Keyphrases
Barth Syndrome
100%
Associated Syndromes
100%
Clinical Presentation
100%
Bone Marrow Failure
100%
Natural History
100%
Phenotypic Abnormalities
100%
MECOM
100%
Hematological Abnormalities
100%
Bleeding Assessment Tool
33%
Cardiomyopathy
20%
X-linked Disorder
20%
Emerging Therapies
20%
Tafazzin
20%
Skeletal Myopathy
20%
Clinical Association
20%
Skeletal Growth
20%
Patient Management
20%
Inner Mitochondrial Membrane
20%
Cardiolipin
20%
Pathogenic Variants
20%
Growth Abnormality
20%
Phospholipids
20%
New Therapies
20%
Neutropenia
20%
Early Identification
12%
Life-threatening Complications
12%
Germ Cells
12%
Radioulnar Synostosis
12%
Stem Cell Self-renewal
12%
Gestational Thrombocytopenia
12%
Self-maintenance
12%
Rapid Molecular Diagnosis
12%
Novel Pathogenic Variant
12%
Genotype-phenotype
12%
Genotype-phenotype Correlation
12%
Clinical Interpretation
12%
Phenotypic Spectrum
12%
Clinical Features
12%
Protein Isoforms
12%
Genetic Counseling
12%
Nonhematologic
12%
Genetic Defects
12%
Hematologic
12%
Hematopoietic Stem Cells
12%
Gene Expression
12%
Multiple Proteins
12%
Improved Genetic
12%
Hospital-acquired VTE
5%
Medicine and Dentistry
Bleeding
100%
Von Willebrand Factor
100%
Barth Syndrome
100%
Diagnosis
100%
Von Willebrand Disease
100%
MDS1 and EVI1 Complex Locus Protein
100%
Disease
86%
Symptom
66%
Laboratory Test
33%
Screening Test
33%
Thrombocyte Function
33%
Thrombocyte Antigen
33%
Blood Clotting Factor 8
33%
Bleeding Disorder
33%
Genetic Screening
33%
Inner Mitochondrial Membrane
20%
Phospholipid
20%
Myopathy
20%
Cardiolipin
20%
Neutropenia
20%
Patient Care
20%
Cardiomyopathy
20%
X Chromosome Linked Disorder
20%
Biochemistry, Genetics and Molecular Biology
MDS1 and EVI1 Complex Locus Protein
100%
Bone Marrow Failure
100%
Enzyme
100%
Phospholipid
100%
Cardiolipin
100%
Inner Mitochondrial Membrane
100%
Thrombocytopenia
12%
Genetics
12%
Genotyping
12%
Protein Isoform
12%
Hematopoietic Stem Cell
12%
Germ Cell
12%
Germline
12%
Stem Cell Self-Renewal
12%
Gene Expression
12%
Genetic Counseling
12%