITH THALASSEMIA INTERMEDIA: INCLUDING EVALUATIONS OF GROWTH, DEVELOPMENT, MATURATION AND PROGNOSIS.

Authors: M E ERLANDSON; R BRILLIANT; C H SMITH
Journal: Ann N Y Acad Sci Date: 1964-10-07 Impact factor: 5.691

2. POSTSPLENECTOMY INFECTION IN COOLEY'S ANEMIA.

Authors: C H SMITH; M E ERLANDSON; G STERN; M W HILGARTNER
Journal: Ann N Y Acad Sci Date: 1964-10-07 Impact factor: 5.691

3. Iron excretion in thalassaemia major after administration of chelating agents.

Authors: R S SMITH
Journal: Br Med J Date: 1962-12-15

4. Studies on congenital hemolytic syndromes, IV. Gastrointestinal absorption of iron.

Authors: M E ERLANDSON; B WALDEN; G STERN; M W HILGARTNER; J WEHMAN; C H SMITH
Journal: Blood Date: 1962-03 Impact factor: 22.113

5. A genetic study of Mediterranean anaemia in Cyprus.

Authors: A H BANTON
Journal: Am J Hum Genet Date: 1951-03 Impact factor: 11.025

6. 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

7. Hypertransfusion regimen in patients with Cooley's anemia.

Authors: S Piomelli; M H Karpatkin; M Arzanian; M Zamani; M H Becker; N Geneiser; S J Danoff; W J Kuhns
Journal: Ann N Y Acad Sci Date: 1974 Impact factor: 5.691

8. Haemoglobinopathies. The pathophysiology of beta-thalassaemia major.

Authors: C B Modell
Journal: J Clin Pathol Suppl (R Coll Pathol) Date: 1974

9. Prenatal diagnosis of homozygous beta-thalassaemia.

Authors: Y W Kan; M S Golbus; R Trecartin
Journal: Lancet Date: 1975-10-25 Impact factor: 79.321

10. Longitudinal growth in thalassemia major. Relationship to hemoglobin level.

Authors: F E Johnston; K P Hertzog; R M Malina
Journal: Am J Dis Child Date: 1966-11

27 in total

1. Immunological abnormalities in thalassaemia major. I. A transfusion-related increase in circulating cytoplasmic immunoglobulin-positive cells.

Authors: A N Akbar; P J Giardina; M W Hilgartner; R W Grady
Journal: Clin Exp Immunol Date: 1985-11 Impact factor: 4.330

Total management of thalassaemia major.

1. COMPARISON OF SIXTY-SIX PATIENTS WITH THALASSEMIA MAJOR AND THIRTEEN PATIENTS WITH THALASSEMIA INTERMEDIA: INCLUDING EVALUATIONS OF GROWTH, DEVELOPMENT, MATURATION AND PROGNOSIS.

2. POSTSPLENECTOMY INFECTION IN COOLEY'S ANEMIA.

3. Iron excretion in thalassaemia major after administration of chelating agents.

4. Studies on congenital hemolytic syndromes, IV. Gastrointestinal absorption of iron.

5. A genetic study of Mediterranean anaemia in Cyprus.

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

7. Hypertransfusion regimen in patients with Cooley's anemia.

8. Haemoglobinopathies. The pathophysiology of beta-thalassaemia major.

9. Prenatal diagnosis of homozygous beta-thalassaemia.

10. Longitudinal growth in thalassemia major. Relationship to hemoglobin level.

1. Immunological abnormalities in thalassaemia major. I. A transfusion-related increase in circulating cytoplasmic immunoglobulin-positive cells.

Review 2. Current concepts in the management of thalassemia.

3. Management of thalassaemia major.

4. Beta-Thalassaemia types in southern Sardinia.

5. Serum ferritin, liver iron stores, and liver histology in children with thalassaemia.

6. Congenital dyserythropoietic anaemia type II (HEMPAS): a family study.

7. Cirrhosis associated with multiple transfusions in thalassaemia.

8. Neocytopheresis: a new approach for the transfusion of patients with thalassaemia major.

9. Partial splenectomy in homozygous beta thalassaemia.

10. Hereditary anaemias: genetic basis, clinical features, diagnosis, and treatment. WHO working group.