Cyclic pamidronate treatment in Bruck syndrome: Proposal of a new modality of treatment
Author:
Publisher
Wiley
Subject
Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.2008.02752.x/fullpdf
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2. Phenotypic and molecular characterization of Bruck syndrome (osteogenesis imperfecta with contractures of the large joints) caused by a recessive mutation in PLOD2;Ha-Vinh;Am. J. Med. Genet. A,2004
3. Bone resorption assessed by immunoassay of urinary cross-linked collagen peptides in patients with osteogenesis imperfecta;Brenner;J. Bone Miner. Res,1994
4. Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: Indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17;Bank;Proc. Natl Acad. Sci. USA,1999
5. Identification of PLOD2 as telopeptide lysyl hydroxylase, an important enzyme in fibrosis;van der Slot;J. Biol. Chem,2003
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