Miwa Yamazaki Selected Research

N- (4'- fluorobutyrophenone)- 4- (4- chlorophenyl)pyridinium (HPP(+))

1/2023	A unique case of childhood hypophosphatasia caused by a novel heterozygous 51-bp in-frame deletion in the ALPL gene.
1/2020	Hypophosphatasia in Japan: ALPL Mutation Analysis in 98 Unrelated Patients.

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Miwa Yamazaki Research Topics

Disease

3	Familial Hypophosphatemic Rickets (X-Linked Hypophosphatemia) 02/2024 - 01/2014
2	Hypophosphatemia 02/2024 - 01/2014
2	Hypophosphatasia 01/2023 - 01/2020
1	Metabolic Bone Diseases (Osteopenia) 01/2023
1	Muscle Weakness 01/2023
1	Rickets (Rachitis) 01/2023
1	Craniosynostoses (Craniosynostosis) 01/2023
1	Hypophosphatemic Rickets 01/2022
1	Inflammation (Inflammations) 01/2022
1	Bone Resorption 05/2015
1	metatarsal type Czech dysplasia 10/2009

Drug/Important Bio-Agent (IBA)

2	Vitamin D FDA LinkGeneric 02/2024 - 01/2014
2	Fibroblast Growth Factor-23IBA 02/2024 - 05/2015
2	N- (4'- fluorobutyrophenone)- 4- (4- chlorophenyl)pyridinium (HPP(+))IBA 01/2023 - 01/2020
2	Proteins (Proteins, Gene)FDA Link 01/2022 - 05/2015
2	Phosphates (Orthophosphate)IBA 01/2022 - 01/2022
1	PHEX Phosphate Regulating Neutral EndopeptidaseIBA 02/2024
1	Alkaline PhosphataseIBA 01/2023
1	EndopeptidasesIBA 01/2022
1	Fibroblast Growth Factor Receptors (Fibroblast Growth Factor Receptor)IBA 01/2022
1	InterleukinsIBA 05/2015
1	Pamidronate (Aredia)FDA LinkGeneric 05/2015
1	Collagen Type II (Type II Collagen)IBA 10/2009

Therapy/Procedure

1	Injections 05/2015