Keyphrases
Congenital Dyserythropoietic Anemia
100%
Anemia Type
83%
Thalassemia
45%
Anemia
36%
Israel
33%
Fanconi Anemia
32%
Israeli
32%
Immune Thrombocytopenia
29%
Diamond-Blackfan Anemia
29%
Thrombocytopenia
27%
Splenectomy
24%
β-Thalassemia (β-thal)
24%
Iron Overload
23%
Bone Marrow
22%
Erythropoiesis
21%
Older Adults
19%
Bedouin
18%
Neutropenia
18%
Platelet Count
17%
Bone Marrow Failure
17%
Macrocytic Anemia
17%
Thrombotic Thrombocytopenic Purpura
16%
Myelodysplastic Syndrome
16%
Novel mutation
16%
Globin
16%
Hemophagocytic Lymphohistiocytosis
15%
Clinical picture
14%
Erythroid
14%
Autosomal Recessive
14%
Hemoglobin
14%
Thalassemia Intermedia
14%
Severe Congenital Neutropenia
14%
Globin Genes
13%
Hematology
13%
Deferoxamine
12%
Hemoglobin Level
12%
Pediatric Patients
11%
Erythroblasts
11%
Clinical Data
11%
Factor VII Deficiency
11%
Causal Factors
11%
Impaired Growth
11%
Bone Marrow Transplantation
11%
Clinical Features
11%
Bleeding Symptoms
11%
Serum Ferritin
11%
Jewish Patients
11%
Founder mutation
11%
Ineffective Erythropoiesis
11%
Pediatric
11%
Medicine and Dentistry
Disease
70%
Congenital Dyserythropoietic Anemia Type 1
56%
Anemia
48%
Idiopathic Thrombocytopenic Purpura
45%
Thalassemia
33%
Pediatrics
29%
Thrombocytopenia
29%
Congenital Dyserythropoietic Anemia
28%
Splenectomy
24%
Bleeding
22%
Neutropenia
20%
Platelet
19%
Diamond-Blackfan Anemia
18%
Symptom
17%
Bone Marrow Failure
16%
Iron Overload
15%
Erythropoiesis
15%
Central Venous Catheter
14%
Thalassemia Major
13%
Hematology
13%
Thrombocytosis
12%
Myelodysplastic Syndrome
12%
Leukemia
12%
Neonatal Infant
11%
Fanconi Anemia
11%
Hemophagocytic Syndrome
11%
Bone Marrow Transplantation
11%
Infection
11%
Ineffective Erythropoiesis
11%
Globin
10%
Sepsis
10%
Macrocytic Anemia
9%
Diagnosis
9%
Next Generation Sequencing
9%
Ferritin
9%
Adolescent
9%
Precursor
8%
Hereditary Spherocytosis
8%
Clinical Feature
8%
Hemochromatosis
8%
Interferon
8%
Cytopenia
8%
Thrombocyte Function
8%
Deferoxamine
8%
Morphology
8%
Genetic Disorder
8%
Granulocyte Colony Stimulating Factor
8%
Bleeding Diathesis
7%
Pediatrics Patient
7%
Hereditary Elliptocytosis
7%
Biochemistry, Genetics and Molecular Biology
Erythropoiesis
40%
Genetics
29%
Diamond-Blackfan Anemia
22%
Thrombocytopenia
21%
Exon
20%
Globin
19%
Haplotype
18%
Heterozygote
16%
Genetic Carrier
16%
Iron Overload
15%
Iron Poisoning
15%
Precursor
15%
Hemoglobins
14%
Mutated Genes
13%
Ferritin Blood Level
13%
Prevalence
12%
Autosomal Recessive Disorder
12%
Bone Marrow Failure
12%
Factor VII
11%
Transcription Factors
11%
Chelation
11%
Hemocyte
10%
Interferon
10%
interferon
10%
Ferritin
10%
Iron Chelation
10%
Globin Gene
10%
Morphology
9%
Myeloid
9%
Allele
9%
Protein Sequencing
9%
Platelet Count
9%
Idiopathic Thrombocytopenic Purpura
8%
Genetic Background
8%
Exome Sequencing
7%
Hypocholesterolemia
7%
DNA Analysis
7%
Hepcidin
7%
Point Mutation
7%
FANCA
7%
KLF1
7%
Chromatin Bridge
7%
G6PC3
7%
Blood Transfusion
7%
Erythropoietin
7%
Homozygosity
7%
Genetic Disorder
7%
Splice Site Mutation
7%
Heterochromatin
7%
DNA Sequence
7%
