Results 71 to 80 of about 6,213,342 (156)

Camurati-Engelmann's disease: a case report.

African health sciences, 2002
Camurati-Engelmann's disease is a rare condition worldwide. No cases have been documented in Uganda. A 26 year old female presented with a history of grinding pain in the limbs for over 20 years. Strong painkillers would temporally relieve the pain. She had an asthenic stature with generalised reduction in muscle bulk.
Kusaba Byanyima, Rosemary, Batuuka Nabawesi, Jennifer   +1 more
openaire   +2 more sources

A case of papilledema in Camurati-Engelmann disease treated effectively with prednisolone. [PDF]

Clin Pediatr Endocrinol, 2023
Asai M, Gomi A, Ibaraki N, Watanabe H, Kikkawa I, Nakamata A, Tajima T.   +6 more
europepmc   +1 more source

Abstracts from the Bone and Muscle Interactions: The Mechanical and Beyond Meeting August 2019

, 2019
JBMR Plus, Volume 3, Issue S4, December 2019.
wiley   +1 more source

Camurati-Engelmann disease combined with transethmoidal meningoencephalocele: illustrative case. [PDF]

J Neurosurg Case Lessons, 2022
Yanagihara W, Wada T, Nomura JI, Saura H, Kubo Y, Ogasawara K.   +5 more
europepmc   +1 more source

CAMURATI ENGELMANN DISEASE

Anais do Congresso Brasileiro de Reumatologia 2020, 2021
Luciana Akita, Viviane Queiroz de Oliveira Maia, Danielly Dantas Pimentel, Viviane Alves Costa, Juliana de Jesus Boscolo, Iane Tamara Dondé, Gustavo Roberto Lourenço, Rita de Cassia Menin, Gizelle Gouvea Rezende   +8 more
openaire   +1 more source

Losartan as a Steroid-Sparing Adjunct in a Patient With Features of Refractory Camurati-Engelmann Disease. [PDF]

AACE Clin Case Rep, 2022
Agarwal K, Rajan R, Paul J, Cherian KE, Kapoor N, Paul TV.   +5 more
europepmc   +1 more source

Psychiatric and neuroradiological aspects in Camurati-Engelmann's disease

, 2000
The Camurati-Engelmann's disease is a rare osteosclerotic dysplasia of bones with usually autosomal dominant inheritance. We describe a case of a 49 years old female patient with a major depression (ICD 10: F 33.2).
Riegel, A., Degner, Detlef, Ruther, Eckart, Bleich, Stefan   +3 more
core   +2 more sources

A mutation affecting the latency-associated peptide of TGF 1 in Camurati-Engelmann disease enhances osteoclast formation in vitro

, 2003
Camurati-Engelmann disease (CED) is a rare autosomal dominant disorder characterized by bone pain and osteosclerosis affecting the diaphysis of long bones.
Janssens, Katrien, Ralston, Stuart H., Van Hul, Wim, Frith, Julie C., Fraser, William D., McGowan, Neil W. A., MacPherson, Heather, Helfrich, Miep H., McGowan, Neil W.A.   +8 more
core   +1 more source

Decompression of the internal auditory canal via the retrosigmoid approach in a patient with Camurati-Engelmann disease: illustrative case. [PDF]

J Neurosurg Case Lessons, 2021
Achahbar SE, Somers T, Van Havenbergh T.
europepmc   +1 more source

A case of Camurati-Engelmann disease from 16th century Sardinia (Italy)

, 2015
The skeletal remains of a male aged 45-55 years, displaying several bone anomalies, were uncovered from a cemetery of Alghero, referable to the plague outbreak of 1582-1583 AD. The skeleton has a stature of about 165 cm.
GIUFFRA, VALENTINA, MILANESE M, BANDIERA P., CARAMELLA, DAVIDE, SPIGA C, TOGNOTTI E, MONTELLA A, BIANUCCI R, FORNACIARI, GINO   +8 more
core