Sideroblastic anaemias

[21] EXCESSIVE ZINC INGESTION - A REVERSIBLE CAUSE OF SIDEROBLASTIC ANEMIA AND BONE-MARROW DEPRESSION [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1990, 264 (11): : 1441 - 1443

[22] BUCHANAN GR, 1980, BLOOD, V55, P109

[23] Soluble transferrin receptor as a potential determinant of iron loading in congenital anaemias due to ineffective erythropoiesis [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1999, 106 (03) : 752 - 755

[24] Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females [J]. BLOOD, 2000, 96 (13) : 4363 - 4365

[25] COOLEY TB, 1945, AM J MED SCI, V209, P561

[26] Anemia in children - With splenomegaly and peculiar changes in the bones - Report of cases [J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1927, 34 (03): : 347 - 363

[27] WIDESPREAD MULTITISSUE DELETIONS OF THE MITOCHONDRIAL GENOME IN THE PEARSON MARROW-PANCREAS SYNDROME [J]. JOURNAL OF PEDIATRICS, 1990, 117 (04) : 599 - 602

[28] Four new mutations in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causing X-linked sideroblastic anemia:: Increased pyridoxine responsiveness after removal of iron overload by phlebotomy and coinheritance of hereditary hemochromatosis [J]. BLOOD, 1999, 93 (05) : 1757 - 1769

[29] ENZYMATIC DEFECT IN X-LINKED SIDEROBLASTIC ANEMIA - MOLECULAR EVIDENCE FOR ERYTHROID DELTA-AMINOLEVULINATE SYNTHASE DEFICIENCY [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (09) : 4028 - 4032

[30] X-LINKED SIDEROBLASTIC ANEMIA - IDENTIFICATION OF THE MUTATION IN THE ERYTHROID-SPECIFIC DELTA-AMINOLEVULINATE SYNTHASE GENE (ALAS2) IN THE ORIGINAL FAMILY DESCRIBED BY COOLEY [J]. BLOOD, 1994, 84 (11) : 3915 - 3924

[21] EXCESSIVE ZINC INGESTION - A REVERSIBLE CAUSE OF SIDEROBLASTIC ANEMIA AND BONE-MARROW DEPRESSION [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1990, 264 (11): : 1441 - 1443

[22] BUCHANAN GR, 1980, BLOOD, V55, P109

[23] Soluble transferrin receptor as a potential determinant of iron loading in congenital anaemias due to ineffective erythropoiesis [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1999, 106 (03) : 752 - 755

[24] Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females [J]. BLOOD, 2000, 96 (13) : 4363 - 4365

[25] COOLEY TB, 1945, AM J MED SCI, V209, P561

[26] Anemia in children - With splenomegaly and peculiar changes in the bones - Report of cases [J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1927, 34 (03): : 347 - 363

[27] WIDESPREAD MULTITISSUE DELETIONS OF THE MITOCHONDRIAL GENOME IN THE PEARSON MARROW-PANCREAS SYNDROME [J]. JOURNAL OF PEDIATRICS, 1990, 117 (04) : 599 - 602

[28] Four new mutations in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causing X-linked sideroblastic anemia:: Increased pyridoxine responsiveness after removal of iron overload by phlebotomy and coinheritance of hereditary hemochromatosis [J]. BLOOD, 1999, 93 (05) : 1757 - 1769

[29] ENZYMATIC DEFECT IN X-LINKED SIDEROBLASTIC ANEMIA - MOLECULAR EVIDENCE FOR ERYTHROID DELTA-AMINOLEVULINATE SYNTHASE DEFICIENCY [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (09) : 4028 - 4032

[30] X-LINKED SIDEROBLASTIC ANEMIA - IDENTIFICATION OF THE MUTATION IN THE ERYTHROID-SPECIFIC DELTA-AMINOLEVULINATE SYNTHASE GENE (ALAS2) IN THE ORIGINAL FAMILY DESCRIBED BY COOLEY [J]. BLOOD, 1994, 84 (11) : 3915 - 3924