Cargando…

Congenital Atypical Microcytic Anemia Accompanied by Hyposideremia and Iron Overload

Detalles Bibliográficos
Autores principales:	Özay, Mustafa, Bıçakcı, Zafer
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Università Cattolica del Sacro Cuore 2022
Materias:	Letter to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9448262/ https://www.ncbi.nlm.nih.gov/pubmed/36119452 http://dx.doi.org/10.4084/MJHID.2022.070

Ejemplares similares

THE INVOLVEMENT OF LACTOFERRIN IN THE HYPOSIDEREMIA OF ACUTE INFLAMMATION
por: van Snick, Jacques L., et al.
Publicado: (1974)

Comparing prevalence of Iron Deficiency Anemia and Beta Thalassemia Trait in microcytic and non-microcytic blood donors: suggested algorithm for donor screening
por: Tiwari, Aseem K., et al.
Publicado: (2009)

Microcytic Anemia Hiding Vitamin B12 Deficiency Anemia
por: Busaleh, Fadi, et al.
Publicado: (2021)

Congenital Diaphragmatic Hernia and Iron Deficiency Anemia
por: Özsoylu, Şinasi
Publicado: (2013)

Erythrocyte Catalase Activity in More Frequent Microcytic Hypochromic Anemia: Beta-Thalassemia Trait and Iron Deficiency Anemia
por: Lazarte, Sandra Stella, et al.
Publicado: (2015)

Multivariable Discriminant Analysis for the Differential Diagnosis of Microcytic Anemia
por: Urrechaga, Eloísa, et al.
Publicado: (2013)

Intravenous Iron in the Treatment of Microcytic Hypochromic Anæmia
por: Mathur, K. S.
Publicado: (1951)

Identification of iron status of blood donors by using low hemoglobin density and microcytic anemia factor
por: Singh, Ashutosh, et al.
Publicado: (2018)

Application of Innovative Hemocytometric Parameters and Algorithms for Improvement of Microcytic Anemia Discrimination
por: Schoorl, Margreet, et al.
Publicado: (2015)

Iron Overload in Hematopoietic Stem Cell Transplantation
por: Yasri, Sora, et al.
Publicado: (2017)

Evaluation of Alpha-Thalassemia Mutations in Cases with Hypochromic Microcytic Anemia: The İstanbul Perspective
por: Karakaş, Zeynep, et al.
Publicado: (2015)

Discrimination Index of Microcytic Anemia in Young Soldiers: A Single Institutional Analysis
por: Huang, Tzu-Chuan, et al.
Publicado: (2015)

Hemoglobin Variants in Patients With Microcytic Hypochromic Anemia: A Review of Indian Studies
por: Kharche, Kaustubh, et al.
Publicado: (2023)

Iron Overload and HFE Mutations: Are They Relevant in Cryptogenic Cirrhosis?
por: Castiella, Agustin
Publicado: (2012)

Severe Iron Deficiency Anemia Due to Late Presentation of Congenital Diaphragmatic Hernia in a Toddler
por: Sarper, Nazan, et al.
Publicado: (2012)

A novel ENU-induced Cpox mutation causes microcytic hypochromic anemia in mice
por: Miyasaka, Yuki, et al.
Publicado: (2022)

Prevalence of common α-thalassemia determinants in south Brazil: Importance for the diagnosis of microcytic anemia
por: Wagner, Sandrine C., et al.
Publicado: (2010)

Glycogen storage disease type Ia: Adult presentation with microcytic anemia and liver adenomas
por: Moest, Wouter, et al.
Publicado: (2018)

Microcytic hypochromic Anemia is a risk factor for postoperative HAEC: A retrospective study
por: Huang, Yuanyuan, et al.
Publicado: (2023)

PB2545: HAEMATOLOGICAL INDICES IN DIFFERENTIAL DIAGNOSIS OF MICROCYTIC ANEMIAS, A REGIONAL STUDY
por: Myrtaj, Rialda, et al.
Publicado: (2023)

HFE Gene Mutations, Iron Overload and Cryptogenic Liver Cirrhosis
por: Eisenbach, Christoph
Publicado: (2012)

Prevalence of Alpha Thalassemia in Microcytic Anemia: a Tertiary Care Experience from North India
por: Sharma, Monica, et al.
Publicado: (2015)

Iron deficiency anemia and its treatment
por: de Souza, Ariani Impieri, et al.
Publicado: (2011)

Effectiveness of Iron Supplementation in Reducing Iron Deficiency Anemia in India
por: Gupta, Aakriti, et al.
Publicado: (2017)

Severe Microcytic Anemia Caused by Complex Hereditary Spherocytosis and X-Linked Sideroblastic Anemia with Mutations in SPTB and ALAS2 Genes
por: Zhou, Jianying, et al.
Publicado: (2023)

Iron deficiency anemia and its treatment - reply
por: Cançado, Rodolfo Delfini
Publicado: (2011)

Not all anemia is solely due to iron deficiency
por: Rössler, Julian, et al.
Publicado: (2020)

Microcytic Anemia: An Insidious Presentation of Sickle Cell Beta+ Thalassemia, a Rare Sickle Cell Variant
por: Shankar, Malavika, et al.
Publicado: (2022)

Alpha‐globin gene mutation spectrum in patients with microcytic hypochromic anemia from Mazandaran Province, Iran
por: Hashemi‐Soteh, Seyed Mohammad Bagher, et al.
Publicado: (2019)

Hemoglobin Andrew-Minneapolis: Hemolytic Erythrocytosis and Severe Iron Overload in Toxic Liver Cirrhosis
por: Zur, Berndt, et al.
Publicado: (2012)

Iron overload assessment in β Thalassemia Major – is T2* Magnetic Resonance Imaging the answer?
por: Ali, Natasha
Publicado: (2017)

Iron overload and fragmented QRS in patients with Thalassemia major: Mechanisms, therapies, and new horizons
por: Karakulak, Uğur Nadir, et al.
Publicado: (2015)

Iron Status in Sickle Cell Anemia: Deficiency or Overload?
por: Patel, Varsha P, et al.
Publicado: (2023)

Efficacy and safety of combined oral iron chelation therapy with deferasirox and deferiprone in a patient with beta-thalassemia major and persistent iron overload
por: Alavi, Samin, et al.
Publicado: (2014)

Deferasirox Might Be Effective for Microcytic Anemia and Neurological Symptoms Associated with Aceruloplasminemia: A Case Report and Review of the Literature
por: Miyake, Zenshi, et al.
Publicado: (2020)

Biallelic mutations in the SARS2 gene presenting as congenital sideroblastic anemia
por: Colin, Elia, et al.
Publicado: (2021)

A Novel ALAS2 Mutation Causes Congenital Sideroblastic Anemia
por: Ding, Yuxi, et al.
Publicado: (2023)

Mitapivat, a pyruvate kinase activator, improves transfusion burden and reduces iron overload in β-thalassemic mice
por: Mattè, Alessandro, et al.
Publicado: (2023)

Effectiveness of iron-fortified infant cereals on prevalence of anemia among children
por: Kumar, Jogender
Publicado: (2018)

A baby with hiatal hernia presenting with severe iron-deficiency anemia
por: Özdemir, Özmert, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_5qp9191gvl4j9mfkrlbile6hqt