These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

352 related articles for article (PubMed ID: 16638728)

  • 1. Camurati-Engelmann disease in conjunction with hypogonadism.
    Gupta S; Cheikh IE
    Endocr Pract; 2005; 11(6):399-407. PubMed ID: 16638728
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hypothalamic amenorrhea in a Camurati-Engelmann disease--a case report.
    Meczekalski B; Czyzyk A; Podfigurna-Stopa A; Rydzewski B; Sroczynski J; Lipinska M; Sokalski J; Krawczynski M; Jamsheer A; Katulski K; Genazzani A
    Gynecol Endocrinol; 2013 May; 29(5):511-4. PubMed ID: 23368730
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment.
    Janssens K; Vanhoenacker F; Bonduelle M; Verbruggen L; Van Maldergem L; Ralston S; Guañabens N; Migone N; Wientroub S; Divizia MT; Bergmann C; Bennett C; Simsek S; Melançon S; Cundy T; Van Hul W
    J Med Genet; 2006 Jan; 43(1):1-11. PubMed ID: 15894597
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Orthopedic Manifestations of Type I Camurati-Engelmann Disease.
    Yuldashev AJ; Shin CH; Kim YS; Jang WY; Park MS; Chae JH; Yoo WJ; Choi IH; Kim OH; Cho TJ
    Clin Orthop Surg; 2017 Mar; 9(1):109-115. PubMed ID: 28261436
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan family.
    Simsek S; Janssens K; Kwee ML; Van Hul W; Veenstra J; Netelenbos JC
    Osteoporos Int; 2005 Sep; 16(9):1167-70. PubMed ID: 15959620
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Camurati-engelmann disease association with hypogonadism and primary hypothyroidism.
    Low SF; Abu Bakar N; Ngiu CS
    Iran Red Crescent Med J; 2014 Aug; 16(8):e9481. PubMed ID: 25389497
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Proband and the Brother.
    B S; Kotha JP
    J Assoc Physicians India; 2023 Jan; 71(1):1. PubMed ID: 37116016
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Rare Sporadic Case of Camurati-Engelmann Disease With Jaw Involvement.
    Fyrgiola M; Lianou V; Katoumas K; Dimopoulos I
    J Oral Maxillofac Surg; 2017 Nov; 75(11):2385-2390. PubMed ID: 28499806
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The first Korean case of Camurati-Engelmann disease (progressive diaphyseal dysplasia) confirmed by TGFB1 gene mutation analysis.
    Park SJ; Yoon CS; Park HW; Choi JR; Chung JS; Lee KA
    J Korean Med Sci; 2009 Aug; 24(4):737-40. PubMed ID: 19654961
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A Case Report of a 44-Year-Old Woman With Camurati-Englemann Disease: A Case Report.
    Owhonda RA; Wells JE; Lloyd EW; Mumm S; Kimonis V
    JBJS Case Connect; 2020; 10(3):e19.00400. PubMed ID: 32668141
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Camurati-Engelmann disease-a rare cause of tetany identified on bone scintigraphy: A case report.
    Xie P; Huang JM; Li HL; Huang XJ; Wei LG
    Medicine (Baltimore); 2017 Jul; 96(27):e7141. PubMed ID: 28682867
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Camurati-Engelmann disease (progressive diaphyseal dysplasia): reports of an Indian kindred.
    Bhadada SK; Sridhar S; Steenackers E; Dhiman V; Mortier G; Bhansali A; Van Hul W
    Calcif Tissue Int; 2014 Feb; 94(2):240-7. PubMed ID: 24154985
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An ENU-induced p.C225S missense mutation in the mouse Tgfb1 gene does not cause Camurati-Engelmann disease-like skeletal phenotypes.
    Ichimura S; Sasaki S; Murata T; Fukumura R; Gondo Y; Ikegawa S; Furuichi T
    Exp Anim; 2017 May; 66(2):137-144. PubMed ID: 27928112
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Camurati-Engelmann Disease.
    Van Hul W; Boudin E; Vanhoenacker FM; Mortier G
    Calcif Tissue Int; 2019 May; 104(5):554-560. PubMed ID: 30721323
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Bone biopsy and densitometry findings in a child with Camurati-Engelmann disease.
    Bondestam J; Mäyränpää MK; Ikegawa S; Marttinen E; Kröger H; Mäkitie O
    Clin Rheumatol; 2007 Oct; 26(10):1773-7. PubMed ID: 17206397
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mild Camurati‑Engelamann disease presenting with exophthalmos as the first and only manifestation: A case report.
    Jiajue R; Wu B; Jiang Y; Wang O; Li M; Xing X; Xia W
    Mol Med Rep; 2016 Sep; 14(3):2710-6. PubMed ID: 27484238
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Camurati-Engelmann Disease Complicated by Hypopituitarism: Management Challenges and Literature Review of Outcomes With Bisphosphonates.
    Das L; Dhiman V; Dutta P; Sood A; Prakash M; Kaur S; Steenackers E; Hendrickx G; Dayal D; Van Hul W; Bhadada SK
    AACE Clin Case Rep; 2022; 8(2):58-64. PubMed ID: 35415221
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenotypic variability at the TGF-beta1 locus in Camurati-Engelmann disease.
    Campos-Xavier B; Saraiva JM; Savarirayan R; Verloes A; Feingold J; Faivre L; Munnich A; Le Merrer M; Cormier-Daire V
    Hum Genet; 2001 Dec; 109(6):653-8. PubMed ID: 11810278
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand.
    Whyte MP; Totty WG; Novack DV; Zhang X; Wenkert D; Mumm S
    J Bone Miner Res; 2011 May; 26(5):920-33. PubMed ID: 21541994
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Camurati-Engelmann disease--a rare cause of bone pain.
    Mundra V; Taxel P
    Conn Med; 2012 Jan; 76(1):33-7. PubMed ID: 22372177
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.