Keyphrases
X-linked Hypophosphatemia
72%
Burosumab
56%
Hypophosphatasia
42%
Conventional Therapy
41%
Rickets
37%
Pediatric
35%
Phase II Trial
25%
Type I Collagen
25%
Skeletal Disorders
25%
Spondyloepiphyseal Dysplasia Tarda
24%
Phosphate
20%
Point mutation
18%
Hypophosphatemic Rickets
18%
Heterozygous mutation
18%
Kindred
18%
X-linked Disorder
18%
Tissue-nonspecific Alkaline Phosphatase
17%
Monoclonal Antibody
17%
Fibroblast Growth Factor 23 (FGF23)
16%
Juvenile Paget's Disease
16%
Sedlin
16%
X-linked Hypophosphataemia
16%
Collagen
16%
RNA Hybrid
16%
RNA-RNA
16%
Osteogenesis Imperfecta
14%
Healing
13%
Osteosclerosis
13%
Pyridoxal 5′-phosphate
13%
Osteoblast
13%
Alkaline Phosphatase
12%
Vitamin D Analogs
12%
Exon
12%
Hyperphosphatasemia
11%
Mucopolysaccharidosis IVA
10%
Fibroblasts
10%
Hybrid Analysis
10%
Metabolic Bone Disease
10%
Autosomal Dominant
10%
Osteoprotegerin
10%
Plasma Parameters
9%
COL1A1
9%
Complementary DNA (cDNA)
9%
Musculoskeletal Disorders
9%
Duplication
9%
Clinical Manifestations
9%
Splice Variant
9%
Exome Sequencing
9%
Arkansas
9%
IFITM5
9%
Medicine and Dentistry
X Linked Hypophosphatemic Rickets
100%
Burosumab
56%
Hypophosphatasia
43%
Rickets
42%
Alkaline Phosphatase
38%
Pediatrics
37%
Diseases
34%
Bone Disease
33%
Vitamin D
20%
Fibroblast Growth Factor 23
19%
Dysplasia
16%
Monoclonal Antibody
15%
Exon
13%
Ossification
13%
Pyridoxal 5 Phosphate
13%
Osteosclerosis
11%
Isoenzyme
11%
Osteogenesis Imperfecta
10%
Metabolic Bone Disease
10%
Autosomal Dominant Inheritance
10%
Base
9%
Cross-Link
9%
Bone Turnover
9%
Pyridoxine
9%
Neonatal Infant
9%
Bone Mass
9%
Osteopathic Medicine
9%
Proteinase
8%
Human Tissue
8%
Hyperphosphatasemia
8%
Pyridoxine Deficiency
8%
Ankylosing Spondylitis
8%
Health Care
8%
Werner Syndrome
8%
Patient-Reported Outcome
8%
Vitamin D Deficiency
8%
Subgroup Analysis
8%
Musculoskeletal Health
8%
Pediatrics Patient
8%
Newborn Screening
8%
Hypovitaminosis D
8%
Patient Care
8%
Plasma Cell Granuloma
8%
Coronary Artery Disease
8%
Oligopeptide
8%
Granulomatosis
8%
Artery Calcification
8%
Spondyloepiphyseal Dysplasia
8%
Cell Transplantation
8%
Low Density Lipoprotein Receptor Related Protein 6
8%
Biochemistry, Genetics and Molecular Biology
Dysplasia
35%
Alkaline Phosphatase
30%
X-Linked Hypophosphatemia
28%
Type I Collagen
25%
Exon
23%
Bone Development
21%
Rickets
18%
PHEX
16%
Vitamin B6
16%
Pyridoxine
16%
RNA RNA Hybridization
16%
Point Mutation
16%
Autosomal Dominant Inheritance
15%
Pyridoxal Phosphate
15%
Fibroblast
12%
Exome Sequencing
12%
RANKL
12%
Enzyme
11%
Osteoblast
11%
Blood Level
11%
Messenger RNA
11%
Allele
10%
Isoenzyme
10%
Osteoclastogenesis
10%
Genetics
10%
Metabolic Pathway
9%
Bone Mass
9%
Isoform
8%
Proband
8%
ALPL
8%
Missense
8%
C-Terminus
8%
Chick
8%
Vitamin D
8%
Transcription Factor Osterix
8%
Mucopolysaccharidosis
8%
Genotyping
8%
Hypovitaminosis D
8%
KRAS
8%
Mosaicism
8%
Osteoprotegerin
8%
LDL Receptor
8%
Lipoprotein Receptor-Related Protein
8%
Marfan's Syndrome
8%
Osteolysis
8%
Polyadenylation
8%
Chromosome 8
8%
Fluorescence in Situ Hybridization
8%
Chromosome Arm
8%
Galactose
8%
