Disease: Hypochromic microcytic anemia with iron overload
- 36-year-old male with X-linked congenital sideroblastic anemia presenting as chronic microcytic anemia with iron overload
- A new case of human atransferrinemia with a previously undescribed mutation in the transferrin gene
- A new mutation of the ALAS2 gene in a large family with X-linked sideroblastic anemia
- A Novel <em>ALAS2</em> Mutation Resulting in Variable Phenotypes and Pyridoxine Response in a Family with X-linked Sideroblastic Anemia
- A Novel ALAS2 Mutation Resulting in Variable Phenotypes and Pyridoxine Response in a Family with X-linked Sideroblastic Anemia
- A novel N491S mutation in the human SLC11A2 gene impairs protein trafficking and in association with the G212V mutation leads to microcytic anemia and liver iron overload
- Abnormal red blood cell morphological changes in thalassaemia associated with iron overload and oxidative stress
- Acquired alpha-thalassemia as early sign for myelodysplastic syndrome (refractory anaemia) with secondary haemochromatosis
- Beta Thalassemia
- Beta Thalassemia
- Beta-Thalassemia
- Case report of idiopathic pulmonary haemosiderosis in a child with recurrent chest infections
- Clinical aspects of the radioimmunological determination of serum ferritin
- Clinical characterization and hematopoietic stem cell transplant outcomes for congenital sideroblastic anemia caused by a novel pathogenic variant in SLC25A38
- Clinicohaematological profile in chronic renal failure
- Co-existing iron deficiency/overload in beta-thalassemia trait
- Congenital hypochromic microcytic anaemia with iron overload of the liver and hyperferraemia
- Congenital Hypotransferrinemia, an Unusual Cause of Iron Deficiency Anemia: Report of Two Cases
- Congenital sideroblastic anemia without clinical iron overload. A case report
- Congenital sideroblastic anemia-a new family with identification of K156E mutation of ALAS2 gene and literature review
- Diagnosis and treatment of iron deficiency anemia
- Diagnosis and treatment of sideroblastic anemias: from defective heme synthesis to abnormal RNA splicing
- Disruption of ferroportin 1 regulation causes dynamic alterations in iron homeostasis and erythropoiesis in polycythaemia mice
- Effects of GlyT1 inhibition on erythropoiesis and iron homeostasis in rats
- Esophagogastric variceal bleeding in a case of liver cirrhosis associated with thalassemia
- Ferrochelatase deficiency in the bone marrow in a syndrome of congenital hypochromic microcytic anemia, hyperferremia, and iron overload of the liver
- Ferrochelatase deficiency of the bone marrow in a syndrome of congenital microcytic anaemia with iron overload of the liver and hyperferraemia
- Genetic defects of iron transport
- Genetic diagnosis history and osteoarticular phenotype of a non-transfusion secondary hemochromatosis
- Glucose metabolism in the Belgrade rat, a model of iron-loading anemia
- H(+)-coupled divalent metal-ion transporter-1: functional properties, physiological roles and therapeutics
- Hematopoietic stem cells in the hereditarily anemic Belgrade laboratory (b/b) rat
- Hepcidin induction by transgenic overexpression of Hfe does not require the Hfe cytoplasmic tail, but does require hemojuvelin
- Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse
- Hereditary hyperferritinemia-cataract syndrome (HHCS) presenting with iron deficiency anemia associated with a new mutation in the iron responsive element of the L ferritin gene in a Swiss family
- Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overload
- How I manage patients with atypical microcytic anaemia
- Identification and treatment of anaemia in older patients
- Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload
- Idiopathic pulmonary haemosiderosis in Swedish children
- Idiopathic Pulmonary Haemosiderosis: An Unusual Case Of Anaemia With Pulmonary Involvement
- Idiopathic pulmonary hemosiderosis
- Idiopathic pulmonary hemosiderosis: alveoli are an answer to anemia
- Increased susceptibility of microcytic red blood cells to in vitro oxidative stress
- Insights into the pathophysiology of iron metabolism in Pythium insidiosum infections
- Intestinal iron absorption studies in mouse models of iron-overload
- Iron deficiency and anaemia in pregnancy: modern aspects of diagnosis and therapy
- Iron in the General Population and Specificities in Older Adults: Metabolism, Causes and Consequences of Decrease or Overload, and Biological Assessment
- Iron management during recombinant human erythropoietin therapy
- Long-term clinical course of patients with idiopathic pulmonary hemosiderosis (1979-1994): prolonged survival with low-dose corticosteroid therapy
- Manuka combinations with nigella sativa and hydroxyurea in treating iron overload of pediatric beta-thalassemia major, randomized clinical trial
- Microcytic hypochromic anemia in idiopathic pulmonary hemosiderosis: a diagnostic pitfall
- Mild copper deficiency alters gene expression of proteins involved in iron metabolism
- Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia
- Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis
- Natural history of recessive inheritance of DMT1 mutations
- NCOA4 Deficiency Impairs Systemic Iron Homeostasis
- Ndfip1-deficient mice have impaired DMT1 regulation and iron homeostasis
- New Cases of Hypochromic Microcytic Anemia Due to Mutations in the <em>SLC11A2</em> Gene and Functional Characterization of the G75R Mutation
- New Cases of Hypochromic Microcytic Anemia Due to Mutations in the SLC11A2 Gene and Functional Characterization of the G75R Mutation
- Not all DMT1 mutations lead to iron overload
- Recent progress in structure-function analyses of Nramp proton-dependent metal-ion transporters
- Recently identified molecular aspects of intestinal iron absorption
- Revisiting beta thalassemia intermedia: past, present, and future prospects
- Role of Hematological Indices as a Screening Tool of Beta Thalassemia Trait in Eastern Uttar Pradesh: An Institutional Study
- Serum Iron and Ferritin Levels in Beta Thalassemia Carriers in Duhok Governorate, Iraq
- Severe hypochromic microcytic anemia in a patient with congenital atransferrinemia
- Severe iron deficiency anemia in transgenic mice expressing liver hepcidin
- Severe iron-deficiency anemia as initial manifestation of pulmonary hemosiderosis in a child
- Sideroblastic anemia: functional study of two novel missense mutations in ALAS2
- The homozygous mutation G75R in the human SLC11A2 gene leads to microcytic anaemia and iron overload
- The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload
- The Role of Ferric Nitrilotriacetate in Renal Carcinogenesis and Cell Death: From Animal Models to Clinical Implications
- The zebrafish mutant gene chardonnay (cdy) encodes divalent metal transporter 1 (DMT1)
- Transgenic HFE-dependent induction of hepcidin in mice does not require transferrin receptor-2
- Two new human DMT1 gene mutations in a patient with microcytic anemia, low ferritinemia, and liver iron overload
- Two novel missense mutations in iron transport protein transferrin causing hypochromic microcytic anaemia and haemosiderosis: molecular characterization and structural implications
- Two Novel α-Thalassemia Mutations CD 39 -C [Thr > Pro] and CD 109 ACC > CCC [Thr > Pro] Identified in Two Chinese Families: A Case Report
- Use of sodium chromate Cr51 in diagnosing childhood idiopathic pulmonary hemosiderosis
- X-linked sideroblastic anaemia due to ALAS2 mutations in the Netherlands: a disease in disguise
- X-linked sideroblastic anemia
- β-Thalassemia Intermedia: A Bird's-Eye View