Results 11 to 20 of about 6,213,342 (156)
Whole‐Body Magnetic Resonance Imaging in Camurati–Engelmann Disease [PDF]
JBMR Plus, 2020 JBMR Plus, Volume 4, Issue 4, April 2020.
Diogo Goulart Corrêa +4 more
doaj +3 more sources
Reply to: Whole‐Body Magnetic Resonance Imaging in Camurati–Engelmann Disease [PDF]
JBMR Plus, 2020 JBMR Plus, Volume 4, Issue 4, April 2020.
Tim Cundy, Peter Hughes
doaj +3 more sources
Camurati–Engelmann Disease [PDF]
Calcified Tissue International, 2019 Camurati-Engelmann disease or progressive diaphyseal dysplasia is a rare autosomal dominant sclerosing bone dysplasia. Mainly the skull and the diaphyses of the long tubular bones are affected. Clinically, the patients suffer from bone pain, easy fatigability, and decreased muscle mass and weakness in the proximal parts of the lower limbs resulting in ...
Wim Van Hul +3 more
openaire +4 more sources
Indian Journal of Radiology and Imaging, 2010 Ribbing disease is a rare sclerosing dysplasia that involves long tubular bones, especially the tibia and femur. It occurs after puberty and is reported to be more common in women.
Mukkada Philson +3 more
doaj +5 more sources
Revista Brasileira de Reumatologia, 2009 A displasia diafisária progressiva ou doença de Camurati-Engelmann é uma doença rara, caracterizada por dor e fraqueza muscular dos membros afetados e espessamento progressivo da cortical diafisária dos ossos longos.
Mónica Bogas +2 more
doaj +2 more sources
Re: Camurati-Engelmann disease
Sri Lanka Journal of Diabetes Endocrinology and Metabolism, 2012 Sri Lanka Journal of Diabetes, Endocrinology and Metabolism 2012; 2: 121 DOI: http://dx.doi.org/10.4038/sjdem.v2i2 ...
HN Rajaratnam
doaj +3 more sources
Bilateral papilloedema in Camurati-Engelmann disease. [PDF]
BMJ Case Rep, 2015 A 23-year-old woman presented with bilateral papilloedema in a setting of Camurati-Engelmann disease (CED). She was investigated with neuroimaging showing no optic nerve canal stenosis or jugular vein canal compromise. Her MRI venogram was normal. Her opening pressure at lumbar puncture and serum alkaline phosphatase were raised.
Popiela M, Austin M.
europepmc +4 more sources
Camurati–Engelmann Disease: A Case-Based Review About an Ultrarare Bone Dysplasia [PDF]
European Journal of Rheumatology, 2023 Philipp Klemm, Iris Aykara, Uwe Lange
doaj +2 more sources
Dual Biologic Therapy in an Adolescent With Camurati-Engelmann Disease and Crohn Disease. [PDF]
JPGN Rep, 2022 Camurati‐Engelmann disease (CED) is a rare disorder caused by activating mutations in the TGF‐β1 gene and characterized by hyperostosis of long bones and bone dysplasia. We describe a case of an adolescent with CED and moderate‐severe Crohn Disease (CD). Infliximab improved gastrointestinal symptoms but was associated with worsening CED‐associated bone
Sami AS, Rosh JR.
europepmc +2 more sources
Hypothalamic Amenorrhea in a Camurati-Engelmann Disease – A Case Report
Gynecological Endocrinology, 2013 A case report of a patient diagnosed with Camurati-Engelmann Disease (CED) in association with the functional hypothalamic amenorrhea disturbances. CED is a very rare genetically determined disorder classified as a type of bone dysplasia.Case report.Department of Gynecological Endocrinology, 3rd grade Medical University Hospital.Twenty-one years old ...
Blazej Meczekalski +2 more
exaly +4 more sources