Zobrazeno 1 - 10
of 423
pro vyhledávání: '"Grill Franz"'
Autor:
Hofstaetter Jochen G, Maurer Kathrin, Biedermann Rainer, Scholl-Buergi Sabine, Al Kaissi Ali, Klaushofer Klaus, Grill Franz
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 9, Iss 1, p 31 (2011)
Abstract Idiopathic osteolysis or disappearing bone disease is a condition characterized by the spontaneous onset of rapid destruction and resorption of a single bone or multiple bones. Disappearing bone disorder is a disease of several diagnostic ty
Externí odkaz:
https://doaj.org/article/b2cecc6bc85b47f7b6aa4ee484144ed1
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 7, Iss 1, p 4 (2009)
Abstract Purpose Stickler syndrome is among the most common autosomal dominant connective tissue disorders but is often unrecognised and therefore not diagnosed by clinicians. Despite much speculation, the cause of osteochondrosis in general and oste
Externí odkaz:
https://doaj.org/article/60b290dacbef4ce9b183a558516ddd53
Publikováno v:
Journal of Medical Case Reports, Vol 2, Iss 1, p 263 (2008)
Abstract Introduction A girl presented with achondroplasia manifested as mild knee pain associated with stiffness of her back. A skeletal survey showed enchondroma-like metaphyseal dysplasia and ossification of the spinal ligaments. Magnetic resonanc
Externí odkaz:
https://doaj.org/article/59687c2d32254acd866ba18fe79ac58b
Publikováno v:
Journal of Medical Case Reports, Vol 2, Iss 1, p 51 (2008)
Abstract Introduction A case of melorheostosis in association with tricho-dento-osseous (TDO) syndrome has been encountered. Case presentation The clinical and the radiographic manifestations of melorheostosis have been encountered in a 41-year-old m
Externí odkaz:
https://doaj.org/article/ad9a06cebc9b486785f5118fc8d071f8
Publikováno v:
Journal of Medical Case Reports, Vol 1, Iss 1, p 142 (2007)
Abstract Endosteal hyperostosis was encountered in a 26-year-old-man and his 6-month-old daughter. Both the father and his daughter presented with fractures. Odontoid process hyperplasia, and progressive sclerosis of the posterior spinal elements, wa
Externí odkaz:
https://doaj.org/article/09f70fe2a7794ba2ab3dfc5232ede794
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 5, Iss 1, p 19 (2007)
Abstract Purpose To present the case of a 14-year-old boy with clinical and radiographic features of pseudorheumatoid chondrodyspalsia with additional, potentially serious, cervical malformations. Methods Detailed clinical and radiological examinatio
Externí odkaz:
https://doaj.org/article/ede72c59a3fe4d638e61eea938eecb70
Autor:
Al Kaissi Ali, Zwettler Elisabeth, Roetzer Katharina M, Haller Joerg, Varga Franz, Klaushofer Klaus, Grill Franz
Publikováno v:
Journal of Medical Case Reports, Vol 1, Iss 1, p 25 (2007)
Abstract This is a case report of a 48-year-old-woman with scoliosis since early childhood. Recent radiographic spinal assessment revealed the presence of distinctive spinal abnormalities. To the best of our knowledge this is the first clinical repor
Externí odkaz:
https://doaj.org/article/6e1913296c174f82902e72cb5585ad71
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 2, Iss 1, p 2 (2007)
Abstract We report a male child with Oromandibular-limb hypogenesis (OMLH), the main features being bilateral sixth and seventh nerve palsies, limb anomalies and hypoplasia of the tongue. Additional features were shortness of the neck associated with
Externí odkaz:
https://doaj.org/article/aad684b13eaa46778a53a68dc746b30f
Publikováno v:
BMC Musculoskeletal Disorders, Vol 7, Iss 1, p 94 (2006)
Abstract Background Progressive non-infectious anterior vertebral fusion is a unique spinal disorder with distinctive radiological features. Early radiographic findings consist of narrowing of the anterior aspect of the intervertebral disk with adjac
Externí odkaz:
https://doaj.org/article/aa3cc36468dd4dbda106b8105c57e8c2
Autor:
Al Kaissi, Ali, Ryabykh, Sergey, Ben Chehida, Farid, Al Kaissi, Hamza, Dougales, Vasileios, Kenis, Vladimir M., Grill, Franz
Publikováno v:
Pediatric Reports; Jun2024, Vol. 16 Issue 2, p410-419, 10p