Results 41 to 50 of about 6,213,342 (156)

Camurati-Engelmann disease : pictorial essay [PDF]

, 2011
Camurati-Engelmann disease (CED), or progressive diaphyseal dysplasia, is a rare sclerosing dysplasia of which 250 cases have been described in the English literature.
Bellew, Neil, Wagener, Georg
core   +1 more source

Orthopedic Manifestations of Type I Camurati-Engelmann Disease. [PDF]

Clin Orthop Surg, 2017
Background: Camurati-Engelmann disease (CED) is a rare genetic skeletal disorder characterized by limb pain, muscle emaciation and weakness, and cortical thickening of the diaphysis of long bones.
Yuldashev AJ, Shin CH, Kim YS, Jang WY, Park MS, Chae JH, Yoo WJ, Choi IH, Kim OH, Cho TJ.   +9 more
europepmc   +2 more sources

Elimination of Pain and Improvement of Exercise Capacity in Camurati-Engelmann Disease With Losartan [PDF]

, 2020
Background: Camurati-Engelmann disease (CED) is a rare disorder, with approximately 250 described cases in the literature.
José G B Derraik, P L H ), Liggins Institute, A A, W S C, Wayne S Cutfield, J G B D, Paul L Hofman, Ahila Ayyavoo   +8 more
core  

Case Report: Camurati-Engelmann Disease and Osteoporosis

Türk Osteoporoz Dergisi, 2011
Nurettin İrem Örnek, Kerem Gün, Murat Uludağ   +2 more
doaj   +1 more source

Skull Base Manifestations of Camurati-Engelmann Disease [PDF]

Archives of Otolaryngology–Head & Neck Surgery, 2010
To describe presenting symptoms, evaluation findings, and surgical management of cranial base hyperostosis in patients with Camurati-Engelmann disease (CED).Retrospective study and literature review.The Mayo Clinic, Rochester, Minnesota.A total of 306 patients diagnosed as having CED, including 12 primarily evaluated at our institution between 1968 and
Matthew L, Carlson, Charles W, Beatty, Brian A, Neff, Michael J, Link, Colin L W, Driscoll   +4 more
openaire   +2 more sources

Century Sardinia (Italy): A Possible Case of Camurati–Engelmann Disease

, 2016
The skeletal remains of a male aged 45–55 years displaying several bone anomalies were unearthed from the Alghero (Sardinia) plague cemetery ‘lo Quarter’, a burial site dating back to the 1582–1583 AD outbreak.
MONTELLA, Andrea Costantino Mario, R. Bianucci, Gino Fornaciari, Tognotti Eugenia, D. Caramella, P. Bandiera, Bianucci Raffaella, MILANESE, Marco, A. Montella, M. Milanese, E. Tognotti, Caramella Davide, G. Fornaciari, BANDIERA, Pasquale, Giuffra Valentina, V. Giuffra   +15 more
core   +2 more sources

The first Korean case of Camurati-Engelmann disease (progressive diaphyseal dysplasia) confirmed by TGFB1 gene mutation analysis. [PDF]

J Korean Med Sci, 2009
Camurati-Engelmann disease (CED) is an autosomal dominant progressive diaphyseal dysplasia caused by mutations in the transforming growth factor-beta1 (TGFB1) gene. We report the first Korean family with an affected mother and son who were diagnosed with
Park SJ, Yoon CS, Park HW, Choi JR, Chung JS, Lee KA.   +5 more
europepmc   +2 more sources

Observations on the Natural History of Camurati-Engelmann Disease [PDF]

Journal of Bone and Mineral Research, 2019
ABSTRACT   Camurati-Engelmann disease (OMIM 31300) is a rare cranio-tubular bone dysplasia characterized by osteosclerosis of the long bones and skull caused by dominantly-inherited mutations in the transforming growth factor beta 1 (TGFB1) gene. A wide variation in phenotype has been recognized, even
Peter, Hughes, Ibrahim, Hassan, Lorna, Que, Patricia, Mead, Jessica Heejong, Lee, Donald R, Love, Debra O, Prosser, Tim, Cundy   +7 more
openaire   +2 more sources

Camurati-Engelmann disease: case report

, 2009
Objetivos: Fornecer informações sobre a doença de Camurati-Engelmann, também conhecida como Displasia Diafisária Progressiva, possibilitando o seu diagnóstico pelo profissional de saúde. Método: Relato de caso associado a revisão da literatura científica
Yamada, Eliane Sayuri, Fernandes, Gisele Cristine Dyonísio, Toledo, Roberto Acayaba de, Souza, Daniela Lima de, Sunahara, Érika Renata Motinaga, Menin, Rita de Cássia   +5 more
core   +1 more source

Tubal Patency Decoction and Its Ingredient β‐Sitosterol Alleviate Tubal Infertility by Inhibiting Inflammation and Promoting Cilia Formation Through PGR

Mediators of Inflammation, Volume 2026, Issue 1, 2026.
Background Tubal infertility is one of the major causes of female infertility. This study aimed to investigate the mechanism of action of tubal patency decoction (TPD) and its active ingredient β‐sitosterol on tubal infertility. Methods The active ingredients of TPD and their potential targets were obtained from the TCMSP and Batman‐TCM databases.
Liang Shao, Nansu Wang, Yan Yan, Qiongfang Tan, Yuying Huang, Qin Wu, Yali Tan, Yue Zhu, Yaqiong Xia, Ling Liu, Jasbir Arora   +10 more
wiley   +1 more source