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2011, ISBN 1405183993, ix, 223
Reproductive hemostasis: A global approach to a global challenge A hemostatic change in women through their reproductive lifetime is emerging as an issue of... 
Medical | Gynecology & Obstetrics | Women | Pregnancy | Hemostasis | Complications | Blood coagulation disorders in pregnancy | Thrombosis | Diseases
Book
Journal of Clinical Pharmacology, ISSN 0091-2700, 07/2016, Volume 56, Issue 7, p. 869
  [beta]-Thalassemia is the most common hereditary disorder characterized by reduced production of [beta]-globin chains of hemoglobin A (HbA). In recent years,... 
Journal Article
Cochrane Database of Systematic Reviews, ISSN 1469-493X, 03/2019, Volume 2019, Issue 3, pp. CD012064 - CD012064
Background Hydroxyurea (hydroxycarbamide) promotes the production of foetal haemoglobin (HbF) by reactivating gamma-genes. Evidence has shown clinical benefits... 
MEDICINE, GENERAL & INTERNAL | EXPERIENCE | THERAPY | EFFICACY | INTERMEDIA | CHILDREN | beta-Thalassemia - drug therapy | Hydroxyurea - adverse effects | Hematinics - therapeutic use | Humans | Hematinics - adverse effects | Hydroxyurea - therapeutic use | Blood Transfusion - statistics & numerical data | Index Medicus
Journal Article
The Journal of Clinical Pharmacology, ISSN 0091-2700, 01/2019, Volume 59, Issue 1, pp. 98 - 106
β‐Thalassemia is a genetic disorder caused by defects in the β‐globin gene resulting in the absence or reduced synthesis of adult hemoglobin (HbA). Hydroxyurea... 
β‐thalassemia | hydroxyurea | transferrin receptor protein | haptoglobin | quantitative proteomics | β-thalassemia | TARGET | PROTEIN | MECHANISMS | IDENTIFICATION | beta-thalassemia | THERAPY | FETAL-HEMOGLOBIN | PHARMACOLOGY & PHARMACY | EXPERIENCE | SICKLE-CELL-DISEASE | PROTEOMICS | Peroxiredoxin | Transferrin | Transfusion | Fetuses | Hemopexin | Thalassemia | Hydroxyurea | Pharmacology | Patients | Proteins | Haptoglobin | Carbonic anhydrase | Proteomics | Hemoglobin | Children
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 378 - 11
Journal Article
Thrombosis journal, ISSN 1477-9560, 2019, Volume 17, Issue 1, pp. 5 - 5
[This corrects the article DOI: 10.1186/s12959-017-0143-3.]. 
Ethnicity | Mutation | Patients | Genes | Deoxyribonucleic acid--DNA | Siblings
Journal Article
Journal Article
Asian Pacific Journal of Cancer Prevention, ISSN 1513-7368, 2016, Volume 17, Issue 4, pp. 2343 - 2344
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 14883 - 10
Acute Leukaemia (AL) is a neoplasm of WBCs (white blood cells). Being an important class of metabolites, alteration in free fatty acids (FFAs) levels play a... 
GC-MS | BIOMARKERS | CELLS | RANDOM FOREST MODELS | METASTASIS | ADIPOCYTES | MULTIDISCIPLINARY SCIENCES | STEARIC-ACID | OLEIC-ACID | IDENTIFICATION | CANCER | Gas chromatography | Acute lymphatic leukemia | Metabolites | Leukemia | Blood cells | Aplastic anemia | Homeostasis | Mass spectroscopy | Leukocytes | Fatty acids | Myelodysplastic syndrome | Cancer
Journal Article
Journal of Clinical Laboratory Analysis, ISSN 0887-8013, 01/2019, Volume 33, Issue 1, pp. e22647 - n/a
Background Differentiation between thalassemia major and thalassemia intermedia at presentation is not uniformly characterized, for which an absolute criteria... 
Xmn1 | genetic mutational combinations | product transfusion | polymorphism | thalassemia | genetic modifiers | Xmn1 polymorphism | MEDICAL LABORATORY TECHNOLOGY | BETA-THALASSEMIA | Thalassemia | Diagnosis | Laboratories | Blood transfusion | Index Medicus
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 16440 - 12
Journal Article
Journal of Oncology, ISSN 1687-8450, 2018, Volume 2018, pp. 2019239 - 5
Background. Most of the hematological disorders are heterogenous with regard to morphology, immunophenotype, and genetic rearrangements. Multiple recurrent... 
EUROPEAN LEUKEMIANET | ONCOLOGY | RECOMMENDATIONS | ACUTE MYELOGENOUS LEUKEMIA | ADULTS | CLASSIFICATION | REFINED CHROMOSOME | ACUTE MYELOID-LEUKEMIA | PROGNOSTIC-SIGNIFICANCE | CYTOGENETICS | MYELODYSPLASTIC SYNDROMES | Medical research | Leukemia | Aplastic anemia | Cytogenetics | Medicine, Experimental | Lymphomas | Diagnosis | Chromosomes
Journal Article
Asian Pacific Journal of Cancer Prevention, ISSN 1513-7368, 2012, Volume 13, Issue 9, pp. 4215 - 4220
AML (Acute myeloid leukemia) is a form of blood cancer where growth of myeloid cells occurs in the bone marrow. The prognosis is poor in general for many... 
AML | ITDs | TKD | FLT3 | Prognostic marker | Leukemia-specific recognition markers | INTERNAL TANDEM DUPLICATION | leukemia-specific recognition markers | ACTIVATION | NORMAL CYTOGENETICS | IDENTIFICATION | MYELODYSPLASTIC SYNDROME | prognostic marker | ONCOLOGY | FLT3 GENE | MYELOGENOUS LEUKEMIA | MUTATIONS | ASSOCIATION | EXPRESSION
Journal Article
Pakistan Journal of Medical Sciences Quarterly, ISSN 1682-024X, 01/2013, Volume 29, Issue 1, p. 10
Journal Article
Cochrane Database of Systematic Reviews, 01/2016, Volume 2016, Issue 1
Journal Article
Asian Pacific Journal of Cancer Prevention, ISSN 1513-7368, 2015, Volume 16, Issue 1, pp. 393 - 393
Journal Article
Pakistan Journal of Medical Sciences, ISSN 1682-024X, 09/2018, Volume 34, Issue 5, pp. 1204 - 1208
Journal Article
Asian Pacific journal of cancer prevention : APJCP, ISSN 1513-7368, 12/2016, Volume 17, Issue 12, pp. 5251 - 5256
Background: Diagnostic karyotyping analysis is routinely used in acute myeloid leukemia (AML) clinics. Categorization of patients into risk stratified groups... 
AML | remission induction chemotherapy | haematological remission | cytogenetics
Journal Article
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