Works matching DE "THALASSEMIA in children"
Results: 257
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
ANALYSIS OF DEFERASIROX AND DEFERIPRON USE IN CHILDREN WITH PEDIATRIC β-THALASSEMIA MAJOR.
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- Folia Medica Indonesiana (2355-8393), 2016, v. 52, n. 1, p. 42
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- Article
CYCLIC RED BLOOD CELL DESTRUCTION IN THALASSEMIA.
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- Chronobiology International: The Journal of Biological & Medical Rhythm Research, 2001, v. 18, n. 4, p. 729, doi. 10.1081/CBI-100106084
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- Article
Unrelated and related donor transplantation for beta‐thalassemia major: A single‐center experience from India.
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- Pediatric Transplantation, 2018, v. 22, n. 5, p. 1, doi. 10.1111/petr.13209
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- Article
Assessment of Iron Overload in Homozygous and Heterozygous Beta Thalassemic Children below 5 Years of Age.
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- Journal of Krishna Institute of Medical Sciences (JKIMSU), 2014, v. 3, n. 2, p. 17
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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
Family Functioning in Children with Thalassemia.
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- Clinical Pediatrics, 2003, v. 42, n. 1, p. 79, doi. 10.1177/000992280304200113
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- Article
A fast hemoglobin variant on newborn screening is associated with α-thalassemia trait.
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- Clinical Pediatrics, 1997, v. 36, n. 2, p. 75, doi. 10.1177/000992289703600203
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- Article
Mothers' Awareness and Experiences of Having a Thalassemic Child: A Qualitative Approach.
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- Pakistan Journal of Social Sciences (PJSS), 2015, v. 35, n. 1, p. 109
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- Article
L-Carnitine ameliorates the iron mediated DNA degradation in peripheral leukocytes of β- thalassemic children.
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- Egyptian Journal of Medical Human Genetics, 2010, v. 11, n. 1, p. 17
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- Article
Haemochromatosis gene mutation H63D is a risk factor for iron overload in Egyptian beta- thalassemic children.
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- Egyptian Journal of Medical Human Genetics, 2008, v. 9, n. 2, p. 149
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- Article
Ocular changes in multi-transfused children with β-thalassaemia receiving desferrioxamine: A case-control study.
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- South African Journal of Child Health, 2011, v. 5, n. 1, p. 11
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- Article
Thalassemia: The Facts and the Controversies.
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- Pediatric Nursing, 2003, v. 29, n. 6, p. 447
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- Article
Echocardiographic evaluation of systolic and diastolic heart function in patients suffering from beta-thalassemia major aged 5-10 years at the Zahedan Research Center for Children and Adolescent Health.
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- Anatolian Journal of Cardiology / Anadolu Kardiyoloji Dergisi, 2010, v. 10, n. 2, p. 150, doi. 10.5152/akd.2010.041
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- Article
A 7-Month-Old Infant Girl With Anemia.
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- Archives of Pathology & Laboratory Medicine, 2006, v. 130, n. 6, p. 879, doi. 10.5858/2006-130-879-amigwa
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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
Seroprevalence of hepatitis C virus markers in multi-transfused children with beta-thalassemia.
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- BMC Infectious Diseases, 2012, v. 12, n. Supplment 1, p. 1, doi. 10.1186/1471-2334-12-S1-P42
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- Article
Oral manifestations and dentofacial anomalies in β-thalassemia major children in Dubai (UAE).
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- 2018
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- journal article
The Effect of α+-Thalassaemia on the Incidence of Malaria and Other Diseases in Children Living on the Coast of Kenya.
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- PLoS Medicine, 2006, v. 3, n. 5, p. e158, doi. 10.1371/journal.pmed.0030158
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- Article
α+-Thalassemia and Protection from Malaria.
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- PLoS Medicine, 2006, v. 3, n. 5, p. e221, doi. 10.1371/journal.pmed.0030221
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- 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
P02-266 A case of selective mutism in an eight-year old girl with thalassaemia major after bone marrow transplantation
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- 2009
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- Abstract
Dental arch morphological and dimensional characteristics in Jordanian children and young adults withβ-thalassaemia major.
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- International Journal of Paediatric Dentistry, 2005, v. 15, n. 2, p. 98, doi. 10.1111/j.1365-263X.2005.00585.x
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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
... Anemia and Mental Problems.
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- Brown University Child & Adolescent Behavior Letter, 2000, v. 16, n. 3, p. 3
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- Article
Vascular Endothelial Growth Factor in Children with Thalassemia Major.
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- Mediterranean Journal of Hematology & Infectious Diseases, 2013, v. 5, n. 1, p. 1, doi. 10.4084/MJHID.2013.044
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- Article
Third Party Cord Blood Transplant Boosts Autologous Hematopoiesis in a Case of Persistent Bone Marrow Aplasia after Double Transplant Failure for Β-Thalassemia Major.
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- 2013
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- Case Study
Genetic Heterogeneity of Beta Globin Mutations among Asian-Indians and Importance in Genetic Counselling and Diagnosis.
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- Mediterranean Journal of Hematology & Infectious Diseases, 2013, v. 5, n. 1, p. 1, doi. 10.4084/MJHID.2013.003
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- Article
T cell depleted haploidentical transplantation: positive selection.
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- Pediatric Reports, 2011, v. 3, p. 38, doi. 10.4081/pr.2011.s2.e14
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- Article
T cell-depleted hla-haploidentical stem cell transplantation in thalassemia young patients.
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- Pediatric Reports, 2011, v. 3, p. 34, doi. 10.4081/pr.2011.s2.e13
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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
Parathyroid hormone in pediatric patients with β-thalassemia major and its relation to βone mineral density; a case control study.
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- Egyptian Journal of Medical Human Genetics, 2017, v. 18, n. 1, p. 75, doi. 10.1016/j.ejmhg.2016.03.004
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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
Current approach to iron chelation in children.
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- British Journal of Haematology, 2014, v. 165, n. 6, p. 745, doi. 10.1111/bjh.12825
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- Article
Health-related quality of life in pediatric and adolescent patients with transfusion-dependent ß-thalassemia in upper Egypt (single center study).
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- 2018
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- journal article
Left ventricular non-compaction in identical twins with thalassaemia and cardiac iron overload.
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- European Journal of Echocardiography, 2009, v. 10, n. 4, p. 509, doi. 10.1093/ejechocard/jen319
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- Article
Tissue Doppler echocardiography reliably reflects severity of iron overload in pediatric patients with β thalassemia.
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- European Journal of Echocardiography, 2008, v. 9, n. 3, p. 368, doi. 10.1016/j.euje.2007.06.003
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- Article
A cephalometric study on craniofacial morphology of Iranian children with beta-thalassemia major.
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- Orthodontics & Craniofacial Research, 2007, v. 10, n. 1, p. 36, doi. 10.1111/j.1601-6343.2007.00380.x
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- Article
Operative Splenectomy for Treatment of Homozygous Thalassemia Major in Afghan Children at a US Military Hospital.
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- AANA Journal, 2010, v. 78, n. 2, p. 129
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- Article
Transfusion-Related Immune Hemolytic Anemia in Two Children with ß-Thalassemia.
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- 2014
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- Case Study
THE KNOWLEDGE OF PARENTS HAVING THALASSEMIA CHILD.
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- Isra Medical Journal, 2016, v. 8, n. 2, p. 79
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- Article
Growth hormone secretion in adult patients with thalassaemia.
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- Clinical Endocrinology, 2005, v. 62, n. 6, p. 667, doi. 10.1111/j.1365-2265.2005.02276.x
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- Article
Bone mineral density, biochemical and hormonal profiles in suboptimally treated children and adolescents with β-thalassaemia disease.
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- Clinical Endocrinology, 2003, v. 58, n. 3, p. 273, doi. 10.1046/j.1365-2265.2003.01707.x
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- Publication type:
- Article
Novel application of IGF-I and IGFBP-3 generation tests in the diagnosis of growth hormone axis disturbances in children with β-thalassaemia.
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- Clinical Endocrinology, 2001, v. 54, n. 2, p. 253, doi. 10.1046/j.1365-2265.2001.01198.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
Homozygous α-thalassemia in a growth retarded, non-hydropic premature newborn.
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- Journal of Perinatology, 2008, v. 28, n. 2, p. 158, doi. 10.1038/sj.jp.7211873
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- Article
The effect of family-centered empowerment model on quality of life of school-aged children with thalassemia major.
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- Iranian Journal of Nursing & Midwifery Research, 2011, v. 16, n. 4, p. 292
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- Article
Confirmation of the validity of using birth MCV for the diagnosis of alpha thalassemia trait.
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- Hematology Reviews, 2009, v. 1, n. 2, p. 103, doi. 10.4081/hr.2009.e20
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- Article