- Home
- Publications
- Publication Search
- Publication Details
Title
How I manage patients with atypical microcytic anaemia
Authors
Keywords
-
Journal
BRITISH JOURNAL OF HAEMATOLOGY
Volume 160, Issue 1, Pages 12-24
Publisher
Wiley
Online
2012-10-11
DOI
10.1111/bjh.12081
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Identification and characterization of the first SLC11A2 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of theSLC11A2gene
- (2012) Luigia De Falco et al. BRITISH JOURNAL OF HAEMATOLOGY
- Aceruloplasminemia
- (2012) Satoshi Kono CURRENT DRUG TARGETS
- Biogenesis of iron-sulfur clusters in mammalian cells: new insights and relevance to human disease
- (2012) T. A. Rouault Disease Models & Mechanisms
- Erythropoietin-driven signaling ameliorates the survival defect of DMT1-mutant erythroid progenitors and erythroblasts
- (2012) M. Horvathova et al. HAEMATOLOGICA
- TMPRSS6, but not TF, TFR2 or BMP2 variants are associated with increased risk of iron-deficiency anemia
- (2012) Peng An et al. HUMAN MOLECULAR GENETICS
- Inactive matriptase-2 mutants found in IRIDA patients still repress hepcidin in a transfection assay despite having lost their serine protease activity
- (2012) Flavia Guillem et al. HUMAN MUTATION
- Candidate Gene Sequencing of SLC11A2 and TMPRSS6 in a Family with Severe Anaemia: Common SNPs, Rare Haplotypes, No Causative Mutation
- (2012) Anita Kloss-Brandstätter et al. PLoS One
- ALAS2 acts as a modifier gene in patients with congenital erythropoietic porphyria
- (2011) J. To-Figueras et al. BLOOD
- Hepcidin regulates ferroportin expression and intracellular iron homeostasis of erythroblasts
- (2011) D.-L. Zhang et al. BLOOD
- A novel type of congenital hypochromic anemia associated with a nonsense mutation in the STEAP3/TSAP6 gene
- (2011) B. Grandchamp et al. BLOOD
- TMPRSS6 rs855791 modulates hepcidin transcription in vitro and serum hepcidin levels in normal individuals
- (2011) A. Nai et al. BLOOD
- Mutation of the gastric hydrogen-potassium ATPase alpha subunit causes iron-deficiency anemia in mice
- (2011) L. Krieg et al. BLOOD
- Responsiveness to oral iron and ascorbic acid in a patient with IRIDA
- (2011) Milena Cau et al. BLOOD CELLS MOLECULES AND DISEASES
- Gastrin-Deficient Mice Have Disturbed Hematopoiesis in Response to Iron Deficiency
- (2011) Suzana Kovac et al. ENDOCRINOLOGY
- Serum hepcidin and prohepcidin concentrations in inflammatory bowel disease
- (2011) Pantelis Oustamanolakis et al. EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
- Response of iron overload to deferasirox in rare transfusion-dependent anaemias: equivalent effects on serum ferritin and labile plasma iron for haemolytic or production anaemias
- (2011) John B. Porter et al. EUROPEAN JOURNAL OF HAEMATOLOGY
- Hemojuvelin is essential for transferrin-dependent and transferrin-independent hepcidin expression in mice
- (2011) T. B. Bartnikas et al. HAEMATOLOGICA
- A pilot trial of deferiprone for neurodegeneration with brain iron accumulation
- (2011) G. Abbruzzese et al. HAEMATOLOGICA
- Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia
- (2011) C. Kannengiesser et al. HAEMATOLOGICA
- Criteria for Early Identification of Aceruloplasminemia
- (2011) Masaro Ogimoto et al. INTERNAL MEDICINE
- Growth differentiation factor 15 in patients with congenital dyserythropoietic anaemia (CDA) type II
- (2011) Guillem Casanovas et al. JOURNAL OF MOLECULAR MEDICINE-JMM
- Congenital Sideroblastic Anemias: Iron and Heme Lost in Mitochondrial Translation
- (2011) M. D. Fleming Hematology-American Society of Hematology Education Program
- A novel TMPRSS6 mutation that prevents protease auto-activation causes IRIDA
- (2010) Sandro Altamura et al. BIOCHEMICAL JOURNAL
- Down-regulation of Bmp/Smad signaling by Tmprss6 is required for maintenance of systemic iron homeostasis
- (2010) K. E. Finberg et al. BLOOD
- Increased susceptibility to iron deficiency of Tmprss6-haploinsufficient mice
- (2010) A. Nai et al. BLOOD
- Transferrin is a major determinant of hepcidin expression in hypotransferrinemic mice
- (2010) T. B. Bartnikas et al. BLOOD
- Detection, evaluation, and management of iron-restricted erythropoiesis
- (2010) L. T. Goodnough et al. BLOOD
- Genetic variability of TMPRSS6 and its association with iron deficiency anaemia
- (2010) Paola Delbini et al. BRITISH JOURNAL OF HAEMATOLOGY
- Two to Tango: Regulation of Mammalian Iron Metabolism
- (2010) Matthias W. Hentze et al. CELL
- Inherited disorders of iron metabolism
- (2010) Clara Camaschella et al. CURRENT OPINION IN PEDIATRICS
- Novel TMPRSS6 mutations associated with iron-refractory iron deficiency anemia (IRIDA)
- (2010) Luigia De Falco et al. HUMAN MUTATION
- Glutaredoxin 5 deficiency causes sideroblastic anemia by specifically impairing heme biosynthesis and depleting cytosolic iron in human erythroblasts
- (2010) Hong Ye et al. JOURNAL OF CLINICAL INVESTIGATION
- Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders
- (2010) Yoshibumi Kaneko et al. JOURNAL OF GASTROENTEROLOGY
- Hepatic but not brain iron is rapidly chelated by deferasirox in aceruloplasminemia due to a novel gene mutation
- (2010) Armin Finkenstedt et al. JOURNAL OF HEPATOLOGY
- A genome-wide association analysis of serum iron concentrations
- (2009) T. Tanaka et al. BLOOD
- Molecular mechanisms of the defective hepcidin inhibition in TMPRSS6 mutations associated with iron-refractory iron deficiency anemia
- (2009) L. Silvestri et al. BLOOD
- Identification of TWSG1 as a second novel erythroid regulator of hepcidin expression in murine and human cells
- (2009) T. Tanno et al. BLOOD
- A Ferroportin Transcript that Lacks an Iron-Responsive Element Enables Duodenal and Erythroid Precursor Cells to Evade Translational Repression
- (2009) De-Liang Zhang et al. Cell Metabolism
- Regulation of serum hepcidin levels in sickle cell disease
- (2009) J. J.C. Kroot et al. HAEMATOLOGICA
- Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis
- (2009) A. Iolascon et al. HAEMATOLOGICA
- Matriptase-2 mutations in iron-refractory iron deficiency anemia patients provide new insights into protease activation mechanisms
- (2009) Andrew J. Ramsay et al. HUMAN MOLECULAR GENETICS
- Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels
- (2009) John C Chambers et al. NATURE GENETICS
- Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
- (2009) Santhi K Ganesh et al. NATURE GENETICS
- Common variants in TMPRSS6 are associated with iron status and erythrocyte volume
- (2009) Beben Benyamin et al. NATURE GENETICS
- Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia
- (2009) Duane L Guernsey et al. NATURE GENETICS
- A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
- (2009) Nicole Soranzo et al. NATURE GENETICS
- The Microcytic Red Cell and the Anemia of Inflammation
- (2009) Siobán B. Keel et al. NEW ENGLAND JOURNAL OF MEDICINE
- SEVERE HYPOCHROMIC MICROCYTIC ANEMIA IN A PATIENT WITH CONGENITAL ATRANSFERRINEMIA
- (2009) Bibi Shahin Shamsian et al. PEDIATRIC HEMATOLOGY AND ONCOLOGY
- Pathogenesis and Management of Iron Deficiency Anemia: Emerging Role of Celiac Disease, Helicobacter pylori, and Autoimmune Gastritis
- (2009) Chaim Hershko et al. SEMINARS IN HEMATOLOGY
- Iron-Refractory Iron Deficiency Anemia
- (2009) Karin E. Finberg SEMINARS IN HEMATOLOGY
- Elevated growth differentiation factor 15 expression in patients with congenital dyserythropoietic anemia type I
- (2008) H. Tamary et al. BLOOD
- Membrane-bound serine protease matriptase-2 (Tmprss6) is an essential regulator of iron homeostasis
- (2008) A. R. Folgueras et al. BLOOD
- Forging a field: the golden age of iron biology
- (2008) N. C. Andrews BLOOD
- Immunoassay for human serum hepcidin
- (2008) T. Ganz et al. BLOOD
- Two nonsense mutations in the TMPRSS6 gene in a patient with microcytic anemia and iron deficiency
- (2008) F. Guillem et al. BLOOD
- Recent advances in the understanding of inherited sideroblastic anaemia
- (2008) Clara Camaschella BRITISH JOURNAL OF HAEMATOLOGY
- The Serine Protease Matriptase-2 (TMPRSS6) Inhibits Hepcidin Activation by Cleaving Membrane Hemojuvelin
- (2008) Laura Silvestri et al. Cell Metabolism
- A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron
- (2008) M. A. Melis et al. HAEMATOLOGICA
- Italian Society of Hematology practice guidelines for the management of iron overload in thalassemia major and related disorders
- (2008) E. Angelucci et al. HAEMATOLOGICA
- Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA)
- (2008) Karin E Finberg et al. NATURE GENETICS
- The Serine Protease TMPRSS6 Is Required to Sense Iron Deficiency
- (2008) X. Du et al. SCIENCE
- Natural History of Recessive Inheritance of DMT1 Mutations
- (2007) A. Iolascon et al. JOURNAL OF PEDIATRICS
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started