Results 101 to 110 of about 1,245,546 (143)

Rare diseases: What rheumatologists need to know? [PDF]

Adv Rheumatol
do Nascimento RRNR, Piotto DGP, Freire EAM, de Souza Neves F, Sztajnbok FR, Bica BERG, Pinheiro FAG, Kozu KT, Pereira IA, Azevedo VF, Cordeiro RA, Giardini HAM, Franco MTM, de Fátima Fernandes Carvalho M, Rosa-Neto NS, Perazzio SF.   +15 more
europepmc   +1 more source

TGF-β/BMP signaling in skeletal biology: molecular mechanisms, regulatory networks, and therapeutic implications in development, regeneration, and disease. [PDF]

Bone Res
Liao J, Wu T, Zhang Q, Shen P, Huang Z, Wang J, Zhang P, Lin S, Pi J, Zhang N, Wang H, Chen G.   +11 more
europepmc   +1 more source

The roles and regulatory mechanisms of TGF-β and BMP signaling in bone and cartilage development, homeostasis and disease. [PDF]

Cell Res
Wu M, Wu S, Chen W, Li YP.
europepmc   +1 more source

Zufallsbefund Einer Progressiven Diaphysären Dysplasie (Camurati-Engelmann-Syndrom)

Nuklearmedizin - NuclearMedicine, 1993
ZusammenfassungWir berichten über eine 35jährige Patientin, bei der als Zufallsbefund während einer Phlebographie vor Varizenoperation hyperostotische Veränderungen in Femur- und Tibiadiaphysen im Sinne eines Camurati-Engelmann-Syndroms aufgefallen waren.
U Büll, C Altehoefer, R Bares
exaly   +3 more sources

Positive Effects of an Angiotensin II Type 1 Receptor Antagonist in Camurati–Engelmann Disease: A Single Case Observation

American Journal of Medical Genetics, Part A, 2014
Camurati-Engelmann disease is characterized by hyperostosis of the long bones and the skull, muscle atrophy, severe limb pain, and progressive joint contractures in some patients.
Koray Boduroglu, Eda Utine, Pelin Ö Şimşek-Kiper   +2 more
exaly   +2 more sources

Some of the next articles are maybe not open access.

Related searches:

Camurati Engelmann Syndrome

International Journal of Contemporary Medicine, 2016
Camurati-Engelmann syndrome or progressive diaphyseal dysplasia is a rare autosomal dominant hereditary disorder, characterized by symmetrical progressive sclerosis of long bones cortical diaphysis. Its presentation and progression is extremely variable.
Sheena Gupta, Sanober Wasim, Neerul Pandita, BP Kalra   +3 more
openaire   +1 more source

Muskel-Funktionsanalyse bei Progressiver Diaphysärer Dysplasie (PDD)/Camurati-Engelmann Syndrom (CES) – eine Fallstudie

Osteologie, 2021
Zusammenfassung Hintergrund Das Camurati-Engelmann Syndrom (CES) ist klinisch durch Muskelfunktionsstörungen, Watschelgang und eingeschränkte Mobilität gekennzeichnet, die möglicherweise durch eine diaphysäre Dysplasie getriggert sind.
Christoph Anders, Ben Abendroth, Klaus Abendroth   +2 more
openaire   +1 more source

Das Camurati-Engelmann-Syndrom, eine seltene Knochenstoffwechselstörung

2016
Deutscher Kongress für Orthopädie und Unfallchirurgie (DKOU 2016)
Pfränger, J, Zajonz, D, Panzert, S, Roth, A, Josten, C, Prietzel, T   +5 more
openaire   +2 more sources

Multiple congenital abnormalities with diaphyseal dysplasia (Camurati—Engelmann's syndrome)

Oral Surgery, Oral Medicine, Oral Pathology, 1969
Abstract A report of a 4 1 2 - year-old child with severe congenital abnormalities consistent with a diagnosis of progeria and associated with Camurati—Engelmann's disease has been presented. Interesting features of the case were the marked sclerotic changes in, and increased density of, the ribs and the mandible.
openaire   +1 more source

[The Camurati-Engelmann syndrome (progressive diaphyseal dysplasia)].

Ceskoslovenska pediatrie, 1992
The presented case-history demonstrates an infant with a rare bone disease with a very serious prognosis. Based on X-ray findings on the skeleton (sclerosis of the diaphyses of long bones, ribs, vertebrae and in particular the base and vault of the skull), the diagnosis of morbus Camurati-Engelmann--progressive diaphyseal dysplasia was established ...
K, Bláhová, J, Horák, I, Marík
openaire   +1 more source