Works matching DE "HEREDITARY spherocytosis"
Results: 72
Clinical and genetic diagnosis of two Turkish patients with hereditary spherocytosis.
- Published in:
- European Research Journal, 2025, v. 11, n. 1, p. 129, doi. 10.18621/eurj.1512399
- By:
- Publication type:
- Article
Membrane Protein Detection and Morphological Analysis of Red Blood Cells in Hereditary Spherocytosis by Confocal Laser Scanning Microscopy.
- Published in:
- Microscopy & Microanalysis, 2023, v. 29, n. 2, p. 777, doi. 10.1093/micmic/ozac055
- By:
- Publication type:
- Article
Zinc toxicosis in a dog secondary to prolonged zinc oxide ingestion.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Positive predictive value of diagnosis coding for hemolytic anemias in the Danish National Patient Register.
- Published in:
- Clinical Epidemiology, 2016, v. 8, p. 241, doi. 10.2147/CLEP.S93643
- By:
- Publication type:
- Article
Novel α-Spectrin Mutation in Trans with α-Spectrin Causing Severe Neonatal Jaundice from Hereditary Spherocytosis.
- Published in:
- Neonatology (16617800), 2014, v. 106, n. 4, p. 355, doi. 10.1159/000365586
- By:
- Publication type:
- Article
Comparison Study of the Eosin-5'-Maleimide Binding Test, Flow Cytometric Osmotic Fragility Test, and Cryohemolysis Test in the Diagnosis of Hereditary Spherocytosis.
- Published in:
- American Journal of Clinical Pathology, 2014, v. 142, n. 4, p. 474, doi. 10.1309/AJCPO7V4OGXLIIPP
- By:
- Publication type:
- Article
Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians.
- Published in:
- Cellular Physiology & Biochemistry (Cell Physiol Biochem Press GmbH & Co. KG), 2021, v. 55, n. 1, p. 117, doi. 10.33594/000000333
- By:
- Publication type:
- Article
Identification of red blood cell membrane defects in a patient with hereditary spherocytosis using next-generation sequencing technology and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
- Published in:
- Molecular Medicine Reports, 2019, v. 19, n. 5, p. 3912
- By:
- Publication type:
- Article
Novel compound heterozygous mutations in the SPTA1 gene, causing hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice.
- Published in:
- Molecular Medicine Reports, 2019, v. 19, n. 4, p. 2801
- By:
- Publication type:
- Article
Combined Hereditary Spherocytosis and β-thalassemia trait: A Rare Co-existence.
- Published in:
- Journal of Clinical & Diagnostic Research, 2018, v. 12, n. 1, p. 9, doi. 10.7860/JCDR/2018/31302.11072
- By:
- Publication type:
- Article
Human parvovirus B19-induced aplastic crisis in an adult patient with hereditary spherocytosis: a case report and review of the literature.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
First experience with single incision laparoscopic surgery in Slovakia: Concomitant cholecystectomy and splenectomy in an 11-year-old girl with hereditary spherocytosis.
- Published in:
- Biomedical Papers of the Medical Faculty of Palacky University in Olomouc, 2014, v. 158, n. 3, p. 479, doi. 10.5507/bp.2013.058
- By:
- Publication type:
- Article
Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Erythrophagocytosis by T-cell lymphoma cells in a patient with hereditary spherocytosis post-splenectomy.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Usefulness of the EMA flow cytometric test in the diagnosis of hereditary spherocytosis post-transfusion.
- Published in:
- British Journal of Haematology, 2017, v. 178, n. 2, p. 180, doi. 10.1111/bjh.14717
- By:
- Publication type:
- Article
A novel L1340P mutation in the ANK1 gene is associated with hereditary spherocytosis?
- Published in:
- British Journal of Haematology, 2014, v. 167, n. 2, p. 269, doi. 10.1111/bjh.12960
- By:
- Publication type:
- Article
Poster Session Red Cell Disorders.
- Published in:
- 2014
- Publication type:
- Abstract
Two different pathogenic gene mutations coexisted in the same hereditary spherocytosis family manifested with heterogeneous phenotypes.
- Published in:
- BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0826-7
- By:
- Publication type:
- Article
Clinical Characteristics and Treatment Outcome of Hereditary Spherocytosis: A Single Center's Experience.
- Published in:
- Medical Bulletin of Sisli Etfal Hospital, 2023, v. 57, n. 4, p. 531, doi. 10.14744/SEMB.2023.60370
- By:
- Publication type:
- Article
Challenges and Results of Laparoscopic Splenectomy for Hematological Diseases in a Developing Country.
- Published in:
- Minimally Invasive Surgery (20901445), 2018, p. 1, doi. 10.1155/2018/4256570
- By:
- Publication type:
- Article
Disorders of the erythrocyte membrane.
- Published in:
- Italian Journal of Medicine, 2015, v. 9, n. 4, p. 323, doi. 10.4081/itjm.2015.470
- By:
- Publication type:
- Article
Correction to: Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis.
- Published in:
- 2019
- By:
- Publication type:
- Correction Notice
Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis.
- Published in:
- Clinical Genetics, 2016, v. 90, n. 1, p. 69, doi. 10.1111/cge.12749
- By:
- Publication type:
- Article
Hereditary spherocytosis: Retrospective evaluation of 65 children.
- Published in:
- Turkish Journal of Pediatrics, 2018, v. 60, n. 3, p. 264, doi. 10.24953/turkjped.2018.03.005
- By:
- Publication type:
- Article
Occurrence of Wilms' tumor in a child with hereditary spherocytosis.
- Published in:
- Turkish Journal of Pediatrics, 2015, v. 57, n. 2, p. 206
- By:
- Publication type:
- Article
Topological Structures and Membrane Nanostructures of Erythrocytes after Splenectomy in Hereditary Spherocytosis Patients via Atomic Force Microscopy.
- Published in:
- Cell Biochemistry & Biophysics, 2016, v. 74, n. 3, p. 365, doi. 10.1007/s12013-016-0755-4
- By:
- Publication type:
- Article
Tuning of Differential Lipid Order Between Submicrometric Domains and Surrounding Membrane Upon Erythrocyte Reshaping.
- Published in:
- Cellular Physiology & Biochemistry (Karger AG), 2018, v. 48, n. 6, p. 2563, doi. 10.1159/000492700
- By:
- Publication type:
- Article
SPLENECTOMY FOR HAEMATOLOGICAL DISORDERS.
- Published in:
- Contributions / Prilozi (1857-9345), 2014, v. 35, n. 1, p. 181
- By:
- Publication type:
- Article
α-thalassaemia combined with hereditary spherocytosis in the same patient.
- Published in:
- Experimental & Therapeutic Medicine, 2018, v. 15, n. 2, p. 1298, doi. 10.3892/etm.2017.5579
- By:
- Publication type:
- Article
Laparoscopic Subtotal Splenectomy in Children and Adolescents With Spherocytosis.
- Published in:
- Deutsches Ärzteblatt International, 2022, v. 119, n. 49, p. 848, doi. 10.3238/arztebl.m2022.0288
- By:
- Publication type:
- Article
A Coincidental Discovery of a New Stable Variant (Hb Hachioji or <italic>HBB</italic>: c.187C>T) in a Patient with Chronic Hemolytic Anemia of Unexplained Origin.
- Published in:
- Hemoglobin, 2018, v. 42, n. 1, p. 1, doi. 10.1080/03630269.2018.1429279
- By:
- Publication type:
- Article
Single-Incision Laparoscopic Splenectomy Using the Suture Suspension Technique for Splenomegaly in Children with Hereditary Spherocytosis.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Open-heart surgery using a centrifugal pump: a case of hereditary spherocytosis.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Detection of red blood cell antibodies in mitogen-stimulated cultures from patients with hereditary spherocytosis.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
A de novo ankyrin mutation (ANK1 Q109X) causing severe hereditary spherocytosis from preterm neonatal period.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
A new frameshift mutation of the β-spectrin gene associated with hereditary spherocytosis.
- Published in:
- 2017
- By:
- Publication type:
- Letter
Comparison and evaluation of three screening tests of hereditary spherocytosis in Chinese patients.
- Published in:
- Annals of Hematology, 2015, v. 94, n. 5, p. 747, doi. 10.1007/s00277-014-2270-2
- By:
- Publication type:
- Article
Automated reticulocyte parameters for hereditary spherocytosis screening.
- Published in:
- Annals of Hematology, 2014, v. 93, n. 11, p. 1809, doi. 10.1007/s00277-014-2127-8
- By:
- Publication type:
- Article
Subtotal Splenectomy in Hereditary Spherocytosis - Advantages and Disadvantages.
- Published in:
- Current Health Sciences Journal, 2016, v. 42, n. 4, p. 408, doi. 10.12865/CHSJ.42.04.11
- By:
- Publication type:
- Article
Quality of life and behavioral functioning in Dutch pediatric patients with hereditary spherocytosis.
- Published in:
- European Journal of Pediatrics, 2014, v. 173, n. 9, p. 1217, doi. 10.1007/s00431-014-2299-1
- By:
- Publication type:
- Article
Previously undiagnosed hereditary spherocytosis in a patient with jaundice and pyelonephritis: a case report.
- Published in:
- Journal of Medical Case Reports, 2016, v. 10, p. 1, doi. 10.1186/s13256-016-1144-8
- By:
- Publication type:
- Article
Identification of a Novel p.Q1772X ANK1 Mutation in a Korean Family with Hereditary Spherocytosis.
- Published in:
- PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0131251
- By:
- Publication type:
- Article
Are the Reference Ranges and Cutoff Values of Eosin-5'-Maleimide (EMA) Binding Test for Hereditary Spherocytosis Specific for Each Age Group?
- Published in:
- Clinical Laboratory, 2018, v. 64, n. 6, p. 1101, doi. 10.7754/Clin.Lab.2018.180124
- By:
- Publication type:
- Article
Evaluation of eosin-5-maleimide flow cytometry test in the diagnosis of hereditary spherocytosis.
- Published in:
- Journal of Medical Laboratory Science & Technology of South Africa, 2021, v. 3, n. 2, p. 56, doi. 10.36303/JMLSTSA.2021.3.2.75
- By:
- Publication type:
- Article
Advances in laboratory diagnosis of hereditary spherocytosis.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2017, v. 55, n. 7, p. 944, doi. 10.1515/cclm-2016-0738
- By:
- Publication type:
- Article
Next-generation osmotic gradient ektacytometry for the diagnosis of hereditary spherocytosis: interlaboratory method validation and experience.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2017, v. 55, n. 3, p. 394, doi. 10.1515/cclm-2016-0290
- By:
- Publication type:
- Article
Eryptosis is induced by hyperthermia in hereditary spherocytosis red blood cells.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2016, v. 54, n. 5, p. e165, doi. 10.1515/cclm-2015-0618
- By:
- Publication type:
- Article
Primary Bilateral Non-Hodgkin’s Lymphoma of the Adrenal Gland Presenting as Incidental Adrenal Masses.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Paraspinal extramedullary hematopoiesis in hereditary spherocytosis with a concurrent follicular lymphoma: case report and review of the literature.
- Published in:
- 2015
- By:
- Publication type:
- Case Study