Works matching DE "HEREDITARY spherocytosis"
Results: 72
The effect of preanalytical phase on the stability of osmotic fragility and morphological changes in bovine (Bos taurus) erythrocytes in cattle.
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- Animal Science & Genetics, 2024, v. 20, n. 1, p. 43, doi. 10.5604/01.3001.0054.4653
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- Article
Spinal Cord Infarction in a Patient with Hereditary Spherocytosis: A Case Report and Discussion.
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- Case Reports in Neurological Medicine, 2016, p. 1, doi. 10.1155/2016/7024120
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- Article
Management of hereditary angioedema in pregnant women: a review.
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- International Journal of Women's Health, 2014, v. 6, p. 839, doi. 10.2147/IJWH.S46460
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- Article
Human parvovirus B19-induced aplastic crisis in an adult patient with hereditary spherocytosis: a case report and review of the literature.
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- 2014
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- 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.
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- Biomedical Papers of the Medical Faculty of Palacky University in Olomouc, 2014, v. 158, n. 3, p. 479, doi. 10.5507/bp.2013.058
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- Article
Comparison Study of the Eosin-5'-Maleimide Binding Test, Flow Cytometric Osmotic Fragility Test, and Cryohemolysis Test in the Diagnosis of Hereditary Spherocytosis.
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- American Journal of Clinical Pathology, 2014, v. 142, n. 4, p. 474, doi. 10.1309/AJCPO7V4OGXLIIPP
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- Article
Gallbladder Disease in Children: A 20-year Single-center Experience.
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- Indian Pediatrics, 2019, v. 56, n. 5, p. 384, doi. 10.1007/s13312-019-1535-1
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- Article
Growth failure in hereditary spherocytosis and the effect of splenectomy.
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- Indian Pediatrics, 2017, v. 54, n. 7, p. 563, doi. 10.1007/s13312-017-1069-3
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- Article
Membrane Protein Detection and Morphological Analysis of Red Blood Cells in Hereditary Spherocytosis by Confocal Laser Scanning Microscopy.
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- Microscopy & Microanalysis, 2023, v. 29, n. 2, p. 777, doi. 10.1093/micmic/ozac055
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- Article
Pulmonary arterial hypertension associated with hereditary spherocytosis and splenectomy in a patient with a mutation in the BMPR2 gene.
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- Clinical Case Reports, 2016, v. 4, n. 8, p. 752, doi. 10.1002/ccr3.610
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- Article
Subtotal Splenectomy in Hereditary Spherocytosis - Advantages and Disadvantages.
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- Current Health Sciences Journal, 2016, v. 42, n. 4, p. 408, doi. 10.12865/CHSJ.42.04.11
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- Article
Particularităţi de management al unui caz de purpură trombocitopenică imună supraacută în sarcină, finalizat cu splenectomie.
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- Romanian Journal of Medical Practice, 2015, v. 10, n. 1, p. 73, doi. 10.37897/rjmp.2015.1.12
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- Article
Comparison and evaluation of three screening tests of hereditary spherocytosis in Chinese patients.
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- Annals of Hematology, 2015, v. 94, n. 5, p. 747, doi. 10.1007/s00277-014-2270-2
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- Article
Automated reticulocyte parameters for hereditary spherocytosis screening.
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- Annals of Hematology, 2014, v. 93, n. 11, p. 1809, doi. 10.1007/s00277-014-2127-8
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- Publication type:
- Article
Two different pathogenic gene mutations coexisted in the same hereditary spherocytosis family manifested with heterogeneous phenotypes.
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- BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0826-7
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- Article
SPLENECTOMY FOR HAEMATOLOGICAL DISORDERS.
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- Contributions / Prilozi (1857-9345), 2014, v. 35, n. 1, p. 181
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- Article
Open-heart surgery using a centrifugal pump: a case of hereditary spherocytosis.
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- 2016
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- Publication type:
- journal article
Hereditary spherocytosis in a patient undergoing coronary artery bypass grafting with cardiopulmonary bypass – a case report.
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- Perfusion, 2015, v. 30, n. 1, p. 77, doi. 10.1177/0267659114529323
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- Article
Iron oxides in human spleen.
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- BioMetals, 2015, v. 28, n. 5, p. 913, doi. 10.1007/s10534-015-9876-2
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- Article
Tuning of Differential Lipid Order Between Submicrometric Domains and Surrounding Membrane Upon Erythrocyte Reshaping.
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- Cellular Physiology & Biochemistry (Karger AG), 2018, v. 48, n. 6, p. 2563, doi. 10.1159/000492700
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- Article
Clinical and genetic diagnosis of two Turkish patients with hereditary spherocytosis.
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- European Research Journal, 2025, v. 11, n. 1, p. 129, doi. 10.18621/eurj.1512399
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- Article
α-thalassaemia combined with hereditary spherocytosis in the same patient.
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- Experimental & Therapeutic Medicine, 2018, v. 15, n. 2, p. 1298, doi. 10.3892/etm.2017.5579
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- Article
Disorders of the erythrocyte membrane.
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- Italian Journal of Medicine, 2015, v. 9, n. 4, p. 323, doi. 10.4081/itjm.2015.470
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- Article
Previously undiagnosed hereditary spherocytosis in a patient with jaundice and pyelonephritis: a case report.
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- Journal of Medical Case Reports, 2016, v. 10, p. 1, doi. 10.1186/s13256-016-1144-8
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- Publication type:
- Article
Novel α-Spectrin Mutation in Trans with α-Spectrin Causing Severe Neonatal Jaundice from Hereditary Spherocytosis.
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- Neonatology (16617800), 2014, v. 106, n. 4, p. 355, doi. 10.1159/000365586
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- Article
Erythrophagocytosis by T-cell lymphoma cells in a patient with hereditary spherocytosis post-splenectomy.
- Published in:
- 2018
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- Publication type:
- Case Study
Usefulness of the EMA flow cytometric test in the diagnosis of hereditary spherocytosis post-transfusion.
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- British Journal of Haematology, 2017, v. 178, n. 2, p. 180, doi. 10.1111/bjh.14717
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- Publication type:
- Article
A novel L1340P mutation in the ANK1 gene is associated with hereditary spherocytosis?
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- British Journal of Haematology, 2014, v. 167, n. 2, p. 269, doi. 10.1111/bjh.12960
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- Article
Poster Session Red Cell Disorders.
- Published in:
- 2014
- Publication type:
- Abstract
Severe chronic thromboembolic pulmonary hypertension in a patient after splenectomy for hereditary spherocytosis: the need for long-term surveillance and closer cooperation between haematologists and cardiologists.
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- Folia Cardiologica, 2021, v. 16, n. 2, p. 130, doi. 10.5603/FC.2021.0015
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- Publication type:
- Article
Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians.
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- Cellular Physiology & Biochemistry (Cell Physiol Biochem Press GmbH & Co. KG), 2021, v. 55, n. 1, p. 117, doi. 10.33594/000000333
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- Article
Zinc toxicosis in a dog secondary to prolonged zinc oxide ingestion.
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- 2018
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- Publication type:
- Case Study
Correction to: Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis.
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- 2019
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- Publication type:
- Correction Notice
Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis.
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- Clinical Genetics, 2016, v. 90, n. 1, p. 69, doi. 10.1111/cge.12749
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- Publication type:
- Article
Laparoscopic Subtotal Splenectomy in Children and Adolescents With Spherocytosis.
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- Deutsches Ärzteblatt International, 2022, v. 119, n. 49, p. 848, doi. 10.3238/arztebl.m2022.0288
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- Publication type:
- Article
Moyamoya disease associated with hereditary spherocytosis.
- Published in:
- 2018
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- Publication type:
- Case Study
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
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- Publication type:
- Article
Characterization of red blood cell microcirculatory parameters using a bioimpedance microfluidic device.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-66693-4
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- Article
Coexistence of Gilbert Syndrome and Hereditary Spherocytosis in a Child Presenting with Extreme Jaundice.
- Published in:
- 2014
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- Publication type:
- Case Study
Ventricular assist device implantation in a young patient with non-compaction cardiomyopathy and hereditary spherocytosis.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Detection of red blood cell antibodies in mitogen-stimulated cultures from patients with hereditary spherocytosis.
- Published in:
- 2015
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- Publication type:
- journal 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.
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- Molecular Medicine Reports, 2019, v. 19, n. 5, p. 3912
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- Publication type:
- Article
Novel compound heterozygous mutations in the SPTA1 gene, causing hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice.
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- Molecular Medicine Reports, 2019, v. 19, n. 4, p. 2801
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- Publication type:
- Article
Positive predictive value of diagnosis coding for hemolytic anemias in the Danish National Patient Register.
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- Clinical Epidemiology, 2016, v. 8, p. 241, doi. 10.2147/CLEP.S93643
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- 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
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
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- 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
Anaesthetic management of a case of hereditary spherocytosis for splenectomy and cholecystectomy.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
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
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- 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
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- Publication type:
- Article