Teriparatide Treatment in Patients withWNT1orPLS3Mutation-Related Early-Onset Osteoporosis - A Pilot Study
Author(s) -
VilleValtteri Välimäki,
Outi Mäkitie,
Renata C. Pereira,
Christine Lainé,
Katherine WesselingPerry,
Jorma A. Määttä,
Mikko Kirjavainen,
Heli Viljakainen,
Matti Välimäki
Publication year - 2016
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.2016-2423
Subject(s) - medicine , teriparatide , osteoporosis , bone remodeling , endocrinology , n terminal telopeptide , bone mineral , femoral neck , urology , osteocalcin , chemistry , alkaline phosphatase , biochemistry , enzyme
We previously identified 2 Finnish families with dominantly inherited, low-turnover osteoporosis caused by mutations in WNT1 or PLS3.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom