نتایج جستجو برای: spondyloepiphyseal dysplasia

تعداد نتایج: 28617  

Journal: :Histology and histopathology 2010
Guo-Wei Zuo Christopher D Kohls Bai-Cheng He Liang Chen Wenli Zhang Qiong Shi Bing-Qiang Zhang Quan Kang Jinyong Luo Xiaoji Luo Eric R Wagner Stephanie H Kim Farbod Restegar Rex C Haydon Zhong-Liang Deng Hue H Luu Tong-Chuan He Qing Luo

The CCN proteins contain six members, namely CCN1 to CCN6, which are small secreted cysteine-rich proteins. The CCN proteins are modular proteins, containing up to four functional domains. Many of the CCN members are induced by growth factors, cytokines, or cellular stress. The CCNs show a wide and highly variable expression pattern in adult and in embryonic tissues. The CCN proteins can integr...

2017
Geetha Wickrematilake

Progressive pseudorheumatoid dysplasia (PPD) or spondyloepiphyseal dysplasia tarda with progressive arthropathy (SEDT-PA) is a rare arthropathy of childhood involving the axial skeleton as well as small peripheral joints. A 10-year-old boy was referred by a general practitioner with pain and deformity in the fingers of hands and limping gait. There was no joint synovitis although the finger joi...

2012
Mathilde Nizon Céline Huber Fabio De Leonardis Rodolphe Merrina Antonella Forlino Mélanie Fradin Beyhan Tuysuz Bassam Y Abu-Libdeh Yasemin Alanay Beate Albrecht Lihadh Al-Gazali Sarenur Yilmaz Basaran Jill Clayton-Smith Julie Désir Harinder Gill Marie T Greally Erkan Koparir Merel C van Maarle Sara MacKay Geert Mortier Jenny Morton David Sillence Catheline Vilain Ian Young Klaus Zerres Martine Le Merrer Arnold Munnich Carine Le Goff Antonio Rossi Valérie Cormier-Daire

Desbuquois dysplasia (DD) is characterized by antenatal and postnatal short stature, multiple dislocations, and advanced carpal ossification. Two forms have been distinguished on the basis of the presence (type 1) or the absence (type 2) of characteristic hand anomalies. We have identified mutations in calcium activated nucleotidase 1 gene (CANT1) in DD type 1. Recently, CANT1 mutations have be...

Journal: :Scoliosis 2007
Konstantinos C Soultanis Alexandros H Payatakes Vasilios T Chouliaras Georgios C Mandellos Nikolaos E Pyrovolou Fani M Pliarchopoulou Panayotis N Soucacos

BACKGROUND Spine deformity can be idiopathic (more than 80% of cases), neuromuscular, congenital or neurofibromatosis-related. However, there are many disorders that may also be involved. We present our experience treating patients with scoliosis or other spine deformities related to rare clinical entities. METHODS A retrospective study of the records of a school-screening study in North-West...

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