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Abbreviation : CED
Long Form : Camurati-Engelmann disease
No. Year Title Co-occurring Abbreviation
2019 Camurati-Engelmann Disease with Good Treatment Response to Losartan. ---
2018 Aberrant activation of latent transforming growth factor-beta initiates the onset of temporomandibular joint osteoarthritis. TGF-beta, TMD, TMJ-OA
2018 Bone-targeted delivery of TGF-beta type 1 receptor inhibitor rescues uncoupled bone remodeling in Camurati-Engelmann disease. TbetaR1I, TGF-beta1
2017 A Rare Sporadic Case of Camurati-Engelmann Disease With Jaw Involvement. ---
2017 An ENU-induced p.C225S missense mutation in the mouse Tgfb1 gene does not cause Camurati-Engelmann disease-like skeletal phenotypes. TGF-beta1
2017 Angioid streaks in a case of Camurati-Engelmann disease. ASs
2017 Clinical diagnosis and mutation analysis of a Chinese family with Camurati-Engelmann disease. TGF-beta1
2017 Orthopedic Manifestations of Type I Camurati-Engelmann Disease. TGFB1
2017 Pain improvement in Camurati-Engelmann disease after anti-TNFalpha therapy. TNF-alpha, UC
10  2017 Repeat Intracranial Expansion After Skull Regrowth in Hyperostotic Disease: Technical Note. ---
11  2017 Significant Improvement of Clinical Symptoms, Bone Lesions, and Bone Turnover after Long-Term Zoledronic Acid Treatment in Patients with a Severe Form of Camurati-Engelmann Disease. ---
12  2016 Mild Camurati‑Engelamann disease presenting with exophthalmos as the first and only manifestation: A case report. TGF-beta1
13  2016 Reduced Dentin Matrix Protein Expression in Camurati-Engelmann Disease Transgenic Mouse Model. TGF-beta1
14  2015 Bilateral papilloedema in Camurati-Engelmann disease. ---
15  2015 Skeletal Dysplasia Presenting as a Neuromuscular Disorder - Report of a Family with Camurati-Engelmann Syndrome. ---
16  2015 Visual and otologic manifestation of Camurati-Engelmann's disease: a case report. ---
17  2014 Camurati-engelmann disease association with hypogonadism and primary hypothyroidism. ---
18  2014 Elimination of pain and improvement of exercise capacity in Camurati-Engelmann disease with losartan. ---
19  2013 A family with Camurati-Engelman disease. The role of the missense p.R218C mutation in TGFB1 in bones and endocrine glands. ---
20  2013 A family with Camurati-Engelman disease: the role of the missense p.R218C mutation in TGFbeta1 in bones and endocrine glands. ---
21  2013 Hypothalamic amenorrhea in a Camurati-Engelmann disease--a case report. ---
22  2013 Transforming growth factor-beta1 gene mutations and phenotypes in pediatric patients with Camurati‑Engelmann disease. TGF-beta1
23  2013 [Camurati-Engelmann disease: a case report]. NSAIDs, PMR, PPIs
24  2011 Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFbeta1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand. IGF, SQSTM1, TNSALP
25  2010 Skull base manifestations of Camurati-Engelmann disease. ---
26  2009 TGF-beta1-induced migration of bone mesenchymal stem cells couples bone resorption with formation. ---
27  2009 The first Korean case of Camurati-Engelmann disease (progressive diaphyseal dysplasia) confirmed by TGFB1 gene mutation analysis. TGFB1
28  2007 A novel mutation of TGF beta1 in a Chinese family with Camurati-Engelmann disease. TGF-beta1
29  2007 Bone biopsy and densitometry findings in a child with Camurati-Engelmann disease. TGF-beta1
30  2006 Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment. TGF
31  2006 The new bone biology: pathologic, molecular, and clinical correlates. CCD
32  2006 Unusual otological manifestations in Camurati-Engelmann's disease. ---
33  2006 [A mutation in TGF beta1 gene encoding the latency-associated peptide in a Chinese patient with Camurati-Engelmann disease]. DHPLC, TGF-beta1
34  2005 Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan family. PDD, TGF, TGFB1
35  2005 Camurati-Engelmann disease in conjunction with hypogonadism. ---
36  2003 A mutation affecting the latency-associated peptide of TGFbeta1 in Camurati-Engelmann disease enhances osteoclast formation in vitro. ---
37  2003 Camurati-Engelmann disease. Review of radioclinical features. ---
38  2001 Domain-specific mutations of a transforming growth factor (TGF)-beta 1 latency-associated peptide cause Camurati-Engelmann disease because of the formation of a constitutively active form of TGF-beta 1. TGF
39  2001 Phenotypic variability at the TGF-beta1 locus in Camurati-Engelmann disease. family 1
40  2000 Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann disease. TGFB1