Works matching DE "THALASSEMIA in children"
Results: 258
A significant proportion of children of African descent with HbSβ<sup>0</sup> thalassaemia are inaccurately diagnosed based on phenotypic analyses alone.
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- Angewandte Chemie, 2019, v. 131, n. 15, p. 153, doi. 10.1111/bjh.15400
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- Article
Hydrops Fetalis in the Stillborn: A Series from the Central Region of Thailand.
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- Pediatric & Developmental Pathology, 2010, v. 13, n. 5, p. 369, doi. 10.2350/09-12-0771-OA.1
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- Article
Immune Response against Hepatitis B Vaccine in Transfusion-dependent Thalassemic Children Vaccinated in Early Infancy.
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- Global Journal of Transfusion Medicine, 2022, v. 7, n. 2, p. 134, doi. 10.4103/gjtm.gjtm_59_22
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- Article
AWARENESS OF PARENTS REGARDING THE BETA THALASSEMIA MAJOR DISEASE.
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- Khyber Medical University Journal, 2015, v. 7, n. 2, p. 72
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- Article
Family care-giving and chronic illness: how parents cope with a child with a sickle cell disorder or thalassaemia.
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- Health & Social Care in the Community, 2000, v. 8, n. 1, p. 57, doi. 10.1046/j.1365-2524.2000.00211.x
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- Article
Renal tubular function in children with β-thalassemia minor.
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- Nephrology, 2005, v. 10, n. 5, p. 427, doi. 10.1111/j.1440-1797.2005.00484.x
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- Article
Influencing of Family Management in Families with Thalassemic Children on Health Related Quality of Life and Family Functioning: SEM approach.
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- Walailak Journal of Science & Technology, 2019, v. 16, n. 1, p. 27
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- Article
HLA-matched sibling stem cell transplantation in children with β-thalassemia with anti-thymocyte globulin as part of the preparative regimen: the Greek experience.
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- Bone Marrow Transplantation, 2012, v. 47, n. 8, p. 1061, doi. 10.1038/bmt.2011.219
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- Article
Recurrence of β-thalassemia major more than 20 years after HLA-identical sibling BMT treated successfully with donor lymphocyte infusion.
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- 2011
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- Letter
Multiple BM harvests in pediatric donors for thalassemic siblings: safety, efficacy and ethical issues.
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- Bone Marrow Transplantation, 2008, v. 42, n. 6, p. 379, doi. 10.1038/bmt.2008.177
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- Article
Quality of life in patients with transfusion-dependent thalassemia after hematopoietic SCT.
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- Bone Marrow Transplantation, 2008, v. 42, n. 5, p. 319, doi. 10.1038/bmt.2008.165
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- Article
Current status of hematopoietic stem cell transplantations in Vietnam.
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- Bone Marrow Transplantation, 2008, v. 42, p. S146, doi. 10.1038/bmt.2008.145
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- Article
PSYCHOSOCIAL PROBLEMS ASSOCIATED WITH TRANSFUSION DEPENDENT THALASSEMIA IN A TRIBAL POPULATION.
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- Pediatric Oncall Journal, 2016, v. 13, n. 4, p. 99, doi. 10.7199/ped.oncall.2016.45
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- Article
SOCIO-DEMOGRAPHIC DETERMINANTS; THALASSIMIC CHILDREN.
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- Professional Medical Journal, 2017, v. 24, n. 8, p. 1170, doi. 10.17957/TPMJ/17.4043
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- Article
Clinical and molecular genetic features of Hb H and AE Bart's diseases in central Thai children.
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- Application of Clinical Genetics, 2018, v. 11, p. 23, doi. 10.2147/TACG.S161152
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- Article
A Severe Case of Hemoglobin H Disease due to Compound Heterozygosity for Deletion of the Major α-Globin Regulatory Element (MCS-R2) and α<sup>0</sup>-Thalassemia.
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- 2017
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- Case Study
Combined Chelation Therapy with Daily Oral Deferiprone and Twice-Weekly Subcutaneous Infusion of Desferrioxamine in Children with β-Thalassemia: 3-Year Experience.
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- Acta Haematologica, 2015, v. 133, n. 2, p. 226, doi. 10.1159/000363210
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- Article
Sequential Use of Deferiprone and Desferrioxamine in Primary School Children with Thalassaemia major in Turkey.
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- Acta Haematologica, 1999, v. 102, n. 1, p. 17, doi. 10.1159/000040962
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- Article
Economic burden of beta-thalassemia/Hb E andbeta-thalassemia major in Thai children.
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- BMC Research Notes, 2010, v. 3, p. 29, doi. 10.1186/1756-0500-3-29
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- Article
Application of an expanded multiplex genotyping assay for the simultaneous detection of Hemoglobin Constant Spring and common deletional α-thalassemia mutations.
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- International Journal of Laboratory Hematology, 2010, v. 32, n. 4, p. 373, doi. 10.1111/j.1751-553X.2009.01197.x
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- Article
Clinical and haematological features in a compound heterozygote (HBB:c.92 + 5G > C/HBB:c.93-2A > C) case of thalassaemia major.
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- International Journal of Laboratory Hematology, 2010, v. 32, n. 3, p. 369, doi. 10.1111/j.1751-553X.2009.01157.x
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- Article
Clinicovirologic analysis of hepatitis C infection in transfusion-dependent β-thalassemia major children.
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- International Journal of Laboratory Hematology, 2010, v. 32, n. 2, p. 184, doi. 10.1111/j.1751-553X.2009.01155.x
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- Article
Hyperhemolysis in a patient with β-thalassemia major.
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- 2009
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- Case Study
Establishment of a thalassaemia screening centre: An initial BMHRC experience.
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- Asian Journal of Transfusion Science, 2008, v. 2, n. 1, p. 26
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- Article
Prevalence of hepatitis C infection among children with β-thalassaemia major in Mid Delta, Egypt: a single centre study.
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- Transactions of the Royal Society of Tropical Medicine & Hygiene, 2013, v. 107, n. 4, p. 224, doi. 10.1093/trstmh/trs024
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- Article
review New insights into haematopoietic stem cell transplantation for patients with haemoglobinopathies.
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- British Journal of Haematology, 2004, v. 125, n. 1, p. 3, doi. 10.1111/j.1365-2141.2004.04842.x
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- Article
Analysis of chimaerism in thalassaemic children undergoing stem cell transplantation.
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- British Journal of Haematology, 2001, v. 114, n. 1, p. 219, doi. 10.1046/j.1365-2141.2001.02931.x
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- Article
Resolution of immune haemolytic anaemia with allogeneic bone marrow transplantation after an unsuccessful autograft.
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- British Journal of Haematology, 1999, v. 106, n. 4, p. 1063, doi. 10.1046/j.1365-2141.1999.01658.x
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- Article
Human neonatal blood: stem cell content, kinetics of CD34[sup +] cell decline andex vivo expansion capacity.
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- British Journal of Haematology, 1999, v. 104, n. 1, p. 178, doi. 10.1046/j.1365-2141.1999.01147.x
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- Article
Response to hydroxycarbamide in pediatric β-thalassemia intermedia: 8 years' follow-up in Egypt.
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- Annals of Hematology, 2014, v. 93, n. 12, p. 2045, doi. 10.1007/s00277-014-2154-5
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- Article
Hemoglobin Lepore EF Bart's disease: a molecular, hematological, and diagnostic aspects.
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- Annals of Hematology, 2011, v. 90, n. 11, p. 1337, doi. 10.1007/s00277-011-1173-8
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- Article
Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis.
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- 2010
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- Letter
Effect of L-carnitine on the physical fitness of thalassemic patients.
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- Annals of Hematology, 2007, v. 86, n. 1, p. 31, doi. 10.1007/s00277-006-0181-6
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- Article
Wrist Deformity in Children and Adolescents with β-thalassemia on Oral Iron Chelation Therapy.
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- Indian Pediatrics, 2019, v. 56, n. 1, p. 41, doi. 10.1007/s13312-019-1465-y
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- Article
Comparative efficacy and safety of oral iron chelators and their novel combination in children with thalassemia.
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- Indian Pediatrics, 2016, v. 53, n. 3, p. 207, doi. 10.1007/s13312-016-0821-4
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- Article
L-carnitine in Beta Thalassemia.
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- Indian Pediatrics, 2010, v. 47, n. 2, p. 165, doi. 10.1007/s13312-010-0025-2
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- Article
Hematopoietic Stem Cell Transplantation in Children with Genetic Defects.
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- Indian Pediatrics, 2009, v. 46, n. 3, p. 241
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- Article
Morphological and dimensional characteristics of dental arch in children with beta thalassemia major.
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- 2018
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- journal article
Relationship between serum ferritin and zinc levels in pediatric thalassemia major patients.
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- Paediatrica Indonesiana, 2019, v. 59, n. 3, p. 144, doi. 10.14238/pi59.3.2019.144-9
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- Article
commentary.
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- Hastings Center Report, 2002, v. 32, n. 3, p. 12
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- Article
'The Child That Might Be Born...'.
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- Hastings Center Report, 2002, v. 32, n. 3, p. 11, doi. 10.2307/3528104
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- Article
Scurvy in a boy with thalassemia major.
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- European Journal of Pediatric Dermatology, 2012, v. 22, n. 2, p. 119
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- Article
Diagnostic performance of hematological discrimination indices to discriminate between βeta thalassemia trait and iron deficiency anemia and using cluster analysis: Introducing two new indices tested in Iranian population.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-54575-3
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- Article
Phylogenetic Analysis of Torque Teno Virus in Thalassemic Children in Egypt.
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- Intervirology, 2017, v. 60, n. 3, p. 102, doi. 10.1159/000480507
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- Article
Impact of splenectomy on quality of life of children with β-thalassemia.
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- International Journal of Medicine & Public Health, 2015, v. 5, n. 4, p. 322, doi. 10.4103/2230-8598.165963
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- Article
Economic Burden of Thalassemia on Parents of Thalassemic Children: A Multi-Centre Study.
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- Pakistan Journal of Medical Research, 2017, v. 56, n. 3, p. 68
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- Article
Prenatal Screening for Rare Co-Inheritance of HbE and β-Thalassaemia Traits in Western India.
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- Journal of Clinical & Diagnostic Research, 2017, v. 11, n. 9, p. 1, doi. 10.7860/JCDR/2017/26068.10674
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- Article
Efficacy of Deferasirox as an Oral Iron Chelator in Paediatric Thalassaemia Patients.
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- Journal of Clinical & Diagnostic Research, 2017, v. 11, n. 2, p. 1, doi. 10.7860/JCDR/2017/22650.9395
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- Article
Compound Heterozygous Sickle and Thalassemia Trait: A Case Report.
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- 2011
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- Case Study
Deferasirox in Indian children with thalassemia major: 3 years experience.
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- Indian Journal of Medical & Paediatric Oncology, 2013, v. 34, n. 1, p. 16, doi. 10.4103/0971-5851.113407
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- Article