Cristina Tau
Overview
Explore the profile of Cristina Tau including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
9
Citations
80
Followers
0
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Recent Articles
1.
Whyte M, Tau C, McAlister W, Zhang X, Novack D, Preliasco V, et al.
Bone
. 2014 Jul;
68:153-61.
PMID: 25063546
Mendelian disorders of RANKL/OPG/RANK signaling feature the extremes of aberrant osteoclastogenesis and cause either osteopetrosis or rapid turnover skeletal disease. The patients with autosomal dominant accelerated bone remodeling have familial...
2.
Zaidman V, Maceiras M, Lazzati J, Kutasz E, DIsa G, Chilleli C, et al.
Clin Chem Lab Med
. 2014 Jan;
52(6):e119-22.
PMID: 24445239
No abstract available.
3.
Kerr N, Cassinelli H, DiMeglio L, Tau C, Tuysuz B, Cundy T, et al.
Arch Ophthalmol
. 2010 Jun;
128(6):698-703.
PMID: 20547946
Objectives: To determine the prevalence and spectrum of retinal changes in juvenile Paget disease. Methods: Observational case series and literature review with analysis. Patients with clinical and molecular evidence of...
4.
Tau C
Medicina (B Aires)
. 2007 Sep;
67(4):389-95.
PMID: 17891938
Treatment with bisphosphonates (BP) improves the quality of life of patients with osteogenesis imperfecta (OI). Beneficial effects are the relief of bone pain, a reduction of fracture incidence, improvement of...
5.
Tau C, Russo R
Medicina (B Aires)
. 2007 Apr;
67(1):53-6.
PMID: 17408022
Glucocorticoids are used for the treatment of inflammatory and autoimmune diseases, cancer, and in prevention of organ rejects. A frequent secondary effect of longterm treatment with corticoids is the loss...
6.
Tau C, Ciriani V, Scaiola E, Acuna M
J Steroid Biochem Mol Biol
. 2007 Jan;
103(3-5):651-4.
PMID: 17257830
In order to improve vitamin D status of children from Ushuaia (55 degrees S), at the South of Argentina, double supplementation with 100.000 IU of vitamin D was administered at...
7.
Cuarterolo M, Ciocca M, Lopez S, Cervio G, Rojas L, Bianco G, et al.
Medicina (B Aires)
. 2005 Nov;
65(5):402-8.
PMID: 16296635
Orthotopic liver transplantation is the only definitive mode of therapy for children with end-stage liver disease. However, it remains challenging because of the necessity to prevent long-term complications. The aim...
8.
Tau C, Mautalen C, Casco C, Alvarez V, Rubinstein M
Bone
. 2004 Jun;
35(1):210-6.
PMID: 15207759
Chronic idiopathic hyperphosphatasia (CIH), or juvenile Paget disease, is a rare disorder characterized by increased bone turnover and progressive enlargement of bones. We report a girl, 6 1/2 years old,...
9.
Chong B, Hegde M, Fawkner M, Simonet S, Cassinelli H, Coker M, et al.
J Bone Miner Res
. 2003 Dec;
18(12):2095-104.
PMID: 14672344
Unlabelled: Homozygous mutations in TNFRSF11B, the gene encoding osteoprotegerin, were found in affected members from six of nine families with idiopathic hyperphosphatasia. The severity of the phenotype was related to...