Keyphrases
Anemia
37%
Anemia Type
83%
Autosomal Recessive
14%
Bedouin
18%
Bleeding Symptoms
11%
Bone Marrow
22%
Bone Marrow Failure
17%
Bone Marrow Transplantation
11%
Causal Factors
11%
Clinical Data
11%
Clinical Features
11%
Clinical picture
14%
Clinical Presentation
11%
Congenital Dyserythropoietic Anemia
100%
Deferoxamine
12%
Diamond-Blackfan Anemia
29%
Erythroblasts
11%
Erythroid
14%
Erythropoiesis
21%
Factor VII Deficiency
11%
Fanconi Anemia
32%
Founder mutation
11%
Globin
17%
Globin Genes
13%
Hematology
13%
Hemoglobin
18%
Hemoglobin Level
12%
Hemophagocytic Lymphohistiocytosis
15%
Immune Thrombocytopenia
29%
Impaired Growth
11%
Ineffective Erythropoiesis
11%
Iron Overload
23%
Israel
33%
Israeli
32%
Jewish Patients
11%
Macrocytic Anemia
17%
Myelodysplastic Syndrome
16%
Neutropenia
18%
Novel mutation
16%
Older Adults
19%
Pediatric Patients
11%
Platelet Count
17%
Serum Ferritin
11%
Severe Congenital Neutropenia
14%
Splenectomy
24%
Thalassemia
45%
Thalassemia Intermedia
14%
Thrombocytopenia
27%
Thrombotic Thrombocytopenic Purpura
16%
β-Thalassemia (β-thal)
24%
Medicine and Dentistry
Adolescent
9%
Anemia
48%
Bleeding
22%
Bleeding Diathesis
7%
Bone Marrow Failure
16%
Bone Marrow Transplantation
11%
Central Venous Catheter
14%
Clinical Feature
8%
Congenital Dyserythropoietic Anemia
28%
Congenital Dyserythropoietic Anemia Type 1
56%
Cytopenia
8%
Deferoxamine
8%
Diagnosis
9%
Diamond-Blackfan Anemia
18%
Disease
70%
Erythropoiesis
15%
Fanconi Anemia
11%
Ferritin
9%
Genetic Disorder
8%
Globin
10%
Granulocyte Colony Stimulating Factor
8%
Hematology
13%
Hemochromatosis
8%
Hemophagocytic Syndrome
11%
Hereditary Elliptocytosis
7%
Hereditary Spherocytosis
8%
Idiopathic Thrombocytopenic Purpura
45%
Ineffective Erythropoiesis
11%
Infection
11%
Interferon
8%
Iron Overload
15%
Leukemia
12%
Macrocytic Anemia
9%
Morphology
8%
Myelodysplastic Syndrome
12%
Neonatal Infant
11%
Neutropenia
20%
Next Generation Sequencing
9%
Pediatrics
29%
Pediatrics Patient
7%
Platelet
19%
Precursor
8%
Sepsis
10%
Splenectomy
24%
Symptom
17%
Thalassemia
33%
Thalassemia Major
13%
Thrombocyte Function
8%
Thrombocytopenia
29%
Thrombocytosis
12%
Biochemistry, Genetics and Molecular Biology
Allele
9%
Autosomal Recessive Disorder
12%
Blood Transfusion
7%
Bone Marrow Failure
12%
Chelation
11%
Chromatin Bridge
7%
Diamond-Blackfan Anemia
22%
DNA Analysis
7%
DNA Sequence
7%
Erythropoiesis
40%
Erythropoietin
7%
Exome Sequencing
7%
Exon
20%
Factor VII
11%
FANCA
7%
Ferritin
10%
Ferritin Blood Level
13%
G6PC3
7%
Genetic Background
8%
Genetic Carrier
16%
Genetic Disorder
7%
Genetics
29%
Globin
19%
Globin Gene
10%
Haplotype
18%
Hemocyte
10%
Hemoglobins
14%
Hepcidin
7%
Heterochromatin
7%
Heterozygote
16%
Homozygosity
7%
Hypocholesterolemia
7%
Idiopathic Thrombocytopenic Purpura
8%
Interferon
10%
interferon
10%
Iron Chelation
10%
Iron Overload
15%
Iron Poisoning
15%
KLF1
7%
Morphology
9%
Mutated Genes
13%
Myeloid
9%
Platelet Count
9%
Point Mutation
7%
Precursor
15%
Prevalence
12%
Protein Sequencing
9%
Splice Site Mutation
7%
Thrombocytopenia
21%
Transcription Factors
11%
