Adult hypophosphatasia treated with reduced frequency of teriparatide dosing
To read more please click on the link below.
Read Article
To read more please click on the link below.
Read Article
To read more please click on the link below. Read Article
Hi, we are twin sisters Amy and Suzanne, we have been dealing with symptoms of HPP for a lifetime. Our diagnosis seemed as though it…
Hi! I’m Denise and I was diagnosed with childhood-onset hypophosphatasia (HPP) at age 50. As a child, I remember that all my permanent teeth…
To read more please click on the link below. Read Article
To read more please click on the link below. Read Article
Mail Address (P.O Box)
The US Hypophosphatasia Foundation
141 Hawkins Place, #267
Boonton, NJ 07005, USA.
Organization
Programs
Community
Office Address (Location for meetings and events)
1719 NJ-10, Suite 315
Parsippany, NJ 07054
Disclaimer: This Website is owned by Soft Bones, Inc. All materials contained in this Website (the “Materials”) are either owned by or licensed to us and are protected by intellectual property and other laws. We retain all proprietary rights to the Materials. This Website is copyrighted. All rights are reserved. Except as expressly authorized by us, any use, copy, reproduction, display, performance, modification or retransmission of the Materials is strictly prohibited.
Responses