Cargando…

Mean reticolocyte hemoglobin content index plays a key role to identify children who are carriers of β-thalassemia

Mostrar otras versiones (1)

Reticulocyte (r) and red blood cell (RBC) indices provide reliable parameters for screening and monitoring iron deficiency anemia (IDA) patients and β-thalassemia trait (BTT) carriers. The aim of this study is to identify a simple method for use to distinguish β-thalassemia trait carriers from IDA a...

Descripción completa

Detalles Bibliográficos
Autores principales:	Vicinanza, Paolo, Vicinanza, Mariella, Cosimato, Vincenzo, Terracciano, Daniela, Cancellario, Sergio, Massari, Angelo, Danise, Paolo, Selleri, Carmine, Serio, Bianca
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Università di Salerno 2018
Materias:	Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6067071/ https://www.ncbi.nlm.nih.gov/pubmed/30083521

Ejemplares similares

Mean reticolocyte hemoglobin content index plays a key role to identify children who are carriers of β-thalassemia
por: Vicinanza, Paolo, et al.
Publicado: (2018)

Mean corpuscular volume/mean corpuscular hemoglobin values are not reliable predictors of the β-thalassemia carrier status among healthy diverse populations of Himachal Pradesh, India
por: Bharti, Omesh Kumar, et al.
Publicado: (2020)

Mirror image phosphoinositides regulate autophagy
por: Vicinanza, Mariella, et al.
Publicado: (2015)

Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population
por: Noor, Farjana Akther, et al.
Publicado: (2020)

Coincidence detection of RAB11A and PI(3)P by WIPI2 directs autophagosome formation
por: Vicinanza, Mariella, et al.
Publicado: (2019)

Function and dysfunction of the PI system in membrane trafficking
por: Vicinanza, Mariella, et al.
Publicado: (2008)

Reticulocyte hemoglobin equivalent to detect thalassemia and thalassemic hemoglobin variants
por: Sudmann, Å A, et al.
Publicado: (2012)

Macrophages and Urokinase Plasminogen Activator Receptor System in Multiple Myeloma: Case Series and Literature Review
por: Manzo, Paola, et al.
Publicado: (2023)

Molecular Analysis of Non-Transfusion Dependent Thalassemia Associated with Hemoglobin E-β-Thalassemia Disease without α-Thalassemia
por: Phanrahan, Paramee, et al.
Publicado: (2019)

Hematologic Features of Alpha Thalassemia Carriers
por: Akhavan-Niaki, Haleh, et al.
Publicado: (2012)

Thalassemia and Hemoglobin E in Southern Thai Blood Donors
por: Nuinoon, Manit, et al.
Publicado: (2014)

Delta beta thalassemia: a rare hemoglobin variant
por: Mansoori, Huma, et al.
Publicado: (2016)

Double heterozygocity for hemoglobin C and beta thalassemia dominant: A rare case of thalassemia intermedia
por: Agapidou, Alexandra, et al.
Publicado: (2018)

Intercontinental Multi-Domain Monitoring for the LHC Optical Private Network
por: Vicinanza, Domenico
Publicado: (2012)

The sonification with video excerp. Presenting the video “History of a Discovery” by Chiara Mariotti
por: Vicinanza, Domenico
Publicado: (2019)

LHChamber Music, listening to the smallest music of the universe
por: Vicinanza, Domenico
Publicado: (2022)

Knowledge, Attitude and Practice of Carrier Thalassemia Marriage Volunteer in Prevention of Major Thalassemia
por: Karimzaei, Tahmineh, et al.
Publicado: (2015)

Innovative Anti-CD38 and Anti-BCMA Targeted Therapies in Multiple Myeloma: Mechanisms of Action and Resistance
por: De Novellis, Danilo, et al.
Publicado: (2022)

Hemoglobin-based oxygen carriers
por: Greenburg, A Gerson, et al.
Publicado: (2004)

Evaluation of the validity of the pre-marriage mean corpuscular volume value as a predictive test for b-thalassemia carrier status
por: Almomani, Ali A., et al.
Publicado: (2023)

Efficacy and safety of splenectomy in adult autoimmune hemolytic anemia
por: Giudice, Valentina, et al.
Publicado: (2016)

Secretory and Membrane-Associated Biomarkers of Mast Cell Activation and Proliferation
por: Parente, Roberta, et al.
Publicado: (2023)

Hemoglobin A(2) Lowered by Iron Deficiency and α-Thalassemia: Should Screening Recommendation for β-Thalassemia Change?
por: Denic, Srdjan, et al.
Publicado: (2013)

In Patients with Minor Beta-Thalassemia, Cognitive Performance Is Related to Length of Education, But Not to Minor Beta-Thalassemia or Hemoglobin Levels
por: Ahmadpanah, Mohammad, et al.
Publicado: (2019)

Effective screening of hemoglobin Constant Spring and hemoglobin Paksé with several forms of α- and β-thalassemia in an area with a high prevalence and heterogeneity of thalassemia using capillary electrophoresis
por: Panyasai, Sitthichai, et al.
Publicado: (2023)

Structural optimization and prospect of constructing hemoglobin oxygen carriers based on hemoglobin
por: Ma, Yuexiang, et al.
Publicado: (2023)

Correlation of BACH1 and Hemoglobin E/Beta-Thalassemia Globin Expression
por: Lee, Tze Yan, et al.
Publicado: (2016)

Updates of the HbVar database of human hemoglobin variants and thalassemia mutations
por: Giardine, Belinda, et al.
Publicado: (2014)

Spontaneous Acute Mesenteric Thrombosis in a Patient With Hemoglobin E Thalassemia
por: Asemota, Joseph, et al.
Publicado: (2022)

Sound and music for science explorations
por: Williams, Genevieve, et al.
Publicado: (2017)

Exploring science with sound: sonification and the use of sonograms as data analysis tool
por: Vicinanza, Domenico, et al.
Publicado: (2017)

Leucine regulates autophagy via acetylation of the mTORC1 component raptor
por: Son, Sung Min, et al.
Publicado: (2020)

Moyamoya syndrome in hemoglobin E-beta thalassemia: A rare presentation and association
por: Doctor, PN, et al.
Publicado: (2018)

A Rare Case of Hemoglobin E/Beta-Thalassemia and Systemic Lupus Erythematosus
por: Khamees, Ibrahim, et al.
Publicado: (2020)

Kaposi’s sarcoma associated with chronic myeloid leukemia and imatinib mesylate therapy
por: D’Addona, Matteo, et al.
Publicado: (2022)

Giant plasma cells with multiple immature nuclei in a young woman with newly diagnosed multiple myeloma
por: Giudice, Valentina, et al.
Publicado: (2022)

Therapeutic Hemoglobin Levels after Gene Transfer in β-Thalassemia Mice and in Hematopoietic Cells of β-Thalassemia and Sickle Cells Disease Patients
por: Breda, Laura, et al.
Publicado: (2012)

67 kDa laminin receptor (67LR) in normal and neoplastic hematopoietic cells: is its targeting a feasible approach?
por: Montuori, Nunzia, et al.
Publicado: (2016)

Efficacy of Decitabine and Venetoclax as Salvage and Bridge Therapy to Haploidentical Hematopoietic Stem Cell Transplantation in a Multiresistant Acute Myeloid Leukemia Patient
por: Serio, Bianca, et al.
Publicado: (2022)

Iron Chelation Therapy in Thalassemia Syndromes
por: Cianciulli, Paolo
Publicado: (2009)

Cannot write session to /tmp/vufind_sessions/sess_tebeo6dt18jvdbtqkgli4dj930