Results 111 to 120 of about 1,245,546 (143)

[An incidental finding of a progressive diaphyseal dysplasia (Camurati-Engelmann syndrome)].

Nuklearmedizin. Nuclear medicine, 1994
In a 35 year-old female diaphyseal hyperostosis of femur and tibia indicative of a Camurati-Engelmann syndrome (progressive diaphyseal dysplasia) were discovered during routine phlebography. This rare disorder belongs to the group of osteochondrodysplasias and affects primarily the diaphyses of long bones.
C, Altehoefer, B, Grün, R, Bares, U, Büll   +3 more
openaire   +1 more source

[Observations on the Camurati-Engelmann syndrome. Demonstration of changes of the petrous bone using high-resolution computed tomography].

RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin, 1989
In Camurati-Engelmann disease HR-CT can impressively demonstrate the involvement of the skull base and also correlate well with the clinical symptoms of deafness, vestibular disturbances and facial paralysis. Since conservative treatment with corticosteroids, calcitonin and diphosphonates is hardly successful and compression of the cranial nerves ...
B, Dannenmaier, B, Weber
openaire   +1 more source

[Diaphyseal dysplasia (Camurati-Engelmann syndrome) with progressive loss of vision: 30-year observations and the effect of prednisolone treatment (author's transl)].

Deutsche medizinische Wochenschrift (1946), 1981
Radiological changes in the skeleton had been present for 30 years in a now 42-year-old man with diaphyseal dysplasia (Camurati-Engelmann syndrome). Because of threatened blindness by bony narrowing of the optic canal prednisolone was administered over several years.
F, Kuhlencordt, H P, Kruse, K A, Hellner, R, Montz   +3 more
openaire   +1 more source

Beobachtungen zum Camurati-Engelmann-Syndrom

RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren, 1989
B. Dannenmaier, B. Weber
openaire   +1 more source

Evidence for locus heterogeneity in the Camurati–Engelmann (DPD1) Syndrome

Clinical Genetics, 2001
J T, Hecht, S H, Blanton, S, Broussard, A, Scott, C, Rhoades Hall, J M, Milunsky   +5 more
openaire   +2 more sources

Progrediente diaphysäre Dystrophie/Camurati-Engelmann-Syndrom (CES) – eine osteologische Modellerkrankung?

Osteologie, 2020
K Abendroth, B Abendroth
openaire   +1 more source

Transitorisches Myelofibrose-Syndrom bei diaphysärer Dysplasie (M. Camurati-Engelmann)

RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren, 1978
D. Emons, D. Hussel, G. Bechrakis, H. Födisch   +3 more
openaire   +1 more source

A 17‐year‐old adolescent with anorexia and gait abnormalities Camurati–Engelmann Syndrome

Acta Paediatrica, 2012
Sascha Meyer, Ludwig Gortner, Raymonda Varon, Karin Ziegler, Georg Kutschke, Alexander Larsen   +5 more
openaire   +1 more source

Analyse der myoelektrischen Aktivität der Gangstörungen bei Progredienter diaphysäre Dystrophie/dem Camurati-Engelmann-Syndrom (CES)

Osteologie, 2020
C Anders, K Abendroth
openaire   +1 more source

Aberrant Activation of TGF-β1 Induces High Bone Turnover via Rho GTPases-Mediated Cytoskeletal Remodeling in Camurati-Engelmann Disease

Frontiers in Endocrinology, 2022
Weihong Hu
exaly